BR102017019397A2 - TUBULAR FORMAT BATTERIES FOR A BIOMEDICAL DEVICE - Google Patents

Abstract

"Tubular-shaped batteries for a biomedical device". The invention relates to designs, strategies and methods for forming tubular batteries. In some instances, airtight seals can be used to seal battery chemistry inside tubular batteries. This can improve the biocompatibility of the energizing elements. In some examples, biocompatible tube-shaped energizing elements may be used in a biomedical device. In still other examples, biocompatible tube-shaped energizing elements may be used in a contact lens.

Description

(54) Title: BATTERIES IN TUBULAR FORMAT FOR A BIOMEDICAL DEVICE (51) Int. Cl .: H01M 2/02; H01M 2/08; G02C 7/04 (30) Unionist Priority: 12/09/2016 US 62 / 393,281 (73) Holder (s): JOHNSON & JOHNSON VISION CARE, INC.

(72) Inventor (s): STUART MICHAEL DAVIS; FREDERICK A. FLITSCH; MILLBURN EBENEZER MUTHU; RANDALL B. PUGH; ADAM TONER (74) Attorney (s): DANNEMANN, SIEMSEN, BIGLER & IPANEMA MOREIRA (57) Summary: Patent for BATTERIES IN TUBULAR FORMAT FOR A BIOMEDICAL DEVICE. The invention relates to designs, strategies and methods for forming batteries in tubular form. In some instances, airtight seals can be used to seal the battery chemistry within tubular batteries. This can improve the biocompatibility of the energizing elements. In some instances, biocompatible tube-shaped energizing elements can be used in a biomedical device. In yet other examples, biocompatible tube-shaped energizing elements can be used on a contact lens.

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Descriptive Report of the Patent of Invention for BATTERIES IN TUBULAR FORMAT FOR A BIOMEDICAL DEVICE. REMISSIVE REFERENCE TO RELATED APPLICATIONS [0001] This patent application claims the benefit of US provisional patent application No. 62 / 393,281, filed on September 12, 2016.

BACKGROUND OF THE INVENTION

1. Field of the invention [0002] Designs and methods for improving the biocompatibility aspects of batteries are described, particularly by the formation of tubular shapes produced from solid structures. In some examples, a field of use for biocompatible batteries may include any biocompatible device or product that requires energy.

2. Description of the related technique [0003] Recently, the number of medical devices and their functionality has started to develop rapidly. Such medical devices may include, for example, implantable pacemakers, electronic pills to monitor and / or test biological function, surgical devices with active components, contact lenses, infusion pumps and neurostimulators. Added functionality and increased performance for many of the aforementioned medical devices have been developed and theorized. However, in order to achieve the theorized added functionality, many of these devices now require their own power means that are compatible with the size and shape requirements of these devices, as well as the requirements for new powered components.

[0004] Some medical devices may include electrical components, such as semiconductor devices that perform a variety of functions, and can be incorporated into many devices

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2/88 biocompatible and / or implantable. However, such semiconductor components need energization and therefore energizing elements should also preferably be included in such biocompatible devices. The topology and relatively small size of biocompatible devices can create innovative and challenging environments for defining various functionalities. In many instances, it is important to provide safe, reliable, compact and low-cost ways to power semiconductor components within biocompatible devices. Therefore, there is a need for biocompatible energizing elements formed for implantation into or under biocompatible devices, where the millimeter structure or smaller energizing elements provide improved function for the energizing element while maintaining biocompatibility.

[0005] Such an energizing element used to energize a device can be a battery. When using a battery for purposes of biomedical applications, it is important that the battery structure and design accommodate aspects of biocompatibility. Therefore, there is a need for innovative examples of forming biocompatible batteries for use in biocompatible energizing elements, which can have significantly improved confinement aspects.

SUMMARY OF THE INVENTION [0006] Consequently, strategies and designs related to improved confinement for use in biocompatible energizing elements are disclosed here.

[0007] A general aspect includes a biomedical device that includes an electroactive component, a biocompatible battery, and a first encapsulation layer. The biocompatible battery in this respect includes a tubular structure, with an internal volume forming a cavity. Petition 870170067406, of 9/11/2017, p. 112/207

3/88 of. The first encapsulation layer encapsulates at least the electroactive component and the biocompatible battery. In some examples, the first encapsulation layer is used to define a contact lens skirt, surrounding internal components of an electroactive lens with a biocompatible hydrogel layer that interacts with the surface of a user's eye. In some instances the nature of the electrolyte solution provides improvements to the biocompatibility of the biomedical device. For example, the composition of the electrolyte solution may have lower electrolyte concentrations than typical battery compositions. In other examples, the composition of electrolytes can mimic the biological environment that the biomedical device occupies, such as the composition of tear fluid in a non-limiting example. In some instances, the biocompatible battery also includes a clad outer metallic coating, the clad outer metallic coating comprising a portion that is clad with autocatalytic cladding, and the thickness of the clad outer metallic cladding is sufficiently thick to act as a barrier against the entry and exit of moisture from the biochemical energizing element. Autocatalytic plating may include a copper-based chemical to deposit a copper layer on the plated outer metallic coating. In some examples, there may be a portion of the biocompatible battery in which a blocking material prevents the outer clad metal coating from forming in the region of one or more between the anode contact and the cathode contact.

[0008] According to one aspect, the present invention is directed to a biomedical device. The biomedical device comprises an electroactive component; a battery comprising an anode current collector, a cathode current collector, an anode, and a cathode; a tube encapsulating the anode and cathode with a priPetition 870170067406, of 9/11/2017, p. 113/207

4/88 first penetration into the anode current collector, a second penetration into the cathode current collector, a first seal between the tube and the anode current collector, and a second seal between the tube and the cathode current collector ; and a first biocompatible encapsulation layer, the first biocompatible encapsulation layer encapsulating at least the electroactive component and the battery.

[0009] According to another aspect, the present invention is directed to a battery. The battery comprises an anode current collector, the anode current collector being a first metal tube closed at a first end; an anode, the anode chemistry being contained within the first metallic tube; a cathode current collector, the cathode current collector being a second metal tube closed at a second end; a cathode, the cathode chemistry being contained within the second metallic tube; a ceramic tube with a first sealing surface that has a sealing interface with the first metal tube, and a second sealing surface that has a sealing interface with the second metal tube; and a sealing material located in the gap between the first sealing surface and the first metal tube.

[0010] In accordance with yet another aspect, the present invention is directed to a battery. The battery comprises an anode current collector, the current collector being a first closed metal tube at a first end; an anode, the anode chemistry being contained within the first metallic tube; a cathode current collector, the cathode current collector being a second metal tube closed at a second end; a cathode, the cathode chemistry being contained within the second metallic tube; a glass tube with a first

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5/88 sealing surface which has a sealing interface with the first metal tube, and a second sealing surface which has a sealing interface with the second metal tube; and a sealing material located in the gap between the first sealing surface and the first metal tube.

[0011] In accordance with yet another aspect, the present invention is directed to a battery. The battery comprises an anode current collector, the anode current collector being a first closed metal tube at a first end; an anode, the anode chemistry being contained within the first metallic tube; a cathode current collector, the cathode current collector being a wire; a ceramic termination with a first sealing surface that has a sealing interface with the first metal tube, and a second sealing surface that has a sealing interface with the cathode current collector; a cathode, the cathode chemistry being deposited on the cathode current collector; and a sealing material located in the gap between the first sealing surface and the first metal tube.

[0013] According to another aspect, the present invention is directed to a method for producing a battery. The method comprises obtaining a cathode collecting tube; fill the cathode collection tube with cathode chemicals; obtain an anode collecting tube; fill the anode collecting tube with anode chemicals; obtain a ceramic insulating piece in tubular shape; forming a first and second sealing surfaces at each end of the tubular ceramic insulating piece; evaporating a metallic film on the first and second sealing surfaces; cover the end of the cathode collection tube with a piece of Nanofoil® material; coating the metallic film on the first and second sealing surfaces with a paste solder; push the pickup tube

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6/88 cathode on the first sealing surface; activate the Nanofoil® material to cause a rapid increase in temperature at the interface between the cathode collecting tube and the first sealing surface, and melt the solder paste.

[0014] The implementations of the batteries described above may include one or more of the features presented below, a sealing material located in a gap between the first sealing surface of a glass or crystal ceramic semiconductor material and a metallic tube or other material semiconductor ceramic or glass.

[0015] Exemplary batteries may also include a battery in which the sealing material located in the gap between the first sealing surface and the first tube includes an epoxy based adhesive. Exemplary batteries can also include a battery in which the sealing material located in the gap between the first sealing surface and the first tube includes an epoxy based adhesive. The battery may also include the battery in which the sealing material located in the gap between the first sealing surface and the first tube includes a first layer that includes particles of molybdenum and manganese, in a mixture with ceramic powders, which is then clad with a metallic film. The battery in which the sealing material located in the gap between the first sealing surface and the first tube includes a first layer that includes particles of molybdenum and manganese, in a mixture with ceramic powders, which is then clad with a metallic film. The battery may also include the battery in which the metallic film includes nickel.

[0016] In some examples, battery examples include the battery in which the sealing material located in the gap between the first sealing surface and the first metal tube includes a first layer of metallic film deposited by POS. The battery may also include a battery in which the metallic film includes titanium. The battery may include

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7/88 also the battery in which a noble metallic film is additionally deposited on the metallic film deposited by PVD.

[0017] Battery examples may also include the battery in which the sealing material located in the gap between the first sealing surface and the first tube includes a plurality of thin layers of metallic films, wherein a first thin layer of metallic film is deposited on a second layer of metallic film, in which the first thin layer of metallic film is chemically reactive with the second layer of metallic film, releasing energy to rapidly heat the layers, and in which the chemical reaction is activated through an energetic pulse power. In some instances, the energy pulse includes photons. In some instances, the energetic pulse includes electrons. In some instances, the energy pulse includes thermal energy.

[0018] In some examples, the battery may also include the battery in which the sealing material located in the gap between the first sealing surface and the first tube includes a conventional solder alloy base with a titanium addition, in which titanium reacts with the surface materials of the first sealing surface upon exposure to ultrasonic energy.

BRIEF DESCRIPTION OF THE DRAWINGS [0019] The above, as well as other features and advantages of the present invention, will be evident from the more specific description, presented below, of the preferred modalities of the invention, as illustrated in the attached drawings.

[0020] Figures 1A to 1B illustrate exemplifying aspects of energizing elements in conjunction with the exemplary application of contact lenses.

[0021] Figures 2A to 2B illustrate an exemplary tubular shape with a metallic confinement and insulating components in a

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8/88 tubular battery design.

[0022] Figure 3 illustrates an exemplary tubular shape with interpenetrating metal confinement and insulating components in a tubular battery design.

[0023] Figure 4 illustrates an exemplary tubular shape with a metallic termination confinement and insulating components in a tubular battery design.

[0024] Figure 5 illustrates an exemplary tubular shape with insulating containment metal contacts in a tubular battery design, with cofacial anode and cathode components.

[0025] Figures 6A to 6F illustrate the formation of a tubular body, according to the present invention.

[0026] Figure 7 illustrates an exemplary sealed metal tube enclosure and insulated wire termination sealed in a tubular battery design.

[0027] Figure 8 illustrates an exemplary sealed tubular metal confinement and insulated wire terminations sealed in a tubular battery design.

[0028] Figure 9 illustrates an exemplary tubular insulator shape with doped semiconductor confinement parts welded together in a tubular battery design.

[0029] Figure 10A illustrates a close view of an exemplary seal.

[0030] Figure 10B illustrates a structure that incorporates welded coated surfaces and a metallic heating sheet.

[0031] Figures 11A to 11E illustrate side cross-sectional views of components in a fully formed exemplary tubular shape.

[0032] Figure 11F illustrates a cross-sectional view of a fully formed example tubular shape.

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9/88 [0033] Figure 11G illustrates a top view of a fully formed exemplary tubular shape in which the tube is formed in a semicircular shape.

[0034] Figure 11H illustrates a cross section of an example of a plated battery in tubular shape completely formed with several clad layers.

[0035] Figure 11J illustrates the blocking of battery portions in an exemplary tubular form with a vinyl tape to inhibit leafing in these regions.

DETAILED DESCRIPTION OF THE INVENTION [0036] Methods of forming batteries in tubular form with improved biocompatibility are disclosed in the present application. In the following sections, detailed descriptions of several examples are described. The descriptions of examples are exemplary modalities only, and various modifications and changes may be evident to those skilled in the art. Therefore, the exemplifying modalities do not limit the scope of the present application. In some instances, these biocompatible batteries can be designed for use in, or close to, the body of a living organism.

Glossary [0037] In the description and claims below, several terms can be used. The following definitions will apply to them:

[0038] Anode, for use in the present invention, refers to an electrode through which electrical current flows into a polarized electrical device. The direction of the electric current is typically opposite to the direction of the electron flow. In other words, electrons flow from the anode to, for example, an electrical circuit.

[0039] Battery, as used here, refers to an electrochemical energy source consisting of a single electrochemical cell or a multiplicity of electrochemical cells, suitably connected to 870170067406, of 9/11/2017, p. 119/207

10/88 connected to each other to provide a desired voltage or current. The cells can be primary (non-rechargeable) or secondary (rechargeable) cells.

[0040] Binder, as used here, refers to a polymer that is capable of exhibiting elastic responses to mechanical deformations and that is chemically compatible with other components of the energizing element. For example, binders can include electroactive materials, electrolytes, polymers, etc. In some examples, the binder may refer to a substance that contains particles and / or particles and liquid together in a cohesive mass.

[0041] Biocompatible, as used here, refers to a material or device that works with an appropriate host response in a specific application. For example, a biocompatible device has no toxic or harmful effects on biological systems. [0042] Cathode, for use in the present invention, refers to an electrode through which electrical current flows out of a polarized electrical device. The direction of the electric current is typically opposite to the direction of the electron flow. Therefore, electrons flow into the cathode of the polarized fixture and out of, for example, the connected electrical circuit.

[0043] Coating, for use in the present invention, refers to a deposit of material in fine forms. In some uses, the term will refer to a thin deposit that substantially covers the surface of a substrate on which it is formed. In other more specialized uses, the term can be used to describe small, thin deposits on smaller regions of the surface.

[0044] Electrode, as used here, can refer to an energy transducer in the energy source. For example, it can include one or both of an anode and a cathode.

[0045] Energized, for use in the present invention, refers to the

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11/88 state of having the capacity to supply electrical current or to have electrical energy stored inside it.

[0046] Energy, for use in the present invention, refers to the ability of a physical system to perform work. Many uses of the energizing elements can refer to the ability to perform electrical actions.

[0047] Power source or energizing element or energizing device, for use in the present invention, refers to any device or layer that has the capacity to supply energy or put a logical or electrical device in an energized state. The energizing elements may include batteries. Batteries may be formed from alkaline cell chemistry, and may be solid state batteries or wet cell batteries, including aqueous alkaline chemistry, aqueous acid, or aqueous saline electrolyte chemistry, or non-aqueous, chemical chemistry. molten salt, or solid-state chemistry. The batteries can be of the dry cell type (immobilized electrolyte) or wet cell (liquid, free electrolyte).

[0048] Charges, as used here, refer to one or more separators of energizing elements that do not react with any one of acid or alkaline electrolytes. Generally, fillers can include substantially water-insoluble materials, such as carbon black; coal powder; graphite; metal oxides and hydroxides such as silicone, aluminum, calcium, magnesium, barium, titanium, iron, zinc and tin; metal carbonates like those of calcium and magnesium; minerals such as mica, montmorolonite, kaolinite, atapulgite and talc; synthetic and natural zeolites like Portland cement; precipitated metal silicates, such as calcium silicate; hollow or solid polymers or glassy microspheres, flakes and fibers; and the like.

[0049] Functionalized, as used here, refers to making a

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12/88 layer or device capable of performing a function that includes, for example, energization, activation and / or control.

[0050] Mold, as used here, refers to a rigid or semi-rigid object that can be used to form three-dimensional objects from uncured formulations. Some exemplifying molds include two mold parts that, when opposed to each other, define the structure of a three-dimensional object.

[0051] Power, as used in this document, refers to the work performed or the energy transferred per unit of time.

[0052] Rechargeable or Reenergizable, as used in the present invention, refers to the ability to restore to a state with greater capacity to perform work. Many uses can relate the ability to restore with the ability of the electric current to flow at a certain rate for certain re-established periods of time.

[0053] Re-energizing or recharging, as used here, refers to restoring to a state with a greater capacity to perform work. Many uses can be related to the restoration of the electrical current flow capacity of a device, at a certain rate during a determined period of time.

[0054] Released, as used here and sometimes called released from a mold, means that a three-dimensional object is either completely separated from the mold or just loosely attached to the mold, so that it can be removed with light agitation.

[0055] Stacked, for use in the present invention, means that at least two layers of component are placed in close proximity to each other so that at least a portion of a surface of one of the layers comes into contact with a first surface of a second layer. In some instances, a coating,

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13/88 which can serve for adhesion or other functions, can reside between the two layers that are in contact with each other through said coating.

[0056] The term trails, as used here, refers to components of energizing elements capable of connecting the components of the circuit. For example, circuit tracks can include copper or gold when the substrate is a printed circuit board and can typically be copper, gold or a film printed on a flexible circuit. A special type of track is the current collector. Current collectors are tracks with electrochemical compatibility that make current collectors suitable for use in conducting electrons to and from a cathode or anode of an electrochemical cell.

[0057] There may be other examples of how to assemble and configure batteries according to the present invention, and some can be described in the following sections. However, for many of these examples, there are parameters and characteristics selected from the batteries that can be described independently. In the following sections, some characteristics and parameters will be analyzed.

Construction of an exemplifying medical device with biocompatible energizing elements [0058] An example of a biomedical device that can incorporate the battery energizing elements of the present invention can be an electroactive focal adjustment contact lens. Referring to Figure 1A, an example of such a contact lens insert can be depicted as a contact lens insert 100. In the contact lens insert 100, there may be an electroactive element 120 that can accommodate changes in focus characteristics in response to control voltages. A circuit 105, to provide these control voltage signals, as well as to provide other functions such as detection of the control environment for external control signals,

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14/88 can be powered by a biocompatible battery element 110. As shown in Figure 1A, battery element 110 can be found as multiple main parts, in this case three parts, and can include the various configurations of battery chemistry elements as was discussed. The battery elements 110 can have several interconnection features to join the parts together, as can be seen underlying the interconnection region 114. The battery elements 110 can be connected to the circuit element 105 which can have its own substrate 115, on the which interconnection characteristics 125 may be located. Circuit 105, which may be in the form of an integrated circuit, may be electrically and physically connected to substrate 115 and its interconnection resources 125. [0059] Referring to Figure 1B, a cross-sectional relief of a contact lens 150 can comprise the contact lens insertion element 100 and its discussed components. The contact lens insert 100 can be encapsulated in a contact lens hydrogel skirt 155 which can encapsulate the contact lens insert 100 and provide a comfortable contact lens interface 150 to a user's eye.

Microbattery electrical requirements [0060] Another area for design considerations may refer to the electrical requirements of the device, which can be supplied by the battery. To function as a power source for a medical device, an appropriate battery may need to meet the total electrical requirements of the system when it is operating in an unconnected or externally powered mode. An emerging field of unconnected or externally powered biomedical devices may include, for example, vision correction contact lenses, health monitoring devices, pill cameras and innovative devices. Recent developments in

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15/88 integrated circuit (Cl) can allow significant electrical operation at very low current levels, for example, current picoamps in standby mode and microamps of the operating current. CIs can also make it possible to create very small devices. [0061] Microbatteries for biomedical applications may be necessary for many simultaneous challenging requirements to be met. For example, the micro-battery may be necessary in order to have the ability to manage an operating voltage suitable for a built-in electrical circuit. This operating voltage can be influenced by several factors, including the Cl process node, the circuit output voltage for another device and a specific current consumption target, which can also refer to the desired life of a device.

[0062] With respect to the Cl process, nodes can typically be differentiated by the minimum size of a transistor, such as the so-called transistor channel. This physical characteristic, together with other parameters of the manufacture of Cl, such as the thickness of the gate oxide, can be associated with a resulting classification standard for connection voltages or limit of the field effect transistors (FET) manufactured in the given node of process. For example, in a node with a minimum dimension of 0.5 microns, it may be common to find FETs with a connection voltage of 5.0 V. However, with a minimum dimension of 90 nm, FETs can connect to 1.2, 1.8 and 2.5 V. The Cl smelter can provide standard digital block cells, for example, inverters and flip-flops that have been characterized and classified for use in certain voltage ranges. Designers chose a Cl process node based on several factors, including the density of digital devices, analog / digital mixed signal devices, leakage current, wiring layers and availability of special devices such as high voltage FETs. Given these aspectsPetition 870170067406, of 9/11/2017, p. 125/207

16/88 parametric components of electrical components, which can consume energy from a micro-battery, it may be important that the micro-battery's power source is compatible with the chosen process node and Cl design requirements, especially in terms of available voltage and current .

[0063] In some examples, an electrical circuit powered by a micro-battery can connect to another device. In non-limiting examples, the micro-battery powered electrical circuit can connect to an actuator or a transducer. Depending on the application, these may include a light-emitting diode (LED), a sensor, a microelectromechanical system pump (MEMS), or various other devices of this type. In some instances, such connected devices may require higher operating voltage conditions than standard Cl process nodes. For example, a variable focus lens may require 35 V to be activated. The operating voltage supplied by the battery can therefore be a critical consideration when designing such a system. In some examples of this type of consideration, the efficiency of a lens driver to produce 35 V from a 1 V battery can be significantly less than it could be when operating from a 2 V battery. Other requirements, such as size of the matrix, can be dramatically different considering also the operating parameters of the micro-battery.

[0064] Individual battery cells can typically be classified with open, load and cut-off voltages. The open circuit voltage is the potential produced by the battery cell with infinite load resistance. The load voltage is the potential produced by the cell with an adequate, and typically specified, load impedance, placed at the cell terminals. The cut-off voltage is typically a voltage at which most of the battery has been discharged. The shear stress can represent a tenPetition 870170067406, from 9/11/2017, p. 126/207

17/88 are, or degree of discharge, below which the battery should not be discharged, in order to avoid harmful effects such as excess gas emission. The cut-off voltage can typically be influenced by the circuit to which the battery is connected, and not just by the battery itself, for example, the minimum operating voltage of the electronic circuit. In one example, an alkaline cell may have an open circuit voltage of 1.6 V, a charge voltage in the range of 1.0 to 1.5 V and a cut-off voltage of 1.0 V. given microbacterial cell design may depend on other factors of the cell chemistry used. Different cell chemistry can therefore have different cell voltages.

[0065] Cells can be connected in series to increase the voltage; however, this combination can come with disadvantages in terms of size, internal resistance, and battery complexity. Cells can also be combined in parallel configurations to decrease resistance and increase capacity; however, such a combination can bring disadvantages to size and life.

[0066] Battery capacity can be the capacity of a battery to supply current or to operate for a period of time. Battery capacity can typically be specified in units such as microampere hours. A battery that can supply 1 microampere of current for 1 hour has 1 microampere-hour of capacity. Capacity can typically be increased by increasing the mass (and thus the volume) of reagents within a battery device; however, it can be considered that biomedical devices can be significantly restricted to the available volume. The capacity of the battery can also be influenced by the electrode and electrolyte material, as well as other factors such as the physical design of the electrodes, the nature and dimensions of any separating material disposed between the electrodes, and the relative anode proportions of the active materials.

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18/88 of cathode, auxiliary conductors and electrolyte.

[0067] Depending on the requirements of the circuit to which the battery is connected, a battery may be required to supply current in a range of values. During storage before active use, a leakage current of the order of picoamps to nanoamps can flow through the circuits, interconnections and insulators. During active operation, the circuit can draw quiescent current for the sample sensors and timers, and perform low-power functions of this type. Quiescent current consumption can range from nanoamps to milliamps. The circuit may also have even higher peak current demands, for example, during flash memory recording or radio frequency (RF) communication. This peak current can extend up to tens of milliamps or more. The resistance and impedance of a micro-battery device can also be important for design considerations.

[0068] Lifetime typically refers to the length of time that a battery can survive in storage while still maintaining useful operating parameters. Service life can be particularly important for biomedical devices for several reasons. Electronic devices can displace unpowered devices, such as the introduction of an electronic contact lens. Products in these existing market spaces may have set life requirements, for example, three years, due to customer, supply chain and other requirements. It may be typically desirable that such specifications are not changed for new products. Lifetime requirements can also be defined by the methods of distribution, inventory and use of a device including a micro-battery. Consequently, micro-batteries for biomedical devices may have specific life requirements

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19/88 useful, which can be, for example, measured in number of years.

[0069] In some examples, the three-dimensional biocompatible energizing elements may be rechargeable. For example, an inductive coil can also be manufactured on the three-dimensional surface. The inductive coil could then be energized with a radio frequency (RF) base. The inductive coil can be connected to the three-dimensional biocompatible energizing element to recharge the energizing element when RF is applied to the inductive coil. In another example, photovoltaics can also be manufactured on the three-dimensional surface and connected to the three-dimensional biocompatible energizing element. When exposed to light or photons, photovoltaics will produce electrons to recharge the energizing element.

[0070] In some examples, a battery can operate to provide electrical energy for an electrical system. In these examples, the battery can be electrically connected to the circuit of the electrical system. The connections between a circuit and a battery can be classified as interconnections. These interconnections can become progressively more challenging in biomedical microbatteries due to several factors. In some instances, energized biomedical devices can be very small, thus providing limited area and volume for interconnections. Size and area restrictions can affect electrical resistance and reliability of interconnections.

[0071] In other respects, a battery may contain a liquid electrolyte that could boil at high temperatures. This restriction can directly compete with the desire to use a weld interconnect that may, for example, require relatively high temperatures like 250 degrees Celsius to melt. However, in some instances, the chemistry of the battery, including the electrolyte, and the heat source used to

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20/88 form weld-based interconnections, can be spatially isolated from one another. In the case of emerging biomedical devices, the small size can prevent the separation between the electrolyte and the solder joints at a sufficient distance to reduce heat conduction.

Modular battery components [0072] In some examples, a modular battery component can be formed according to some aspects and examples of the present invention. In these examples, the modular battery pack can be a separate component from other parts of the biomedical device. In the example of an ophthalmic contact lens device, a design of the type may include a modular battery that is separate from the rest of a media insert. There may be several advantages to forming a modular battery component. For example, in the contact lens example, a modular battery component can be formed in a separate, non-integrated process that can alleviate the need to handle three-dimensionally formed rigid optical plastic components. In addition, the manufacturing sources can be more flexible and can operate in a manner more parallel to the manufacture of other components in the biomedical device. In addition, the manufacture of modular battery components can be decoupled from the characteristics of devices in three-dimensional (3D) format. For example, in applications requiring final three-dimensional shapes, a modular battery system can be manufactured in a flat or approximately two-dimensional (2D) perspective, and then molded into the correct three-dimensional shape. In some instances, the battery may be small enough not to interfere with a three-dimensional shape, even if it is not curved. In some other examples, a coupling of multiple small batteries may fit into a three-dimensional space. A component

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21/88 modular battery can be tested independently of the rest of the biomedical device, and the loss of performance due to battery components can be resolved prior to assembly. The resulting modular battery component can be used in various media insertion constructs that do not have a suitable rigid region on which the battery components can be formed; and in yet another example, the use of modular battery components can facilitate the use of different options for manufacturing technologies that would otherwise be used, such as, for example, a blanket-based (roll-to-roll) technology, blade-based (blade-by-blade) printing, lithography, and squeegee processing. In some examples of a modular battery, the distinct confinement aspect of such a device may result in additional material being added to the construction of the biomedical device in general. Such effects can define a restriction for the use of modular battery solutions when parameters of available space require reduced thickness or volume of the solutions.

Tubes as design elements in the design of a battery component [0073] In some examples, battery elements can be designed so that they segment the active chemical regions of the battery with robust seals. In some instances, these fences may be airtight. There can be numerous advantages from dividing active battery components into hermetically sealed segments, which can commonly take the form of tubes. Tubular batteries with external components made from metals, glass or ceramics can form an aspect of ideal architectural design. In some examples, the materials can be chosen in such a way that seals that are formed between the materials can be considered hermetic in the sense that the diffusion 870170067406, of 9/11/2017, p. 131/207

22/88 are molecules through the seal may be below a specification according to a test protocol for the type of seal, or type of process used to create the seal. For example, electronic components such as batteries can have an air volume or volume equivalent to an amount of air inside, and an airtight specification can refer to a seal that has a leak rate lower than a certain level that it would replace 50% of the volume of the device with air outside the seal. A broad form of a tubular battery can be formed through one or more processes to be discussed in the following sections of the specification, in which a low level of leakage can be measured to determine whether the seal is airtight for the particular battery. In practice, small tubular batteries or micro-batteries, such as those according to the present description, may have a volume in the order of 10 ' ⁴ cm' ³ in some examples. The ability of leak detection equipment to measure a leak rate that is low enough to ensure that a micro-battery seal is airtight may be beyond current leak detection technology; however, the sealing of the micro-battery can be called hermetic, since the same processing and materials, when applied to a wide battery format, results in a low measurable leakage rate, sufficient to consider the processing and sealing materials to be hermetic.

[0074] With reference to Figure 2A, a basic example of a battery in formatubular can be found, a basic metal compartment with an isolated battery 200. In the example, two metallic components, the anode contact 211 and the cathode contact 221, form metal tubes that surround the material. Anode chemicals 212 can be located inside anode contact 211. And, cathode chemicals 222 can be located inside anode

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23/88 cathode contact 221. In some examples, cathode chemicals 222 and anode chemicals 212 can be separated by a separator 240. The battery contacts must be isolated from each other to form a functional battery, a since an electrical connection could cause the battery chemistry to be consumed. In the basic example of Figure 2A, an insulator 230 electrically separates the anode and cathode.

[0075] As illustrated, the insulator 230 can be a physical part that acts by itself in the confinement of the material inside the battery, and as part of the diffusion barrier to inhibit chemical transfer into or out of the battery. In a section below, a description of several types of fences, including hermetic seals and techniques for forming them, is discussed. Examples of seals in the example in Figure 2A can be metal to ceramic seals, or metal to glass seals. The example in Figure 2A has at least two such seals on seal 231 and seal 232, for example.

[0076] Now with reference to Figure 2B, an alternative tubular battery 250 with a similar structure to the device of Figure 2A is illustrated. The alternative tubular shaped battery 250 may have an anode region 260 with anode contact 261 and anode chemicals 262. It may also have a cathode region 270 with a metallic tubular shape containing the cathode chemicals 272 and defining a cathode contact 271. The insulating part 280 separating the anode contact 261 and the cathode contact 271 can have metal insulating seals, as shown in seal 281 and seal 282. As in the example in Figure 2A, the seals from insulator to metal can be hermetic seals in some examples. The insulator can electrically separate anode 260 and cathode 270, but separator 290 can physically separate anode 260 and cathode 270. In this second example, there are again materials 870170067406, from 9/11/2017, p. 133/207

24/88 solids that comprise the anode contact, the cathode contact, and the insulating device, which significantly blocks the diffusion of molecules and atoms through their contour. Hermetic seals on seal 281 and seal 282 can generally result in a hermetically sealed tubular battery.

[0077] Now with reference to Figure 3, another example of a tubular battery is illustrated. In an overlapping tubular battery 300, a metal can over the anode or cathode can significantly overlap an insulating part, which can be significantly overlaid by a metal can over the other region of the battery. Specifically, in the illustrated form, anode 310 has a metal can that also acts as anode contact 311 and surrounds anode chemicals 312. The anode metal can, in the illustrated design, also significantly overlaps the insulating part 330, which in itself is significantly subposed by the metal can from the cathode region 320. The metal cathode can surrounds the cathode chemicals 322 and is the cathode contact 321. The cathode chemicals 322 and the chemicals anode 312 are physically separated in the example by the separator 340. In the tube illustrations, one or both of the anode or cathode chemicals can be shown in a block form for the purposes of illustration; while in some examples, the physical form may look like the illustration, in other examples the chemicals themselves may be films that cover a portion of the space. The example of the overlapping tubular battery 300 can demonstrate a maximum number of sealing surfaces between the metal and the insulating parts. These seals are shown on seal 331 and seal 332, which, as can be seen, overlap a significant fraction of the size of the tubular battery.

[0078] With reference to Figure 4, an alternative tubular shape

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25/88

400 is illustrated. In examples of this type, a central insulating part

430 interfaces with metal terminations for external contacts. The exemplary anode region 410 may include anode metal contact 411 and anode chemicals 412. A seal

431 of the central insulating part 430 can be made with the anode metal contact 411. In the exemplary cathode region 420 there can be a cathode metal contact 421 and cathode chemicals 422, as well as a seal 432 between the central insulating part 430 and the metal contact of cathode 421. This type of configuration may have the smallest area for a seal to act among the various examples. The central insulating part electrically separates the cathode and anode contact, a separator 440 physically separates the anode chemicals 412 and the cathode chemicals 422.

[0079] With reference to Figure 5, an alternative battery in tubular shape 500 is illustrated, with a side layout of the anode and cathode chemicals. Such a layout can also be formed in a tube-shaped micro-battery and can allow the area in the highest cross section for the separator 550 that interfaces with and separates the anode chemicals 512 and the cathode chemicals 522. In illustration, the top region can be anode region 510 with anode chemicals 512 and anode contact 511, and an anode seal 531 around anode contact 511. In some examples, a single insulating part 530 can be formed with holes at one end for the anode and cathode contacts, in some other examples there may be two or more insulating parts, where the top part may be a separate part with holes for the anode and cathode contacts. In the illustration, the bottom region can be the cathode region 520 with the cathode chemicals 522, a cathode contact 521, and a cathode seal 532 around the cathode contact 521.

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26/88 [0080] Referring to Figures 6A to 6F, the formation of a tubular battery is illustrated. A tube 610 in Figure 6A of an insulating material, such as glass or ceramic, can be cut to a desired length, as shown in Figure 6B. In some examples, glass may include borosilicate, sealing glasses for Kovar and other metals, quartz, soda-lime, aluminum silicate, neutral glass, and lead glass, as non-limiting examples. In some instances, tube 610 may be ceramic, and examples of ceramic types may include alumina, silica, zirconia, stabilized zirconia, zirconia, mullite, cordierite, magnesia, silicon carbide, porcelain. In Figure 6C an example of an electrical wire contact, which can be anode contact 621, is illustrated. In some instances, the metal wire may be a zinc wire. In other examples, it may be a wire from another metal such as brass, which may be coated with 620 zinc. The wire may be encircled and sealed with a 622 sealing material.

[0081] In the following sections, various types of sealing are discussed, many examples of which are compatible with the illustrated 622 sealing material. In Figure 6D another metallic wire 630 can be used to form a cathode contact. In some instances, the metallic wire may be a titanium wire. The wire may have a deposit of cathode material 631 surrounding it. Another sealing material 632 can surround cathode wire 630. Referring to Figure 6E, tube 610 can have a wick 641 which can be a polyolefin film or a cellulosic film. In some instances, it can be a cellulosic fiber that spans from the anode region to the cathode region. The wick 641 can be positioned in a volume of electrolyte 640 placed inside the tube. In some instances, the electrolyte may be an aqueous solution, such as a ZnCI ₂ solution. In some other examples, the electrolyte may be a polymeric electrolyte.

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27/88

Some aspects of the different electrolyte options will be discussed in later sections of the present invention. Proceeding to Figure 6F, the various components illustrated in Figures 6E, 6D and 6C can be assembled to form a tube-shaped battery. The seals between the sealing material 622 and the pipe 610, and the sealing material 632 and the pipe 610, may comprise various types of seals, as discussed in the following sections. In some examples, the wick 641 may be a complete separator that can keep the most densely packed battery chemicals separate, as opposed to physical separation, as shown in Figures 6A to 6F.

[0082] In some examples, metal endings can be added as a design variation. The two metallic wires can be embedded in an insulating adhesive body in tubular shape at either end. The tubular shaped adhesive can be partially contained within the insulating tubular battery container, and can also protrude partially beyond the battery container. In some instances, adhesives can adhere and seal the wire terminals and the insulating container. The insulating adhesive can contain battery fluids and prevent leakage of fluids to the outside. The adhesive can be a thermoset, thermoplastic, or a combination of the two.

[0083] With reference to Figure 7, an example of a tube-shaped battery, which includes a wire-shaped cathode contact, is illustrated. The example can comprise two tubes, a hollow tube 711 and a can-shaped tube 710, which together can form the anode contact. Anode chemicals 715 can be deposited or otherwise used to fill can-shaped tube 710. In some examples, anode chemicals 715 can include zinc plated. The can-shaped tube 710 can be sealed to the hollow tube 711 with a metal-to-metal seal 720.

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For example, there may be a metal wire 740 that can be coated with cathode chemicals 730. In some examples, cathode chemicals 730 may include clad manganese dioxide. The metallic wire 740 can form a cathode contact. The metallic wire 740 can be formed of titanium, in some examples. An insulating ceramic piece 760 can form the electrical insulation between the cathode formed by the metal wire 740 and the anode contact produced by combining the hollow tube 711 with the can-shaped tube 710. A ceramic seal with metal 761 can be formed between the hollow tube 711 and the insulating ceramic piece 760. Thus, a seal 762 can be formed between the insulating ceramic piece 760 and the metallic wire 740.

[0084] Referring to Figure 8, yet another example of a tube-shaped battery that includes a wire-shaped cathode contact and a wire-shaped anode contact is illustrated. The example may comprise two tubes, a first hollow tube 800, and a second hollow tube 840, which together can contain anode and cathode chemicals, and electrolyte formulations. In the illustrated example, a zinc wire 820 can form both anode contact and anode chemicals. In some instances, the zinc wire 820 may also be thickened in parts, including zinc plated. The first hollow tube 800 can be sealed to the second hollow tube 840 with a metal-to-metal seal 830. In the example, there may be a metal wire 850 that can be coated with cathode chemicals, as shown, with deposit 860. In in some instances, cathode chemicals may include clad manganese dioxide. The metallic wire can form a cathode contact. The metallic wire can be formed of titanium, in some examples. An insulating ceramic piece 870 can form the electrical insulation between the cathode formed of metal wire 850 and the second hollow tube 840. On the other hand, the battery

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An example may be the anode contact wire formed from a zinc wire 820, which can be insulated by a second piece of insulating ceramic 810. A ceramic seal with metal 871 can be formed between the hollow tube 840 and the insulating ceramic piece 870. Likewise, a seal 872 can be formed between insulating ceramic piece 870 and metal wire 850. A ceramic seal with metal 811 can also be formed between hollow tube 800 and the ceramic piece insulating 810. Likewise, a seal 812 can be formed between the insulating ceramic piece 810 and the metallic wire 800.

[0085] Referring to Figure 9, yet another example of a tube-shaped battery that includes a doped semiconductor is illustrated. The use of doped semiconductors can drastically reduce the amount of sealing edge, which is required in the battery, since electrical contact is made through the tube through the highly doped region. Non-doped regions can form insulators between the anode and cathode regions. During manufacture, the battery may consist of two canned semiconductor pieces, highly doped at the ends, which can be joined by a 930 semiconductor to semiconductor junction. A highly doped semiconductor, when coated with a metallic film such as titanium, or when reacted to form a silicide such as titanium silicide, can form a low resistance ohmic contact. Since the semiconductor can be relatively thin, the result can be a low resistance contact devoid of any joints. If the semiconductor-to-semiconductor junction 930 is located in a region of a separator, there may be little overlap of internal chemistry with a junction. Again with reference to Figure 9, the exemplifying device may comprise two tubes, a first hollow semiconductor can 900 and a second hollow semiconductor can 950, which together may contain

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30/88 anode and cathode chemicals, and electrolyte formulations. In the illustrated example, a metallic film 915 can form an internal anode contact. The first hollow semiconductor can 900 may have a highly doped region 910. In some instances, the highly doped region may be doped with a type N dopant, such as phosphorus. An outer layer of metal 925 can form the outer anode contact. Anode 920 chemicals can be located in the can. The anode can be composed of deposited films, aqueous paste, or solid plugs in the examples. The first hollow semiconductor can 900 can be sealed to the second hollow semiconductor can 950 with a semiconductor to semiconductor junction 930, and in some instances a colocalized separator 960. In the example, there may be a metallic film 975 that can be coated with chemicals, as illustrated with deposit 940. In some examples, cathode chemicals may include clad manganese dioxide. A highly doped region 970 may form electrical contact through the second hollow semiconductor can 950, and may have an external metal deposit to form cathode contact 965. Internal seals of the battery element [0086] In some examples of battery elements for use in biomedical devices, the chemical action of the battery involves aqueous chemistry, where water or moisture is an important constituent to be controlled. Thus, it may be important to incorporate sealing mechanisms that slow or prevent the transit of moisture both outside and inside the battery body. Moisture barriers can be designed to keep the internal moisture content at a designated level, within a certain tolerance. In some instances, a moisture barrier can be divided into two sections or components; specifically, packaging and sealing.

[0087] The packaging can refer to the main material of invoPetição 870170067406, of 9/11/2017, p. 140/207

Profit 31/88. In some examples, the package may comprise a bulk material. The water vapor transmission rate (WVTR) can be an indicator of performance, with ISO and ASTM standards controlling the test procedure, including the environmental conditions operating during the test. Ideally, the WVTR for good battery packaging can be zero. Exemplary materials with an almost zero WVTR can be glass and metal laminates, as well as ceramic and metal parts. Plastics, on the other hand, can be inherently porous to moisture and can vary significantly with different types of plastic. Projected, laminated, or co-extruded materials can generally be hybrids of common packaging materials.

[0088] The seal can be the interface between two of the packaging surfaces. The connection of the sealing surfaces ends the enclosure together with the packaging. In many instances, the nature of seal designs can make them difficult to characterize in relation to the seal's WVTR due to the difficulty of making measurements using an ISO or ASTM standard, for example, sample size or surface area may not be compatible with these procedures. In some examples, a practical way of testing the seal integrity can be a functional test of the actual seal design, against some defined conditions. The performance of the seal may be a function of the seal material, the thickness of the seal, the length of the seal, the seal width and the adhesion or intimacy of the seal to the packaging substrates.

[0089] In some examples, seals may be formed by a welding process that may involve thermal, laser, solvent, friction, ultrasonic or arc processing. In other examples, seals can be formed through the use of sealants

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32/88 adhesives such as glues, epoxies, acrylics, natural rubber, synthetic rubber, resins, tar, or bitumen. Other examples may derive from the use of trim-type material that can be formed from natural and synthetic rubber, poly (tetrafluoroethylene) (PTFE), polypropylene and silicones, to mention some non-limiting examples. In some examples, the sealing material can be a thermoset, a thermoplastic, or a combination of a thermoset and a thermoplastic.

[0090] In some examples, batteries according to the present invention can be designed to have a specified operating life. Operating life can be estimated by determining a practical amount of moisture permeability that can be obtained using a particular battery system and then estimating when such a moisture leak can result in an end-of-life condition for the drums. For example, if a battery is stored in a humid environment, then the difference in partial pressure between the battery's internal and external parts will be minimal, resulting in a reduced rate of moisture loss and thus the battery life can be extended. The same exemplary battery stored in a particularly dry and hot environment can have a significantly shortened life cycle due to the strong drive function for moisture loss.

Metal / Metal Fences, Metal / Glass, Metal / Ceramics, Glass / Glass,

Semiconductor / Semiconductor and Metal / Semiconductor [0091] There can be several ways to form a hermetic or well-formed interface between solid materials that can act as confinement for battery chemistry. Typical means for forming a suitable hermetic mechanical bond between solid materials include brazing, brazing, and welding. These methods can be seen as largely similar, since all of them

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33/88 include heat treatment of both base materials (the materials to be bonded, which can be homogeneous or heterogeneous materials) and the filler material that links the two base materials. The main distinctions that exist between these methods can be seen as the specific temperatures that are used to heat the materials in each method, and how these temperatures affect the properties of each material, when applied over a period of time. More specifically, both brazing (brazing) and welding (weak brazing) can use a temperature that is above the liquid temperature of the filler material, but below the solid temperature of both base materials. The main distinction that can exist between brazing and welding can be seen as the specific temperature that is applied. For example, if the applied temperature is below 450Ό, the method can be called welding, and can be called brazing if the applied temperature is above 450Ό. Welding, however, can use an applied temperature that is above the liquid temperature of the filler and base materials.

[0092] Each of the aforementioned methods can operate for a variety of material combinations, and specific material combinations have the ability to be linked to one another using more than one of these methods. The best choice among these methods for joining two materials can be determined by any number of characteristics, including, but not limited to, specific material properties and net temperatures of the desired materials, other thermal properties of the bond or materials desired load, practice, timing, and precision of the worker or machine connection of the two materials, and an acceptable level of mechanical or surface damage to the materials connected through each method. In some examples, consistent with the

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In the present invention, the materials used for joining two materials can include pure metals, such as gold, silver, indium and platinum. They may also include alloys such as silver-copper, silver-zinc, copper-zinc, copper-zinc-silver, copper-phosphorus, silver-copper-phosphorus, gold-silver, gold-nickel, gold-copper, indium, and aluminum- silicon. They may also include active brazing alloys such as active titanium brazing alloys, which may include gold, copper, nickel, silver, vanadium or aluminum. There may be other welding materials that may be consistent with the sealing needs mentioned in the present disclosure. [0093] Different material combinations for each of these bonding methods can include metal / metal, metal / glass, metal / ceramic, glass / glass, semiconductor / semiconductor, and metal / semiconductor. [0094] In a first type of example, a metal seal with metal seal can be formed. Welding, brazing, and welding are all very commonly used for metal / metal connections. Since the material properties of various metals can vary widely from metal to metal, the liquid temperature of a metal can typically be the decisive feature of the bonding method to be used with a desired metal, for example, a base metal it can have a liquid temperature so low that it will melt quickly at brazing temperatures, or a base metal can have a liquid temperature so high that it does not chemically respond to welding temperatures to form a suitable bond.

[0095] In another type of example, a metal-to-glass (or glass-to-metal) bond can be formed. Due to the inhomogeneity of metal and glass as materials, typical metal / metal bonding methods may not be useful for bonding metals with glass. For example, typical filler materials used in metal / metal welding may bond well to a metal, but may not react with glass to bond to its surface under heat treatment. An

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35/88 The possibility to overcome this problem may be the use of other materials, such as epoxies, which bind to both materials. Typical epoxies have hydroxyl groups pending in their structure, which can allow them to bond with inorganic materials. Epoxy can be applied easily and inexpensively between materials, bonding ubiquitously to many types of surfaces. Epoxies can be easily cured, both before and after application, using many methods, such as a mixture of chemicals that are then quickly applied, thermal, optical radiation, or other types that introduce energy to the epoxy to induce a bonding / curing reaction, or through other methods. Several different types of epoxies may have different desires for different applications, based on several different properties, including, but not limited to, bonding strength, ease of application, curing method, curing time, bondable materials, and many others . In order to obtain a true hermetic seal with epoxy, it is important to consider the leakage rates of certain fluids through the epoxy. An airtight seal with epoxy, however, offers the flexibility to use copper alloys for wires or pins, while maintaining an airtight seal, unlike materials that are less conductive than are required for other types of connections or airtight seal. Epoxy seals, however, are typically viable under much more restricted operating temperature ranges than other bonding methods, and can also have substantially lower bond strength.

[0096] In another type of example, a metal-to-ceramic (or ceramic-to-metal) bond can be formed. Brazing can be seen as a typical method for obtaining a bond between metal and ceramic, and there are a large number of tested and approved methods for obtaining an airtight seal between the materials. This can

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36/88 include the molybdenum-manganese / nickel plating method, where molybdenum and manganese particles are mixed with glass additives and volatile vehicles to form a coating that is applied to the ceramic surface to be brazed. This coating is processed and then coated with nickel and further processed, to now be readily welded by brazing using standard methods and filler materials.

[0097] The deposition of a thin film can also be seen as another commonly used brazing method. In this method, a combination of materials can be applied to a non-metallic surface using the physical vapor deposition (PVD) method. The choice of materials applied may depend on the material properties or the desired layer thicknesses, and occasionally multiple layers are applied. This method has several advantages, including a wide variety of possible metals for application, as well as speed and consistent success proven with standard materials. There are disadvantages, however, including the need for specialized PVD equipment to apply coatings, the need for complicated masking techniques if masking is desired, and geometric constraints with ceramics that can prevent uniform coating thicknesses. The PVD layer can include constituents such as titanium, zirconium and hafnium, and in some instances, it can be between 100 nanometers and 250 nanometers thick. In some examples, a noble overlay may be deposited, which comprises constituents such as gold, palladium, platinum or silver, as non-limiting examples.

Linking Nanofoil® material [0098] A commercially available product called Nanofoil®, a nanotechnology material available from Indium Corporation, can provide a meaningful example when it is needed Petition 870170067406, from 9/11/2017, p. 146/207

37/88 seals a metal, ceramic and / or semiconductor confinement for batteries. In some instances, it may be desirable that any thermal effects on the formation of the seal are located as close as possible to the seal itself. Composite materials such as Nanofoil® material can provide significant thermal localization during the formation of hermetically sealed seals. Composite films of the Nanofoil® type can be produced in hundreds or thousands of levels of nanoscale film. In one example, a reactive multilayer sheet is manufactured by vapor deposition of thousands of alternating layers of aluminum (Al) and nickel (Ni). These layers can be nanometers thick. When activated by a small pulse of local energy from electrical, optical or thermal sources, the metal sheet reacts exothermically. The resulting exothermic reaction produces a quantifiable amount of energy in milliseconds, which heats up to very high local temperatures on the surfaces, but can be controlled so as not to provide a total amount of energy that would increase the temperature in metal, ceramic or semiconductors being sealed. Proceeding to Figure 10A, a portion of the battery seal 830 shown in Figure 8 is detached. In Figure 10B, an example of layers related to the seal is produced before activation of a nanofoil. A first hollow tube 800 and a second hollow tube 840 can be coated with a pre-moistened solder layer on each side, for a first 1010 solder layer and a second 1030 solder layer. A piece of Nanofoil® 1020 material can be located between the two weld layers. When Nanofoil® material is activated, it can fuse the weld layers locally and form an 830 seal. The illustration represents a top-type joint, but many other joint structures may be possible, including overlap designs, pleated designs, and other types of junPetition 870170067406, of 9/11/2017, p. 147/207

38/88 tions, where a piece of Nanofoil can be located between two surfaces to be sealed and which have surfaces coated with weld. Bonding S-Bond® [0099] An example similar to bonding Nanofoil® material can be bonding S-Bond® material. The S-Bond material may comprise a conventional welding alloy base with the addition of titanium or other rare earth elements to the material, and is available from S-Bond Technologies. Active materials such as titanium react with oxides or other inert materials at a bonding interface, and either chemically bond to them or transport them to the weld melt. Upon heating, SBond® materials can fuse, but still have a thin surface oxide on them. When the surface oxide is broken, active material reactions occur with the surface regions of the bond / seal. The oxide can be broken by scraping processes, but it can also be broken by ultrasound. Therefore, a surface reaction can be initiated at a relatively low temperature, and a bond can be made to materials that could be difficult to bond otherwise. In some examples, the S-Bond® material can be combined with the Nanofoil® material to form a structure that can be bonded locally, without significant thermal load on the rest of the battery system.

Silicon bonding [0100] In some examples, a silicon bonding can be achieved with the S-Bond® material. The S-Bond® 220M composition can be used in some examples to form a weldable interface. The S-Bond® 220M material can be deposited on the silicon surface to be bonded / sealed at temperatures in the range of 115 to 400Ό. Therefore, tin-shaped silicon pieces can be heavily doped at the closed end, or through the use of doped films

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39/88 as POCI, through implantation, or through other means of doping. Other means may include oxidation of the semiconductor body and then thinning / chemical attack of the oxide in regions where doping is desired. The doped regions can then be exposed to titanium and heated to form a silicide. The regions of the silicon cans that are used to form the seals can have SBond 220M material applied to them, and heated to moisten the silicon surface, or the silicon surface. In some instances, a film of Nanofoil® material can be applied to the sealing region for subsequent activation. Battery chemistry, electrolyte and other structures can be formed in the can halves, and then the two halves can be put together. Through simultaneous activation by ultrasound and activation of the Nanofoil® material, a fast, low temperature hermetic seal can be formed.

Battery module thickness [0101] When designing battery components for biomedical applications, trade-offs between the various parameters can be made to balance technical, safety and functional requirements. The thickness of the battery component can be an important and limiting parameter. For example, in an optical lens application, the ability of a device to be used comfortably by a user can critically depend on the thickness by the biomedical device. Therefore, there may be critical permissive aspects when designing the battery seeking finer results. In some examples, the thickness of the battery can be determined by the combined thicknesses of the thicknesses of the upper and lower sheets, spacer blades and adhesive layer. Practical aspects of manufacture can motivate certain parameters of the film thickness to standard values in the available sheet stock. In addition, films can have minimum thickness values to which they can be specified based

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40/88 in technical considerations related to chemical compatibility, gas / moisture impermeability, surface finish and compatibility with coatings that can be deposited on film layers.

[0102] In some examples, a desired or target thickness of a finished battery component may be a component thickness that is less than 220 pm. In these examples, this desired thickness can be motivated by the three-dimensional geometry of an exemplary ophthalmic lens device, and the battery component may need to be fitted within the available volume defined by the end user's comfort in the shape of a hydrogel lens, by biocompatibility and acceptance restrictions. This volume and its effect on the thickness requirements of the battery component can be a function of specifying the total thickness of the device, as well as specifying the device regarding its width, tapered angle and internal diameter. Another important design consideration for the resulting battery component design may refer to the volume available for chemicals and active battery materials in a given battery component design with respect to the resulting chemical energy that may result from this design. This resulting chemical energy can then be balanced against the electrical requirements of a functional biomedical device, in relation to its target life and operating conditions.

Battery module width [0103] There may be several applications in which the biocompatible energizing elements or batteries of the present invention can be used. In general, the battery width requirement can largely be a function of the application in which it is applied. In an exemplary case, a contact lens battery system may have restricted requirements for the specification in relation to home. Petition 870170067406, of 9/11/2017, p. 150/207

41/88 of a modular battery component. In some examples of an ophthalmic device where the device has a variable optical function powered by a battery component, the variable optical portion of the device may occupy a central spherical region of about 7.0 mm in diameter. The exemplary drum elements can be considered a three-dimensional object, which fits like a conical annular skirt around the central optics and formed in the shape of a truncated conical ring. If the maximum required diameter of the rigid insert is a diameter of 8.50 mm and tangency to a certain sphere of the diameter can be targeted (as, for example, in a diameter of approximately 8.40 mm), then the geometry can dictate the allowable battery width. There may be geometric models that can be useful in calculating desirable specifications for the resulting geometry which, in some instances, may be called a flattened tapered trunk in a sector of a ring.

[0104] The width of the flattened battery can be motivated by two characteristics of the battery element, the active battery components and sealing width. In some examples related to ophthalmic devices, a target thickness can be between 0.100 mm and 0.500 mm per side, and the active battery components can be targeted at approximately 0.800 mm in width. Other biomedical devices may have different design restrictions, but the principles for flexible flat battery elements can be applied in a similar way.

Flexibility of the battery module [0105] Another dimension of relevance to the design of the battery and the design of related devices that use battery-based power sources is the flexibility of the battery component. There can be several advantages conferred by flexible battery forms. For example, a flexible battery module can facilitate the capacity

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42/88 previously mentioned of making the shape of the battery in a flat two-dimensional (2D) shape. The flexibility of the shape can allow the two-dimensional battery to then be formed into an appropriate 3D shape to fit into a biomedical device such as a contact lens.

[0106] In another example of the benefits that can be conferred by the flexibility in the battery module, if the battery and the subsequent device are flexible, then there may be advantages regarding the use of the device. In one example, a contact lens shape of a biomedical device may have advantages over inserting / removing the contact lens based on a media insert, which may be closer to inserting / removing a hydrogel contact lens. not filled standard.

[0107] The number of push-ups can be important in the design of the battery. For example, a battery that can flex only once, from a flat shape to a shape suitable for a contact lens, can have a significantly different design than a battery capable of multiple flexions. Battery flexion can also go beyond the ability to mechanically survive the flexion event. For example, an electrode may be physically capable of flexing without breaking, but the electrode's mechanical and electrochemical properties can be alternated by flexing. The changes induced by flexion can appear instantly, for example, as changes in impedance, or flexion can introduce changes that are only evident in long-term life tests.

Battery format aspects [0108] The battery format requirements can be motivated, at least in part, by the application in which the battery is to be used. Traditional battery shape factors can be cylindrical shapes or rectangular prisms made of metal and can be turned

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43/88 for products that require large amounts of energy for long durations. These orders can be large enough to understand large form factor batteries. In another example, flat solid-state (2D) batteries are thin rectangular prisms, typically formed on silicon or inflexible glass. These flat solid-state batteries can be formed, in some instances, through the use of silicon wafer processing technologies. In another type of battery form factor, flexible low-power batteries can be formed into a pouch construct, using thin metal sheets or plastic to contain the battery's chemistry. These batteries can be made flat (2D), and can be designed to work when curved to a modest curvature outside the plane (3D).

[0109] In some of the examples of battery applications in the present invention in which the battery can be used in a variable optical lens, the form factor may require a three-dimensional curvature of the battery component, the radius of which can be approximately 8.4 mm. The nature of such a curvature can be considered relatively steep and for reference it can approximate the type of curvature observed on a human fingertip. The nature of a relative steep curvature creates challenging aspects for manufacturing. In some examples of the present invention, a modular battery component can be designed so that it can be manufactured in a flat two-dimensional shape and then formed into a three-dimensional shape of high relative curvature. Battery element separators [0110] Batteries of the type described in the present invention can use a separating material that physically and electrically separates the anode and current collector portions of the anode from the cathode and current collector portions of the cathode. The separator can be a

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44/88 membrane that is permeable to water and dissolved electrolyte components; however, it can typically be electrically non-conductive. While a myriad of commercially available separator materials can be known to those skilled in the art, the innovative form factor of the present invention may present unique restrictions on the task of separator selection, processing and handling.

[0111] Since the designs of the present invention may have ultra-thin profiles, the choice may be limited to the finest separating materials typically available. For example, separators approximately 25 microns thick may be desirable. Some examples that can be advantageous can be about 12 microns thick. There may be several acceptable commercial separators that include microfibrillated microporous polyethylene and / or polypropylene-polyethylene-polypropylene (PP / PE / PP) monolayer separating membranes, such as those produced by Celgard (Charlotte, NC, USA). A desirable example of separating material may be the Celgard M824 PP / PE / PP trilayer membrane having a thickness of 12 microns. Alternative examples of separating materials useful for examples of the present invention can include separating membranes including regenerated cellulose (e.g., cellophane).

[0112] While PP / PE / PP three-layer separating membranes can have advantageous thickness and mechanical properties due to their polyolefinic character, they can also have several disadvantages that may have to be overcome to make them useful in the examples of the present invention. The roll or blade stock of PP / PE / PP three layer separator materials may have various wrinkles or other shape errors that may be detrimental to the micron tolerances applicable to the batteries described here. In addition disPetition 870170067406, of 9/11/2017, p. 154/207

45/88 so, polyolefin separators may need to be cut to ultra-precise tolerances for inclusion in the present designs, which may imply laser cutting as an exemplary method for forming discrete current collectors in desirable shapes with strict tolerances. Due to the polyolefinic character of these separators, certain cutting lasers useful for micro fabrication may employ laser wavelengths, for example, 355 nm, which are not capable of cutting polyolefins. Polyolefins do not absorb laser energy considerably and are thus without ablation. Finally, polyolefin separators may not be inherently humidifiable in the aqueous electrolytes used in the batteries described herein.

[0113] However, there may be methods to overcome these limitations inherent in polyolefin-type membranes. In order to present a microporous separating membrane to a high precision cutting laser to cut parts in arc segments or other advantageous separator designs, the membrane may need to be flat and free of wrinkles. If these two conditions are not met, the separating membrane may not be completely cut, as the cutting beam may be inhibited as a result of the defocusing or dispersion of the incident laser energy. In addition, if the separating membrane is not flat and free of wrinkles, the precision of the shape and geometric tolerances of the separating membrane may not be sufficiently achieved. The allowable tolerances for the separators of the current examples can be, for example, +0 microns and -20 microns with respect to the characteristic lengths and / or radii. There may be advantages in stricter tolerances of +0 microns and -10 microns and also for tolerances of +0 microns and -5 microns. It is possible to make the stock material separator flat and free of wrinkles by temporarily laminating the material in a float glass vehicle with an appropriate low volatility liquid. Low fluids

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46/88 volatility may have advantages over temporary adhesives due to the fragility of the separating membrane and due to the amount of processing time that may be required to release the separating membrane from an adhesive layer. In addition, in some examples, it has been observed that obtaining a flat, wrinkle-free separating membrane in the float glass using a liquid is much easier than using an adhesive. Before lamination, the separating membrane can be made free of particulates. This can be achieved by ultrasonic cleaning the separating membrane to dislodge any particulate adhering to surfaces. In some instances, the handling of a separating membrane can be done in a suitable environment with low particle presence, such as a laminar flow hood or a clean room of at least class 10,000. In addition, the floating glass substrate can be made to be free of particulates by rinsing with an appropriate solvent, ultrasonic cleaning and / or scrubbing with clean room cleaning cloths.

[0114] While a wide variety of low volatility liquids can be used for the mechanical purpose of laminating microporous polyolefin separating membranes on a floating glassy vehicle, specific requirements can be imposed on the liquid to facilitate subsequent laser cutting of the separator shapes discreet. A requirement may be that the liquid has a surface tension low enough to penetrate the pores of the separating material, which can be easily checked by visual inspection. In some instances, the separating material changes from a white color to a translucent appearance when the liquid fills the material's micropores. It may be desirable to choose a liquid that can be benign and safe for workers who will be exposed to separator preparation and cutting operations. It may be desirable to choose a liquid whose prescription 870170067406, of 9/11/2017, p. 156/207

47/88 vapor pressure can be low enough that considerable evaporation does not occur during the processing time scale (on the order of 1 day). Finally, in some instances, the liquid may have sufficient solvating power to dissolve the advantageous UV absorbers that can facilitate the laser cutting operation. In one example, it was observed that a 12 percent (w / w) solution of avobenzone UV absorber in benzyl benzoate solvent can meet the previously mentioned requirements and can serve to facilitate laser cutting of high-grade polyolefin separators precision and tolerance in short order without an excessive number of passes of the cutting laser beam. In some examples, separators can be cut with a solid-state laser pumped by an 8W 355 nm nanosecond diode using this approach, with the laser having low energy attenuation settings (for example, 3 percent energy), a moderate speed of 1 to 10 mm / s, and only 1 to 3 passes of the laser beam. While this oily UV absorbing composition has been proven to effectively assist the lamination and cutting process, other oily formulations can be designed by those skilled in the art and used without limitation.

[0115] In some examples, a separator can be cut while attached to a float glass. An advantage of laser cut separators while attached to a floating glassy vehicle may be that a very high density of separators can be cut from a separator stock blade, in the same way that the semiconductor matrix can be densely arranged together in a silicon wafer. Such an approach can provide economies of scale and parallel processing advantages inherent in semiconductor processes. In addition, the generation of excess separating membrane can be reduced. Once the separators have been cut, the oily process assist fluid can be removed by

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48/88 a series of extraction steps with miscible solvents, the last extraction can be carried out with a highly volatile solvent, such as isopropyl alcohol, in some examples. Discrete separators, once extracted, can be stored indefinitely in any suitable environment with low particle presence.

[0116] As previously mentioned, polyolefin separating membranes may be inherently hydrophobic and may need to be wetted to aqueous surfactants used in the batteries of the present invention. One approach to making the separating membranes moist may be oxygen plasma treatment. For example, separators can be treated for 1 to 5 minutes on 100 percent oxygen plasma in a wide variety of energy settings and oxygen flow rates. While this approach can improve wettability for a while, it can be well known that the plasma surface modifications provide a temporary effect that may not last long enough to effect robust humidification of electrolyte solutions. Another approach to improve the wettability of the separating membranes may be to treat the surface by incorporating a suitable surfactant into the membrane. In some cases, the surfactant can be used in conjunction with a hydrophilic polymeric coating that remains within the pores of the separating membrane.

[0117] Another approach to provide more permanence to the hydrophilic capacity conferred by an oxidative plasma treatment may be the subsequent treatment with a suitable hydrophilic organosilane. In this way, oxygen plasma can be used to activate and distribute functional groups over the entire surface area of the microporous separator. The organosilane can then covalently bond and / or adhere non-covalently to the plasma treated surface. In examples using an organosilane, inherent porosity Petition 870170067406, of 9/11/2017, p. 158/207

49/88 te of the microporous separator cannot be considerably changed, and the monolayer surface coverage can also be possible and desired. Prior art methods that incorporate surfactants in conjunction with polymeric coatings may require strict control over the actual amount of coating applied to the membrane, and may therefore be subject to process variability. In extreme cases, pores of the separator can become blocked, thus adversely affecting the usefulness of the separator during the operation of the electrochemical cell. An exemplary organosilane useful for the present invention can be (3-aminopropyl) triethoxy silane. Other hydrophilic organosilanes can be known to those skilled in the art and can be used without limitation.

[0118] Another method to make the separating membranes moist with aqueous electrolyte may be the incorporation of a suitable surfactant in the electrolyte formulation. A consideration when choosing a surfactant to make the separating membranes moist may be the effect that the surfactant can have on the activity of one or more electrodes within the electrochemical cell, for example, by increasing the electrical impedance of the cell. In some cases, surfactants may have advantageous anti-corrosion properties, specifically in the case of zinc anodes in aqueous electrolytes. Zinc can be an example of a material known to undergo a slow reaction with water to release hydrogen gas, which may be unwanted. Various surfactants can be known to those skilled in the art for limiting the rates of said reaction to advantageous levels. In other cases, the surfactant may interact so strongly with the zinc electrode surface that battery performance may be impaired. Consequently, great care may be required in the selection of appropriate surfactant types and load levels to ensure that separator wetting can be achieved without affecting damage 870170067406, of 9/11/2017, p. 159/207

50/88 initially the electrochemical performance of the cell. In some cases, a plurality of surfactants can be used, one being present to impart moisture to the separating membrane, and the other being present to facilitate the anti-corrosion properties of the zinc anode. In one example, no hydrophilic treatment is done to the separating membrane, and a surfactant, or a plurality of surfactants, is added to the electrolyte formulation in an amount sufficient to influence the wetting of the separating membrane.

[0119] Separate separators can be integrated into a tubular micro-battery through direct positioning on a portion of one or sides of a tube set.

Battery element polymerized separators [0120] In some battery designs, the use of a discrete separator (as described in a previous section) can be prevented due to a variety of reasons such as cost, material availability, quality of materials, or the complexity of processing some material options, as non-limiting examples.

[0121] One method of obtaining a molded separator in uniform and mechanically robust place can be to use UV curable hydrogel formulations. Various water-permeable hydrogel formulations can be known in several industries, for example, the contact lens industry. An example of a hydrogel common in the contact lens industry may be cross-linked poly (hydroxy-ethyl methacrylate) gel, or simply pHEMA. For various applications of the present invention, pHEMA can have many attractive properties for use in Leclanché and zinc-carbon batteries. PHEMA typically can maintain a water content of approximately 30 to 40 percent in the hydrated state, while maintaining an elastic modulus of about 100 psi or greater. In addition, property 870170067406, of 9/11/2017, p. 160/207

51/88 modulus and water content of the crosslinked hydrogels can be adjusted by those skilled in the art by incorporating additional hydrophilic monomeric components (for example, methacrylic acid) or polymeric components (for example, polyvinylpyrrolidone). In this way, the water content, or, more specifically, the ion permeability of the hydrogel can be adjusted through formulation.

[0122] Particularly advantageous in some examples, a polymerizable and moldable hydrogel formulation may contain one or more diluents to facilitate processing. The diluent can be chosen to be volatile, so that the moldable mixture can be spread into a cavity and then dried for a period sufficient for the volatile solvent component to be removed. After drying, bulk photopolymerization can be initiated by exposure to actinic radiation of suitable wavelength, such as blue UV light at 420 nm, for the chosen photoinitiator, such as CGI 819. The volatile diluent can adjust to provide an application viscosity in order to facilitate the casting of a uniform layer of the polymerizable material in the cavity. The volatile diluent can also provide beneficial surface tension reduction effects, particularly in the case where strongly polar monomers are incorporated into the formulation. Another aspect that may be important to obtain the melting of a uniform layer of polymerizable material in the cavity may be the viscosity of the application. Common reactive monomers with small molar mass typically do not have very high viscosities, and can typically be only a few centipoise. In an effort to provide beneficial control of the viscosity of the moldable and polymerizable separating material, a polymeric component of high molar mass known to be compatible with the polymerizable material can be selected for incorporation into the formulation.

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Examples of high molecular weight polymers that may be suitable for incorporation into exemplary formulations, may include polyvinylpyrrolidone and poly (ethylene oxide).

[0123] In some examples, the moldable and polymerizable separator can be advantageously applied in a designed cavity, as previously described. In alternative examples, there may be no cavities at the time of polymerization. Instead, the moldable and polymerizable separator formulation can be coated on a substrate containing electrode, for example, zinc plated shaped brass and then subsequently exposed to actinic radiation with the use of a photomask to selectively polymerize the separating material into target areas. The separating material can then be removed by exposure to appropriate rinsing solvents. In these examples, the separator material can be designed as a photo-moldable separator.

Multi-component separator formulations [0124] The useful separator, according to the examples of the present invention, can have numerous properties that may be important for its function. In some instances, the separator may desirably be formed in such a way as to create a physical barrier, so that the layers on either side of the separator do not come into physical contact. The layer can thus have an important characteristic of uniform thickness, since, while a thin layer may be desirable for various reasons, an empty space or gap may be essential. In addition, the thin layer may desirably have a high permeability to allow free flow of ions. In addition, the separator requires optimal water intake to optimize the mechanical properties of the separator. Thus, the formulation can contain a cross-linking component, a hydrophilic polymer component and a solvent component.

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53/88 [0125] A crosslinker can be a monomer with two or more polymerizable double bonds. Suitable crosslinkers can be composed of two or more polymerizable functional groups. Examples of suitable hydrophilic crosslinkers may further include compounds with two or more polymerizable functional groups, as well as hydrophilic functional groups, such as polyether, amide or hydroxyl groups. Specific examples can include TEGDMA (tetraethylene glycol dimethacrylate), TrEGDMA (triethylene glycol dimethacrylate), ethylene glycol dimethacrylate (EGDMA), ethylenediamine dimetaacrylamide, glycerol dimethacrylate and combinations thereof.

[0126] The amounts of crosslinker that can be used in some examples can vary, for example, from about 0.000415 to about 0.0156 mol per 100 grams of reactive components in the reaction mixture. The amount of hydrophilic crosslinker used can generally be about 0 to about 2 weight percent and, for example, about 0.5 to about 2 weight percent. Hydrophilic polymer components capable of increasing the viscosity of the reactive mixture and / or increasing the degree of hydrogen bonding with the slow-reacting hydrophilic monomer, such as high molecular weight hydrophilic polymers, may be desirable.

[0127] High molecular weight hydrophilic polymers provide optimum wettability and, in some examples, can improve wettability for the separator of the present invention. In some non-limiting examples, high molecular weight hydrophilic polymers are believed to be hydrogen bonding receptors that, in aqueous environments, bind hydrogen to water, thus effectively becoming more hydrophilic. The absence of water can facilitate the incorporation of the hydrophilic polymer in the reaction mixture. In addition to the specifically named hydrophilic high molecular weight polymers, any high molecular weight polymer can be expected

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54/88 is useful in the present invention, provided that, when said polymer is added to an exemplary silicone hydrogel formulation, the hydrophilic polymer (a) does not substantially separate in phases of the reaction mixture and (b) provides wettability to the resulting cured polymer.

[0128] In some examples, the high molar hydrophilic polymer may be soluble in the diluent under processing temperatures. Manufacturing processes that use water or water-soluble diluents, such as isopropyl alcohol (IPA), can be desirable examples due to their simplicity and low cost. In these examples, high molecular weight hydrophilic polymers that are soluble in water at processing temperatures may also be desirable. [0129] Examples of high molecular weight hydrophilic polymers may include, but are not limited to, functionalized polyamides, polylactones, polyimides, polylactams and polyamides, polylactones, polyimides, polylactams, such as PVP and copolymers thereof, or, alternatively, functionalized DMA by copolymerization with a smaller molar amount of a hydroxyl-functional monomer, such as HEMA, followed by reaction of the hydroxyl groups of the resulting copolymer with materials containing radical polymerizable groups, such as ethyl methacrylate isocyanate or methacryloyl chloride. High molecular weight hydrophilic polymers may include, but are not limited to, poly-N-vinyl pyrrolidone, poly-N-vinyl-2-piperidone, poly-N-vinyl-2-caprolactam, poly-N-vinyl3-methyl-2 -caprolactam, poly-N-vinyl-3-methyl-2-piperidone, poly-N-vinyl-4-methyl-2-piperidone, poly-N-vinyl-4-methyl-2-caprolactam, poly-N-vinyl-3-ethyl -2-pyrrolidone and poly-N-vinyl-4,5-dimethyl-2-pyrrolidone, polyvinylimidazole, poly-N - N-dimethylacrylamide, polyvinyl alcohol, polyacrylic acid, polyethylene oxide, poly 2 ethyl oxazoline, heparin polysaccharides , polysaccharides, mixtures and copolymers (including block or random, branched, multi-stranded, comb-shaped or star-shaped) of

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55/88 same where poly-N-vinylpyrrolidone (PVP) can be a desirable example where PVP has been added to a hydrogel composition to form an interpenetration network that shows a low degree of surface friction and a low rate of dehydration.

[0130] Additional components or additives, which can generally be known in the art, can also be included. Additives may include, but are not limited to, ultraviolet absorbing compounds, photoinitiators, such as CGI 819, reactive toners, microbicidal compounds, pigments, photochromics, release agents, combinations thereof and the like.

[0131] The method associated with these types of separators may also include receiving CGI 819; and then mix with PVP, HEMA, EGDMA and IPA; and then cure the resulting mixture with a source of heat or exposure to photons. In some instances, photon exposure can occur where the photon energy is consistent with a wavelength that occurs in the ultraviolet portion of the electromagnetic spectrum. Other methods of initiating polymerization generally carried out in polymerization reactions are within the scope of the present invention.

Interconnections [0132] Interconnections can allow current to flow to and from the battery in connection with an external circuit. These interconnections can interface with the environments inside and outside the battery, and can cross the boundary or fence between these environments. These interconnections can be considered as tracks, making connections with an external circuit, passing through the battery seal and then connecting to the current collectors inside the battery. Thus, these interconnections can have several requirements. Outside the battery, the interconnects may resemble typical printed circuit tracks. They can be welded or otherwise connected to other tracks. On a

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56/88 example where the battery is a physical element separate from a circuit board comprising an integrated circuit, the interconnection of the battery may allow connection to the external circuit. This connection can be formed with solder, conductive tape, epoxy or conductive paint, or other means. Interconnect trails may need to survive in the environment outside the battery, for example, without corrosion in the presence of oxygen.

[0133] As an interconnection passes through the battery seal, it may be of critical importance that the interconnection coexists with the seal and allows the seal. Adhesion may be required between the seal and the interconnect in addition to the adhesion that may be required between the seal and the battery packaging. The integrity of the seal may need to be maintained in the presence of electrolyte and other materials contained in the battery. Interconnections, which can typically be metallic, can be known as points of failure in the battery pack. The electrical potential and / or the current flow can increase the tendency of the electrolyte to deform along the interconnection. Consequently, an interconnect may need to be built to maintain the integrity of the seal.

[0134] Within the battery, interconnections can interface with current collectors or can actually form current collectors. In this sense, the interconnection may need to meet the requirements of the current collectors, as described here, or it may need to form an electrical connection with these current collectors. [0135] One class of candidate interconnects and current collectors is that of sheet metal. These foils are available in thicknesses of 25 microns or less, which makes them suitable for very thin batteries. These metal sheets can also be purchased with a low degree of surface roughness and contamination, two factors that can be critical to the performance of the batPetition 870170067406, of 9/11/2017, p. 166/207

57/88 laugh. The metal sheets can be of zinc, nickel, brass, copper, titanium, other metals and various alloys.

Current and electrode collector [0136] Many of the current and electrode collector designs are designed to be formed by depositing metallic film on a side wall, or by using metallic wires as substrates to form the current and electrode collectors. Examples of these have been illustrated. However, there may be some designs that use other current collector or electrode designs in a tubular battery format.

[0137] In some examples of zinc and Leclanche carbon cells, the cathode current collector may be a sintered carbon rod. This type of material can face technical obstacles for fine electrochemical cells of the present invention. In some examples, printed carbon inks can be used in thin electrochemical cells to replace a sintered carbon rod for the cathode current collector, and in these examples, the resulting device can be formed without significant damage to the resulting electrochemical cell. Typically, said carbon inks can be applied directly to packaging materials, which may comprise polymeric films or, in some cases, metal sheets. In examples where the packaging film may be a foil, the carbon paint may need to protect the underlying foil from chemical degradation and / or corrosion by the electrolyte. In addition, in these examples, the current collector of the carbon ink may need to provide electrical conductivity from within the electrochemical cell to the outside of the electrochemical cell, which implies a seal around or through the carbon ink.

[0138] Carbon inks can also be applied in layers that are relatively small and finite in thickness, for example,

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58/88 to 20 microns. In a thin electrochemical cell design in which the total packaging thickness can be only about 100 to 150 microns, the thickness of a layer of carbon paint can assume a significant fraction of the total internal volume of the electrochemical cell, thus negatively impacting on the electrical performance of the cell. In addition, the thin nature of the entire battery and the current collector, in particular, can imply a small cross-sectional area for the current collector. Since the resistance of a track increases with the track length and decreases with the cross-sectional area, there may be a direct disadvantage between the thickness and the resistance of the current collector. The bulk resistivity of the carbon ink may be insufficient to satisfy the strength requirement of thin batteries. Paints filled with silver or other conductive metals can also be considered to reduce strength and / or thickness, but they can introduce new challenges, such as incompatibility with new electrolytes. In consideration of these factors, in some examples, it may be desirable to make efficient and high-performance thin electrochemical cells of the present invention using a thin metal sheet as the current collector, or to apply a thin metallic film to a packaging layer of underlying polymer to act as the current collector. Such metal sheets can have significantly lower resistivity, thus allowing them to meet electrical resistance requirements with much less thickness than printed carbon inks.

[0139] In some examples, one or more of the tubular shapes can be used as a substrate for the electrodes and current collectors, or as the current collectors themselves. In some instances, metals in a tubular shape may have deposits on their surfaces. For example, tubular metal parts can serve

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59/88 as a substrate for a metal or metal pile of the ion-bombarded current collector. Exemplary metal batteries useful as cathode current collectors can be Ti-W (titanium-tungsten) adhesion layers and conductive Ti (titanium) layers. Exemplary metal cells useful as anode current collectors can be Ti-W adhesion layers, Au conductive layers (gold) and In deposition layers (indium). The thickness of the PVD layers can be less than 500 nm in total. If multiple layers of metals are used, the electrochemical and barrier properties may need to be compatible with the battery. For example, copper can be galvanized on top of an initial particle layer to cultivate a thick conductive layer. Additional layers can be clad over copper. However, copper can be electrochemically incompatible with certain electrolytes, especially in the presence of zinc. Consequently, if copper is used as a layer on the battery, it may need to be sufficiently isolated from the battery electrolyte. Alternatively, copper can be excluded or replaced with another metal.

[0140] Wires produced from numerous materials can also be used to form current collectors and / or substrates for the electrodes. In some instances, the metal conductor may penetrate an insulating material, such as glass or ceramic, to provide contact with the isolated electrical current collector. In some instances, the wire may be produced from titanium. In other examples, other base metals including, but not limited to, aluminum, tungsten, copper, gold, silver, platinum, may be used, and may have films applied to their surface.

Cathode mixtures and depositions [0141] There may be several chemical cathode mixtures that can be consistent with the concepts of the present invention. In some

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60/88 examples, a cathode mixture, which can be a term for a chemical formula used to form a battery cathode, can be applied as a paste, gel, suspension or aqueous paste, and can comprise a transition metal oxide, such as manganese dioxide, some in the form of a conductive additive, which, for example, can be a conductive powder form, such as carbon black or graphite, and water-soluble polymer, such as polyvinylpyrrolidone (PVP) or some other binding additives. In some examples, other components may be included, such as one or more of binders, electrolyte salts, corrosion inhibitors, water or other solvents, surfactants, rheology modifiers and other conductive additives, such as conductive polymers. Once formulated and appropriately mixed, the cathode mixture can have a desirable rheology that allows it to either be dispensed over desired portions of the cathode current separator and / or collector, or spread across a screen or stencil in a similar manner. In some examples, the cathode mixture may be dried before being used in future cell assembly steps, while in other examples, the cathode may contain some or all of the electrolyte components, and may only be partially dried to a selected moisture content.

[0142] The transition metal oxide may, for example, be manganese dioxide. Manganese dioxide, which can be used in the cathode mixture, can be, for example, electrolytic manganese dioxide (DME), due to the additional specific beneficial energy that this type of manganese dioxide provides over other forms, such as dioxide of natural manganese (NMD) or chemical manganese dioxide (CMD). In addition, the DME useful in batteries of the present invention may need to have a particle size and a particle size distribution that can be conductive for the formation of aqueous paste / paste of printable or depositable cathodes.

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Specifically, DME can be processed to remove components of significantly large particles, which can be considered large in relation to other characteristics such as internal battery dimensions, separator thickness, dispensing tip diameters, stencil opening sizes, or sizes of screen mesh. Particle size optimization can also be used to improve battery performance, for example, internal impedance and discharge capacity.

[0143] Grinding is the reduction of solid materials from an average particle size to a smaller average particle size, by crushing, grinding, cutting, vibrating, or other processes. Milling can also be used to release useful materials from the matrix materials in which they can be incorporated, and to concentrate minerals. A mill is a device that breaks solid materials into smaller pieces by grinding, grinding or cutting. There may be several means for grinding and many types of materials processed therein. Such grinding media may include: ball mill, mill mill, mortar and pestle, roller press and jet mill, among other grinding alternatives. An example of grinding may be jet grinding. After grinding, the state of the solid is changed, for example, the particle size, the particle size arrangement and the particle shape. Aggregate grinding processes can also be used to remove or separate contamination or moisture from the aggregate to produce dry fillings prior to transportation or structural filling. Some equipment can combine various techniques to classify a solid material into a mixture of particles whose size is limited by both a minimum and a maximum particle size. Such processing can be referred to as classifiers or classification. [0144] Milling can be an aspect of producing a mixture of

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62/88 cathodes for uniform particle size distribution of the cathode mixture ingredients. The uniform particle size in a cathode mixture can aid in viscosity, rheology, electroconductivity and other properties of a cathode. Grinding can assist these properties by controlling the agglomeration, or a mass collection, of the cathode mixing ingredients. Agglomeration - the grouping of dispersed elements that, in the case of the cathode mixture, can be carbon allotropes and transition metal oxides - can negatively affect the filling process, leaving empty spaces in the desired cathode cavity, as illustrated in the Figures 11A to 11J described in detail below. [0145] Still, filtration can be another important step for the removal of agglomerated or undesirable particles. Undesirable particles can include huge particles, contaminants, or other particles not explicitly taken into account in the preparation process. Filtration can be achieved by means, such as paper filter filtration, vacuum filtration, chromatography, microfiltration and other filtration media.

[0146] In some examples, DME can have an average particle size of 7 microns with a large particle content that can contain particles up to about 70 microns. In alternative examples, the DME can be sieved, ground further, or otherwise separated or processed to limit the content of large particles below a certain threshold, for example, 25 microns or less. [0147] The cathode may also comprise silver oxides, silver chlorides, or nickel oxy-hydroxides. Such materials can offer high capacity and less decrease in voltage charged during discharge compared to manganese dioxide, both properties desirable in a battery. Batteries based on these cathodes may have current examples present in industry and literaturePetition 870170067406, of 9/11/2017, p. 172/207

63/88 tura. An innovative micro-battery that uses a silver dioxide cathode may include a biocompatible electrolyte, for example, one that comprises zinc chloride and / or ammonium chloride instead of potassium hydroxide.

[0148] Some examples of the cathode mixture may include a polymeric binder. The binder can serve many functions in the cathode mixture. The primary function of the binder can be to create a sufficient interparticle electrical network between DME particles and carbon particles. A secondary function of the binder may be to facilitate mechanical adhesion and electrical contact with the cathode current collector. A third function of the binder may be to influence the rheological properties of the cathode mixture for distribution and / or printing with advantageous stencil / canvas. In addition, a fourth function of the binder may be to increase the absorption and distribution of the electrolyte within the cathode.

[0149] The choice of the binder polymer, as well as the amount to be used, can be beneficial for the function of the cathode in the electrochemical cell of the present invention. If the polymer binder is too soluble in the electrolyte to be used, then the primary function of the binder - electrical continuity - can be dramatically impacted to the point of non-functionality of the cell. Conversely, if the binder polymer is insoluble in the electrolyte to be used, portions of DME can be ionically isolated from the electrolyte, resulting in reduced cell performance, such as reduced capacity, lower open circuit voltage and / or high internal resistance.

[0150] The binder can be hydrophobic; it can also be hydrophilic. Examples of binder polymers useful for the present invention include PVP, polyisobutylene (PIB), rubbery tri-block copolymers comprising styrene end blocks, such as those manufactured by Kraton Polymers, block copolymers

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64/88 of styrene-butadiene latex, polyacrylic acid, hydroxyethylcellulose, carboxymethylcellulose, fluorocarbon solids, such as poly (tetrafluoroethylene), cements including Portland cement, among others.

[0151] A solvent can be a component of the cathode mixture. A solvent can be useful for moistening the cathode mixture, which can assist in the distribution of particles in the mixture. An example of a solvent can be toluene. Also, a surfactant can be useful to moisten and thus distribute the cathode mixture. An example of a surfactant can be a detergent, such as Triton ™ QS-44, available from Dow Chemical Company. Triton ™ QS-44 can assist in the dissociation of aggregate ingredients in the cathode mixture, allowing for a more uniform distribution of the ingredients in the cathode mixture.

[0152] A conductive carbon can normally be used in the production of a cathode. Carbon is capable of forming many different allotropes or structural modifications. Different carbon allotropes have different physical properties, allowing variation in electroconductivity. For example, the viscosity of carbon black can assist in adhering a mixture of cathodes to a current collector. However, in energizing elements that require relatively low amounts of energy, these variations in electroconductivity may be less important than other favorable properties, such as density, particle size, heat conductivity and relative uniformity, among other properties. Examples of carbon allotropes include: diamond, graphite, graphene, amorphous carbon (informally called carbon black), buckminsterfulerane, glassy carbon, carbon airgel and other possible forms of carbon capable of conducting electricity. An example of a carbon allotrope can be graphite.

[0153] In some examples, the cathode may be deposited on

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65/88 a wall of the tube or a cathode collector in the form of wire. The tube walls and wires may be metallic, in some instances, and may have cathode chemicals such as electrodeposited manganese dioxide on them. In other examples, electrolytic manganese dioxide coatings can be formed on cathode collectors.

Anode and anode corrosion inhibitors [0154] The anode for the tubular battery of the present invention can comprise, for example, zinc. In traditional zinc-carbon batteries, a zinc anode can take the physical form of a container in which the electrochemical cell contents can be contained. For the battery of the present invention, a zinc container may be an example, but there may be other physical forms of zinc that may be desirable for projects to create ultra-small batteries.

[0155] Zinc electroplating is a type of process in several uses in industries, for example, for the protective or aesthetic coating of metal parts. In some examples, galvanized zinc can be used to form thin and insulating anodes useful for batteries of the present invention. In addition, electrogalvanized zinc can be standardized in many different configurations, depending on the design intent. An easy way to standardize electroplated zinc can be processing using a photomask or a physical mask. In the case of the photomask, a photoresist can be applied to a conductive substrate, the substrate on which the zinc can subsequently be galvanized. The desired galvanizing pattern can then be designed for photoresist by means of a photomask, thereby curing selected areas of photoresist. The uncured photoresist can then be removed with suitable solvent and cleaning techniques. The result can be a standardized area of conductive material that

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66/88 can receive galvanized zinc treatment. While this method can provide benefits for the shape or design of the zinc to be plated, the approach may require the use of available photovoltaic materials, which may have limited properties for the overall construction of the cell packaging. Consequently, new and innovative methods for standardizing zinc may be required to carry out some of the fine micro-battery designs of the present invention. [0156] The zinc mask can be put on and then the galvanization of one or more metallic materials can be carried out. In some instances, zinc can be galvanized directly into an electrochemically compatible anode current collecting sheet, such as bronze. In alternative design examples, where the side anode package comprises a polymer metallic foil or multilayer polymer metallic foil on which the initial metallization has been applied, zinc and / or the foil solutions used to deposit zinc may not be chemically compatible with the underlying underlying metallization. Manifestations of lack of compatibility may include cracking, corrosion and / or exacerbated evolution of H ₂ in the film upon contact with the cell electrolyte. In this case, additional metals can be applied to the parent metal to better affect the overall chemical compatibility in the system. A metal that may find specific use in the construction of electrochemical cells may be indium. Indium can be widely used as an alloy component in the battery's zinc grade with its primary function being to provide an anti-corrosion property to zinc in the presence of the electrolyte. In some examples, the Indian can be successfully deposited in several initial metallizations, such as Ti-W and Au. The films resulting from 1 to 3 microns of indium in said layers of initial metallization can be low-tension and adherent. Thus, the packaging film on the side

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67/88 of the anode and the attached current collector that has a top layer of indium can be conformable and durable. In some examples, it may be possible to deposit zinc on the surface treated by indium, and the resulting deposit may be very non-uniform and nodular. This effect can occur in low current density configurations, for example, at 20 amps per square foot (ASF). As seen under a microscope, the formation of zinc nodules can be seen in the underlying smooth indium deposit. In certain electrochemical cell designs, the vertical space gap for the zinc anode layer can be up to about 5 to 10 microns in thickness, but in some instances, lower current densities can be used for zinc plating, and the resulting nodular growths can be greater than the maximum vertical anode thickness. It may be because the development of nodular zinc stems from a combination of the high excess potential of indium and the presence of a layer of indium oxide.

[0157] In some instances, higher current density DC plating can overcome relatively large nodular zinc growth patterns on indium surfaces. For example, 100 ASF leaf conditions can result in nodular zinc, but the size of the zinc nodules can be drastically reduced compared to 20 ASF leaf conditions. In addition, the number of nodules can be immensely greater under 100 ASF leaf conditions. The resulting zinc film can finally bond to a more or less uniform layer, with only a few residual characteristics of nodular growth, while reaching the provision of vertical space of about 5 to 10 microns.

[0158] An added benefit of indium in the electrochemical cell can be the reduction of the formation of H ₂ , which can be a lenPetition process 870170067406, of 9/11/2017, p. 177/207

68/88 to what occurs in aqueous electrochemical cells containing zinc. Indium can be beneficially applied to one or more of the anode current collectors, the anode itself, as a component of a corked alloy, or as a surface coating on galvanized zinc. For the latter case, indium surface coatings can desirably be applied in-situ by means of an electrolyte additive, such as indium trichloride or indium acetate. When these additives can be added to the electrolyte in small concentrations, the Indian can spontaneously galvanize on exposed zinc surfaces as well as portions of the exposed anode current collector. [0159] Zinc anodes and the like, commonly used in commercial primary batteries, can typically be found in the form of leaves, stems, and pastes. The anode of a miniature, biocompatible battery can be similarly shaped, for example thin sheet, or can be galvanized as mentioned earlier. The properties of this anode can differ significantly from those in existing batteries, for example, due to differences in contaminants or surface finishes, attributed to the machining and leafing processes. Consequently, electrodes and electrolyte may require special handling to meet capacity, impedance and life requirements. For example, special electroplating process parameters, electroplating bath composition, surface treatment and electrolyte composition may be required to optimize the electrode performance.

Battery architecture and manufacturing [0160] Battery architecture and manufacturing technology can be closely intertwined. As discussed in previous sections of the present invention, a battery can have the following elements: cathode, anode, separator, electrolyte, cathode current collector, anode current collector, and tube-shaped confinement. In

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69/88 some examples, the designs may have dual-use components, such as the use of a metal can in the form of a can or a tube that can act as a current collector. From a point of view of relative volume and thickness, these elements can be approximately all of the same volume, except the cathode. In some examples, the electrochemical system may require about two (2) to ten (10) times the cathode volume as an anode due to significant differences in mechanical density, density energy, discharge efficiency, material purity and the presence of binders , fillers and conducting agents.

Aspects of battery biocompatibility [0161] According to the present invention, batteries can have important aspects related to safety and biocompatibility. In some instances, batteries for biomedical devices may need to meet the requirements above and beyond those for typical usage scenarios. In some instances, design aspects can be considered to be related to stressful events. For example, the safety of an electronic contact lens may need to be considered when a user breaks the lens during insertion or removal. In another example, design aspects may consider the potential for a user to be hit in the eye by a foreign object. Still other examples of stress conditions that can be considered when developing design parameters and restrictions may refer to the potential for a user to wear lenses in challenging environments, such as the underwater environment or the high altitude environment, as non-limiting examples.

[0162] The security of such a device can be influenced by: materials with which the device was formed, or from it; the quantities of these materials used in the manufacture of the device; and for the packaging applied to separate the devices from the ambiPetição 870170067406, of 9/11/2017, p. 179/207

70/88 around or inside the body. In one example, pacemakers can be a typical type of biomedical device that can include a battery and can be implanted in a user for an extended period of time. In some instances, such pacemakers may typically be packaged with hermetically sealed, welded titanium wrappers or in other examples, multiple layers of encapsulation. Emerging energized biomedical devices may present new challenges in relation to packaging, specifically battery packaging. These new devices can be much smaller than existing biomedical devices, for example, an electronic contact lens or pill camera can be significantly smaller than a pacemaker. In these examples, the volume and area available for packaging can be greatly reduced. An advantage of limited volume may be that the amount of materials and chemicals can be so small that it inherently limits a user's potential for exposure to a level below a safe limit.

[0163] The tube-based approach, particularly when it includes airtight seals, can provide a means to improve biocompatibility. Each of the tubular components can provide a significant barrier against the entry and exit of materials. Additionally as with many of the hermetic sealing processes that have been described here, a battery that has superior biocompatibility can be formed.

Contact lens skirts [0164] In some examples, a preferred encapsulation material that can form an encapsulation layer in a biomedical device may include a component containing silicone. In one example, this encapsulation layer can form a lens contour for a contact lens. A component containing

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71/88 silicone is one that contains at least one unit of [-Si-O-] in a monomer, macromer or prepolymer. Preferably, total Si and O-bound Si are present in the silicone-containing component in an amount greater than about 20 weight percent, and more preferably greater than 30 weight percent of the total molecular weight of the silicone-containing component . Useful silicone-containing components preferably comprise polymerizable functional groups such as acrylate, methacrylate, acrylamide, methacrylamide, vinyl, Nvinyl lactam, N-vinylamide and styryl functional groups.

[0165] In some examples, the ophthalmic lens skirt, also called the insertion element encapsulation layer, which surrounds the insertion element may comprise ophthalmic lens formulations with standard hydrogel. Exemplary materials with characteristics that can provide an acceptable resemblance to various materials of the insertion element may include, for example, the Narafilcon family (including Narafilcon A and Narafilcon B) and the Etafilcon family (including Etafilcon A). A more technically inclusive discussion follows the nature of the materials consistent with the technique of the present invention. The person skilled in the art with ordinary skill may recognize that material other than those discussed may also form an acceptable wrapper or partial wrapper of sealed and encapsulated inserts and should be considered consistent and included in the scope of the claims.

[0166] Suitable silicone-containing components include compounds of formula I

tram

R1 is independently selected from monoPetition groups 870170067406, from 9/11/2017, p. 181/207

72/88 reactive valentes, monovalent alkyl groups, or monovalent aryl groups, any of the above, which may additionally comprise functionalities selected from hydroxyl, amino, oxa, carboxyl, alkylcarboxyl, alkoxy, amide, carbamate, carbonate, halogen or the their combinations; and monovalent siloxane chains comprising from 1 to 100 Si-0 repeat units that may additionally comprise functionalities selected from alkyl, hydroxy, amino, oxa, carboxy, carboxyalkyl, alkoxy, starch, carbamate, halogen or combinations thereof;

where b = 0 to 500, and where it is understood that, when b is different from 0, b is a distribution having a mode equal to an established value;

wherein at least one R1 comprises a reactive monovalent group, and in some instances between one and 3 R1 comprise reactive monovalent groups.

[0167] As used here, monovalent reactive groups are groups that can undergo free radical polymerization and / or cationic polymerization. Some non-limiting examples of reactive free radical groups include (meth) acrylates, styryl, vinyls, vinyl ethers, C1-6alkyl (meth) acrylates, (meth) acrylamides, C1-6alkyl (meth) acrylamides, N-vinylactams, N -vinylamides, C2-12alkenyls, C2-12alkenylphenyls, C2-12alkenylnaphthylates, C2-6alkenylphenyl C1-6alkyls, O-vinylcarbamates and O-vinylcarbonates. Non-limiting examples of reactive cationic groups include vinyl ethers or epoxide groups and mixtures thereof. In one embodiment, the reactive free radical groups comprise (meth) acrylate, acryloxy, (meth) acrylamide, and mixtures thereof.

[0168] Suitable monovalent alkyl and aryl groups include unsubstituted monovalent C1 to C16alkyl groups, C6C14 aryl groups such as methyl, ethyl, propyl, butyl, 2-hydroxy-propyl, propoxyPetition 870170067406, from 9/11/2017, pg. 182/207

73/88 substituted and unsubstituted propyl, polyethyleneoxypropyl, combinations thereof and the like.

[0169] In one example, b is zero, an R1 is a reactive monovalent group, and at least 3 R1 are selected from monovalent alkyl groups that have one to 16 carbon atoms, and, in another example, from monovalent alkyl groups that have one to 6 carbon atoms. Non-limiting examples of silicone components of this modality include 2-methyl-, 2-hydroxy-3- [3- [1,3,3,3tetramethyl-1 - [(trimethylsilyl) oxy] disyloxanil] propoxy] propyl ester (SiGMA) ,

2- hydroxy-3-methacryloxypropyloxypropyl-tris (trimethylsiloxy) silane,

3-methacryloxypropyltris (trimethylsiloxy) silane (TRIS), 3-methacryloxypropylbis (trimethylsiloxy) methylsilane and 3-methacryloxypropylpentamethyldisiloxane.

[0170] In another example, b is 2 to 20, 3 to 15 or, in some examples, 3 to 10; at least one terminal R1 comprises a reactive monovalent group and the remaining R1 are selected from monovalent alkyl groups with 1 to 16 carbon atoms and, in another embodiment, from monovalent alkyl groups with 1 to 6 carbon atoms. In yet another embodiment, b is 3 to 15, one terminal R1 comprises a monovalent reactive group, the other terminal R1 comprises a monovalent alkyl group having 1 to 6 carbon atoms and the remaining R1 comprises monovalent alkyl groups having 1 to 3 carbon atoms. Non-limiting examples of silicone components of this modality include ether-terminated polydimethylsiloxane (mono- (2-hydroxy-3-methacryloxypropyl) -propyl (molecular weight 400 to 1,000)) (OH-mPDMS), mono-n- terminated polydimethylsiloxanes butyl terminated in monomethacryloxypropyl (molecular weight 800 to 1,000), (mPDMS).

[0171] In another example, b is 5 to 400 or 10 to 300, both terminal R1s comprise monovalent reactive groups and R1

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The remaining 74/88 are independently selected from monovalent alkyl groups that have 1 to 18 carbon atoms, which may have ether bonds between carbon atoms and may also comprise halogen.

[0172] In one example, where a silicone hydrogel lens is desired, the lens of the present invention will be produced from a reactive mixture that comprises at least about 20 and preferably between about 20 and 70%, by weight, of silicone-containing components based on the total weight of the reactive monomeric components from which the polymer is made.

[0173] In another modality, one to four R1 comprise a vinyl carbonate or carbamate with the following formula:

Formula II

R O

H ₂ C = C- (CH ₂ ) _q -OCY where: Y denotes O-, S- or NH-,

R denotes hydrogen or methyl, d is 1,2, 3 or 4; and q is 0 or 1.

[0174] The vinyl carbonate or vinyl carbamate monomers containing silicone specifically include: 1,3-bis [4- (vinyloxycarbonyloxy) but-1-yl] tetramethyldisiloxane; 3- (vinyloxycarbonylthio) propyl [tris (trimethylsiloxy) silane]; 3- [tris (trimethylsiloxy) silyl] propyl allyl carbamate; 3- [tris (trimethylsiloxy) silyl] propyl vinyl carbamate; trimethylsilylethyl and vinyl carbonate; trimethylsilylmethyl vinylcarbonate, and çh ₃

H ₂ C = C — OCO (CH ₃ ) ₄ -Si — oH I ch ₃ çh ₃

-Si-O ch ₃

-125 çh ₃

-Si- (CH ₂ ) ₄ OCO — c = ch ₂ ch ₃ [0175] When biomedical devices with a module below about 200 are desired, only one R1 should comprise a monovalent reactive group and no more than two of the R1 groups restanPetição 870170067406, of 9/11/2017, p. 184/207

75/88 will comprise monovalent siloxane groups.

[0176] Another class of components containing silicone includes polyurethane macromers with the following formulas:

Formula IV-VI (* D * A * D * G) to * D * D * E1;

E (* D * G * D * A) to * D * G * D * E1 or;

E (* D * A * D * G) a * D * A * D * E1 where:

D denotes an alkyl diradical, an alkylcycloalkyl diradical, a cycloalkyl diradical, an aryl diradical or an alkylaryl diradical that has 6 to 30 carbon atoms,

G denotes an alkyl diradical, a cycloalkyl diradical, an alkylcycloalkyl diradical, an aryl diradical or an alkylaryl diradical which has 1 to 40 carbon atoms and which may contain ether, uncle or amine bonds in the main chain;

* denotes a urethane or ureid bond; a is at least 1;

A denotes a divalent polymeric radical of the formula: Formula VII r- _R m> 11

R

II - (CH ₂ ) _y fSiO-Si- (CH ₂ ) _y SiO

R ¹¹

R11 independently denotes a fluoro-substituted alkyl or alkyl group having 1 to 10 carbon atoms, which may contain ether bonds between the carbon atoms; y is at least 1; and p provides a portion weight of 400 to 10,000; each of E and E1 independently denotes a polymerizable unsaturated organic radical represented by the Formula:

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76/88

Formula VIII

R12

Ri3ChH = C- (CH2) _w - (X) x— (Z) _z - (Ar) y-Ri4— where: R12 is hydrogen or methyl; R13 is hydrogen, an alkyl radical that has 1 to 6 carbon atoms, or a —CO — Y— R15 radical where Y is —O—, Y — S— or —NH—; R14 is a divalent radical that has 1 to 12 carbon atoms; X represents —CO— or —OCO—; Z stands for —O— or —NH—; Ar denotes an aromatic radical having 6 to 30 carbon atoms; w is 0 to 6; x is 0 or 1; y is 0 or 1; ez is 0 or 1.

[0177] A preferred silicone-containing component is a polyurethane macromer, represented by the following formula:

Formula IX

CH2 = C-COCH ₂ CI-l · CHj

CHb CH ₃ ο ο ο ο / | \ | • OCN- R16— NCCCH ₂ CH ₂ OCH2CH ₂ OaJ- R16- NCCXC ^ nj- SOja— (CH ₂ ) _n

Η Η Η Η \ I / pl

CHj CH ₃

ÇHj

OCN- R ₁₆ - NCCCH ₂ CH ₂ OCH2CH ₂ OCN— r ¹⁶ - nco-ch ₂ ch ₂ cooc Η Η Η H where R16 is a diisocyanate diradical after removal of the isocyanate group, such as the isophorone diisocyanate diradical . Another suitable silicone-containing macromer is the compound of formula X (in which x + y is a number in the range 10 to 30) formed by the reaction of fluorether, hydroxy-terminated polydimethyl siloxane, isophorone diisocyanate and isocyanatoethylmethacrylate.

Formula X

[0178] Other silicone-containing components suitable for use in the present invention include macromers containing polysiloxane groups, polyalkylene ether, diisocyanate, polyfluoro hydrocarbons, polyfluoro ether and polysaccharides; polysiloxanes with a group 870170067406, of 9/11/2017, p. 186/207

77/88 lateral poles or a polar fluoride graft having a hydrogen atom attached to a carbon atom replaced by terminal difluoro; hydrophilic siloxanil methacrylates containing ether and siloxanil bonds and crosslinkable monomers containing polyether and polysiloxanil groups. In some examples, the polymer base may have zwitterions incorporated into it. These zwitterions can exhibit charges of both polarities along the polymer chain when the material is in the presence of a solvent. The presence of zwitterions can improve the wettability of the polymerized material. In some examples, any of the polysiloxanes mentioned above can also be used as an encapsulating layer in the present invention. Autocatalytic cladding of metal layers to seal battery structures [0179] Metal cladding is very useful in several applications, for aesthetic purposes in jewelry or metal devices, to add corrosion resistance to industrial machinery, or to surfaces of devices or materials , or even to add electrical conductivity to a surface, as non-limiting examples. In a biocompatible energizing element, the foil surrounding the battery body can be useful to form a sealed barrier against the entry or exit of the material. There may be several methods for applying a layer of metal to a battery structure, but the basic premise may involve the deposition of a coating or layer of a metallic material on the surface of the external surfaces of the battery. Metal plating can be done with various types of metals, including copper, nickel, platinum, rhodium, and many others. The result of metal plating can be the deposition of metals on various types of other materials, including, but not limited to, other metals, semiconductors, or plastics. [0180] Typical examples of metal cladding methods

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78/88 may include electroplating and autocatalytic leafing; both involve coating a material with a layer of metal. However, electroplating may involve an induced electrical charge on the material to be coated, whereas autocatalytic plating may not involve electricity, and may involve a chemical reaction that deposits the metal.

[0181] Electroplating can involve numerous steps to achieve a desired finish, consistent deposited material thickness and other desired qualities in a successful coating. In some instances, a part can first be carefully pre-treated to ensure effective veneering. Pre-treatment steps may include, but are not limited to, polishing, masking, chemical roughing, washing, steam cleaning, rinsing, ultrasonic washing, or electrolubbing, as some non-limiting examples. In some instances, pretreatment can remove oil, grease, or other contaminants from the surface of a part to be coated.

[0182] After successful pre-treatment, the object to be clad can be placed in a bath solution containing the metal to be deposited in ionic form. Typically, electroplating methods may involve inducing a positive electrical charge to the bath solution, and a negative electrical charge to the object to be plated. This difference in electrical charge can induce a force of electrical attraction between the metal particles in the bath solution and the clad object. The attraction force can chemically modify the ionic state of and bind the metal particles in the bath solution to the object, coating its surface.

[0183] Depending on the composition of the material to be veneered and the bath solution, certain conditions including, but not limited to, tension, pH of the bath solution, metal concentration in the solution,

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79/88 duration of leafing and room temperature, should preferably be maintained, in order to ensure effective leafing. Adjusting these conditions can alter various aspects of the veneer, including, but not limited to, the finish of the resulting metal surface, the color of the deposited metal, the rate of deposition, or the thickness of the deposited metal. Other ambient conditions, such as air bubbles or contaminants in the bath solution, can also affect the resulting finish; these imperfections can be resolved by shaking the bath or applying a carbon treatment to the bath, as non-limiting examples. In some instances, it may be important to reduce all causes of imperfections on a veneered surface over a biocompatible energizing element; as such imperfections can reduce the effectiveness of a seal.

[0184] Various forms of post-treatment may also be necessary to ensure the success of electroplating, including, but not limited to, rinsing, steam cleaning, heating drying, or other methods.

[0185] Autocatalytic veneering can involve numerous steps to obtain a desired finish, consistent thickness of the deposited material and other desired qualities in a successful coating. Autocatalytic veneering can have the same requirements related to the coating and sealing of a biocompatible energizing element that was discussed in relation to electroplating. First, a part to be coated can be carefully pre-treated to ensure effective veneering. Pre-treatment steps can include, but are not limited to, cleaning. Cleaning can remove contaminants and / or debris remaining from any of the previous processing steps of the object to be coated, as well as oil, grease, or other surface contaminants

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80/88 of a part to be coated. Cleaning can be achieved with acids or other types of cleaning solutions; when choosing a suitable cleaning solution, it may be important to consider what material or debris needs to be removed, the temperature at which the cleaned part (and thus the solution) will be maintained during cleaning, the desired concentration of the cleaning solution , the amount of mechanical work (agitation, etc.) that may be required for the cleaning product, as well as other possible aspects.

[0186] The pre-treatment steps can also include steps of chemical thinning, masking, rinsing, drying, and immersing the object to be plated in a pre-immersion activation solution, as well as an activation solution, as non-limiting examples. . Chemical thinning may involve the use of a chemical and / or mechanical product, as non-limiting examples, to engrave a profile on a work object to be leafed, which will serve as a prescribed leafing location. A pre-immersion solution may contain ions common to those in the activation solution, which will prepare the workpiece for leafing itself; this pre-immersion solution can typically be designed to be applied to the workpiece, and not rinsed before being added to the activation solution. A pre-immersion solution may be less sensitive to metal ion contamination than an associated activation solution. There can be numerous advantages regarding the use of a pre-immersion solution, including, in a non-limiting sense, a result that is less expensive, and that can save the metal ion contamination activation solution, to help the process be more efficient. and create higher quality results.

[0187] After pre-immersion, an activation solution can be applied to the workpiece. An activator may contain certain ions maintained in a reduced state by other ions in the solution; in practice,

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81/88 reduced ions can be maintained mechanically at the bonding surface, acting as a catalyst for the chemical reaction that will facilitate autocatalytic leafing. While a sufficient layer of activation solution on the workpiece surface is important to catalyze the autocatalytic leafing process, it may be important to note that a layer of very thick activation solution can possibly act as a barrier against proper adhesion of the clad metal, and needs to be avoided. [0188] The pre-treatment steps can also include a post-activation step, or acceleration, as it is also commonly called. This step can serve to allow activation species, deposited from the activation solution in the pre-immersion step, to be as 'active' as possible, before the autocatalytic leafing step itself. This step can allow the activation species to interact more readily with the autocatalytic leafing solution in the leafing step itself; this can not only decrease the start time of the autocatalytic leafing reaction, but also minimize the possibility of activation species contaminating the autocatalytic leafing solution, increasing the quality of the resulting leafing. If this post-activation step is left out, the activation solution deposited on the workpiece may contain marginally adherent species, which can result in contamination of the autocatalytic leafing solution and prolong the start of the autocatalytic leafing reaction. In some examples, post-activation solutions can be acidic and act to remove metal oxides that can form on work surfaces due to rinsing steps between the activator and the post-activator; while this is satisfactory for the object of work, it can serve to contaminate the post-activator, and the bath solution may need to be reconstituted after becoming excessive Petition 870170067406, of 9/11/2017, p. 191/207

82/88 concentrated with these metals or other contaminants.

[0189] After pre-treatment, a work object can be submerged in a chemical bath, which contains the following possible ingredients as non-limiting examples: metal salts (of the desired metal for deposition), a reducing agent, an alkaline hydroxide , chelating agents, stabilizers, brighteners, and, optionally, wetting agents. The reducing agent and hydroxide ions can provide the necessary reduction force for depositing the metal contained in the bath solution. The deposition reaction can be initiated by the catalytic species that may have been applied to the surface of the work object during the activation step. Typical autocatalytic bath bath choices may depend on several factors, including, but not limited to, temperature, desired leaf speed, desired leaf thickness, and metal concentration (and thus the repeatability of the leaf reaction to multiple work objects in a single bath, although it can be seen that this repeatability also depends on many other factors).

Improved mechanical strength through autocatalytic plating [0190] In some examples, a desirable solution to improve mechanical strength may involve autocatalytic plating as a technique for creating a shaped barrier coating. The principles of autocatalytic leafing have been discussed in the present invention. Autocatalytic veneering can deposit a shaped metal layer on a conductive or non-conductive coating. Autocatalytic leaf baths were developed to deposit metals such as nickel, copper, and tin on plastic surfaces. The autocatalytically plated metal can then be additionally clad through the use of autocatalytic plating or electroplating with a wide variety of metals, including nickel,

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83/88 copper, tin, gold, silver, cadmium, and rhodium. In some cases, due to cost, corrosion, and / or mechanical problems, it may be desirable to use a layered structure that incorporates more than one galvanized layer.

[0191] The coating can be arbitrarily thick, and can mechanically reinforce the battery in addition to acting as a barrier. This mechanical reinforcement can force hydrogen out of the sides of the cell, reducing or eliminating its expansion due to the production of hydrogen gas during zinc corrosion. To avoid creating a short circuit between the battery terminals due to leafing, it may be necessary to mask one or both terminals with the use of a non-conductive material during the leafing process. [0192] In some examples, a layer may be formed by autocatalytic plating, in which autocatalytic plating and / or electroplating can be used to create a shaped copper coating of approximately 25 microns (1 mil) thereon. A vinyl tape can be used to mask both terminals of these batteries during leafing, to avoid short-circuiting the batteries during the leafing process.

[0193] The tape can then be removed from the terminals, and then the batteries can be aged at room temperature to 50% relative humidity.

Tubular plastic batteries [0194] Autocatalytic veneering of sealing layers can allow tube-shaped batteries that comprise plastic tubes, to be formed in a usable manner. Referring to Figures 11A to 11F, an illustration of the formation of a plastic tube-shaped battery is illustrated. A 1110 plastic tube that can comprise polyethylene, or a plastic composite of the Mylar type, and metal layers is shown in Figure 11 A. It can be cut up to

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84/88 a desired length, as illustrated in Figure 11B, or in other examples can be melted deformed or encircled in other tubes formed to be curved in shape. In some instances, a flat piece of plastic or Mylar can be wrapped around a tube while processing a tube-shaped battery. As illustrated in the following discussion, the shape of the plastic tube can be shaped at a later processing stage.

[0195] In Figure 11C an example of an electrical wire contact, which can be anode contact 1121, is illustrated. In some instances, the metal wire may be a zinc wire. In other examples, it may be a wire from another metal such as brass, which may be coated with zinc 1120. The wire may be encircled and sealed to an 1122 sealing material. In the present invention, various types of sealing are discussed, many examples of which are compatible with the sealing material 1122 illustrated.

[0196] In Figure 11 D, another 1130 metal wire can be used to form a cathode contact. In some instances, the metallic wire may be a titanium wire. The wire may have a deposit of cathode material 1131 that surrounds it. Another sealing material 1132 can surround the cathode wire 1130.

[0197] With reference to Figure 11E, the tube 1110 can have a wick 1141 which can be a polyolefin film or a cellulosic film. In some instances, it may be a cellulosic yarn that ranges from the anode region to the cathode region. The wick 1141 can be positioned in a volume of electrolyte 1140 that can be located in the tube in a further processing step.

[0198] Proceeding to Figure 11F, the various components illustrated in Figures 11E, 11D and 11C can be assembled to form a tube-shaped battery. The seals between the sealing material 1122 and the tube 1110, and the sealing material 1132 and the tube

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1110, can comprise various types of seals, as discussed in the following sections. In some examples, wick 1141 can be a complete separator or plug of separating material that can keep the most densely packed battery chemicals separate, as opposed to physical separation, as shown in Figures 11A to 11F.

[0199] In some examples, metal endings can be added as a design variation. The two metallic wires can be embedded in an insulating adhesive body in tubular shape at each end. The tubular shaped adhesive can be partially contained within the insulating tubular battery container, and can also protrude partially beyond the battery container. In some instances, adhesives can adhere and seal the wire ends and the insulating container. The insulating adhesive can contain battery fluids and prevent leakage of fluids to the outside. The adhesive can be a thermoset, thermoplastic, or a combination of the two.

[0200] In some examples, there may be a supply port or a reserved port port along the body of the plastic tube. After the battery is assembled, a supply port can be cut at the supply port location, and the battery can be charged with electrolyte. In some instances, the electrolyte may be an aqueous solution, such as a ZnCI ₂ solution. In some other examples, the electrolyte may be a polymeric electrolyte. Different electrolyte options that were discussed earlier can be used.

Leafing of biocompatible batteries [0201] Any one of a number of tube-shaped batteries can be further processed for electrocatalytic leafing of barrier films to the battery structure. In one example, a fully formed tubular plastic battery could be laPetição 870170067406, from 9/11/2017, p. 195/207

86/88 with electrocatalytic deposition, followed by electroplating. In a non-limiting example, the battery structure in Figure 11F can be further processed with electroplating. As shown in a top-down view of Figure 11G, the plastic battery 1150 can be flexed in a curved shape, with a cathode contact 1152 and an anode contact 1153. The shape of the battery is illustrated in the cross section of the Figure 11H. The cross section is illustrated along the region indicated by the dotted line 1151. [0202] The tube-shaped surface can be cleaned and treated with a pre-immersion in an acid bath, to remove contaminants like a residual slurry. Other washes and cleanings may include RCA-type cleanings, peroxide-based cleanings of types SC1 and SC2, hydrofluoric acid, sulfuric acid, and combinations of acids. An accelerator or sensitizer may include proprietary formulations such as the Transene Company's Type C solution. An activator can then be used to treat the surface. As a non-limiting example, a Type D solution from Transene Company can be used. With reference to Figure 11 Η, the result of this treatment is illustrated as layer 1161 on the fully formed biocompatible energizing element of Figure 11F.

[0203] Then, the pretreated surface can be immersed in baths for autocatalytic leafing, in this example, of copper. The battery body that has been pre-treated and activated can now be immersed in a mixture of Type A and Type B autocatalytic copper bath solution, at an elevated temperature of approximately 40 C over a period of time, to form several microns of deposition. The resulting deposition is illustrated as layer 1162. In some examples, the surface can be washed later in acids to stabilize the surface.

[0204] In some examples, a thicker layer of deposition 870170067406, of 9/11/2017, p. 196/207

87/88 sition, perhaps 10 microns or more in thickness, can be deposited on the autocatalytic layer, through the use of electroplating with a copper bath. The resulting copper layer is illustrated as layer 1163. In some instances, a rhodium electroplating treatment may follow the galvanized copper layer like layer 1164. Rhodium can stabilize and protect the copper surface; therefore, a thin layer can be added as the top surface in some examples.

[0205] If a complete battery element were clad in a copper layer, the two battery contacts would be shorted and the battery would not be functional. Therefore, one or both battery contacts can be protected prior to leafing, to prevent their formation around the contacts and isolate the contact. Referring to Figure 11J, an example top view of a laminated battery prior to leafing is illustrated on the battery in Figure 11G, with anode connection 1152 and cathode connection 1153. A protective film, such as a vinyl tape , can be placed around the anode contact at location 1171, and the cathode contact at location 1172. The remaining surface 1170 of the battery can be coated with the autocatalytic and galvanized layers, as illustrated in Figure 11 A. The fact that the contact region may have a non-veneered surface of the uncoated laminated structure may not be a problem for battery sealing. In some instances, contacts can be made long enough so that there is a relatively large seal close to the contact. In another sense, the operation of a primary battery can result in the production of gases, such as hydrogen gas. The presence of a region around one or more of the contacts that is also not sealed can be advantageous, as it can create a path that allows the generated gases to dissipate slowly.

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88/88 [0206] Biocompatible batteries can be used in biocompatible devices such as implantable electronic devices, such as pacemakers and microenergy collectors, electronic pills to monitor and / or test a biological function, surgical devices with active components, devices ophthalmic, micro-sized pumps, defibrillators, stents, and the like.

[0207] Specific examples have been described to illustrate the sample modalities for the cathode mixture for use in biocompatible batteries. These examples are for the purpose of illustrating mentioned and are not intended to limit the scope of the claims in any way. Consequently, the description is intended to encompass all examples that may be evident to those skilled in the art.

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Claims (39)

1. Biomedical device, characterized by the fact that it comprises: an electroactive component; a battery comprising: an anode current collector; a cathode current collector; an anode; a cathode; a tube encapsulating the anode and cathode with a first penetration into the anode current collector, a second penetration into the cathode current collector, a first seal between the tube and the anode current collector, and a second seal between the tube and the cathode current collector; and a first biocompatible encapsulation layer, the first biocompatible encapsulation layer encapsulating at least the electroactive component and the battery. 2. Battery, characterized by the fact that it comprises: an anode current collector, wherein the anode current collector is a first closed metal tube at a first end; an anode, in which the anode chemistry is contained within the first metallic tube; a cathode current collector, wherein the cathode current collector is a second metal tube closed at a second end; a cathode, in which the chemistry of the cathode is contained within the second metallic tube; a ceramic tube with a first sealing surface that has a sealing interface with the first metal tube, and a Petition 870170067406, of 9/11/2017, p. 199/207 2/8 second sealing surface that has a sealing interface with the second metal tube; and a sealing material located in a gap between the first sealing surface and the first metal tube. 3. Battery according to claim 2, characterized by the fact that the sealing material located in the gap between the first sealing surface and the first metal tube comprises an epoxy based adhesive. 4. Battery according to claim 2, characterized by the fact that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a first layer comprising molybdenum and manganese particles, in a mixture with powders ceramic, which is then clad with a metallic film. 5. Battery, according to claim 4, characterized by the fact that the metallic film comprises nickel. 6. Battery according to claim 2, characterized by the fact that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a first layer of a metallic film deposited by PVD. 7. Battery according to claim 6, characterized by the fact that the metallic film comprises titanium. 8. Battery, according to claim 7, characterized by the fact that a noble metallic film is additionally deposited on the metallic film deposited by PVD. 9. Battery according to claim 2, characterized in that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a plurality of thin layers of metallic films, in which a first thin layer of metallic film is deposited on a second layer Petition 870170067406, of 9/11/2017, p. 200/207 3/8 of metallic film, in which the first thin layer of metallic film is chemically reactive with the second layer of metallic film, releasing energy to rapidly heat the layers, and in which the chemical reaction is activated by an energetic pulse of energy. 10. Battery, according to claim 9, characterized by the fact that the energetic pulse comprises photons. 11. Battery according to claim 9, characterized by the fact that the energetic pulse comprises electrons. 12. Battery, according to claim 9, characterized by the fact that the energy pulse comprises thermal energy. 13. Battery, according to claim 2, characterized by the fact that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a conventional solder alloy base with a titanium addition, in which the titanium reacts with ceramic surface materials upon exposure to ultrasonic energy. 14. Battery, characterized by the fact that it comprises: an anode current collector, in which the anode current collector is a first metal tube closed at a first end; an anode, in which the anode chemistry is contained within the first metallic tube; a cathode current collector, wherein the cathode current collector is a second metal tube closed at a second end; a cathode, in which the chemistry of the cathode is contained within the second metallic tube; a glass tube with a first sealing surface that has a sealing interface with the first metal tube, and a second sealing surface that has a sealing interface with section 870170067406, from 9/11/2017, p. 201/207 4/8 second metal tube; and a sealing material located in a gap between the first sealing surface and the first metal tube. 15. Battery according to claim 14, characterized by the fact that the sealing material located in the gap between the first sealing surface and the first metal tube comprises an epoxy based adhesive. 16. Battery according to claim 14, characterized by the fact that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a first layer comprising particles of molybdenum and manganese, in a mixture with powders ceramic, which is then clad with a metallic film. 17. Battery according to claim 16, characterized by the fact that the metallic film comprises nickel. 18. Battery according to claim 14, characterized in that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a first layer of a metallic film deposited by PVD. 19. Battery, according to claim 18, characterized by the fact that the metallic film comprises titanium. 20. Battery, according to claim 19, characterized by the fact that a noble metallic film is additionally deposited on the metallic film deposited by PVD. 21. Battery according to claim 14, characterized in that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a plurality of thin layers of metallic films, in which a first thin layer of metallic film is deposited on a second layer of metallic film, in which the first thin layer of film mePetição 870170067406, of 9/11/2017, p. 202/207 5/8 tálico is chemically reactive with the second layer of metallic film, releasing energy to quickly heat the layers, and in which the chemical reaction is activated by an energetic pulse of energy. 22. Battery, according to claim 21, characterized by the fact that the energetic pulse comprises photons. 23. Battery, according to claim 21, characterized by the fact that the energetic pulse comprises electrons. 24. Battery according to claim 21, characterized by the fact that the energy pulse comprises thermal energy. 25. Battery, according to claim 14, characterized by the fact that the sealing material located in the gap between the first sealing surface and the first metal tube comprises a conventional welding alloy base with a titanium addition, in which the titanium reacts with glass surface materials upon exposure to ultrasonic energy. 26. Battery, characterized by the fact that it comprises: an anode current collector, in which the anode current collector is a first metal tube closed at a first end; an anode, in which the anode chemistry is contained within the first metallic tube; a cathode current collector, where the cathode current collector is a wire; a ceramic termination with a first sealing surface that has a sealing interface with the first metal tube, and a second sealing surface that has a sealing interface with the cathode current collector; a cathode, in which the cathode chemistry is deposited on the cathode current collector; and a sealing material located in a gap between the first Petition 870170067406, of 9/11/2017, p. 203/207 6/8 sealing surface and the first metal tube. 27. Battery, characterized by the fact that it comprises: an anode current collector, in which the anode current collector is a first semiconductor tube, closed at the first end and doped at the first end; an anode, in which the anode chemistry is contained within the first semiconductor tube; a cathode current collector, wherein the cathode current collector is a second semiconductor tube closed at a second end and doped at the second end; a cathode, in which the cathode chemistry is deposited on the cathode current collector; and a sealing material located in a gap between the first semiconductor tube and the second semiconductor tube. 28. Battery according to claim 27, characterized in that the sealing material located in the gap between the first semiconductor tube and the second semiconductor tube comprises an epoxy based adhesive. 29. Battery according to claim 27, characterized in that the sealing material located in the gap between the first semiconductor tube and the second semiconductor tube comprises a first layer comprising molybdenum and manganese particles, in a mixture with powders ceramic, which is then clad with a metallic film. 30. Battery, according to claim 29, characterized by the fact that the metallic film comprises nickel. 31. Battery according to claim 27, characterized by the fact that the sealing material located in the gap between the first semiconductor tube and the second semiconductor tube comprises a first layer of a metallic film deposited by PVD. Petition 870170067406, of 9/11/2017, p. 204/207 7/8 32. Battery, according to claim 31, characterized by the fact that the metallic film comprises titanium. 33. Battery, according to claim 32, characterized by the fact that a noble metallic film is additionally deposited on the metallic film deposited by PVD. 34. Battery according to claim 27, characterized in that the sealing material located in the gap between the first semiconductor tube and the second semiconductor tube comprises a plurality of thin layers of metallic films, wherein a first thin layer of metallic film is deposited on a second layer of metallic film, in which the first thin layer of metallic film is chemically reactive with the second layer of metallic film, releasing energy to rapidly heat the layers, and in which the chemical reaction is activated by a energetic pulse of energy. 35. Battery, according to claim 34, characterized by the fact that the energetic pulse comprises photons. 36. Battery, according to claim 34, characterized by the fact that the energetic pulse comprises electrons. 37. Battery according to claim 34, characterized by the fact that the energy pulse comprises thermal energy. 38. Battery, according to claim 27, characterized by the fact that the sealing material located in the gap between the first semiconductor tube and the second semiconductor tube comprises a conventional welding alloy base with a titanium addition, in which the titanium reacts with the surface materials of the first semiconductor tube and the second semiconductor tube, upon exposure to ultrasonic energy. 39. Method for making a battery, characterized by the fact that it comprises: Petition 870170067406, of 9/11/2017, p. 205/207 8/8 obtain a cathode collecting tube; loading the cathode collecting tube with cathode chemicals; obtain an anode collecting tube; load the anode collecting tube with anode chemicals; obtain a ceramic insulating piece in the form of a tube; forming a first and a second sealing surface at each end of the tube-shaped ceramic insulating part; evaporating a metallic film on the first and second sealing surfaces; cover the end of the cathode collection tube with a piece of Nanofoil; apply the metallic film as a coating on the first and second sealing surfaces with a paste solder; position the cathode collecting tube on the first sealing surface; activate the Nanofoil to cause a rapid increase in temperature at an interface between the cathode collecting tube and the first sealing surface, and melt the solder paste. Petition 870170067406, of 9/11/2017, p. 206/207 1/15 100