Solid-state structures with volatile sintering aids, and methods for fabrication and use thereof
US-2024429439-A1 · Dec 26, 2024 · US
US2016372786A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016372786-A1 |
| Application number | US-201615172641-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 3, 2016 |
| Priority date | Jun 16, 2015 |
| Publication date | Dec 22, 2016 |
| Grant date | — |
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A process for making a superionic conducting salt includes: combining a primary salt and an impact member, the primary salt including an ordered phase and being an ionic conductor; impacting the primary salt with the impact member; and converting the primary salt to the superionic conducting salt in response to impacting the primary salt with the impact member at a conversion temperature to make the superionic conducting salt, the conversion temperature optionally being less than a thermally activated transition temperature that thermally converts the primary salt to the superionic conducting salt in an absence of the impacting the primary salt, and the superionic conducting salt including a superionic conductive phase in a solid state at less than the thermally activated transition temperature.
Opening claim text (preview).
What is claimed is: 1 . A superionic conducting salt comprising: a plurality of salt cations; a plurality of salt anions; and a superionic conductive phase that is present in a solid state at ambient temperature, the superionic conducting salt being a mechanical milling product of a primary salt or a drying product of a drying composition comprising the primary salt. 2 . The superionic conducting salt of claim 1 , wherein that salt cations comprise: a cation of an alkali metal, an alkaline earth metal, a transition metal, a rare earth metal, or a combination comprising at least one of the foregoing metals. 3 . The superionic conducting salt of claim 2 , wherein the salt anions comprise: a closo-borate anion of formula B n H (n-z) R z 2− , wherein n is an integer greater than or equal to 10; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a closo-carborate anion of formula CB n H (n+1)-z R z 1− , wherein n is an integer greater than or equal to 9; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a closo-dicarborate anion of formula C 2 B n H (n+3)-z R z 1− , wherein n is an integer greater than or equal to 9; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a carborate anion of formula CB n H (n+3)-z R z 1− , wherein n is an integer greater than or equal to 9; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a borate of formula B 11 H (14-z) R z −1 , wherein z is an integer from 0 to 11; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a closo-ammonioborate anion of formula ((R′R″R′″)NB n Z n-1 ) 1− , wherein n is an integer greater than or equal to 10, N is bonded to B; and R′, R″, R′″, and Z independently comprise a hydrogen, a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; or a combination comprising at least one of the foregoing salt anions. 4 . The superionic conducting salt of claim 3 , wherein the salt anions comprise: a plurality of first salt anions; and a plurality of second salt anions. 5 . A battery comprising: an electrolyte composition comprising: a superionic conducting salt that comprises: a plurality of salt cations; a plurality of salt anions; and a superionic conductive phase that is present in a solid state at ambient temperature; and optionally, a binder in which the superionic conducting salt is disposed; a first electrode; and a second electrode separated from the first electrode by interposition of the electrolyte composition. 6 . The battery of claim 5 , wherein that salt cations comprise: a cation of an alkali metal, an alkaline earth metal, a transition metal, a rare earth metal, or a combination comprising at least one of the foregoing metals. 7 . The battery of claim 6 , wherein the salt anions comprise: a closo-borate anion of formula B n H (n-z) R z 2− , wherein n is an integer greater than or equal to 10; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a closo-carborate anion of formula CB n H (n+1)-z R z 1− , wherein n is an integer greater than or equal to 9; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a closo-dicarborate anion of formula C 2 B n H (n+3)-z R z 1− , wherein n is an integer greater than or equal to 9; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a carborate anion of formula CB n H (n+3)-z R z 1− , wherein n is an integer greater than or equal to 9; z is an integer from 0 to n; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a borate of the formula B 11 H (14-z) R z −1 , wherein z is an integer from 0 to 11; and each R independently comprises a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; a closo-ammonioborate anion of formula ((R′R″R′″)NB n Z n-1 ) 1− , wherein n is an integer greater than or equal to 10; N is bonded to B; and R′, R″, R′″; and Z independently comprise a hydrogen, a hydrocarbon substituent, a halogenated-hydrocarbon substituent, a halogen, an amine, a cyano, a hydroxyl, a thiol, a carbonyl, a carboxylate, a carboxylic acid, an epoxide, an ester, an amide, an ether, or a combination comprising at least one of the foregoing groups; or a combination comprising at least one of the foregoing salt anions. 8 . The battery of claim 7 , wherein the salt anions comprise: a plurality of first salt anions; and a plurality of second salt anions. 9 . A process for making a superionic conducting salt, the process comprising: combining a primary salt and an impact member, the primary salt comprising an ordered phase and being an ionic conductor; impacting the primary salt with the impact member; and converting the primary salt to the superionic conducting salt in response to impacting the primary salt with the impact member at a conversion temperature to make the superionic conducting salt, the conversion temperature optionally being less than a thermally activated transition temperature that therm
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