Solid-state structures with volatile sintering aids, and methods for fabrication and use thereof
US-2024429439-A1 · Dec 26, 2024 · US
US2024222697A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024222697-A1 |
| Application number | US-202318537953-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 13, 2023 |
| Priority date | Dec 30, 2022 |
| Publication date | Jul 4, 2024 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A method for preparing a sodium super ionic conductor solid electrolyte by low-dimensional crystallization belongs to a field of energy materials. The method is based on the theory of negative ion coordination polyhedron growth unit, and uses low-temperature plasma as a protective gas of a spray drying equipment. While evaporating the solvent in a sodium super ionic conductor solid electrolyte precursor slurry, plasma active groups modify the particle surface of the sodium super ionic conductor solid electrolyte precursor particles in-situ. A free space dimension of crystal growth in the crystallization process is reduced, and directional growth of crystals in the solid phase sintering process is induced. Secondly, the dispersion stability of the sodium super ionic conductor solid electrolyte precursor particles is improved. Compared with the traditional high-temperature solid-state sintering process, the method has the advantages of fast crystallization speed, high crystal purity and integrity, good compactness, and uniform particles.
Opening claim text (preview).
What is claimed is: 1 . Method for preparing a sodium super ionic conductor solid electrolyte by low-dimensional crystallization, comprising the following steps: Precursor slurry preparation: Weigh raw materials according to a preset chemical formula Na x Zr 2 Si x-1 P 4-x O 12 (wherein, 1≤x≤4); a grinding solvent is added, followed by ball milling pretreatment and sand milling nano treatment to obtain a sodium super ionic conductor solid electrolyte precursor slurry. Plasma-assisted spray drying granulation: The sodium super ionic conductor solid electrolyte precursor slurry is spray-dried and granulated in a spray drying tower, and the plasma atmosphere is passed into the spray drying tower simultaneously to obtain sodium super ionic conductor solid electrolyte precursor particles with surfaces modified in-situ by plasma active groups. Sodium super ionic conductor solid electrolyte precursor particle sintering: Sodium super ionic conductor solid electrolyte precursor particles are put into a muffle furnace for sintering so as to obtain the sodium super ionic conductor solid electrolyte. 2 . The method according to claim 1 , wherein, a sodium source in the raw material is one or more of sodium chloride, sodium carbonate, sodium thiosulfate, sodium bicarbonate, sodium nitrate, and trisodium phosphate dodecahydrate; a zirconium source is zirconium dioxide; a silicon source is silicon dioxide; a phosphorus source is one or more of ammonium dihydrogen phosphate, sodium hydrogen phosphate, and trisodium phosphate dodecahydrate. 3 . The method according to claim 1 , wherein, the grinding solvent is one or more of ethanol, water, acetone, and isopropanol. 4 . The method according to claim 1 , wherein, in the step of precursor slurry preparation, a rotational speed of the ball milling pretreatment is 50 r/min-1000 r/min, and ball milling time is 0.5 h-48 h. 5 . The method according to claim 1 , wherein, a speed of the sand-milling nano-treatment is 50 r/min-1500 r/min, and sand-milling time is 0.5 h-48 h. 6 . The method according to claim 1 , wherein, the plasma atmosphere is one or more of nitrogen, argon, helium, nitrogen-argon mixed gas, nitrogen-helium mixed gas, and argon-helium mixed gas. 7 . The method according to claim 1 , wherein, in the step of plasma-assisted spray drying and granulation, a spray drying temperature is 50° C.-300° C., and a pressure is 0 Mpa-1 Mpa. 8 . The method according to claim 1 , wherein, in the step of sodium super ionic conductor solid electrolyte precursor particle sintering, a sintering temperature is 700° C.-1400° C., and sintering time is 2 h-36 h. 9 . The method according to claim 1 , wherein, the sodium super ionic conductor solid electrolyte is in a form of regular hexahedral crystals with a particle size of 3 μm-4 μm. 10 . A sodium super ionic conductor solid electrolyte, wherein the sodium super ionic conductor solid electrolyte is prepared by the preparation methods in claim 1 .
Solid materials · CPC title
Energy storage using batteries · CPC title
inorganic · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.