US20040055875A1 - Nanodevice for charged particle flow and method for producing same - Google Patents
Nanodevice for charged particle flow and method for producing same Download PDFInfo
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- US20040055875A1 US20040055875A1 US10/254,947 US25494702A US2004055875A1 US 20040055875 A1 US20040055875 A1 US 20040055875A1 US 25494702 A US25494702 A US 25494702A US 2004055875 A1 US2004055875 A1 US 2004055875A1
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- 150000001768 cations Chemical group 0.000 claims description 5
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- 229910001451 bismuth ion Inorganic materials 0.000 claims description 4
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- 238000000151 deposition Methods 0.000 claims description 4
- 229910003437 indium oxide Inorganic materials 0.000 claims description 4
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 claims description 4
- 229920000515 polycarbonate Polymers 0.000 claims description 4
- 239000004417 polycarbonate Substances 0.000 claims description 4
- 229920001721 polyimide Polymers 0.000 claims description 4
- 102000004877 Insulin Human genes 0.000 claims description 3
- 108090001061 Insulin Proteins 0.000 claims description 3
- 229940125396 insulin Drugs 0.000 claims description 3
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- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
- C25F3/00—Electrolytic etching or polishing
- C25F3/02—Etching
- C25F3/14—Etching locally
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D57/00—Separation, other than separation of solids, not fully covered by a single other group or subclass, e.g. B03C
- B01D57/02—Separation, other than separation of solids, not fully covered by a single other group or subclass, e.g. B03C by electrophoresis
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/42—Electrodialysis; Electro-osmosis ; Electro-ultrafiltration; Membrane capacitive deionization
- B01D61/425—Electro-ultrafiltration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0023—Organic membrane manufacture by inducing porosity into non porous precursor membranes
- B01D67/003—Organic membrane manufacture by inducing porosity into non porous precursor membranes by selective elimination of components, e.g. by leaching
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0023—Organic membrane manufacture by inducing porosity into non porous precursor membranes
- B01D67/0032—Organic membrane manufacture by inducing porosity into non porous precursor membranes by elimination of segments of the precursor, e.g. nucleation-track membranes, lithography or laser methods
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/02—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/487—Physical analysis of biological material of liquid biological material
- G01N33/48707—Physical analysis of biological material of liquid biological material by electrical means
- G01N33/48721—Investigating individual macromolecules, e.g. by translocation through nanopores
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/02—Details relating to pores or porosity of the membranes
- B01D2325/022—Asymmetric membranes
Definitions
- the present invention relates to an apparatus having a nanodevice for controlling the flow of charged particles in electrolytes and method for producing same.
- FIG. 1 shows a schematic drawing of an apparatus having a nanodevice for controlling the flow of charged particles in electrolytes.
- FIG. 2 shows principles of the functioning of the nanodevice for controlling the flow of charged particles in electrolytes.
- FIG. 3 shows a scheme of an experimental set-up for evaluating the performance of the nanodevice.
- FIG. 4 shows current-voltage characteristics of a single conical pore in a polyethylene terephthalate (PET) foil with a gold layer on the side of the small or narrow opening of a pore, applying 0.1 m KF on both sides of the membrane foil.
- PET polyethylene terephthalate
- FIGS. 5 a and 5 b show examples of time series without and with applied “gate voltage” for two directions of the potassium ion flow.
- an apparatus having a nanodevice for controlling the flow of charged particles in electrolytes comprising an electrolytic bath container, divided by a polymeric foil into a first and a second compartment. Each compartment comprises an electrode connected to a voltage supply. Further, the nanodevice comprises at least an asymmetric pore forming a via hole through said foil, wherein said pore provides a narrow opening of a diameter in the range of several nanometers down to about one nanometer on a front side of said foil and a wide opening in the range of several ten nanometers up to several hundred nanometers on a back side of said foil.
- the polymeric foil is covered on its front side by an electrically conductive layer surrounding said narrow opening.
- a gate voltage supply is connected to said electrically conductive layer on said front side of said foil controlling the flow of charged particle within said nanodevice from said first compartment to said second compartment and vice versa.
- This nanodevice has the advantage to control or to switch on and off a charged particle flow of heavy ions, ions of macromolecules, ions of bio-molecules, ionized dimeric, ionized oligomeric or ionized polymeric DNA or ionized insulin.
- the spatial distribution of electric potential inside the pore is changed by the gate voltage on the electrically conductive layer of the polymeric foil in order to advantageously tune the flow of ion through the pore.
- the electrically conductive layer forms a gate close to the narrow opening of the conical, funnel-like, or trumpet-like pore, where the pore has its highest resistance. Such a gating ion flow would allow to control ionic current through the asymmetric pore.
- the polymeric foil comprises polyethylene terephthalate, polyimide or polycarbonate.
- polyethylene terephthalate, polyimide or polycarbonate These materials have the advantage, that an ion trace can be performed through said foil by a high accelerated ion like bismuth.
- Such a trace across a foil material can be etched in an electrolytic cell consisting of two cell halves filled with an electrolytic solution and being divided by said foil comprising said ion trace.
- These materials have further the advantage that a nanodevice made of same is cation selective.
- Another preferred embodiment comprises a gold layer as electrically conductive layer surrounding said narrow opening of said front side.
- a gold layer as a gate electrode has the advantage, that it is resistive against corrosion and oxidation. Therefore, such gold layer can be used in different electrolytic bathes to control and/or switch on an off a flow of charged particles.
- Another preferred material for the gate electrode is a semiconductor like indium oxide or ITO.
- Indium oxide has the advantage, that it is erosion and oxidation resistant in almost any electrolytic bath.
- the back side of said foil is covered by an electrically conductive layer surrounding said wide opening.
- an electrically conductive layer surrounding said wide opening.
- the nanodevice is not limited either to polymer films or to a gold layer, since any asymmetric and charged nanopores together with a conductive layer, which can be charged by a voltage, can be potentially used to accomplish the present invention.
- One preferred mode of operation of the nanodevice is to provide a direct current voltage supply for the electrolytic bath and a direct current voltage supply for the gate voltage.
- Another preferred mode of operation is to apply an alternating voltage to the gate, which enables to achieve a pulse-like flow of charged molecules through said nanodevice with at least one asymmetric pore.
- the invention is further related to a method for producing a nanodevice. Such a method comprises the steps of:
- This method has the advantage that a conical, a funnel-like or a trumpet-like nanopore is performed along the ion trace through the polymeric foil dependent on the parameters of an electrolytic process in an electrolytic cell consisting of two cell halves filled with an electrolytic solution.
- At least a single bismuth ion is accelerated to an energy in the range of 10 to 15 MeV and irradiated toward said polymeric foil to form said ion trace.
- This bismuth ion is particularly advantageous if applied to foils made of polyethylene terephthalate, polyimide and/or polycarbonate.
- This trace is preferably etched by a caustic solution, where such a solution can comprise 9 m NaOH.
- This caustic solution has the advantage that the ion trace can be etched at room temperature. After etching along the ion trace an asymmetric pore, the front side of the foil is deposited with a electrically conductive layer like a gold or indium oxide layer by a sputter technique.
- FIG. 1 shows an embodiment of an apparatus having a nanodevice 1 for controlling the flow of charged particles (ion+ or ion ⁇ ) in an electrolyte.
- This device comprises an electrolytic bath container 2 divided by a polymeric foil 3 into a first 4 and a second 5 compartment. Each compartment 4 and 5 comprises an electrode 6 and 7 connected to a voltage supply 8 , which supplies in this embodiment a direct current voltage U1.
- the electrolytic current I is measured by a current meter 18 .
- the potential of electrode 6 is positive, positive charged particles like ion+are forced through the asymmetric pore 9 of the foil 3 from a wide opening 12 on the back side 13 of the foil 3 to a narrow or small opening 10 on the front side of said foil 3 .
- the foil itself is a circular disc having a diameter D of about 30 mm and a thickness d of 12 ⁇ m.
- the material of the foil in this embodiment is polyethylene terephthalate which was irradiated in its center with a single bismuth ion of 11.4 MeV specific energy and etched from one side in a 9 m NaOH at room temperature to form said pore 9 .
- the polymeric foil 3 is covered on the front side 11 by a gold layer surrounding the narrow opening 10 of said pore 9 .
- This gold layer functions as a gate electrode 17 , which is supplied by a gate voltage U2 supply 15 . If this gate voltage U2 is negative, the charged particles in the first compartment 4 like ion+are accelerated, so that the flow through the nanodevice 1 is increased toward the second compartment 5 . When Increasing U2 toward a positive gate voltage the flow of positive charged particles (ion+) is decreased and can even be switched off.
- FIG. 2 shows principles of the functioning of the nanodevice 1 for controlling the flow of charged particles (ion+, ion ⁇ ) in electrolytes.
- Components with the same functions as in FIG. 1 are characterized by the same reference signs and an explanation of same is omitted.
- FIG. 2 shows in detail the principles of operating a device shown in FIG. 1.
- a thin layer 14 of metal or semiconductor is sputtered on the front side 11 of the foil 3 having such narrow openings 10 .
- This layer 14 can be charged via an independent electric circuit U2. If the pore is very narrow, the passage of the ions through the pore will be influenced by such a “gate”.
- the pore produced by a track-etching technique in a foil 3 made of polyethylene terephthalate, polyimide or polycarbonate are negatively charged due to formation of carboxylate groups, therefore they are cation-selective. This means that cations are the main charged carriers.
- FIG. 3 shows a scheme of an experimental set-up of evaluating the performance of the nanodevice 1 .
- Components having the same functions as in FIG. 1 or in FIG. 2 are characterized by the same reference signs and an explanation of same is omitted.
- the evaluation of the performance of the nanodevice 1 is made for a single pore within a 12 ⁇ m thick circular disc of 30 mm diameter.
- this disc or membrane is inserted in an electrolytic cell consisting of two cell halves of KF and sealed hermetically by applying pressure onto the two cell halves.
- the polymer foil 3 is removed from the cell and dried.
- a gold layer 14 is sputtered on the front side 11 with its narrow opening 10 .
- a piece of a conductive tape is attached to the front side onto the gold layer. Now, the foil is inserted back into the electrolytic cell, which chambers are now filled with potassium fluoride.
- FIG. 4 shows a current-voltage characteristic of a single conical pore 9 in a PET-foil.
- the abscissa of said diagram shows the voltage U1 in V and the ordinate shows the current in nA.
- the dotted curves shows the effect of the parameters: +0.6 V at the metal gate electrode, 0V at the metal gate and ⁇ 0.6 V at the metal gate.
- FIGS. 5 a and 5 b show examples of time series without and with applying a gate voltage for two directions of the potassium ion flow. If a voltage of +2V is applied across the membrane a voltage of +1.5V at the gate will decrease the current drastically, whilst a gate voltage of ⁇ 1.5 will increase the current up to 1 nA.
- the abscissa shows the time in seconds and one can see that after three seconds the current is relatively constant.
Abstract
The present invention relates to an apparatus having a nanodevice for controlling the flow of charged particles in an electrolyte. Such apparatus comprises an electrolytic bath container divided by a polymeric foil into a first and a second compartment, wherein each compartment comprises an electrode connected to a voltage supply. Further the apparatus comprises at least one asymmetric pore forming a via hole through said foil, wherein said pore provides a narrow opening of a diameter in the range of several nanometers down to about one nanometer on a front side of said foil and a wide opening in the range of several ten nanometers up to several hundred nanometers on a back side of said foil. Further, the apparatus comprises an electrically conductive layer surrounding said narrow opening on said front side and a gate voltage supply connected to said electrically conductive layer on said front side of said foil controlling the flow of charged particles within said nanodevice from said first compartment to said second compartment vice versa. The invention further relates to a method for producing such a nanodevice.
Description
- 1. Field of the Disclosure
- The present invention relates to an apparatus having a nanodevice for controlling the flow of charged particles in electrolytes and method for producing same.
- 2. Brief Description of Related Technologies
- In many electrolytic systems the problem of controlling ion flow, rather than flow of electrons, is crucial. For the flow of electrons diodes and transistors are the basic elements controlling, switching on and off and amplifying the signal. For the ionic current there exist very limited possibilities to tune the ion flow. From German patent application 100 44 565.9 an electrochemical rectifier is known, based on preparation of asymmetric pores in a polymeric foil. One mode of operation entails applying a constant voltage across a membrane with asymmetric pores, however changing the current would require changing the concentration and/or the pH-value of the electrolyte. Since this changing of concentration and/or pH-value is time consuming and disturbs the condition of operation, this option may not be applicable for a given system.
- Therefore, it is the object of the present invention to provide an independent “switch”, which would be able to modulate the ion current through the pore with a minimum disturbance of the operation conditions. Further, it is an object of the present invention to control the transport of charged or ionized large molecules.
- FIG. 1 shows a schematic drawing of an apparatus having a nanodevice for controlling the flow of charged particles in electrolytes.
- FIG. 2 shows principles of the functioning of the nanodevice for controlling the flow of charged particles in electrolytes.
- FIG. 3 shows a scheme of an experimental set-up for evaluating the performance of the nanodevice.
- FIG. 4 shows current-voltage characteristics of a single conical pore in a polyethylene terephthalate (PET) foil with a gold layer on the side of the small or narrow opening of a pore, applying 0.1 m KF on both sides of the membrane foil.
- FIGS. 5a and 5 b show examples of time series without and with applied “gate voltage” for two directions of the potassium ion flow.
- According to the invention an apparatus having a nanodevice for controlling the flow of charged particles in electrolytes is provided, comprising an electrolytic bath container, divided by a polymeric foil into a first and a second compartment. Each compartment comprises an electrode connected to a voltage supply. Further, the nanodevice comprises at least an asymmetric pore forming a via hole through said foil, wherein said pore provides a narrow opening of a diameter in the range of several nanometers down to about one nanometer on a front side of said foil and a wide opening in the range of several ten nanometers up to several hundred nanometers on a back side of said foil.
- The polymeric foil is covered on its front side by an electrically conductive layer surrounding said narrow opening. A gate voltage supply is connected to said electrically conductive layer on said front side of said foil controlling the flow of charged particle within said nanodevice from said first compartment to said second compartment and vice versa.
- This nanodevice has the advantage to control or to switch on and off a charged particle flow of heavy ions, ions of macromolecules, ions of bio-molecules, ionized dimeric, ionized oligomeric or ionized polymeric DNA or ionized insulin. In such a nanodevice with such a pore the spatial distribution of electric potential inside the pore is changed by the gate voltage on the electrically conductive layer of the polymeric foil in order to advantageously tune the flow of ion through the pore. The electrically conductive layer forms a gate close to the narrow opening of the conical, funnel-like, or trumpet-like pore, where the pore has its highest resistance. Such a gating ion flow would allow to control ionic current through the asymmetric pore.
- In a preferred embodiment the polymeric foil comprises polyethylene terephthalate, polyimide or polycarbonate. These materials have the advantage, that an ion trace can be performed through said foil by a high accelerated ion like bismuth. Such a trace across a foil material can be etched in an electrolytic cell consisting of two cell halves filled with an electrolytic solution and being divided by said foil comprising said ion trace. These materials have further the advantage that a nanodevice made of same is cation selective.
- Another preferred embodiment comprises a gold layer as electrically conductive layer surrounding said narrow opening of said front side. Such a gold layer as a gate electrode has the advantage, that it is resistive against corrosion and oxidation. Therefore, such gold layer can be used in different electrolytic bathes to control and/or switch on an off a flow of charged particles.
- Another preferred material for the gate electrode is a semiconductor like indium oxide or ITO. Indium oxide has the advantage, that it is erosion and oxidation resistant in almost any electrolytic bath.
- In a further preferred embodiment the back side of said foil is covered by an electrically conductive layer surrounding said wide opening. Such a second metal layer on the back side of the polymeric foil enables the nanodevice to make the ion current changes finer and better controlled.
- The nanodevice is not limited either to polymer films or to a gold layer, since any asymmetric and charged nanopores together with a conductive layer, which can be charged by a voltage, can be potentially used to accomplish the present invention.
- One preferred mode of operation of the nanodevice is to provide a direct current voltage supply for the electrolytic bath and a direct current voltage supply for the gate voltage. Another preferred mode of operation is to apply an alternating voltage to the gate, which enables to achieve a pulse-like flow of charged molecules through said nanodevice with at least one asymmetric pore.
- Preferred applications of the apparatus having a nanodevice are
- 1. Separation processes for the pharmaceutical industry,
- 2. Controlled release of bio-molecules like insulin,
- 3. Voltage-controlled nanosystems,
- 4. Tuning of the ion current signal,
- 5. Gating of ionic bio-molecule in microfluicid lab-on-a-chip devices.
- The invention is further related to a method for producing a nanodevice. Such a method comprises the steps of:
- irradiating a membrane of a polymeric foil by at least one high accelerated ion to form an ion trace through said foil;
- etching said ion trace from a back side of said foil toward a front side of said foil to form a pore having a wide opening on said back side in the range several ten nanometers up to several hundred nanometers and a narrow opening on said front side in the range of several nanometers down to about one nanometer;
- drying said etched foil;
- depositing an electrically conductive layer on said front side by diminishing the narrow opening;
- reopen said narrow opening to a predetermined diameter by etching said conductive layer from its back side.
- This method has the advantage that a conical, a funnel-like or a trumpet-like nanopore is performed along the ion trace through the polymeric foil dependent on the parameters of an electrolytic process in an electrolytic cell consisting of two cell halves filled with an electrolytic solution.
- In a preferred method at least a single bismuth ion is accelerated to an energy in the range of 10 to 15 MeV and irradiated toward said polymeric foil to form said ion trace. This bismuth ion is particularly advantageous if applied to foils made of polyethylene terephthalate, polyimide and/or polycarbonate. This trace is preferably etched by a caustic solution, where such a solution can comprise 9 m NaOH. This caustic solution has the advantage that the ion trace can be etched at room temperature. After etching along the ion trace an asymmetric pore, the front side of the foil is deposited with a electrically conductive layer like a gold or indium oxide layer by a sputter technique.
- To increase the adhesiveness of an electrically conductive layer like a gold layer or a semiconductor layer on the polymer surface of the foil, it is an advantage to roughened the surface of the polymer foil before etching the irradiated film.
- During said deposition of a metal or a semiconductor on said front side the narrow opening is diminished. To reopen said narrow opening a piece of a conductive tape is attached to cover the conductive layer. After that it is an advantage to reinsert said foil with its electrically conductive layer and said piece of a conductive tape in an electrolytic cell, wherein the two cell halves are filled with potassium fluoride, whilst a conductive tape stays attached to the conductive layer.
- Further embodiments, features and advantages of the invention are now discussed with reference to the attached drawings.
- FIG. 1 shows an embodiment of an apparatus having a nanodevice1 for controlling the flow of charged particles (ion+ or ion−) in an electrolyte. This device comprises an
electrolytic bath container 2 divided by apolymeric foil 3 into a first 4 and a second 5 compartment. Eachcompartment electrode 6 and 7 connected to avoltage supply 8, which supplies in this embodiment a direct current voltage U1. The electrolytic current I is measured by acurrent meter 18. - If the potential of
electrode 6 is positive, positive charged particles like ion+are forced through theasymmetric pore 9 of thefoil 3 from awide opening 12 on theback side 13 of thefoil 3 to a narrow orsmall opening 10 on the front side of saidfoil 3. The foil itself is a circular disc having a diameter D of about 30 mm and a thickness d of 12 μm. The material of the foil in this embodiment is polyethylene terephthalate which was irradiated in its center with a single bismuth ion of 11.4 MeV specific energy and etched from one side in a 9 m NaOH at room temperature to form saidpore 9. - The
polymeric foil 3 is covered on the front side 11 by a gold layer surrounding thenarrow opening 10 of saidpore 9. This gold layer functions as agate electrode 17, which is supplied by a gatevoltage U2 supply 15. If this gate voltage U2 is negative, the charged particles in thefirst compartment 4 like ion+are accelerated, so that the flow through the nanodevice 1 is increased toward thesecond compartment 5. When Increasing U2 toward a positive gate voltage the flow of positive charged particles (ion+) is decreased and can even be switched off. - FIG. 2 shows principles of the functioning of the nanodevice1 for controlling the flow of charged particles (ion+, ion−) in electrolytes. Components with the same functions as in FIG. 1 are characterized by the same reference signs and an explanation of same is omitted.
- FIG. 2 shows in detail the principles of operating a device shown in FIG. 1. A
thin layer 14 of metal or semiconductor is sputtered on the front side 11 of thefoil 3 having suchnarrow openings 10. Thislayer 14 can be charged via an independent electric circuit U2. If the pore is very narrow, the passage of the ions through the pore will be influenced by such a “gate”. The pore produced by a track-etching technique in afoil 3 made of polyethylene terephthalate, polyimide or polycarbonate are negatively charged due to formation of carboxylate groups, therefore they are cation-selective. This means that cations are the main charged carriers. - Applying a positive voltage U2 slows down the flow of cations observed as lower current. Applying a negative voltage U2 has an opposite effect, the current will be larger. Accordingly, this device will be the first device, which can control the ion flow, based on asymmetry of electric potential introduced by the conical, funnel-like or trumpet-like shape of a charged nanopore in combination with applying locally electric fields. Since this layer can be charged positively or negatively by means of the voltage applied via an independent circuit, this results in changes of the profile of the electric potential at the pore constriction, which influences the ion current flow.
- FIG. 3 shows a scheme of an experimental set-up of evaluating the performance of the nanodevice1. Components having the same functions as in FIG. 1 or in FIG. 2 are characterized by the same reference signs and an explanation of same is omitted.
- The evaluation of the performance of the nanodevice1 is made for a single pore within a 12 μm thick circular disc of 30 mm diameter. For the purpose of etching such a pore in a 9 m NaOH this disc or membrane is inserted in an electrolytic cell consisting of two cell halves of KF and sealed hermetically by applying pressure onto the two cell halves. When the etching process is completed, the
polymer foil 3 is removed from the cell and dried. In a next step, agold layer 14 is sputtered on the front side 11 with itsnarrow opening 10. Then, a piece of a conductive tape is attached to the front side onto the gold layer. Now, the foil is inserted back into the electrolytic cell, which chambers are now filled with potassium fluoride. - The current through the
pore 9 is measured with electrodes of Ag/AgCl. An independent circuit is built, which applies a voltage to the gold layer via the conductive tape. The scheme of the experimental set-up is shown in FIG. 3. The use of fluoride ions in a KF solution increases the effect of the applied voltage during the electrolytic procedure. Actually, it is possible to perform this treatment of the device in any electrolyte etching a gold layer. - FIG. 4 shows a current-voltage characteristic of a single
conical pore 9 in a PET-foil. The abscissa of said diagram shows the voltage U1 in V and the ordinate shows the current in nA. The dotted curves shows the effect of the parameters: +0.6 V at the metal gate electrode, 0V at the metal gate and −0.6 V at the metal gate. As one can see from this evaluation it is possible to enhance the current through the asymmetric pore at a voltage U1 of 0.4 V by a gate voltage U2 of −0.6 V up to around 1 nA, whilst with a positive gate voltage of 0.6 V the ionic current is decreased to 0 or shut off. - FIGS. 5a and 5 b show examples of time series without and with applying a gate voltage for two directions of the potassium ion flow. If a voltage of +2V is applied across the membrane a voltage of +1.5V at the gate will decrease the current drastically, whilst a gate voltage of −1.5 will increase the current up to 1 nA. In these diagrams of FIGS. 5a and 5 b the abscissa shows the time in seconds and one can see that after three seconds the current is relatively constant.
- In FIG. 5b the voltage across the membrane or across the pore is changed to −2V, so that the current is also negative. By applying negative gate voltage of about −1.5V the current is decreased, whilst applying a positive gate voltage of 1.5V the current is increased to −1 nA. This diagrams show that this nanodevice is quite sensitive and works like a transistor for ions in an electrolytic bath.
Claims (23)
1. An apparatus having a nanodevice for charged particles flow comprising:
(a) an electrolytic bath container, divided by a polymeric foil into a first and a second compartment, wherein each compartment comprises an electrode connected to a direct current voltage (U1) supply;
(b) at least one asymmetric pore forming a via hole through said foil, wherein said pore provides a narrow opening of a diameter in a range of about one nanometer to several nanometers on a front side of said foil, and a wide opening in a range of ten nanometers to several hundred nanometers on a back side of said foil;
(c) an electrically conductive layer surrounding said narrow opening on said front side; and
(d) a gate voltage (U2) supply connected to said electrically conductive layer on said front side of said foil controlling the flow of charged particles within said nanodevice from said first compartment to said second compartment and vice versa.
2. The apparatus of claim 1 , wherein said asymmetric pore is a conical pore.
3. The apparatus of claim 1 , wherein said asymmetric pore is a funnel-like pore from said wide opening toward said narrow opening.
4. The apparatus of claim 1 , wherein said asymmetric pore is a straight trumpet-like pore from said narrow opening toward said wide opening.
5. The apparatus of claim 1 , wherein said foil comprises polyethylene terephthalate.
6. The apparatus of claim 1 , wherein said foil comprises polyimide.
7. The apparatus of claim 1 , wherein said foil comprises polycarbonate.
8. The apparatus of claim 1 , wherein said nanodevice is cation selective.
9. The apparatus of claim 1 , wherein said electrically conductive layer comprises gold.
10. The apparatus of claim 1 , wherein said electrically conductive layer comprises indium oxide.
11. The apparatus of claim 1 , wherein said electrically conductive layer is a gate electrode.
12. The apparatus of claim 1 , wherein said back side of said foil is covered by an electrically conductive layer surrounding said wide opening.
13. The apparatus of claim 1 , wherein said nanodevice is applied to control or to switch on and off a charged particle flow of heavy ions, ions of macromolecules, ions of bio-molecules, ionized dimeric, ionized oligomeric or ionized polymeric DNA or ionized insulin.
14. A method of making the nanodevice apparatus of claim 1 , the method comprising the steps of:
(a) irradiating a membrane of a polymeric foil by at least one highly accelerated ion to form an ion trace through said foil;
(b) etching said ion trace from a back side of said foil toward a front side of said foil to form a pore having a wide opening on said back side and a narrow opening on said front side in a range of about one nanometer to several nanometers;
(c) drying said etched foil;
(d) depositing an electrically conductive layer on said front side by diminishing the narrow opening;
(e) reopening said narrow opening to a predetermined diameter by etching said conductive layer from its back side.
15. The method of claim 14 , wherein a single bismuth ion is accelerated to an energy in the range of 10 to 15 MeV and irradiated toward said polymeric foil to form said ion trace.
16. The method of claim 14 , wherein step (b) further comprises etching said ion trace by a caustic solution.
17. The method of claim 16 , wherein said caustic solution comprises 9 m NaOH.
18. The method of claim 14 , wherein step (b) further comprises etching said ion trace at room temperature.
19. The method of claim 14 , wherein said deposition is carried out by sputtering a metal or a semiconductor on to said front side.
20. The method of claim 14 , further comprising roughening said front side of said foil before etching said ion trace.
21. The method of claim 14 , wherein said membrane is inserted in an electrolytic cell comprising two cell halves filled with a KF solution and being divided by said membrane and sealed hermetically to etch said ion trace.
22. The method of claim 14 , wherein a conductive tape is attached to the conductive layer before said reopening of said narrow opening is performed.
23. The method of claim 22 , wherein said foil covered on its front side by a conductive tape is reentered to said electrolytic cell, which cell halves are now filled with NaF.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
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US10/254,947 US20040055875A1 (en) | 2002-09-25 | 2002-09-25 | Nanodevice for charged particle flow and method for producing same |
DE60308535T DE60308535T2 (en) | 2002-09-25 | 2003-09-24 | METHOD FOR PRODUCING A NANOVA DIRECTION FOR A CONTROLLED FLOW OF LOADED PARTICLES |
AT03798180T ATE340017T1 (en) | 2002-09-25 | 2003-09-24 | METHOD FOR PRODUCING A NANODEVICE FOR A CONTROLLED FLOW OF CHARGED PARTICLES |
EP03798180A EP1542788B1 (en) | 2002-09-25 | 2003-09-24 | Method for producing a nanodevice for controlled charged particle flow |
AU2003275981A AU2003275981A1 (en) | 2002-09-25 | 2003-09-24 | Nanodevice for controlled charged particle flow and method for producing same |
PCT/EP2003/010631 WO2004028673A1 (en) | 2002-09-25 | 2003-09-24 | Nanodevice for controlled charged particle flow and method for producing same |
JP2004539005A JP2006502839A (en) | 2002-09-25 | 2003-09-24 | Nanodevice for controlling the flow of charged particles and fabrication method thereof |
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US10/254,947 US20040055875A1 (en) | 2002-09-25 | 2002-09-25 | Nanodevice for charged particle flow and method for producing same |
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US10/254,947 Abandoned US20040055875A1 (en) | 2002-09-25 | 2002-09-25 | Nanodevice for charged particle flow and method for producing same |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070048437A1 (en) * | 2002-09-24 | 2007-03-01 | Junji Kido | Display element and method for producing the same |
US20110132762A1 (en) * | 2009-12-03 | 2011-06-09 | O' Brien Kevin C | Nanoengineered field induced charge separation membranes manufacture thereof |
US9403128B2 (en) | 2009-12-03 | 2016-08-02 | Lawrence Livermore National Security, Llc | Nanoengineered field induced charge separation membranes manufacture thereof |
US10345289B2 (en) * | 2013-04-18 | 2019-07-09 | The Board Of Trustees Of The University Of Illinois | Method and apparatus for analyzing a target material |
US10677752B2 (en) | 2013-04-18 | 2020-06-09 | The Board Of Trustees Of The University Of Illinois | Method and apparatus analyzing a target material |
US11035847B2 (en) | 2017-06-29 | 2021-06-15 | President And Fellows Of Harvard College | Deterministic stepping of polymers through a nanopore |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4555274A (en) * | 1982-03-15 | 1985-11-26 | Fuji Photo Film Co., Ltd. | Ion selective electrode and process of preparing the same |
-
2002
- 2002-09-25 US US10/254,947 patent/US20040055875A1/en not_active Abandoned
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4555274A (en) * | 1982-03-15 | 1985-11-26 | Fuji Photo Film Co., Ltd. | Ion selective electrode and process of preparing the same |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070048437A1 (en) * | 2002-09-24 | 2007-03-01 | Junji Kido | Display element and method for producing the same |
US9379351B2 (en) * | 2002-09-24 | 2016-06-28 | Dai Nippon Printing Co., Ltd. | Display element and method for producing the same |
US20110132762A1 (en) * | 2009-12-03 | 2011-06-09 | O' Brien Kevin C | Nanoengineered field induced charge separation membranes manufacture thereof |
US8696882B2 (en) | 2009-12-03 | 2014-04-15 | Lawrence Livermore National Security, Llc. | Nanoengineered field induced charge separation membranes and methods of manufacture thereof |
US9403128B2 (en) | 2009-12-03 | 2016-08-02 | Lawrence Livermore National Security, Llc | Nanoengineered field induced charge separation membranes manufacture thereof |
US10345289B2 (en) * | 2013-04-18 | 2019-07-09 | The Board Of Trustees Of The University Of Illinois | Method and apparatus for analyzing a target material |
US10677752B2 (en) | 2013-04-18 | 2020-06-09 | The Board Of Trustees Of The University Of Illinois | Method and apparatus analyzing a target material |
US11035847B2 (en) | 2017-06-29 | 2021-06-15 | President And Fellows Of Harvard College | Deterministic stepping of polymers through a nanopore |
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