Electrode forming process for metal-ion battery with hexacyanometallate electrode

Patent metadata

Field	Value
Publication number	US-9269953-B2
Application number	US-201213432993-A
Country	US
Kind code	B2
Filing date	Mar 28, 2012
Priority date	Mar 28, 2012
Publication date	Feb 23, 2016
Grant date	Feb 23, 2016

Abstract

A method is provided for forming a metal-ion battery electrode with large interstitial spacing. A working electrode with hexacyanometallate particles overlies a current collector. The hexacyanometallate particles have a chemical formula A m M1 x M2 y (CN) 6 .zH 2 O, and have a Prussian Blue hexacyanometallate crystal structure, where A is either alkali or alkaline-earth cations. M1 and M2 are metals with 2+ or 3+ valance positions. The working electrode is soaked in an organic first electrolyte including a salt including alkali or alkaline earth cations. A first electric field is created in the first electrolyte between the working electrode and a first counter electrode, causing A cations and water molecules to be simultaneously removed from interstitial spaces in the Prussian Blue hexacyanometallate crystal structure, forming hexacyanometallate particles having the chemical formula of A m′ M1 x M2 y (CN) 6 .z′H 2 O, where m′<m and z′<z, overlying the working electrode.

First claim

We claim:

1. A method for forming a metal-ion battery electrode with large interstitial spacing, the method comprising:
forming a working electrode with hexacyanometallate particles overlying a current collector, the hexacyanometallate particles having a chemical formula A m M1 x M2 y (CN) 6 .zH 2 O, and having a Prussian Blue hexacyanometallate crystal structure,
where A is selected from a group consisting of alkali and alkaline-earth cations;
where M1 is a metal selected from a group consisting of 2+ and 3+ valance positions;
where M2 is a metal selected from a group consisting of 2+ and 3+ valance positions;
where m is in a range of 0 to 2;
where x is in a range of 0.5 to 1.5;
where y is in a range of 0.5 to 1.5;
where z is in a range of 0 to 10;

soaking the working electrode in an organic first electrolyte including a salt selected from the group consisting of alkali and alkaline earth cations;
accepting a first electric field in the first electrolyte between the working electrode and a first counter electrode;
in response to the first electric field, simultaneously removing A cations and water molecules from interstitial spaces in the Prussian Blue hexacyanometallate crystal structure;
forming hexacyanometallate particles having a chemical formula of A m′ M1 x M2 y (CN) 6 .z′H 2 O, where m′<m and z′<z, overlying the working electrode;
subsequent to forming A m′ M1 x M2 y (CN) 6 .zH 2 O, soaking the working electrode in an organic second electrolyte including a salt with A′ cations, where A′ is selected from a group consisting of alkali and alkaline-earth cations;
accepting a second electric field in the second electrolyte between the working electrode and a second counter electrode including A′ elements;
in response to the second electric field, adding A′ cations into the interstitial spaces of the A m′ M1 x M2 y (CN) 6 .zH 2 O crystal structure; and,
forming hexacyanometallate particles with the chemical formula A′ n A m′ M1 x M2 y (CN) 6 .z′H 2 O the metal current collector, where n is in a range of 0.5 to 2.

2. The method of claim 1 wherein soaking the working electrode in the second electrolyte including a salt with A′ cations includes the A′ cations being selected from a group consisting the same material as the A cations and a different material other than the A cations.

3. The method of claim 1 wherein forming hexacyanometallate particles having the chemical formula of A m′ M1 x M2 y (CN) 6 .z′H 2 O includes forming hexacyanometallate particles having the chemical formula of M1 x M2 y (CN) 6 , where m′=z=0.

4. The method of claim 1 wherein the A cations are selected from a group consisting of Na + , K + , Mg 2+ , and Ca 2+ .

5. The method of claim 1 wherein the A′ cations are selected from a group consisting of Na + , K + , Mg 2+ , and Ca 2+ .

6. The method of claim 1 wherein simultaneously removing A cations and water molecules from interstitial spaces in the Prussian Blue hexacyanometallate crystal structure in response to the first electric field includes forming a solid-electrolyte interphase (SEI) layer overlying the working electrode.

7. The method of claim 1 wherein soaking the working electrode in an organic second electrolyte, and accepting the second electric field in the second electrolyte between the working electrode and the second counter electrode includes soaking the working electrode in an assembled battery, where the second counter electrode is selected from a group consisting of an anode and a cathode, the working electrode is unselected from the group, and the second electric field inserts A′ cations into the interstitial spaces of the A m′ M1 x M2 y (CN) 6 .z′H 2 O crystal structure.

Assignees

• Lu Yuhao
• Lee Jong-Jan
• Sharp Lab Of America Inc

Inventors

• Lu Yuhao
• Lee Jong-Jan

Classifications

• H01M10/054

  Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium · CPC title

• H01M4/0438

  by electrochemical processing (electroless electrochemical plating C23C18/54) · CPC title

• H01M4/0459

  Electrochemical doping, intercalation, occlusion or alloying · CPC title

• H01M4/58 Primary

  of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates · CPC title

• Y02P70/50

  Manufacturing or production processes characterised by the final manufactured product · CPC title