Solid-state structures with volatile sintering aids, and methods for fabrication and use thereof
US-2024429439-A1 · Dec 26, 2024 · US
US2016028105A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016028105-A1 |
| Application number | US-201414782151-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 4, 2014 |
| Priority date | Apr 5, 2013 |
| Publication date | Jan 28, 2016 |
| Grant date | — |
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The present disclosure relates to novel compositions, electrodes, electrochemical storage devices (batteries) and ionic conduction devices that use cubic ionic conductor (“CUBICON”) compounds, such as nitridophosphate compounds. The cubic ionic conductor compound have a framework formula [MT 3 X 10 ] n− (1) and a general formula A x MT 3 X 10 (2), where M is a cation in octahedral coordination, T is a cation in tetrahedral coordination, X is an anion, and the framework has a net negative charge of −n, a net charge of +n. The framework of this class of compounds can accept excess ions.
Opening claim text (preview).
1 . An electrode, comprising: a cubic ionic conductor compound having a framework of formula (1) with a general chemical formula (2) [MT 3 X 10 ] n− (1) A x MT 3 X 10 (2) where M is a cation in octahedral coordination, T is a cation in tetrahedral coordination, X is an anion, n is a net charge of the framework between 0 and 16, A is a variable number of additional non-framework chemical species that can fit into an open space within the framework with a net charge of +n, and x is less than 10, wherein a T 3 X 10 trimer of three TX 4 tetrahedra share one common X anion, organized around an octahedral MX 6 site such that each MX 6 octahedron is connected to three different T 3 X 10 trimers by two bridging X anions connected to two different TX 4 tetrahedra within the T 3 X 10 trimer and wherein the framework can accept excess ions. 2 - 3 . (canceled) 4 . The electrode of claim 1 , wherein A species is a monopositive cation. 5 . The electrode of claim 1 , wherein A is loosely bound and can move through an electrode lattice. 6 . The electrode of claim 1 , wherein A is selected from wholly or partially mobile cations (A M ), or a combination of partially mobile and partially immobile cations (A M A I ). 7 . The electrode of claim 6 , wherein A M is Li present within the framework at about 90% or more. 8 . (canceled) 9 . The electrode of claim 1 , wherein TX 4 tetrahedra comprises PO 3 N, PO 4 , PO 2 N 2 , PON 3 , PN 4 , SiO 4 , VO 4 , MoO 4 , VO 3 N, SO 3 N, and SiO 3 N. 10 . The electrode of claim 1 , wherein the cubic ionic conductor compound is crystalline and has a space group of P2 1 3 or a space group which represents a slight distortion away from P2 1 3 symmetry. 11 . The electrode of claim 1 , wherein the cubic ionic conductor compound belongs to a structural family of Na 3 Ti(PO 3 ) 3 N. 12 . The electrode of claim 1 , wherein the cubic ionic conductor compound further comprises dopants selected from the group of cations, anions, neutral atoms, or small molecules having a radius of less than 2 Å in a manner that preserves the framework. 13 . The electrode of claim 12 , wherein the dopant is selected from the group consisting of H, H 2 O, H 3 O, OH, NH 3 , NH 4 , N 2 , O 2 , Li, Na, K, Rb, Cs, Be, Mg, Ca, Sr, Ba, Y, La, Zr, Hf, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Th, Pa, U, Np, and Pu and populates one or more A sites within voids of the framework. 14 . The electrode of claim 12 , wherein the dopant is selected from the group consisting of Li, Na, Mg, Al, Si, P, S, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, In, Sn, Sb, Hf, Ta, W, Re, Os, Ir, Pt, Au, and Hg and can substitute the octahedral M sites of the framework. 15 . The electrode of claim 1 , wherein T is phosphorus (P), X is oxygen (O), nitrogen (N), or a combination thereof, and n is 6. 16 . The electrode of claim 15 , wherein T 3 X 10 trimer of the formula (1) is P 3 O 9 N forming a nitridophosphate compound having a general formula (3) A x M(PO 3 ) 3 N (3) where x≦3 and a combination of A x M yields a net charge of +6. 17 - 26 . (canceled) 27 . The electrode of claim 16 , wherein the nitridophosphate compound is partially or fully crystalline and has a cubic non-centrosymmetric structure with the space group of P2 1 3. 28 . (canceled) 29 . The electrode of claim 16 , wherein a N(PO 3 ) 3 6− anion in the nitridophosphate compound of formula (3) is formed by a trimer of three PO 3 N tetrahedra sharing one N vertex and each pair of PO 3 N tetrahedra within the trimer share two corners with an MO 6 octahedron. 30 . The electrode of claim 29 , wherein each corner of the MO 6 octahedron is shared with a PO 4 tetrahedron allowing connections with two neighboring tetrahedra in three different P 3 O 10 trimers of the tetrahedra. 31 - 41 . (canceled) 42 . A solid electrolyte comprising a cubic ionic conductor compound having a framework of formula (1) with a general chemical formula (2) [MT 3 X 10 ] n− (1) A x MT 3 X 10 (2) where M is a cation in octahedral coordination, T is a cation in tetrahedral coordination, X is an anion, n is a net charge of the framework between 0 and 16, A is a variable number of additional non-framework chemical species that can fit into an open space within the framework with a net charge of +n, and x is less than 10, wherein a T 3 X 10 trimer of TX 4 tetrahedra share one common X anion, organized around an octahedral MX 6 site such that each MX 6 octahedron is connected to three different T 3 X 10 trimers by two bridging X anions connected to two different TX 4 tetrahedra within the trimer and wherein the framework can accept excess ions. 43 . The solid electrolyte of claim 42 , wherein the T 3 X 10 trimer of formula (1) is P 3 O 9 N forming a nitridophosphate compound having a general formula (3) A x M(PO 3 ) 3 N (3) where x≦3, and A is an ionic or neutral species and the combination of A and M species produce a +6 charge that results in a net charge neutrality. 44 - 60 . (canceled) 61 . A method of synthesizing substantially pure crystalline nitridophosphate having a framework that can accept excess ions, the method comprising mixing the stoichiometric amounts of a metal oxide, a metaphosphate, and urea; heating the mixture to about 300 to 400° C. under flowing ammonia gas for about 1 to 10 hours; heating the mixture to about 700 to 800° C. for about 10 to 30 hours under flowing ammonia; and collecting the crystalline nitridophosphate. 62 . The method of claim 61 , further comprising grinding or milling the mixture before either or both heating steps. 63 . The method of claim 61 , wherein the urea has a mole fraction of 10-90% of the starting mixture. 64 . The method of claim 63 , wherein the urea has a mole fraction of 33 mole % of the starting mixture. 65 - 69 . (canceled)
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