Batteries with replaceable zinc cartridges
10608243 ยท 2020-03-31
Assignee
Inventors
Cpc classification
H01M4/62
ELECTRICITY
H01M8/188
ELECTRICITY
Y02E60/10
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
Y02E60/50
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
H01M10/4235
ELECTRICITY
International classification
H01M4/62
ELECTRICITY
H01M8/18
ELECTRICITY
H01M10/42
ELECTRICITY
Abstract
This application proposes the use of rechargeable and replaceable zinc cartridges to expand cycle life and lifetime of nickel-zinc and silver-zinc batteries. Two types of possible battery cell assemblies are demonstrated: a battery that includes face-to-back arrangement of cells, and side-by-side linked flat batteries that can be used as wall mounted batteries. An improved composition of the replaceable zinc electrode is suggested.
Claims
1. A mechanically rechargeable battery cell comprising a) at least one zinc anode comprising an anode current collector, and a zinc electroactive composition that includes zinc particles and additives in contact with said anode current collector, b) at least one doped nickel hydroxide cathode that includes a cathode current collector, and a nickel hydroxide electroactive composition with additives in contact to said cathode current collector, c) an ion conducting electron blocking separator between said zinc anode and nickel hydroxide cathode, d) an electrolyte, and e) a case that includes a body, a cap, and an optional relief valve in the cap, and accommodates said zinc anode, said nickel hydroxide cathode, said separator and said electrolyte, wherein f) said zinc anode is preconditioned before assembling the battery by in situ electrochemical oxidation in a separate electrochemical cell to produce doped zinc oxide layers on the surfaces of the zinc particles, and g) said zinc anode is hermetically sealed with said ion conducting separator, and h) the zinc anode includes additives selected from the group consisting of graphite, carbon, bismuth, lead, aluminum, indium, carboxymethylcellulose, polyacrylic acid and polyvinyl alcohol, and i) the zinc anode further includes polyaminodiphenylamine, and zirconia fibers in amount 0.1 w %-15 w %, whereby the battery is electrochemically rechargeable.
2. The battery of claim 1 wherein said separator is ion-selective, and forms a layer on the zinc anode.
3. The battery of claim 1 wherein the case includes plurality of zinc and nickel hydroxide electrodes.
4. The battery of claim 1 wherein the nickel hydroxide cathode is electrochemically rechargeable and mechanically replaceable.
5. The battery of claim 1 wherein the case is made of materials selected from the group consisting of plastic, plastic composition, rubber, rubber composition, ceramic, ceramic composition, metal foil, and metal foil composition.
6. The battery of claim 1 wherein the zinc anode current collector is made of a) material selected from the group consisting of copper, nickel, silver, gallium, lead, bismuth, indium, antimony, and their alloys, and b) stainless steel, and c) materials listed in a) and b) and covered with a layer of material selected from the group consisting of zinc, tin, indium, lead, copper, bismuth, antimony, nickel, silver and their alloys.
7. The battery of claim 1 wherein the anode current collector and the cathode current collector are made of low surface area materials on one side, and large surface area materials on the other side.
8. The battery cell assembly of the battery cells of claim 1.
9. The battery cell assembly of the battery cells of claim 1 wherein the cases a) are united via their vertical edges to form modules, and b) the modules are assembled in racks to form flat wall mounted batteries.
10. The battery cell assembly of the battery cells of claim 1 wherein the cell assemblies are united using rotational joints.
11. The battery cell assembly of the battery cells of claim 1 wherein multiple zinc anodes and multiple nickel hydroxide cathodes are arranged consequently face-to-back, and the case includes a spring means for compression said zinc anodes and nickel hydroxide cathodes to each-other.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
(4)
(5)
(6)
DETAILED DESCRIPTION OF THE INVENTION
(7) A horizontal cross section of a nickel zinc battery cell with two nickel cathodes and a replaceable zinc cartridge is shown in
(8) Main components of the nickel-zinc battery cell presented in
(9) An example of a battery assembly made of four cells packed in a case is shown in
(10) The battery can also work as flow battery by adding at least one outside pump, filter and two tubes connected to the battery. Possible purpose of using a flow battery is conditioning the electrolyte by filtering and eliminating impurities.
(11) The collectors to zinc and nickel electrodes are made of low surface area conducting sheet on one side, and high surface area conducting sheet on the other side. For example, the current collector to the nickel electrode can be produced by soldering or welding a piece of nickel foam to a nickel foil of appropriate thickness, for example in the range 0.05 mm-0.5 mm. Then electroactive nickel composition is imbedded into nickel foam to produce a rechargeable nickel electrode.
(12) The zinc electrode of the first cell, and the nickel electrode of the last one are attached to the battery output connectors (not shown in
(13) The possible outer view of a nickel-zinc battery is shown in
(14)
(15) A foldable version of the flat battery is shown in
(16) A battery case can be produced from polyethylene, polypropylene, polymethylmetacrylate, or any other plastic stable in alkaline solutions. Metal sheet, for example stainless steel, or steel covered by nickel, rubber or casted ceramic can be also used. Possible materials for sliding lid 18 include metals, rubbers, plastics, ceramic materials and their composites.
(17) The material of the collector 2 to the zinc electrode 1 can be selected from copper, copper alloys, nickel, nickel alloys, lead, lead alloys, steel, stainless steel, bismuth, bismuth alloys, tin, tin alloys, carbon, graphite, expanded graphite, graphene, composites of graphite materials, plastics and rubber.
(18) The current collector can be made of metal foil, corrugated metal foil, mesh, expanded metal sheet, foam, and the combination of these materials. A dual current collector includes low surface area material on one side, and high surface area material on the other side. For example metal foil can be soldered to metal foam, expanded foil or metal mesh with two parts connected to each other by welding, soldering, ultrasonic or laser welding. The metals can be similar or different depending on application requirement. For example copper foil is prime choice when high conducting collector is needed. Dual type collector can be used for both nickel and zinc electrodes.
(19) The current collector can be covered by an additional layer to increase conductivity, to protect from corrosion, to improve mechanical, chemical or physical properties as required by the system. The current collector can be covered by zinc, tin, lead indium, bismuth, antimony, nickel, silver or their alloys. The amount of the second component of alloy is about 0.1%-50%. Said layer can be deposited by electroplating, electroless plating, hot metallization, painting, liquid metal pulverization, rubbing, and dipping.
(20) The third component can be added to alloy if required. For example a three component current collector based on ZnCuBi alloy can be used for replaceable zinc electrode. Three component current collector can be prepared similar to two component collector described above. For example, a zinc electrode current collector has been produced by casting ZnBiCu alloy with mass content 80% Zn, 15% Bi and 5% Cu on brass mesh at 550 C.
(21) Current collector for nickel hydroxide electrode is produced from nickel, titanium, stainless steel, cobalt, lead, and alloys of mentioned metals. The current collector can be formed as mesh, foam, corrugated metal sheet, or expanded metal. Corrosion stability of current collectors can be improved by anodic treatment of stainless steel and other metals in the electrolytes that include amines and their derivatives, for example diphenylamine. To improve this process a soluble complex between amine and platinum group metal, for example ruthenium, can be used. Complexes of other platinum group metals with conjugated amines can be applied.
(22) The zinc electrode can be formed from zinc powder or zinc oxide doped with indium, aluminum, lead, bismuth to inhibit zinc corrosion. Zinc or/and zinc oxide paste can also include carboxymethylcellulose, polyvinyl alcohol, polyacrylic acid, polyamines, surface active compounds, carbons, graphite to insure stable operation. The zinc electrode can further include materials that improve its performance, for example zirconia fibers in the amount 0.1%-5% or hydroxides of second group metals, for example calcium or barium hydroxides. The zinc electrode can be wrapped in the battery separator and ion selective membrane. The upper end and lower ends of the separator or membrane can be sealed with material stable in the alkaline electrolyte.
(23) Another approach is to cover the surface of the zinc electrode with a layer of anion selective membrane. For this purpose a composition is prepared from anion selective material by mixing with an adhesive, for example soluble ptfe. Ptfe is added in the amount 0.5%-10%. The zinc electrode with a current collector are dipped into liquid suspension, and dried at elevated temperature about 60 C.-70 C.. The layer can be made partially porous by adding a water soluble component to be dissolved when the zinc electrode is introduced in water. An example of the additive is ammonium carbonate, which can be also eliminated by heat treatment. The example of an anion exchange material for deposition is quaternary ammonia polysulfone.
(24) For the purpose of this patent application the zinc cartridge should be as cheap as possible. Therefore the design of the zinc electrode (or cartridge) is the simplest, and does not include any expensive compound. In this case the cost of replacement can be decreased to 5%-15% of the nickel-zinc battery cost.
(25) Nickel oxide-hydroxide electrode can be formed from nickel hydroxide that can be oxidized to nickel oxide-hydroxide. The electrode includes 1%-10% of cobalt and 1%-7% of zinc. The electrode can also include aluminum in the amount 1%-20%. The electrode might contain a binder in the amount 0.1%-5%. Possible binder is ptfe.
(26) Electrolyte includes one of several ion conducting materials selected from the group consisting of potassium hydroxide, sodium hydroxide, lithium hydroxide, tetrabutylammonium hydroxide in total concentration in the range 1 M/L to 7 M/L. Following materials can be added to improve properties of the electrolyte: borates, fluorides, acetates, citrates, carbonates, polyacrylic acid, or carboxymethylcellulose. In certain cases electrolyte in the pH range 3-13 can be used.
(27) What is written above in relation to the nickel-zinc battery is applicable to the silver-zinc battery. In this case the applicability of the replaceable cartridges for extending cycle life and lifetime of silver-nickel battery depends on performance of the silver electrode.
(28) An Example of Practical Implementation.
(29) Nickel hydroxide doped with Zn 2% and Co 5% has been prepared by the addition of nitrate salts to ammonia and alkaline solutions. Precipitated nickel hydroxide was washed with distilled water three times. Then hydroxide was precipitated in a centrifuge at 1500 rpm, and dried in vacuum at 70 C for 5 h. Nickel hydroxide was mixed with nickel powder 15%, ptfe 1% and distilled water to form a paste. The paste was impregnated into nickel foam current collector, which was oxidized at 0.25 A for approximately 5 h in a three electrode cell with a nickel foil electrode as a counter electrode, and zinc wire as a pseudo reference electrode.
(30) The zinc paste was prepared by mixing of the zinc powder doped with Bi 0.5% and In 0.5% with graphite 5%, ptfe 1% and 2% polyaminodiphenylamine. The paste was attached to the lead current collector and wrapped into polypropylene separator. The case was prepared by gluing two polypropylene sheets to a polypropylene base. The cap was made of polysilicon rubber. The zinc electrode and the nickel electrode were placed into case, filled with 30% of KOH and sealed with the cap. The battery voltage was 1.7V, the voltage under 0.5 A current was 1.66V, and voltage under 3 A load 1.52V. The zinc cartridge could be removed from the battery and exchanged by another one to achieve similar performance.