Printed silver oxide batteries
An energy storage device, such as a silver oxide battery, can include a silver-containing cathode and an electrolyte having an ionic liquid. An anion of the ionic liquid is selected from the group consisting of: methanesulfonate, methylsulfate, acetate, and fluoroacetate. A cation of the ionic liquid can be selected from the group consisting of: imidazolium, pyridinium, ammonium, piperidinium, pyrrolidinium, sulfonium, and phosphonium. The energy storage device may include a printed or non-printed separator. The printed separator can include a gel including dissolved cellulose powder and the electrolyte. The non-printed separator can include a gel including at least partially dissolved regenerate cellulose and the electrolyte. An energy storage device fabrication process can include applying a plasma treatment to a surface of each of a cathode, anode, separator, and current collectors. The plasma treatment process can improve wettability, adhesion, electron and/or ionic transport across the treated surface.
1. A method of manufacturing an energy storage device, the method comprising:
printing a first electrode over a substrate, wherein the first electrode comprises an ionic liquid comprising an anion selected from the group consisting of: methanesulfonate, methylsulfate, acetate, and fluoroacetate,
wherein the energy storage device comprises a silver oxide battery.
2. The method of claim 1 , wherein the ionic liquid is a basic ionic liquid.
3. The method of claim 1 , wherein the ionic liquid comprises a cation selected from the group consisting of: imidazolium, pyridinium, ammonium, piperidinium, pyrrolidinium, sulfonium, and phosphonium.
4. The method of claim 3 , wherein the cation comprises at least one of a butyltrimethylammonium, 1-ethyl-3-methylimidazolium, 1-butyl-3-methylimidazolium, 1-methyl-3-propylimidazolium, 1-hexyl-3-methylimidazolium, choline, ethylammonium, tributylmethylphosphonium, tributyl(tetradecyl)phosphonium, trihexyl(tetradecyl)phosphonium, 1-ethyl-2,3-methylimidazolium, 1-butyl-1-methylpiperidinium, diethylmethylsulfonium, 1-methyl-3-propylimidazolium, 1-ethyl-3-methylimidazolium, 1-methyl-1-propylpiperidinium, 1-butyl-2-methylpyridinium, 1-butyl-4-methylpyridinium, 1-butyl-1-methylpyrrolidinium, or diethylmethylsulfonium.
5. The method of claim 1 , wherein the first electrode serves as a cathode of the energy storage device.
6. The method of claim 5 , wherein the cathode comprises at least one of silver(I) oxide (Ag 2 O), silver(I,III) oxide (AgO), or silver nickel oxide (AgNiO 2 ).
7. The method of claim 5 , wherein the cathode comprises at least one of manganese(IV) oxide (MnO 2 ) or nickel oxyhydroxide (NiOOH).
8. The method of claim 6 , wherein the cathode further comprises at least one of manganese(IV) oxide (MnO 2 ) or nickel oxyhydroxide (NiOOH).
9. The method of claim 1 , wherein the first electrode serves as an anode of the energy storage device.
10. The method of claim 9 , wherein the anode comprises at least one of zinc, cadmium, iron, nickel, aluminum, metal hydrate, or hydrogen.
11. The method of claim 1 , further comprising:
forming a second electrode over the first electrode; and
forming a separator comprising at least partially dissolved cellulose, the separator between the first electrode and the second electrode.
12. The method of claim 11 , wherein the second electrode comprises zinc.
13. The method of claim 1 , further comprising,
forming a separator over the first electrode;
forming a second electrode over the separator; and
plasma treating a surface of the energy storage device prior to one or more of printing the first electrode, forming the separator, or forming the second electrode.
14. The method of claim 13 , comprising:
prior to printing the first electrode, plasma treating a surface of the substrate;
prior to forming the separator, plasma treating a surface of the first electrode; and
prior to forming the second electrode, plasma treating a surface of the separator.
15. The method of claim 13 , wherein plasma treating comprises applying a plasma comprising one or more of oxygen gas, nitrogen gas, hydrogen gas, or carbon tetrafluoride gas to the surface of the energy storage device.
16. The method of claim 13 , wherein plasma treating comprises directing a plasma source at the surface of the energy storage device at a temperature of about 25° C. and under atmospheric pressure.
17. The method of claim 13 , wherein the energy storage device comprises a current collector, and wherein plasma treating comprises applying a plasma to a surface of the current collector.