Information
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Patent Application
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20230299279
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Publication Number
20230299279
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Date Filed
April 28, 2023a year ago
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Date Published
September 21, 2023a year ago
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Inventors
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Original Assignees
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CPC
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International Classifications
- H01M4/485
- C01G33/00
- H01M4/66
- H01M10/0525
- H01M10/0565
Abstract
Processes for preparing a niobate material are provided, in which the processes include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.
Claims
- 1. An anode, comprising: an anode-composition including an active anode species comprising at least one niobate compound, the at least one niobate compound comprising at least one transition-metal-niobate (TMN), at least one post-transition-metal-niobate (PTMN), or both, wherein
the at least one niobate compound is prepared by:
(i) providing a water-soluble niobium-containing source;(ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both;(iii) dissolving (a) the water-soluble niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate aqueous solution;(iv) forming an intermediate paste by admixing an inert support material with the intermediate aqueous solution;(v) optionally coating the intermediate paste on a support substrate; and(vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing the TMN and/or the PTMN.
- 2. The anode of claim 1, wherein the anode composition comprises from about 80 wt.% to about 95 wt.% of the at least one niobate compound.
- 3. The anode of claim 1, wherein the at least one niobate compound comprises a titanium niobate, a copper niobate, a tungsten niobate, an aluminum niobate, or any combination thereof.
- 4. The anode of claim 1, wherein the water-soluble niobium-containing source is a water-soluble niobium oxalate.
- 5. The anode of claim 1, wherein the TMS comprises one or more of titanium, copper, and tungsten, and the PTMS comprises aluminum.
- 6. The anode of claim 1, further comprising adding an organic acid during step (iii).
- 7. The anode of claim 6, wherein the organic acid comprises oxalic acid.
- 8. The anode of claim 1, wherein the inert support material comprises a material that does not react with (i) the niobium-containing source or (ii) the TMS or PTMS.
- 9. The anode of claim 8, wherein the inert support material comprises a plurality of particles.
- 10. The anode of claim 9, wherein the inert support material comprises carbon black.
- 11. The anode of claim 1, wherein the intermediate paste comprises from about 20 wt.% to about 80 wt.% on a dry basis of the inert support material.
- 12. The anode of claim 11, wherein the intermediate paste comprises a diphasic system containing both a liquid phase comprising the intermediate aqueous solution and a solid phase comprising the inert support material.
- 13. The anode of claim 1, wherein
the at least one niobate compound is further prepared by a step of drying the intermediate paste prior to the calcination process to form a dry-intermediate paste, wherein the dry-intermediate paste comprises from about 0 to about 5 wt.% of water, andthe calcination process comprises subjecting the intermediate paste to a calcination temperature from about 800° C. to about 1400° C.
- 14. The anode of claim 1, wherein the TMN comprises a titanium niobate, a copper niobate, or a tungsten niobate, and the PTMN is an aluminum niobate.
- 15. The anode of claim 1, wherein the TMN, the PTMN, or both comprise a plurality of particulates having an average diameter from about 1 to about 100 microns.
- 16. The anode of claim 15, wherein the plurality of particulates comprise a platelet-like morphology having an aspect ratio from about 2:1 to about 20:1.
- 17. The anode of claim 1, wherein the water-soluble niobium-containing source is a niobium (V) oxalate hydrate.
- 18. The anode of claim 1, wherein the inert support material comprises a plurality of particles having an average diameter from about 5 nm to about 200 nm.
Provisional Applications (1)
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Number |
Date |
Country |
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63061282 |
Aug 2020 |
US |
Divisions (1)
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Number |
Date |
Country |
Parent |
17346495 |
Jun 2021 |
US |
Child |
18140670 |
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US |