GB2588943A

GB2588943A - Method of manufacturing a thin crystalline layer of material on a surface

Info

Publication number: GB2588943A
Application number: GB1916631.3A
Authority: GB
Inventors: Edward Rendall Michael; Ian Joseph Gruar Robert
Original assignee: Dyson Technology Ltd
Current assignee: Dyson Technology Ltd
Priority date: 2019-11-15
Filing date: 2019-11-15
Publication date: 2021-05-19
Also published as: GB201916631D0; WO2021094769A1

Abstract

A method of manufacturing a crystalline layer of material on a surface comprises generating a sputter plasma B remote from at least one sputter target 104 and depositing the sputtered material on a surface 128 to form a crystalline layer, wherein the surface has a roughness of 100 nm or less, and the crystalline layer has a thickness of between 0.01 and 10 microns and a surface roughness of no more than between one and two times the surface roughness of the surface on which it is deposited. The substrate preferably comprises a polymer material and may comprise embedded particles. The method preferably comprises a step of unrolling the substrate from a roll of material. A method of manufacturing an electronic component, preferably an energy storage device or a cell of a battery, comprises performing the method of the invention to form a multilayer sheet of different materials, wherein at least one of the layers is a conducting, semiconducting or dielectric material.

Description

Method of manufacturing a thin crystalline layer of material on a surface

Background of the Invention

[0001] The present invention concerns a method of manufacturing a layer of crystalline material on a surface. More particularly, but not exclusively, this invention concerns making a relatively thin crystalline layer using a plasma deposition process on a relatively thin substrate.

[0002] Many technologies rely on layers of crystalline material to be formed on a thin substrate for the end product to have a given size or mass (i.e. when the substrate forms a part of the end-product). It may therefore be desirable to have a substrate that is as thin as possible. When forming a fine layer of crystalline material on a substrate using a method of sputtering material from a target, a large amount of energy may typically be required in order to form the desired crystal structure. This energy is often supplied as heat, either in the form of preheating the substrate, or in the form of an annealing step provided after the film is deposited.

[0003] Additionally, certain processes provide for the modulation of ad atom arrival energy. A substrate may therefore need to be of a certain thickness or chemical composition to not deteriorate as a result of thermal loading at the surface of the substrate. At thicknesses 25 microns or less substrate materials made from polymer material such as PET tend to suffer from deformation and wrinkling, and are otherwise difficult to handle as a result of the increasing significance of surface forces/electrostatic forces in relation to the mass of material present. In order to improve material properties, insofar as handling thin film polymer material is concerned, it is known to add particles to the material. Such particles are typically embedded, at least to some extent, within the bulk of the polymer material.

[0004] The inventors have been exploring the possibility of forming a layer of crystalline material on a substrate without a subsequent annealing step. This could open up the possibility of using thin substrates, for example of polymer material, having a thickness of no more than 100p.m (for example around lOpm or less), and potentially down to thickness being of the order of lum thickness or lower. The thickness of crystalline material formed on such a thin substrate may have a comparable thickness, for example being of the order of 100pm (for example around lOpm or less), and potentially down to thicknesses at the sub-pm scale. At such thicknesses, the inventors have encountered significant difficulties in forming ordered crystalline material with sufficiently good structural properties to allow for commercial applications. In order to form crystalline material on a substrate there is typically a need for there to be sufficient energy available in order for crystals to form. Annealing of material is often required. There is therefore a conflicting requirement of balancing the need of sufficient energy to form crystalline material of the desired quality and the need to avoid Delamination of crystalline material from the overheating the substrate material substrate is a further issue.

[0005] The present invention seeks to mitigate one or more of the above-mentioned problems. Alternatively or additionally, the present invention seeks to provide an improved method of manufacturing a layer of crystalline material on a substrate.

Summary of the Invention

[0006] The present invention provides, according to a first aspect, a method of manufacturing a layer of crystalline material on a substrate using a sputter deposition technique to deposit material directly onto a surface of or supported by the substrate to form a first crystalline layer, preferably having a thickness of from 0.01 to I Ottm. The surface of the substrate preferably has a surface roughness of Xs or less, where Xs = 100 nm. The surface of the substrate may have a surface roughness of greater than 1% of Xs, for example greater than 5% of Xs.

[0007] It has been found that the roughness of the surface of the substrate is an important factor in manufacturing products incorporating a thin layer of crystalline material on the substrate. Ensuring that the surface of the substrate is extremely smooth has produced surprisingly good results. Conversely, when the surface of the substrate is relatively rough there is a surprisingly profound effect on the likelihood of delaminati on of the layer of crystalline material from the substrate. If the surface of the substrate is too smooth however the substrate can become too difficult to handle and process. The method is able to produce good results, particularly when the first crystalline layer has a thickness of from 50nm to 10µm, including for example the range from 100nm to 5pm.

[0008] In some cases the first crystalline layer may have a thickness of 500nm or more. The method may be used to form the crystalline layer having a surface roughness of no -3 -more than Xi, where Xi equals the product of F and Xs. and where F is a factor from 1.0 to 2.0.

[0009] Some applications that utilise thin film crystalline layers may require or otherwise benefit from the surface of the crystalline material being smooth. A relatively rough layer may have an adverse impact on the function or performance of the crystalline layer and/or may cause mechanical/structural issues with the formation of other layers in a multi-layer product. As increased risk of delamination may be an issue for example. A deposited layer having a surface roughness of more than twice the surface roughness of the supporting substrate, particularly when the substrate has a surface roughness of close to or greater than 100nm, may be undesirable for many applications of thin layer crystalline films. The surface roughness of the substrate has been found to have a surprisingly large impact on the quality of the thin layer films being deposited thereon.

[0010] The material deposited may include material from one or more sputter targets. [0011] It may be that the substrate forms a part of an end product. In such a case, it is preferred that the substrate is relatively thin. In such a case it is preferred that the substrate has a thickness of less than lOpm, optionally less than 5pm and possibly 1µm or less. There is a lower limit on how thin the substrate can be before its mechanical strength and other physical properties make it unsuitable for use. The lower limit depends on various factors, but typically the substrate will be at least 500nm thick and possibly 1pm or thicker. It may be that Xs is no more than 10 % of the thickness of the substrate. It may be that Xs is no more than 10 % of the thickness of the first crystalline layer. For very thin crystalline layers, from say lOnm to 100nm thick, it may be that Xs is no more than 50 % of the thickness of the first crystalline layer. For crystalline layers, with a thickness of from 100nm to 1p.m thick, it may be that Xs is no more than 10 % of the thickness of the first crystalline layer.

[0012] Particularly in applications where the substrate is stored in layers that are in contact with each other, for example then the substrate is an elongate film supplied on a drum or roller, it may be that the roughness surface needed for easing handling decreases as the thickness of the substrate increases. For thick films, the minimum roughness required may be lower than for very thin films. It may be the case that the product of the thickness of the substrate and Xs (i.e. the thickness of the substrate multiplied by Xs) is no more than 105 nm2. Preferably, the product of the thickness of the substrate and Xs is no more than 5 x 104 nm2.

[0013] The surface roughness may be measured by a profilometer. The surface roughness may be measured by means of calculating the RMS roughness. The RMS roughness may be calculated as the deviation in height from a perfectly smooth external surface. It will be understood that a perfectly smooth external surface is perfectly flat when the mid-plane of the substrate is transformed onto a flat plane. The surface roughness may be measured by means of calculating the arithmetic average of the absolute values of profile heights (above the minimum height measured) over an evaluation length of a sample.

[0014] The surface onto which material is deposited may be a surface of the substrate itself The surface onto which material is deposited may be a surface of an intermediate layer on top of the substrate, such an intermediate layer possibly being formed directly onto the substrate. Such an intermediate layer may for example comprise a metal layer, preferably having a conductivity greater than or equal to that of selenium.

[0015] The substrate may be provided as a film. The substrate may be carried by a carrier device, for example of glass. In such case, the substrate and material deposited thereon may be removed or released from the carrier after one or more layer(s) of material are deposited on the substrate.

[0016] The substrate may comprise or be in the form of a semiconductor wafers, plastic film, metal foil, thin glass, mica or a poly imide material. The substrate may be a polymer material. The substrate may be a thin film of polymer material. The substrate may comprises polyethylene terephthalate (PET), or polyethylene naphthalate (PEN). PEN and PET are reasonably flexible, and relatively high tensile strength due to their semi-crystalline structure.

[0017] The polymer material may be provided with embedded particles within or on the surface of polymer material, the majority of those that contribute to surface roughness of the substrate optionally having a median size of from 10% to 125% of Xs. Such particles may be provided to prevent or reduce the polymer material sticking to itself during processing, for example as a result of electrostatic forces. The size of the embedded particles is therefore optionally roughly of the same size or less than the desired roughness, allowing the particles to be at or very close to the boundary of the substrate bulk material which forms the outer surface of the substrate. -5 -

[0018] The polymer material may be provided with embedded particles and of all of the embedded particles within or on the polymer material, the majority of those that contribute to surface roughness of the substrate optionally having a median size of greater than 150% of Xs. It may be that the size of embedded particle representing the 95th centile is no more than 150% of Xs.

[0019] The size of a particle in this context may be the largest distance from one side of the particle to the opposite side as measured in the direction through the thickness of the substrate. For spherical or near spherical particles this may be approximated to the mean diameter of the particles.

[0020] The majority of the embedded particles may have a shape that is generally spherical. The majority of the embedded particles may have a shape that is generally plate-like. The longest dimension of the embedded particles may be more than twice and possibly more than three times the shortest dimension. The majority of the embedded particles may have a shape that is generally rod-like.

[0021] The material of the embedded particles may be a silica oxide. The material of the embedded particles may be silicon dioxide. The material of the embedded particles may be polystyrene. The material of the embedded particles may be calcium carbonate. The material of the embedded particles may be a ceramic, such as for example aluminium silicate or magnesium silicate. The material of the embedded particles may be diamond. The material of the embedded particles may be titanium dioxide. The material of the embedded particles may be PTFE.

[0022] The method may comprise depositing sputtered material on a first portion of substrate, thereby forming crystalline material on the first portion of the substrate. The method may also comprise subsequently moving the substrate, and depositing sputtered material on a second portion of substrate, thereby forming crystalline material on the second portion of the substrate. The substrate may be stationary for some of the time during which material is deposited onto it.

[0023] At least one of the substrate and the target may be moving as crystalline layer is being formed on the surface of or supported by the substrate. For example, the substrate may be continuously moving while material is being deposited onto it. The substrate may be moving relative to the target when the crystalline layer is formed on the substrate. The target(s) may additionally move. The target(s) may move slower than the substrate, so that the substrate also moves relative to the target(s). -6 -

[0024] The substrate may comprise, or be in the form of, a sheet, optionally an elongate sheet. Such a sheet may be provided in the form of a roll. This facilitates simple storage and handling of the substrate. The substrate may comprise, or be in the form of, a sheet, optionally an elongate sheet. Such a sheet may be provided in the form of a roll. This facilitates simple storage and handling of the substrate. Alternatively, the substrate may be supplied in discrete sheets that are handled and stored in relatively flat sheets. The substrate may be planar in shape as the material is deposited thereon. This may be the case, when the substrate is provided in the form of discrete sheets, not being transferred to or from a roll. The sheets may each be mounted on a carrier, having greater structural rigidity. This may allow for thinner substrates to be used than in the case of substrate film held on a roller.

[0025] The substrate may be movably mounted to facilitate movement of the substrate (optionally in the form of a sheet). The substrate may be mounted in a roll-to-roll arrangement. Substrate upstream of the plasma deposition process may be held on a roller or drum. Substrate downstream of the plasma deposition process may be held on a roller or drum. This facilitates simple and rapid handling of flexible sheets of substrate. A shutter may be provided to allow for a portion of the substrate to be exposed to the remotely generated plasma.

[0026] The plasma deposition process optionally takes place in a chamber. An upstream drum or roller for carrying the substrate may be located inside or outside the chamber. A downstream drum or roller for carrying the substrate may be located inside or outside the chamber.

[0027] The use of a roll-to-roll arrangement has a number of potential benefits. It facilitates a high material throughput and allows a large cathode area to be deposited on one large substrate, though a series of depositions at a first portion of the substrate, followed by a second portion of the substrate, and so on. One of the main benefits of a roll-to-roll processing is that it may allow for a number of depositions to occur without breaking vacuum. This saves both time and energy compared to systems in which the chamber needs to be taken to back up to atmospheric pressure from vacuum after deposition, in order to load a new substrate.

[0028] There may be a step of unrolling the substrate from a roll of material. There may be a step of conveying the substrate to a location at which the step of depositing material onto the substrate is performed. The substrate held under tension, preferably -7 -at least at the location at which material is deposited onto the surface of the substrate by the sputter deposition. The tension may be greater than 10N.

[0029] Remote plasma -particularly plasma for forming crystalline layer in situ [0030] Embodiments of the present invention include a step of generating a plasma, remote from a sputter target or targets, suitable for plasma sputtering and may be considered as utilising a remote plasma system. In a remote plasma system, the plasma is generated remotely from, and independently of, the sputter target(s). In conventional plasma deposition, it is the biasing of the target(s) which both generate and sustain the plasma. In a remote plasma deposition system, the plasma is generated elsewhere, and then confined to the targets by various electronic and or magnetic fields.

[00311 Embodiments of the invention can be used to manufacture crystalline material in situ on the surface of or supported by the substrate. It may for example be that the step of using the sputter deposition technique to deposit material directly onto the substrate is performed such that crystalline material is formed in situ as the material is deposited.

[0032] Such crystalline material may comprise lithium ions and have a structure which provides excellent lithium ion mobility and thus suitable for forming cathode material for energy cells in lithium ion batteries for example. (While mention is made of batteries herein, it will be understood that the invention may have application in other products or devices which might benefit from the use or inclusion of crystalline material, for example on thin film substrates).

[0033] Thus, with embodiments of the invention, it is possible to form crystalline films, for example of LiCo02, directly onto substrates. In "directly", what is meant is that the film forms a crystalline film with substantially no annealing step. The method has been shown to work on a wide range of substrate materials. For example, by careful control of temperature (i.e. not exceeding certain temperatures locally), a thin film polymer substrate can be used to form such crystalline forms thereon without damaging or deforming the substrate.

[0034] The plasma preferably comprises argon ions. A remotely generated plasma allows for control of plasma energy independently of the target(s) of the system. High energy plasma can be generated, contained and controlled without interaction with a target, in contrast with prior art techniques which generate the plasma via target biasing. Sputtering may be achieved by applying a negative, accelerating voltage to the target -8 - (referred to herein alternatively as "bias power"), which accelerates plasma ions towards and into the target, generating energised ions to sputter from the target. The sputter threshold (the plasma energy at which sputtering starts) depends on the target material and the plasma energy. In general terms, the bias power applied dictates the accelerating field for ions in the plasma and hence their bombardment energy and therefore the amount/rate of material sputtered. The biasing of the target(s) allows for control of the rate of sputtering.

[0035] Thus, the use of remotely generated plasma separates the plasma generation process and the rate of sputtering, allowing the kinetic energy of the sputtered material and the rate of sputtering to be finely controlled.

[0036] The deposited material is crystalline. At least a portion of and optionally all of the deposited material may have a hexagonal crystal structure. At least a portion of and optionally all the deposited material may have a crystalline "layered oxide" structure. Such "layered oxide" structures are important when manufacturing solid-state batteries. A layered oxide structure allows for lithium ions to more easily de-intercalate from the crystal structure, resulting in a faster charging, higher capacity solid-state battery. It will be understood that intercalation refers to a property of a material that allows ions to readily move in and out of the material without the material changing its phase (chemical and crystalline structure). For example, a solid-state intercalation film remains in a solid state during discharging and charging of an energy-storage device. [0037] The crystalline material formed on the surface may comprise a metal (for example an alkali metal such as lithium), at least one different metal and at least one counter-ion. The crystalline material may be in the form of a layered oxide structure (or framework), defined by the formula ABO2, where A is lithium for example, B is the different metal and the oxide is formed from said at least one counter-ion. The different metal ("B") may be one or more redox active transition metals, one or more transition metals or a mixture thereof Elemental metals in the so called "post-transition metals" group such as aluminium, can also be incorporated into layered oxide frameworks. The different metal may comprise one or more of Fe, Co, Mn, Ni, Ti, Nb, Al, and V. Cobalt is a preferred choice, for example producing crystalline LiCoO2 [0038] In the case where the material deposited is LiCoO2, the material is optionally deposited with a hexagonal and/or rhombohedral lattice structure, optionally having a form which is in the R3m space group (also referred to as the "R 3(bar) 2/m" space -9 -group or space group 166). This structure has a number of benefits, particularly when the LiCoO2 material is being used as the cathode of an energy cell or battery, such as having a relatively greater accessible capacity and high rate of charging and discharging compared to the low energy structure of LiCoO2, which has a structure in the Fd3m space group (a face centred cubic structure). The R3m space group is regarded as having better performance in typical battery applications due to enhanced reversibility and fewer structural changes on lithium intercalation and de-intercalation. Therefore crystalline LiCoO2 in the R7m space group is favoured for solid state battery applications.

[0039] During performance of the method, crystalline material may grow substantially epitaxially from the surface on or supported by the substrate. Epitaxial growth is favoured, particularly when the crystalline material is being used for electrical devices, as it allows for ions to intercalate and de-intercalate more easily. The crystals of the crystalline material are optionally aligned with the (101) and (110) planes substantially parallel to the substrate. This may be beneficial as it means that the ion channels of a thin film crystalline material are orientated perpendicular to the substrate, making for easier intercalation and de-intercalation of the ions. With a lithium ion battery for example, this can improve the working capacity and the speed of charging of the battery.

[0040] Embodiments of the invention may be used to deposit crystalline I material of the general formula LiaNI1bNI2c02, wherein the amount of Lithium, "a" is from 0.5 to 1.5 (optionally 1), NI1 is one or more transition metals (optionally one or more of cobalt, iron, nickel, niobium, manganese, titanium, and vanadium), b being the total of transition metal, and M2 is, for example, aluminium, with c being the total of M2 (optionally zero). Optionally, a is 1, b is 1, and c is O. Optionally, M1 is one of cobalt, nickel, vanadium, niobium and manganese.

[0041] Optionally, a is more than 1-such materials are sometimes known as "lithium-zi 0, rich" materials. Such lithium-rich materials may be -with x = 0, 0.06, 0.12, 0.2, 0.3 and 0.4, for example.

[0042] Another such material is wherein y has a value greater than 0.12 and equal to or less than 0.4.

[0043] Another such material is,wherein x has a value equal to or greater than 0.175 and equal to or less than 0.325; and y has a value equal to or greater than 0.05 and equal to or less than 0.35.

[0044] is another such material, wherein x is equal to or greater than 0 and equal to or less than 0.4; y is equal to or greater than 0.1 and equal to or less than 0.4; and z is equal to or greater than 0.02 and equal to or less than 0.3.

[0045] The first crystalline layer may comprise, and optionally be formed of, LiCoO2. LiCoO2 is a material suitable for use as cathode material in batteries for example. [0046] The thickness of the deposited LiCoO2 on completion of the method is optionally no more than 1.0 micron.

[0047] There may be a step of depositing material directly onto the substrate using sputter deposition to form a second layer. The second layer may have a thickness of from 0.01 to lOpm. The second layer may have a thickness of between 20% and 500% of the thickness of the first layer, and optionally between 40% and 250% of the thickness of the first layer. The second layer may have a surface roughness of no more than 200% of Xs, and optionally no more than 150% of Xs. The material composition of the first layer may be different from the material composition of the second layer. At least part of the second layer is optionally deposited upon the first layer.

[0048] The second layer of material may comprise, and optionally be formed of UPON. LiPON is a material suitable for use as electrolyte material in batteries for example.

[0049] The method may include a step of depositing material onto the substrate to form a third layer. The material composition of the third layer is preferably different from the material composition of the second layer. The third layer may be made from material that is suitable for use as an anode in a battery. At least part of the third layer may be deposited upon the second layer.

[0050] There may be a current collector layer between the substrate and the first layer of crystalline material. Such a current collector layer may be considered as being part of the substrate in some embodiments.

[0051] Material may be deposited simultaneously, on opposite sides of the substrate.

[0052] There may be further layers of material deposited under, between or on top of the above-mentioned first, second and/or third layers.

[0053] The method of depositing one or more of the layers onto the substrate, whether directly or indirectly, may comprise providing target material for sputtering and also generating a plasma remote from such target material. The method may comprise exposing such target material to the plasma to generate sputtered material therefrom. [0054] There may be one or more targets. There may be a target which comprises Lithium. There may be a target (optionally the same target) which comprises at least one different metal. There may be a target which comprises at least two different chemical elements and optionally three different chemical elements. There may be one or more targets which comprise a distinct region of elemental material, for example elemental lithium or elemental cobalt. A "distinct region" can mean either its own target, or an area of a target. There may be a composite target body comprises multiple distinct regions of different materials.

[0055] The surface of the target which faces the substrate may be planar. In some embodiments the surface of the target may be curved, for example being either convex or concave.

[0056] Particularly in the case where the substrate is moved during the sputter deposition process, the substrate may be held under tension. It is preferred of course that the substrate does not exceed its temperature corrected yield strength at any point as it moves during the sputter deposition process. As the polymer heats up, its yield strength may begin to lower. Also, if the polymer increases in temperature too much, the polymer may begin to deform. This can lead to buckles, jams, and/or uneven deposition onto the substrate.

[0057] It may be that the temperature of the substrate does not exceed 500 degrees Celsius at any point during the plasma deposition process, and optionally does not exceed 200 degrees Celsius.

[0058] It may be that the step of using the sputter deposition technique to deposit material onto the substrate is performed at temperatures such that the maximum temperature reached at any given time by any given square of substrate material having an area of 1 cm2 as measured on the surface opposite to said surface on which the material is deposited and as averaged over a period of 1 second, may be no more than -12 - 500°C, optionally no more than 300°C, optionally no more than 200°C, optionally no more than 150°C, optionally no more than 120°C and optionally no more than 100°C. [0059] The step of depositing material directly onto the substrate may be performed at a deposition rate of from 1 nm to 10000 nm per second, optionally from 5 nm to 500 nm per second, optionally 10 nm to 100 nm per second, and possibly no less than 10 nm per second.

[0060] The ratio of the power used to generate the plasma to the power associated with the bias on the target may be greater than or equal to 1:1, optionally less than or equal to 7:2 and is optionally less than or equal to 3:2. The applicant has discovered that such power ratios may be beneficial in depositing crystalline materials without the need to anneal the material so deposited.

[0061] The actual power in the plasma may be less than the power used to generate the plasma. In this connection, the efficiency of the generation of the plasma ([actual power in the plasma/power used to generate the plasma] x 100) may typically be from 50% to 85%, typically about 50%.

[0062] The method may also optionally comprise the sputtering of material under a reactive sputtering regime, using oxygen or nitrogen as a reactive gas.

[0063] In a reactive sputtering method, a reactive gas is introduced into the process, along with an inert sputter gas. The inert sputter gas may be Argon. This allows elemental targets to be used, and oxides to form as part of the plasma sputtering process. Generally, the structure and form of the oxide produced may be adjusted, by providing the reactive oxygen gas at a higher or lower flow rate.

[0064] It may be that electron density distribution of the plasma is relatively uniform for different cross-sections taken across it volume. The plasma may be constrained to have a certain overall shape that has a width and/or length much greater than its thickness. The width and length of the plasma cloud may each be at least five times greater than the thickness. The plasma may have a width which is aligned with the width of the substrate. There may be a pair of antennae on opposing sides of plasma separated by distance L (the lengthwise direction of the plasma) each having length, W (the widthwise direction of the plasma). The thickness of plasma may be defined either by the maximum extent of the glow in visible spectrum or the largest distance as measured in the direction perpendicular to both L and W which covers 90% of the free electrons in the plasma.

-13 - [0065] The generating of plasma may be performed by at least one antenna extending in a direction parallel to the width of the substrate. There are preferably a pair of such antennae. Preferably the or each antenna extends across the majority of the width of, possibly at least substantially the entire width of, the substrate.

[0066] Magnetic and/or electrostatic fields may be used to contain and shape the plasma, for example so as to be close to the target and to extend and propagate between the target and the substrate.

[0067] The magnetic and/or electrostatic fields may contain and shape the plasma by propagating the plasma in a direction transverse to the width of the substrate.

[0068] The method preferably comprises containing and shaping the plasma using magnetic and/or electrostatic fields so that the shape of the electron density distribution of the plasma forms a blanket of plasma (i.e. one, not necessarily planar in shape but with a thickness that does not vary significantly along at least one of the width and the length of the blanket). The plasma may be shaped to form a blanket of plasma that extends in a direction along the width of the substrate and in a direction along the length of the substrate.

[0069] The working distance between at least one of the sputter target(s) and the substrate may be within +1-50% of the theoretical mean free path of the system.

[0070] Without wishing to be bound by theory, it is believed that the working distance has an influence on the "ad atom" energy of the sputtered material as it deposits onto the substrate. In a case where the working distance is greater than the mean free path of the system, it is thought that it is more likely that an ion in the sputter flux would be involved in a collision before reaching the substrate, resulting in relatively low ad atom energy. Conversely, if the working distance is shorter than the mean free path of the system, the ad atom energy is relatively high. The separation of a target from the substrate may be used as an additional control over rate of the material deposited. [0071] A definition of the mean free path is the average distance between collisions for an ion in the plasma. The mean free path is calculated based on the volume of interaction (varied by the working distance), and the number of molecules per unit volume (varied by the working pressure).

[0072] The working distance is optionally at least 3.0cm, optionally at least 4.0cm and optionally 5.0cm. The working distance is optionally no more than 20cm, optionally no more than 15cm and optionally no more than 13cm. The working distance may be from -14 - 4.0cm to 13cm, optionally from 6.0cm to 10cm, and optionally from 8.0cm to 9.0cm. It may be that the working distance between the target and the substrate is from 5cm to 20cm.

[0073] The working pressure may be from 0.00065 mBar to 0.010 mBar, optionally from 0.001 to 0.007mBar. A higher working pressure in this range may result in a higher deposition rate. This is because a higher working pressure results in a larger number of process ion (usually Ar+) bombardments on the surface of the target, and hence material is sputtered from the target at a higher rate.

[0074] When the working distance is from 8.0 to 9.0 cm, the range of crystallite sizes available may be narrower, for example, if a working pressure of from 0.0010 mBar to 0.0065 mBar is used. The crystallite size may be from 14 to 25 nm. This is evidence that within these parameter ranges, it is possible to form films with narrow and predictable thin film ranges.

[0075] It may be that the substrate is retained as a part of the electronic product.

[0076] It may be that the substrate is a sacrificial substrate. It may be that the substrate is removed before the layer(s) of material. Part or all of the substrate may be removed before integrating the crystalline layer or a part thereof in an electronic product package or other end product.. For example, the layer of crystalline material may be lifted off from the substrate. There may be a layer of other intervening material between the base substrate and the crystalline material. This layer may lift off with the crystalline material or assist in the separation of the crystalline material from the base substrate. A laser-based lift-off technique may be used. The substrate may be removed by a process that utilises laser ablation.

[0077] Similar techniques are described in the prior art. For example, K R20130029488 describes a method of making a battery including using a sacrificial substrate and laser radiation to harvest a battery layer.

[0078] According to a further aspect of the invention there is provided a method of manufacturing a layer of crystalline material on a surface, wherein the method comprises using a sputter deposition technique to deposit material directly onto a surface of or supported by a polymer substrate film, preferably having a thickness of from 0.5 to 10um, the polymer substrate film comprising embedded particles, to form a first crystalline layer, such that crystalline material is formed in situ as the material is deposited. Said surface preferably has a surface roughness of no more than 50 nm.

Said first crystalline layer may have a thickness of from 0.01 pm to 10 pm, possibly a thickness of from 0.5 pm to 10 pm. The step of using the sputter deposition technique to deposit material onto the substrate is preferably performed such that the maximum temperature reached at any given time by any given square of substrate material having an area of I cm' as measured on the surface opposite to said surface on which the material is deposited and as averaged over a period of I second, may be no more than 500°C, optionally no more than 300°C, optionally no more than 200°C, optionally no more than 150°C, optionally no more than 120°C and optionally no more than 100°C According to a yet further aspect of the invention there is provided a method of manufacturing an electronic product comprising performing the deposition method of the invention as described or claimed herein. A multilayer sheet of different materials may thus be made. There may be a step of integrating the multilayer sheet or a part thereof in an electronic product package. It is preferred that at least one of the layers of the sheet is both formed by the step of using a sputter deposition technique and is a conducting, a semiconducting material or a dielectric material. The electronic product may be a battery, an energy storage device, or a cell of battery. The substrate, or optionally a part only thereof, may be retained as a part of the electronic product.

[0079] According to a yet further aspect of the invention there is provided a battery, an energy storage device, or a cell of battery, for example made by the performance of the method of the invention as described or claimed herein. Such a battery may comprise multiple stacked cathode layers, multiple stacked electrolyte layers, and multiple stacked anode layers. At least one (optionally at least three) of the layers in the battery is made by performing the method of the invention as described or claimed herein.

[0080] It will of course be appreciated that features described in relation to one aspect of the present invention may be incorporated into other aspects of the present invention. For example, the method of the invention may incorporate any of the features described with reference to the apparatus of the invention and vice versa.

Description of the Drawings

[0081] Embodiments of the present invention will now be described by way of example only with reference to the accompanying schematic drawings which can be briefly summarised as follows.

Figure 1 a is a schematic side-on view of a plasma deposition chamber used in accordance with a first example; Figure lb shows the steps of a method of manufacturing a battery cathode in accordance with the first example; Figures lc to lh are schematic illustrations of various polymer substrate materials in cross-section; Figure 2a is a schematic side-on view of a plasma deposition chamber used in accordance with a second example method; Figure 2b is an X-ray diffraction (XRD) spectra of a first sample of a battery cathode made in accordance with the method of the second example; Figure 2c is a Raman spectra of a battery cathode from which the XRD data of Figure 2b are obtained; Figure 2d is an XRD spectra of a second sample of a battery cathode made in accordance with a method of the second example; Figure 2e is a Raman spectra of the battery cathode from which the XRD data of Figure 2d are obtained; Figure 3a is a schematic side view of a plasma deposition chamber used in a method in accordance with a third example; Figure 3b is a schematic plan view of the plasma deposition chamber shown in Figure 3a; Figure 3c is a further schematic side view of the plasma deposition chamber shown in Figures 3a and 3b; Figure 3d is a graph comparing sputter yields of cobalt and lithium as a function of energy; Figure 3e is a schematic side view of a plasma deposition chamber used in a method in accordance with a fourth example; Figure 4a is a cross-sectional scanning electron micrograph of a battery cathode relating to a first sample made using in accordance with the method of the second example; Figure 4b is a birds-eye view of a scanning electron micrograph of a battery cathode relating to a second sample made in accordance with the method of the second example; Figure 5a is a schematic cross-section through a battery cathode relating to a first sample made using a method of a fifth example; Figure 5b is a schematic cross-section through a battery cathode relating to a second sample made using the method of the fifth example; Figure 5c shows the steps of a method of manufacturing a battery cathodic half-cell in accordance with the fifth example; Figure 6 is a schematic representation of an example of a method of making a battery cell in accordance with a sixth example; Figure 7a is a schematic representation of an example of a method of manufacturing a solid-state thin film battery in accordance with a seventh example; Figure 7b is a schematic cross-section through a solid-state thin film battery in accordance with a first sample of the seventh example; Figure 7c is a schematic cross-section through a sample solid state thin film battery made in accordance with a second sample of the seventh example; Figure 8a is a schematic representation of a method of determining an optimum working distance for a remote plasma deposition system configured for the deposition of layered oxide materials in accordance with an eighth example; Figure 8b shows a number of X-Ray diffraction spectra collected as part of the method of Figure 8a, where the characterisation technique is X-Ray diffraction and the characteristic feature is a characteristic X-Ray diffraction peak associated with a layered oxide structure; Figure 9a is a micrograph of a sample film formed in accordance with the first example of the invention,; Figure 9b is an X-ray diffraction spectra obtained from the film shown in Figure 9a; Figure 10a a schematic representation of an example of a method of determining an optimum working pressure for a remote plasma deposition system configured for the deposition of layered oxide materials in accordance with a ninth example; Figure 106 shows two X-Ray diffraction spectra collected as part of the method as described with reference to Figure 10a, where the characterisation technique is X-Ray diffraction and the characteristic feature is a characteristic X-Ray diffraction peak associated with a layered oxide structure; Figure 1 la is an example of the steps of a method of determining the crystallite size of layered oxide materials in accordance with a tenth example; Figure 1 lb is a graph showing how to determine the crystallite size at different working pressures in accordance with the tenth example, for a working distance of 16 cm, showing the crystallite size for a number of films deposited in accordance with the first example; Figure 1 lc is a graph showing how to determine the crystallite size at different working pressures in accordance with the tenth example, for a working distance of 8.5 cm, the crystallite size for a number of films deposited in accordance with the first example; Figure 12 is a schematic representation of a method of depositing a material on a substrate in accordance with an eleventh example of the invention; Figure 13 is a schematic representation of an example of a method of manufacturing a component for an electronic device in accordance with a twelfth example; Figure 14 is a schematic representation of an example of a method of manufacturing a component for an electronic device, in accordance with the thirteenth example of the invention; Figure 15 is a schematic representation of an example of a method of manufacturing a Light Emitting Diode (LED) in accordance with a fourteenth example of the invention; Figure 16 is a schematic representation of an example of a method of manufacturing a permanent magnet in accordance with a fifteenth example of the invention; and Figure 17 is a schematic representation of an example of a method of manufacturing an electronic device comprising a layer of Indium Tin Oxide (ITO) in accordance with a sixteenth example of the invention.

Detailed Description

[0082] Figure la is a schematic side-on view of a plasma deposition process apparatus which is used in a method of depositing a (crystalline) material onto a substrate in accordance with a first example. The method is denoted generally by reference numeral 1001 and is shown schematically in Figure lb, and comprises generating 1002 a plasma remote from one or more targets, exposing 1003 the plasma target or targets to the plasma such that target material is sputtered from one or more targets, and exposing 1004 a first portion of a substrate to sputtered material such that the sputtered material is deposited onto the first portion of the substrate, thereby forming crystalline material onto the first portion of the substrate. The method of depositing a (crystalline) material onto the substrate may be performed as a part of a method of manufacturing a battery cathode.

[0083] The crystalline material in this example takes the form ABO2. In the present example, the ABO2 material takes a layered oxide structure. In the present example, the ABO2 material is LiCo02. However, the method of the present example has been shown to work on a wide range of ABO2 materials. In other examples, the ABO2 material structure comprises at least one of the following compounds (described here with nonspecific stoichiometry): LiCoO, LiCoAIO, LiNiCoA10, LiMnO, Li Ni MnO, LiNiMnCoO, LiNiO and LiNiCoO. These materials are potential candidates for manufacturing a battery cathode. Those skilled in the art will realise that the stoichiometry may be varied.

[0084] In this example, the ABO2 material is LiCoO2 and is deposited as a layer that is approximately 1 micron thick. In other examples, the ABO2 material is deposited as layer that is approximately 5 microns thick. In yet further examples, the ABO2 material is deposited as a layer that is approximately 10 microns thick.

[0085] With reference to Figure la, the plasma deposition process apparatus is denoted generally by reference numeral 100 and comprises a plasma target assembly 102 comprising a target 104, a remote plasma generator 106, a series of electromagnets 108 for confining the plasma generated by the remote plasma generator 106, a target power supply 110, a remote plasma source power supply 112 and a housing 114. Remote plasma generator 106 comprises two pairs of radio frequency (RF) antennae 116. Housing 114 comprises a vacuum outlet 120 which is connected to a series of vacuum pumps located outside the chamber so that the chamber 122 defined by housing 114 can be evacuated. Housing 114 is also provided with a gas inlet 124 which may be connected to a gas supply (not shown) for the introduction of one or more gases into the chamber 122. In other examples, the gas inlet 124 may be positioned over the surface of the target assembly 102. As can be seen from Figure la, the plasma is generated remote from the target 104.

[0086] In this example, the target 104 comprises material LiCoO2. Briefly, the chamber 122 is evacuated until a sufficiently low pressure is reached. Power provided by power supply 112 is used to power the remote plasma generator 106 to generate a plasma. Power is applied to the target 104 such that plasma interacts with target 104, causing LiCoO2 to be sputtered from the target 104 and onto the substrate 128. In the present example, the substrate 128 comprises a polymer sheet which is introduced into the housing 114 via inlet 130 and out of the housing 114 via outlet 132. A powered roller 134 is used to help move the substrate 128. The LiCoO2 is deposited onto the substrate 128 as a crystalline (non-amorphous) material.

[0087] The apparatus 100 also comprises a shutter 136, for restricting deposition of sputtered material onto the substrate 128, and an input 138 for cooling the drum. Shutter 136 allows a portion of the substrate 128 to be exposed to the sputtered material.

[0088] As mentioned above, a powered roller 134 is used to help move the substrate 128 into and out of the plasma deposition apparatus 100. Powered roller 134 is part of a roll-to-roll substrate handling apparatus (not shown) which comprises at least a first storage roller upstream of the plasma deposition apparatus 100 and a second storage roller downstream of the plasma deposition apparatus 100. The roll-to-roll substrate handling apparatus is a convenient way of handling, storing and moving thin, flexible substrates such as the polymer substrate used in this example. Such a roll-to-roll system has a number of other advantages. It allows for a high material throughput and allows a large cathode area to be deposited on one substrate, throughout a series of depositions at a first portion of the substrate, followed by a second portion of the substrate, and so on. Furthermore, such roll-to-roll processing allows for a number of depositions to occur without breaking vacuum. This saves both time and energy compared to systems in which the chamber needs to be taken back up to atmospheric pressure from vacuum after deposition in order to load a new substrate. In other examples, sheet-to-sheet processing is used instead of roll-to-roll processing, wherein the substrate is provided with a support. Alternatively, the substrate may be supplied in discrete sheets that are handled and stored in relatively flat sheets. The substrate may be planar in shape as the material is deposited thereon. This may be the case, when the substrate is provided in the form of discrete sheets, not being transferred to or from a roll. The sheets may each be mounted on a carrier, having greater structural rigidity. This may allow for thinner substrates to be used than in the case of substrate film held on a roller. It may be that the substrate is a sacrificial substrate. It may be that the substrate is removed before the layer(s) of material. Part or all of the substrate may be removed before integrating the crystalline layer or a part thereof in an electronic product package, component or other end product. For example, the layer of crystalline material may be lifted off from the substrate. There may be a layer of other intervening material between the base substrate and the crystalline material. This layer may lift off with the crystalline material or assist in the separation of the crystalline material from the base substrate. A laser-based liftoff technique may be used. The substrate may be removed by a process that utilises laser ablation.

[0089] Similar techniques are described in the prior art. For example, KR20130029488 describes a method of making a battery including using a sacrificial substrate and laser radiation to harvest a battery layer. In other examples, another suitable processing regime is used, provided it is capable of sufficiently high production throughput.

[0090] The polymer substrate 128 is under tension when moving through the system, for example withstanding a tension of at least 0.001N during at least part of the processing. The polymer is robust enough such that when the polymer is fed through the roll-to-roll machine, it does not experience deformation under tensile stress. In this example, the polymer is Polyethylene terephthalate (PET), and the substrate 128 has a thickness of 1 micron or less, in examples the thickness is 0.9 microns. The substrate 128 is pre-coated with a current collecting layer, which is made of an inert metal. In this example, the inert metal used as the current collecting layer is platinum. The yield strength of the PET film is sufficiently strong that the substrate does not yield or plastically deform under the stresses of the roll-to-roll handling apparatus. The inert metal used in other examples can alternatively be gold, iridium, copper, aluminium or nickel.

-22 - [0091] The use of such thin polymer substrates is beneficial because this facilitates batteries with a higher energy density to be manufactured. In other examples, a material, which is not polymeric, is used, providing that it can be manufactured in a sufficiently thin and flexible manner to allow for a high battery density and ease of handling post-deposition.

[0092] The plasma deposition process and subsequent manufacturing processes are however subject to the technical challenges that working with such thin layers impose. [0093] Before the substrate 128 is so pre-coated, it has a surface roughness that is carefully engineered so as (a) to be great enough to mitigate the undesirable effects that would otherwise result from electrostatic forces (such as increasing the force required to unwind the polymer film from the drum on which it is held) and (b) to be small enough that the roughness does not cause problems when depositing material onto the substrate. In this example, the surface roughness is engineered to be about 50 nm. It will be noted that the product of the thickness of the substrate (0.9 microns) and the surface roughness is 4.5 x 101 nm2 and is therefore less than 105 min' and less than 5 x 104 nm2 in this example. It has been found that that the roughness needed for easing handling of thin films rises with decreasing thickness. Generally, it has been found that the roughness required to improve handling of thinner substrates (i.e. less than 10 microns, particularly less than 1 micron) increases as the substrate thickness decreases. [0094] Figure lc shows (not to scale) a typical thin-film polymer being about 1 micron thick and having embedded particles providing roughness. The roughness of the surface features provided by the particles is at least 90 nm and possibly higher. This is too rough for the particular example envisaged (although may be acceptable for other examples).

[0095] Figure ld shows (not to scale) one way in which the desired roughness can be achieved. Spherical particles of polystyrene are embedded in the substrate material such that at least 90% of those which contribute to the roughness of the substrate protrude from the local substrate surface by no more than half the volume of the particle. The particles have a diameter of about 90 nm. Thus, a majority of the embedded particles that contribute to surface roughness of the substrate have a median size of about 180% of the surface roughness of the substrate. In other examples, the embedded spherical particles are made of different material, such as silicon oxide.

-23 - [0096] Figure le shows (not to scale) an alternative way in which a desired roughness can be achieved. Spherical embedded particles of polystyrene are present on the surface of the substrate material such that at least 90% of those which contribute to the roughness of the substrate protrude from the local substrate surface by more than half the volume of the particle. The particles used in the example of Fig. le are smaller than those used in the example of Fig. ld.

[0097] Examples such as those of Fig. ld and le enable good quality films to be deposited, as crystalline material, on thin substrates in a manufacturing environment. The advantages of the presence of embedded particles are retained, but by careful control of the location and size distribution of such particles, the potential disadvantages can be avoided or reduced. Figures if to lh show schematically a cross-section corresponding to the substrate shown in Figures lc to le after a layer of crystalline material has been formed on the substrate surface. The intermediate layer of metal current collector is omitted from Figures if to lh. The roughness of the substrate shown in Figures lc and if is such that problems arise. The dominating protrusions caused by certain embedded particles 152 cause shadowing and competing crystal growth, which are illustrated schematically by means of the contrasting shading 154 in Figure 11 This competing crystal growth which is aligned in a conflicting direction gives rise to discontinuities in the layer that affects performance of the final product. Also, there is a surprisingly profound effect on the likelihood of delamination of the layer of deposited material from the substrate. This may be as a result of poor contact between the deposited layer and the underlying substrate in the region near to any embedded particles that protrude far from the median plane of the surface (illustrated schematically by the voids 156 in Figure 1f), where the local asperity radius is small. In contrast, it can be seen from Figure lg and lh that no such problems arise. The roughness of the surface of the material deposited on the substrate is approximately 50 nm.

[0098] The roughness of the substrate can be measured with a profilometer. This instrument has a stationary stylus. The surface to be measured is translated under the stylus, and the deflections of the stylus measure the surface profile, from which various roughness parameters are calculated.

-24 - [0099] Roughness can also be measured using "non-contact" methods. A suitable machine for measuring roughness is the "Omni scan MicroXAM 5000B 3d" which uses optical phase shift interference to measure the surface profile.

[0100] The roughness, Ra, can be calculated using the formula where the deviation y from a smooth surface is measured for n data points.

[0101] The surface roughness, Sa, of an area A extending in the x-and y-directions can be calculated using the formula: where Z is the deviation from a mathematically perfectly smooth surface.

[0102] In the present example, the average surface roughness is measured with a non-contact method.

[0103] The remotely generated plasma is created by the power supplied to the antennae 116 by power supply 112. There is therefore a measurable power associated with that used to generate the plasma. The plasma is accelerated to the target by means of electrically biasing the target 104, there being an associated electrical current as a result. There is thus a power associated with the bias on the target 104. In this example, the ratio of the power used to generate the plasma to the power associated with the bias on the target is greater than 1:1, and optionally greater than 1.0:1.0. Note that in this example, the ratio is calculated on the assumption that the power efficiency of the plasma-generating source is taken to be 50%. The power associated with the bias on the target is at least 1 Wcm-2.

[0104] In further examples, the ratio of the power used to generate the plasma to the power associated with the bias on the target is greater than 1:1, and no more than 7:2, optionally 7.0:2.0. In yet further examples, the power associated with the bias on the target is greater than 1:1 and no more than 3:2, optionally 3.0:2.0. In some examples, the power efficiency of the plasma generating source is taken to be 80%. In some examples, the power associated with the bias on the target is 10 Wcm-2. In yet further examples, the power associated with the bias on the target is 100 Wm'. In yet further examples, the power associated with the bias on the target is 800 Wein'. In other examples, the efficiency of the plasma generating source may be different, and the power ratio may also be different.

[0105] When the LiCoO2 film is deposited onto the substrate, it forms a crystalline film of LiCoO2. The crystalline structure which forms onto the substrate is in the R7m space group. This structure is a layered oxide structure. This structure has a number of benefits, such as having a high accessible capacity and high rate of charge and discharge compared to the low energy structure of LiCoO2, which has a structure in the Fd3m space group. Crystalline LiCoO2 in the R3m space group is often favoured for solid state battery applications.

[0106] Throughout the plasma deposition process, the temperature of the substrate 128 does not exceed the degradation point of the polymer substrate 128. Moreover, the temperature of the substrate is sufficiently low throughout the deposition process such that the temperature adjusted yield stress of the polymer substrate remains sufficiently high such that the polymer substrate does not deform under the stresses exerted by the roll-to-roll processing machine.

[0107] The general shape of the confined plasma made from the remote plasma generator 106 is shown by the dashed lines B in Figure I a. The series of electromagnets 108 is used to and confine the plasma to a desired shape/volume.

[0108] It should be noted that, whilst in this first example, substrate 128 is fed into the chamber at inlet 130, and exits the chamber at outlet 132, alternative arrangements are possible. For example, the roll or other store upstream of shutter 136 may be inside the process chamber 122. The roll or other store downstream of shutter H6 may be inside or could be stored inside the process chamber 122.

[0109] In addition the means 112 of powering the plasma source, may be of RF, (Direct Current) DC, or pulsed-DC type.

[0110] In this first example, the target assembly 102 comprises only one target 104. This target is made of LiCoO2. It should be appreciated that alternative and/or multiple target assemblies may be used, for example, comprising a distinct region of elemental lithium, a distinct region of elemental cobalt, a distinct region of lithium oxide, a distinct region of cobalt oxide, a distinct region of a LiCo alloy, a distinct region of LiCoO2, or any combination thereof In other examples, the ABO2 material may not be LiCo02. In these examples, the target assembly or assemblies contain distinct regions of A, distinct regions of B, distinct regions of a compound containing A and/or B, and/or distinct regions containing ABO2.

[0111] For the avoidance of doubt, the target 104 of the target assembly 103 acts as a source of material alone and does not function as a cathode when power is applied to it from the RF, DC or pulsed DC power supply.

[0112] In this example, the working pressure of the system is 0.0050 mBar. The theoretical mean free path of the system is approximately 10 cm. The theoretical mean free path is the average distance between collisions for an ion in the plasma. The working distance between the target 104 and substrate 128 is approximately 8.5 cm. This working distance is therefore approximately 85% of the theoretical mean free path of the system.

[0113] In this example, the working pressure is above a lower bound below which crystalline material in the layered oxide structure does not form, but below an upper bound above which observable damage is caused to the substrate. The working distance is shorter than an upper bound above which crystalline material in the layered oxide structure does not form, and longer than a lower bound below which the energy of the deposition causes observable damage to the substrate, or unfavourable oxide states to form.

[0114] The average crystallite size of the crystallites which form on the film in this example is around 20 nm. In other examples, the average crystallite size of the crystallites which form on the film is around 50 nm.

[0115] In an alternative example, the working pressure of the system is 0.0020 mBar. The theoretical mean free path of the system is approximately 12 cm. The working distance between the target 104 and substrate 128 is approximately 9 cm. This working distance is therefore approximately 75% of the theoretical mean free path of the system. [0116] In an alternative example, the working pressure of the system is 0.0065 mBar. The theoretical mean free path of the system is approximately 15 cm. The working distance between the target 104 and substrate 128 is approximately 7.5 cm. This working distance is therefore approximately 50% of the theoretical mean free path of the system.

-27 - [0117] A second example method uses the apparatus shown in Figure 2a. The main differences between the apparatus of Figure 1 a and the apparatus of Figure 2a will now be described. Figure 2a shows that instead of the flexible substrate 128 presented in the first example, an inflexible planar glass substrate 228 is used. Furthermore, no shutter is present in this example. The thickness of the glass substrate is in the order of millimetres. A single target 204 is used in this example. A thermal indicator sticker was attached to the face of the glass slide opposite to that on which the cathode material was deposited. The thermal indicator sticker is configured to indicate whether or not the substrate 228 experienced a temperature of 270°C or more during the plasma deposition process. After deposition, the sticker indicated that the substrate did not experience a temperature of 270°C or more during the deposition process. The general shape of the plasma is indicated by the area enclosed by the broken line B' in Figure 2a.

[0118] Table 1 shows the properties of the resultant exemplary battery cathodes produced in accordance with the second example: Example Target Measured film Plasma source power OM Sputtering Process Ar process flow rate (SCCM) Film Film yep identifier composition Composition (At%) Power (kW) pressure thickness Roughness Sa (nm) time (mBar) (nm) (min) 0 Co Li Sample 1 LiCo02 56 21 23 1800 500 3.90e-03 52 910 51.8 100 Sample 2 LiCoO, 55 21 24 1800 800 3.90e-03 52 915 106 100 Table 1 -properties of Li Co02 cathode films as a function of deposition parameters [0119] In Table 1 above, the elemental film composition was determined by x-ray photoelectron spectroscopy using a Themo Fisher K-alpha spectrometer with a MAGCIS ion gun. Quoted compositions were taken from depth profiling measuring at about 10 levels with a film. Plasma source power is the electrical power supplied to generate the plasma. Sputtering power is the electrical power applied to the target 204. Process pressure is the pressure in the chamber. Film thickness and roughness measurements were taken after deposition, using an Omniscan MicroXAM 5000b 3d optical profiler. Film thicknesses were measured after deposition, as step-heights at masked edges and roughness measurements were taken from sample areas of about 400microns x 500microns.

[0120] Figure 2b shows an X-ray diffraction (XRD) spectra of the battery cathode of Sample 1. The structure of the film was characterised by X-ray diffraction using a diffractometer (Rigaku-Smartlab) with nickel filtered CuKa radiation (X= 1.5406A). The diffraction pattern was taken at room temperature in the range 10° < 2 0 < 80° using a fixed incident angle of < 5°. Data were collected using step scans with a resolution of 0.04 °/step and a count time of 0.5s/step. The peak at approximately 37° is associated with the (101) plane of the crystals being substantially orientated parallel to the substrate surface. The peak at approximately 66° is associated with the crystals being substantially oriented such that the (110) plane is parallel to the substrate. The peak at approximately 55° is associated with the glass substrate, and for the purposes of determining the crystal structure of the LiCoO2, should be ignored.

[0121] The absence of extra reflections associated with the Fd3m space group is an initial indicator that the LiCoO2 deposited is in the RXrn space group.

[0122] Also notably absent is the peak associated with the (003) plane. This implies that very few crystals are orientated in such a way that the (003) plane is parallel to the substrate surface. It is beneficial that very few crystals are orientated in this way. A detailed explanation is beyond the scope of the present application, but briefly, the accessible capacity of a cathode increases when a higher proportion of the crystals are aligned such that the (101) and (110) planes are parallel to the substrate, as opposed to being aligned such that the (003) plane is parallel to the substrate as the apparent resistance to ion migration is lower. The crystals have formed such that the longitudinal axis of the crystals is normal to the substrate. In other words, the crystals have formed in an epitaxial manner.

[0123] The applicant has discovered that if the ratio of the power used to generate the plasma to the power associated with the biasing of the target is more than 1:1, then generally a crystalline material is deposited. In Sample 1, the ratio is 1800:500 (3.6:1) and in Sample 2, the ratio is 1800:800 (9:4). Note that in this example, the ratio is calculated on the assumption that the power efficiency of the plasma-generating source is taken to be 50%.

[0124] In a comparative example, the experiment was repeated with a plasma source power of IkW and a power associated with bias to the target of lkW. The material deposited was substantially amorphous. The performance of the film of the comparative example as a cathode was investigated by depositing an electrolyte (in this case, LiPON) and an anode metal on top of the cathode layer, thereby making a solid state battery. The charge-discharge characteristics of the battery were investigated and were found to be poor, with a cathode specific capacity of about 10m Ah/g. When analogous batteries were made using crystalline LiCoO2 such as that formed in Sample 1 and Sample 2, the charge-discharge characteristics were far superior, with typical cathode specific capacities of about 120mAh/g.

[0125] Figure 2c shows a Raman spectra of the battery cathode of Sample 1. The bonding environment of the films was characterised by Raman Spectrocopy. Raman spectra were collected using a JY Horiba LabRANI ARAMIS imaging confocal Raman microscope using 532 nm excitation. Note that the strong sharp peak at 600 cm-1 can be considered as anomalous due to the unphysical nature of the sharpness of the peak. The strong, characteristic peak observed at 487 cm -1 is well known in the art to be associated with the R3m space group crystal structure of LiCo02.

[0126] Figure 2d shows an XRD spectra (collected in the same way as that for Sample 1) of the cathode of Sample 2. The spectra shown is similar to that shown in Figure 2b. However, in Figure 2d, the relative intensity of the peak at approximately 66° is far stronger than that of the peak at 37°. This indicates that the number of crystals with their (110) planes parallel to the substrate is higher than the number of crystals with their (101) planes parallel to the substrate for Sample 2. This is beneficial as it means that the ion channels of the thin film are orientated perpendicular to the substrate, making for easier for intercalation and de-intercalation of the ions from their interstitial sites from within the crystal structure of the cathode. This improves the accessible capacity and the rate of charge of the cathode. Figure 2e is a Raman spectra of the cathode of Sample 2; the same comments apply to Figure 2e that apply to Figure 2c. [0127] Figures 3a to 3c show an alternative example of an apparatus for use in another example of a method of manufacturing a layer of crystalline material on a surface using plasma sputtering according to a third example. The apparatus and method of manufacture employed is similar to that described with reference to the first example. Only the significant differences will now be described. The same parts are labelled with reference numerals sharing the same last two digits. For example, rotating drum 334 in Fig. 3a is the same as rotating drum 134 in Fig. la. The apparatus of Fig. 3a comprises a rotating drum 334 on which a polymer substrate 328 is supported within a region defined by a process chamber 322 (the walls of the chamber being omitted for the sake of clarity). The target assembly 302 comprises a plurality of targets. There is provided a first target 304 consisting of elemental lithium and a plurality of targets 303 consisting of elemental cobalt (referred to now as the second targets). The targets are all positioned at a working distance of about 10 cm from the substrate 328 (the working distance being shortest separation therebetween). The surface of each target 303, 304 facing the drum 334 is flat (and planar). The radius of the drum 334 is significantly greater than the working distance (the size of the drum 334 being shown in the Figures as being relatively smaller than it is in reality for the sake of the illustration). The targets 303, 304 are arranged circumferentially around the circumference of the drum 334. The apparatus also comprises a shutter 336, for restricting deposition of sputtered material onto the substrate 328.

[0128] A plasma of argon ions and electrons is generated by means of two electrically powered spaced apart antennae 316. The plasma is confined and focussed by a magnetic field controlled by two pairs of electromagnets 308, each pair being positioned proximate to one of the antennae 316 and the electric field generated by the system. The overall shape of the plasma (the 90% highest concentration of which being illustrated in highly schematic fashion in Figure 3c by the plasma cloud B") is that of a blanket, in that the length and width of the plasma cloud are much greater than the thickness. The width of the plasma is controlled in part by the length of the antennae 316. The two pairs of antennae 316 are separated by a distance that is comparable to the length of the plasma. The length and width of the plasma are in the same general direction as the length and width, respectively, of the substrate.

[0129] The plasma source is spaced apart from the targets, and may thus be considered as a remotely generated plasma. The theoretical mean free path of the system (that is, the average distance between collisions for an ion in the plasma) is about 12 cm, meaning that the majority of particles travel from the target to the substrate without colliding with any argon ions in the plasma.

[0130] Figure 3a is a partial schematic cross-sectional view showing part of the substrate travelling on the drum 334 and also shows schematically the trajectories of particles that travel from the targets 303, 304 to the substrate. Thus, there is a first plume corresponding to the trajectories of particles from the first target 304 to the surface of the substrate 328 and a second plume corresponding to the trajectories of particles from the second target 303 to the surface of the substrate 328. The first plume is shown as a spotted region and each second plume is shown as a solid grey region. It will be seen from Figure 3a that the first plume and the second plume converge at a region proximate to the substrate. It will also be seen in Figure 3a that the first target 304 faces towards the substrate in a first direction (defined in this example by the notional line extending from the centre of the surface of the target 304) and the adjacent second target 303 to the left as shown in Figure 3a, faces towards the substrate in a second direction (defined in this example by the notional line extending from the centre of the surface of the target 303). The first and second directions converge towards the substrate and intersect at a location just beyond the substrate (the location being about 3 cm beyond the substrate). Oxygen gas is supplied at a controlled rate into the process chamber 322 through inlets 325. The targets are stationary as the substrate moves with rotation of the drum. In other examples, the inert sputtering gas is introduced through the gas inlet (not shown here, but substantially the same configuration as that shown in Figure la).

[0131] The amount of oxygen introduced into the chamber may be reduced in some other examples if distinct regions of lithium oxide and cobalt oxide are present in targets 304, 303, and the oxygen content in such targets may be sufficiently high in some examples such that no additional oxygen gas need be introduced into the chamber 322 at all.

[0132] Figure 3b is a view looking from the drum towards the targets. Figure 3c is a cross-sectional view that includes sections of the first target 304, the second targets 303 and the substrate 328 on the drum 334.

[0133] It will be seen that in Figure 3c (the view of the cross-section) the first target 304 is angled relative to each of the second targets 303.

[0134] In performance of the method, the plasma generated is used to sputter material from the first target and from the second targets onto the substrate.

[0135] As shown in Figure 3d, elemental lithium material has a lower sputter yield than cobalt as measured in atoms yielded per ion received at the surface at a given energy (less than half at 10keV). As such, the (negative) potential applied to the first target has a magnitude greater than the potential applied to the second targets. The first target also has a slightly larger surface area exposed to the plasma than the sum area of the second targets. As such, the number of ionised Li atoms arriving at the substrate per unit is substantially the same as the number of ionised Co atoms arriving at the substrate per unit. Ionised oxygen atoms are also present as are electrons from the plasma. The high energy particles made possible by the remote plasma allows for crystalline LiCo02 -32 -material, having a hexagonal crystal structure, to be formed in situ on the surface of the substrate.

[0136] A greater number of high energy particles from the plasma are received at the first target 304 (over the whole surface area of the target) than at the second targets 303 (summed over the whole surface area of both second targets).

[0137] Figure 3e shows a schematic cross-section through a further example of an apparatus in accordance with a fourth example, similar to that shown in Figures 3a to 3c, but in which the targets move and are arranged in pairs, circumferentially around the drum 334. Each pair of targets (i.e. each assembly 302) is arranged to be angled to face towards a location very near to the substrate on the drum. Each pair 302 comprises a first target 304 of elemental lithium and a second target of elemental cobalt 303. The targets are all positioned at a working distance of about 15 cm from the substrate, the working distance being theshortest separation therebetween. The theoretical mean free path of the system (that is, the average distance between collisions for an ion in the plasma) is about 20 cm. For each pair of targets (302), in use there is a first plume of particles from the first target (304) and a second plume of particles from the second target (303) which converge at a region proximate to the substrate. The centre of rotation of the main drum 334 is also the centre of rotation of the targets. The targets move with an angular velocity about the centre of rotation slower than the drum. Targets may be replaced when they have moved out of the plasma on a rotating basis, thus allowing for constant deposition of material on the moving substrate.

[0138] An example of a battery cathode made in accordance with the second example will now be described with reference to Figures 4a, 4b and 5a. The substrate 428, 528 comprises a current collecting layer 429, 529, in this case, a layer of platinum, on which a layer of LiCoO2 442, 542 is deposited. In other examples, another inert metal is used as a current collecting layer, for example gold, iridium, copper, aluminium or nickel. In yet further examples, the current collecting layer may be carbon based. In some examples, the current collecting layer is surface modified, and in some examples, the current collecting layer comprises rod-like structures.

[0139] As shown on the Scanning Electron Microscope (SEM) image of Figure 4a (cross sectional view of a first sample deposited film) and Figure 4b (bird's-eye view a second sample deposited film), the LiCoO2 film layer 442, 542 of both samples is -33 -polycrystalline in nature. The battery cathodes of Figures 4a, 4b and 5a can also be made in accordance with the methods of the third or fourth example.

[0140] A method of making a cathodic half-cell in accordance with a fifth example will now be described with reference to Figure 5a (a first sample), Figure 5b (a second sample), and Figure 5c. The method, generally described by reference numeral 3001, comprises depositing 3002 a battery cathode material 542 onto a substrate (which in this example comprises a current collecting layer 529), and depositing 3003 onto said battery cathode material 542 battery electrolyte material 544. In this example, the material deposited for the electrolyte 544 is lithium phosphorous oxy-nitride (LiPON). In other examples, the material deposited is another suitable electrolyte material. In some samples of the fifth example of the invention (such as the second sample), the half-cell may comprise an electrode material 544, and in other samples of the fifth example, the half-cell may not comprise an electrode material 544 (such as the first sample).

[0141] In this example, the LiPON is deposited in substantially the same way as the ABO2 materials in the first, second, third or fourth examples, using a remotely-generated plasma. However, in this example, the target material used is Li3PO4, with deposition occurring in a reactive nitrogen atmosphere. In other examples, the target assembly may include a number of targets, with distinct regions of lithium and/or phosphorous containing compounds, elemental lithium, or lithium oxide. In other examples, the deposition additionally occurs in a reactive oxygen atmosphere.

[0142] An example of a method of making a solid-state battery cell in accordance with a sixth example will now be described with reference to Figure 6. The method is denoted generally by reference numeral 5001 and comprises making 5002 a cathodic half-cell in accordance with the fifth example (for example, as described above with reference to Figure 5b and 5c) and contacting 5003 said cathodic half-cell with an anode. In this example, the anode is deposited by a convenient method, including remote plasma sputtering, magnetron sputtering, CVD etc. In other examples, the anode is deposited by thermal evaporation, e-beam evaporation, pulsed laser deposition, or simple DC-sputtering.

[0143] An example of a method of making a solid-state battery in accordance with a seventh example will now be described with reference to Figure 7a. The method is denoted generally by reference numeral 6001 and comprises making 6002 a plurality -34 -of cathodic half-cells of a solid state thin film battery, making 6003 a plurality of anodic half cells of a solid state thin film battery and bringing 6004 said cathodic and anodic half cells into contact with one another, thereby forming at least one battery. A battery so made according to a first sample of the seventh example of the present invention is shown schematically in Figure 7b. Referring to Figure 7b, 628 and 628' are substrate materials, 629 and 629' are current collecting layers, 642 is the cathode material, in this case, LiCoO2, and 644 is LiPON, which acts as both electrolyte and anode.

[0144] Alternatively, in other examples the current collector material acts as an anode material. Alternatively, in a second sample of the seventh example of the invention a further anode material may be deposited. This is shown schematically in Figure 7c. Referring to Figure 7c, 628 and 628' are substrate materials, 629 and 629' are current collecting layers, 642 is the cathode material, in this case, LiCoO2, 644 is LiPON, which acts as electrolyte, and 646 is a suitable anode material.

[0145] An example of a method of determining an optimum working distance for a remote plasma deposition system configured for the deposition of layered oxide materials in accordance with an eighth example will now be described with reference to Figure 8a. The method is generally described by numeral 7001 and comprises: * Selecting 7002 a range of working distances, wherein a working distance within said range is +/-50% of the theoretical mean free path of the system, * for a number of test specimens, for each respective specimen, performing 7003 the method of depositing material according to the first example at different working distances within the selected range, * performing 7004 a characterisation technique capable of determining a characteristic feature of a layered oxide structure on each of the test specimens after deposition has occurred, * identifying 7005 specimens where said characteristic property is present; * from those specimens, selecting 7006 the specimen wherein the (normalised) intensity of said characteristic peak is highest, and subsequently selecting 7007 the working distance for the system to that which was used during deposition of said test specimen.

[0146] In this eighth example, the characterisation technique used is X-ray diffraction, and the characteristic property is a diffraction peak or series of diffraction peaks. Figure 8b shows a number of X-Ray diffraction patterns recorded of films deposited at different working distances. From the top diffraction pattern to the bottom diffraction pattern the working distances were 5 cm (ref no. 731), 8 cm (733), 12 cm (735) and 15 cm (737), respectively. As can be seen from the figure, a working distance of 8 cm shows the highest intensity peak 733 at 19 degrees 2theta (which is one of the required peak positions 739 for hexagonal LiCoO2, this particular peak not being present in cubic or spinel structures of LiCo02). Therefore, in this example, 8 cm is chosen as the working distance. In other examples, a different characterisation technique may be used other than X-Ray diffraction. The intensity of the diffraction pattern 731 measured for a working distance of 5cm is less intense at 19 degrees 2theta than the diffraction pattern 733 at a working distance of 8cm. The diffraction patterns collected for a working distance of 12 cm 735 and 15 cm 737 do not show the characteristic peak for hexagonal Li Co02 at 19 degrees 2theta at all.

[0147] In some examples, the test specimens of the method are replaced with an average value for a number of test specimens, comprising a number of test specimens, wherein the method of the first example has been performed a number of times at the same working distance, and an average taken. In some examples the method may be performed a number of times such that a range of optimal working distances can be found for operating the system.

[0148] Figure 9a shows a sample formed in accordance with the first example, during performing the method of the eighth example, and shows a damaged substrate surface (with undesirable oxides) which forms due to the deposition when the working distance is too short. In this example, the working distance was 5 cm, and the material deposited was LiCoO2. As can be seen from the figure, crystallites have not formed over the whole substrate surface, and deformation of the substrate can be seen. In addition, regions of Co(II)O, an undesirable phase of cobalt oxide, can be seen forming on the substrate at this working distance. This is confirmed by the spectra as shown in Figure 9b, which shows peaks relating to Co(II)O phases (identified at two values 843 of 2theta) being detected in a diffraction pattern 831 obtained for a sample at which the working distance was 5 cm, in addition to hexagonal LCO, peaks (identified at 5 values 839 of 2theta). A structural refinement model 831' containing both hexagonal LiCoO2 and Co(11)0 phases, was obtained from the collected diffraction pattern of 831. The difference between the diffraction pattern 831 and the refinement model 831' is illustrated by the difference line 841. Thus, during the method of the eighth example, overly short working distances cannot be selected as the optimum working distance.

[01491 An example of a method of determining an optimum range of working pressures for a remote plasma deposition system configured for the deposition of layered oxide materials in accordance with a ninth example will now be described with reference to Figure 10a. The method is generally described by numeral 8001 wherein the method comprises: * Selecting 8002 an initial range of working pressures, from 0.00065 mBar to 0.01 mBar (and optionally from 0.001 to 0.007mBar), * for a number of test specimens, for each respective specimen, performing 8003 the method of depositing material according to the first example at different working pressures within the selected range, * performing 8004 a characterisation technique capable of determining a characteristic property of a layered oxide structure on each of the test specimens after deposition has occurred, * selecting 8005 the test specimen which was deposited at the lowest working pressure from the group of test specimens which display a characteristic feature of a layered oxide material, and setting 8006 this working pressure as the lower bound of the range, * selecting 8007 the test specimen which was deposited at the highest working pressure from the group of test specimens which do not show observable signs of damage to the substrate, and setting 8008 this working pressure as the higher bound of the range.

[01501 In this ninth example, the characterisation technique used is X-ray diffraction, and the characteristic feature is a feature comprises a characteristic X-Ray diffraction peak of a layered oxide material. Figure 10b shows an example X-Ray spectra showing how below a certain working pressure, this characteristic feature is not present. In this example, the presence of a peak at 19 degrees 2theta in the pattern 947 for the sample deposited at 0.0046mBar resulted in the formation of a hexagonal crystalline phase, whereas the pattern 945 for the sample deposited at 0.0012mBar did not lead to the formation of a hexagonal crystalline phase, as shown by the absence of the peak. In other examples, a characterisation technique may be used other than X-Ray diffraction.

-37 - [0151] In further examples, the test specimens of the method are replaced with an average value for a number of test specimens, comprising a number of test specimens wherein the method of the first example has been performed a number of times at the same working pressure, and an average taken.

[0152] In some examples, the method also comprises selecting the optimum working pressure of the system within the desired range. In this example, the optimum working pressure is the working pressure within the range that results in the highest deposition rate.

[0153] An example of a method of determining the crystallite size for deposition of layered oxide materials in accordance with a tenth example will now be described with reference to Figure 1 la. The method is generally described by numeral 9001 wherein the method comprises: * selecting 9002 an initial range of working pressures, from 0.00065 mBar and 0.01 mBar, * for a number of test specimens, for each respective specimen, performing 9003 the method of depositing material according to the first example at different working pressures within the selected range, * performing 9004 a characterisation technique capable of determining the crystallite size of each film for each of the test specimens after deposition has occurred, [0154] The selected range of working pressures may be from 0.001 to 0.007 mBar, for example.

[0155] Figure 1 lb is a graph showing, after performing the method of the tenth example over a given range of working pressures, for a working distance of 16 cm, that the range of crystallite size that forms for a number of films deposited in accordance with the first example at different working pressures between 0.001 mBar and 0.0065 mBar, is relatively broad in comparison to Figure 11c.

[0156] Figure llcisa graph showing, after performing the method of the tenth example over a given range of working pressures, for a working distance of 8.5 cm, that the range of crystallite size that forms for a number of films deposited in accordance with the first example at different working pressures between 0.001 mBar and 0.0065 mBar is relatively narrow in comparison to Figure 1 1 b.

[0157] It is beneficial to have a narrow distribution of crystallite sizes, as this makes the crystallite size of films deposited on an industrial scale both predictable and repeatable.

[0158] An example of a method of depositing a material on a substrate in accordance with an eleventh example of an example will now be described with reference to Figure 12. The method is generally described by numeral 1101 and comprises: * generating 1102 a plasma remote from a plasma target or targets suitable for plasma sputtering, * exposing 1103 the plasma target or targets to the plasma, thereby generating sputtered material from the target or targets, * depositing 1104 the sputtered material on a first portion of the substrate.

[0159] The method of depositing material on a substrate as described by the eleventh example comprises all of the features of the deposition of the first example, although in this example, the target material may be any material. In this example, the target material is crystalline, however in other examples the deposited material may take a semi-crystalline form, or be amorphous.

[0160] Also presented is a twelfth example, which relates to a method of manufacturing a component for an electronic device comprising a substrate, which will now be described with reference to Figure 13. The method is generally described by numeral 1201 and comprises depositing 1202 a material onto the substrate using a method of the as described in the eleventh example. The method of the eleventh example in this example is performed a plurality of times 1203 in order to deposit multiple layers. In this example, at least some of the multiple layers may are semi-conducting layers. In this example, the method is therefore a method of manufacturing a semi-conducting device or part thereof In this example adjacent layers are be deposited with differing parameters and/or target materials used for the deposition of each layer, in order to produce an electronic device. In other examples, multiple layers of a plurality of layers of material are deposited with substantially the same target materials and parameters. [0161] In this example, the substrate comprises one intermediate layer, which may optionally act as a current collecting layer. In other examples, there are more intermediate layers, which help with adhesion during deposition steps. In some other examples, there is no intermediate layer. The deposition of the intermediate layer onto the substrate is be performed in accordance with the method as described in the eleventh example. In other examples, deposition of the intermediate layer onto the substrate is performed by another appropriate deposition technology such as sputtering, thermal evaporation, electron beam evaporation, pulsed laser deposition, or other thin film deposition technology.

[0162] In this example, the method comprises depositing a first semiconducting layer of material. In this example, the first semiconducting layer is deposited onto an intermediate layer of material. In other examples, the first semiconducting layer is deposited directly onto the substrate. In this example, the first semiconducting layer comprises silicon. In other examples, the first semiconducting layer comprises aluminium, and in some further examples, gallium nitride. In examples where the semiconducting layer of material is gallium nitride, the deposition occurs under a reactive nitrogen atmosphere. In this example, the first semiconducting layer of material is doped n-type. This is achieved in this example by sputtering of a target comprising a compound containing phosphorous. In other examples, this is achieved by use of a different dopant such as arsenic, antimony, bismuth or lithium. In some further examples, the semiconducting layer of material is doped p-type, with dopants such as boron, aluminium, gallium or indium. In further examples, the semiconducting layer of material is not doped, and is an intrinsic semi-conductor. In some of these examples, the dopant material is not introduced as a target which can be sputtered, and is instead introduced as a gas after deposition, such that the dopant diffuses into the surface of the semiconducting layer.

[0163] In this example, the method comprises depositing a second semiconducting layer of material, onto the first semiconducting layer of material. In other examples, the second semi-conducting layer of material is deposited directly onto the substrate or the intermediate layer (if present). In this example, the second semiconducting layer of material is an intrinsic semiconductor. In this example, the second semiconducting layer of material is gallium nitride. In further examples, the second semiconducting layer of material is doped n-type with dopants such as phosphorous, arsenic, antimony, bismuth or lithium. In some further examples, the second semiconducting layer of material is doped p-type, with dopants such as boron, aluminium, gallium or indium. In some of these examples, the dopant material is not introduced as a target that can be sputtered, and is instead introduced as a gas after deposition, such that the dopant diffuses into the surface of the semiconducting layer.

[0164] In this example, the method comprises depositing a third semiconducting layer of material. In this example, the third semiconducting layer is deposited onto the second semi-conducting layer of material. In other examples, the third semiconducting layer is deposited directly onto the first semiconducting layer, second semiconducting layer, the intermediate layer or the substrate. In this example, the third semiconducting layer comprises silicon. In other examples, the third semiconducting layer comprises aluminium, and in some further examples, gallium nitride. In some examples where the semiconducting layer of material is gallium nitride, the deposition occurs under a reactive nitrogen atmosphere. In this example, the third semiconducting layer of material is doped p-type. This is achieved in this example by sputtering of a target comprising a compound containing boron. In other examples, this is achieved by use of a different dopant such as aluminium, gallium or indium. In some further examples, the third semiconducting layer of material is doped n-type, with dopants such as phosphorus, arsenic, antimony, bismuth or lithium. In further examples, the third semiconducting layer of material is not doped, and is an intrinsic semi-conductor. In some of these examples, the dopant material is not introduced as a target, which can be sputtered, and is instead introduced as a gas after deposition, such that the dopant diffuses into the surface of the semiconducting layer.

[0165] The method of this example may therefore be used to form a p-n or p-i-n junction.

[0166] In this example, no further dopants are introduced into some of the semiconducting layers hitherto described. In some examples, germanium is introduced as a dopant in the first, second and/or third layers. Germanium alters the band gap of the electronic device, and improves the mechanical properties of each semiconducting layer of material. In some examples, nitrogen is introduced as a dopant in the first, second and/or third layers of material. Nitrogen is used to improve the mechanical properties of the semiconducting layers formed.

[0167] Also presented is a thirteenth example, which relates to a method of manufacturing a crystalline layer of Yttrium Aluminium Garnet (Y AG), which will now be described with reference to Figure 14. The method is generally described by numeral 1301 and comprises using the method as described in the eleventh example 1302, wherein the YAG is doped 1303 with at least one f-block transition metal.

[0168] In this example, the dopant material is a lanthanide.

[0169] In this example, the dopant material comprises neodymium. In other examples, the dopant material comprises chromium or cerium in addition to neodymium. In this example, the crystalline layer of material comprises 1.0 molar percent neodymium. In some examples, the material also comprises 0.5 molar percent cerium.

[0170] In yet further examples, the dopant material comprises erbium. In this example, the dopant material is provided as a target, and sputtered as described in the eleventh example. The crystalline layer of material in this further example comprises 40 molar percent erbium. In one example, the crystalline layer of material comprises 55 percent erbium.

[0171] In yet further examples, the dopant material comprises ytterbium. In one of these examples, the crystalline layer of material comprises 15 molar percent ytterbium. [0172] In yet further examples, the dopant material comprises thulium. In further examples, the dopant material comprises dysprosium. In further examples, the dopant material comprises samarium. In further examples, the dopant material comprises terbium.

[0173] In yet further examples, the dopant material comprises cerium. In some examples where the dopant material comprises cerium, the dopant material also comprises gadolinium.

[0174] In some examples, instead of the dopant material being provided as a distinct region of a target or targets, the dopant material is, at least in part, introduced after the deposition of the layer of crystalline material, by providing the dopant material as a gas, such that it diffuses into the layer of crystalline material.

[0175] According to a fourteenth example, a method of manufacturing a light emitting diode is presented, which will now be described with reference to Figure 15. The method is generally described by numeral 1401 and comprises performing the method according to the twelfth example 1402, and thereafter or therein performing the method according to the thirteenth example 1403, in the case where the dopant used during the method of the thirteenth example comprises cerium 1404. The layer of cerium-doped YAG is used as a scintillator in an LED in this example.

-42 - [0176] The methods according to the twelfth and thirteenth examples may be performed inside the same process chamber.

[0177] According to a fifteenth example, a method of manufacturing a permanent magnet is presented, which will now be described with reference to Figure 16. The method is generally described by numeral 1501 and comprises comprising performing the method according to the eleventh example 1502, wherein the distinct regions of the target or targets provided comprise neodymium, iron, boron and dysprosium 1503, and the method comprises processing the film 1504 such that the layer of material becomes a permanent magnet.

[0178] In this example, the final layer of material comprises 6.0 molar percent dysprosium. In further examples, the molar percentage of dysprosium is less than 6.0. [0179] The high target utilisation that the current method provides is beneficial when constructing electronic devices from rare elements such as dysprosium. Dysprosium is available in limited Earth abundancy, and so a deposition system with a high target utilisation results in less material waste.

[0180] According to a sixteenth example, a method of manufacturing a layer of Indium Tin Oxide (ITO) is presented, which will now be described with reference to Figure 17. The method is generally described by numeral 1601 and comprises performing the method according to the eleventh example 1602, wherein the distinct regions of the targets provided comprise indium and tin 1603. The layer of ITO is deposited in such a way that it directly forms a transparent crystalline layer of material on deposition 1604 onto the substrate. In other examples, a composite target is used, which comprises both indium and tin. In yet further examples, the composite target comprises an oxide of indium and tin. The number of targets used thus may differ in further examples, and a single target may be used.

[0181] In yet further examples the targets may comprise an oxide of indium, or an oxide of tin. The deposition process in further examples comprises providing oxygen, such that the sputtered material from the targets reacts with the oxygen in order to form Indium Tin Oxide on the substrate.

[0182] According to a seventeenth example, not separately illustrated, a method of manufacturing a photovoltaic cell is presented. In this example, the method further comprises the deposition of an ITO, as described in the fifteenth example. In further examples, no layer of ITO is deposited. In this example, the method also comprises the deposition of a layer of perovskite material in between a n-type doped layer of semiconducting material and a p-type doped layer of semiconducting material. The perovskite layer of material is in this case deposited as described by the method of the eleventh example. In further examples, it is deposited by another suitable means such as physical vapour deposition, or wet chemistry techniques. In further examples, no perovskite layer of material is deposited.

[0183] In alternative examples, the method comprises the deposition of a layer of copper indium gallium selenide in accordance with the eleventh example. The copper, indium, gallium, and selenide is provided as distinct regions of the target or targets. In this example the copper is provided as an elemental target, and the indium, gallium, and selenide are provided as oxide targets. Other combinations of oxide, elemental, compound or composite targets are used in further examples. The number of targets used thus may differ in further examples, and a single target may be used.

[0184] In some examples, the method comprises the deposition of a layer of cadmium sulphide in accordance with the eleventh example. In this example, the cadmium and sulphide are provided as distinct regions of the targets in oxide form. Other combinations of oxide, elemental, compound or composite targets are used in further examples. The number of targets used thus may differ in further examples, and a single target may be used.

[0185] In some examples, the method comprises deposition of a layer of cadmium telluride in accordance with the eleventh example. The cadmium and telluride is provided as distinct regions of elemental targets in tis example. In other examples, the cadmium and telluride is provided as distinct regions of the target or targets in elemental, an oxide, a composite or any combination thereof. The number of targets used thus may differ in further examples, and a single target may be used.

[0186] Whilst the forgoing description has been described and illustrated with reference to particular examples, it will be appreciated by those of ordinary skill in the art that the invention lends itself to many different variations not specifically illustrated herein.

[0187] Where in the foregoing description, integers or elements are mentioned which have known, obvious or foreseeable equivalents, then such equivalents are herein incorporated as if individually set forth. Reference should be made to the claims for determining the true scope of the example, which should be construed so as to -44 -encompass any such equivalents. It will also be appreciated by the reader that integers or features of the invention that are described as preferable, advantageous, convenient or the like are optional and do not limit the scope of the independent claims. Moreover, it is to be understood that such optional integers or features, whilst of possible benefit in some embodiments of the invention, may not be desirable, and may therefore be absent, in other embodiments.

Claims

Claims 1. A method of manufacturing a crystalline layer of material on a surface, wherein the method comprises the following steps generating a sputter plasma remote from at least one sputter target, and depositing material from the sputter target directly onto a surface of or supported by a substrate to form a crystalline layer, wherein said surface has a surface roughness Xs or less, where Xs = 100 nm, and the crystalline layer has a thickness of from 0.01 to lOttm and a surface roughness of no more than Xi, where Xi equals the product of F and Xs, where F is a factor in the range of 1 to 2.
A method according to claim 1, wherein Xs is no more than 10% of the thickness of the substrate and the product of the thickness of the substrate and Xs is no more than 10' nm2.
3. A method according to claim 1 or claim 2, wherein the substrate comprises a polymer material.
4. A method according to claim 3, wherein the polymer material is provided with embedded particles and of all of the embedded particles within or on the polymer material, the majority of those that contribute to surface roughness of the substrate have a median size from 10% to 125% of Xs.
5. A method according to claim 3, wherein the polymer material is provided with embedded particles and of all of the embedded particles within or on the polymer material, the majority of those that contribute to surface roughness of the substrate have a median size of no less than 150% of Xs.
6. A method according to any preceding claim, wherein the method includes a step of unrolling the substrate from a roll of material, and a step of conveying the substrate to a location at which the sputter deposition technique is performed.
7. A method according to any preceding claim, wherein the substrate is held under tension at least at the location at which sputter deposition technique is performed.
8. A method according to any preceding claim, wherein the method includes a step of depositing material onto the surface using sputter deposition to form a further layer having a thickness of from 0.01 to 10um and a surface roughness of no more than 150% of Xs, the material composition of the crystalline layer being different from the material composition of the further layer.
9. A method according to any preceding claim, wherein the step of depositing material from the sputter target directly onto the surface is performed such that crystalline material is formed in situ as the material is deposited.
10. A method according to any preceding claim, wherein the step of depositing material from the sputter target directly onto the surface is performed at temperatures such that the maximum temperature reached at any given time by any given square of substrate material having an area of lcm2 as measured on the surface opposite to said surface on which the material is deposited and as averaged over a period of 1 second, is no more than 500 degrees C.
11. A method according to any preceding claim, wherein the step of depositing material directly onto the surface is performed at a deposition rate of from 1 nm to 10000 nm per second.
12. A method of manufacturing a crystalline layer of material on a surface, wherein the method comprises the following steps generating a plasma remote from at least one sputter target, -47 -depositing material from the sputter target directly onto a surface of or supported by a polymer substrate film to form crystalline material in situ as the material is deposited thus forming the crystalline layer of material on the surface, the polymer substrate film having a thickness of from 0.5 to lOttm and being provided with embedded particles, wherein said surface has a surface roughness of no more than 50 nm, and the crystalline layer has a thickness of from 0.01 to 10pm.
13. A method according to claim 12, wherein depositing material onto the surface is performed at temperatures such that the maximum temperature reached at any given time by any given square of substrate material having an area of lcm2 as measured on the surface opposite to said surface on which the material is deposited and as averaged over a period of I second, is no more than 350 degrees C.
14. A method of manufacturing an electronic component comprising performing the method of any of claims 1 to 13, to form a multilayer sheet of different materials, integrating the multilayer sheet or a part thereof in an electronic product, wherein at least one of the layers of the sheet is one formed by the step of using a sputter deposition technique and is a conducting, semiconducting or dielectric material and wherein the substrate is retained as a part of the electronic component.
15. A method according to claim 14, wherein the electronic product is a battery, an energy storage device or a cell of battery.
16. A battery comprising one or more layers of crystalline material formed by performing the method according to any of claims 1 to 15.
17. A battery comprising multiple stacked cathode layers, multiple stacked electrolyte layers, and multiple stacked anode layers, wherein at least one of the layers in the device is made by performing the method according to any of claims 1 to 15.