Sodium transition metal silicate and method of forming same

Patent metadata

Field	Value
Publication number	US-2016365578-A1
Application number	US-201514738120-A
Country	US
Kind code	A1
Filing date	Jun 12, 2015
Priority date	Jun 12, 2015
Publication date	Dec 15, 2016
Grant date	—

Abstract

A macroporous sodium transition metal silicate material includes a composition represented by A a M 1 b M 2 c X d O e , wherein A is sodium or a mixture of sodium with lithium and/or potassium; M 1 is one or more transition metals; M 2 is one or more metals and/or metalloids; X is silicon or a mixture containing silicon and one or more elements selected from phosphorus, boron and aluminium; a is >0; b is >0; c is ≧0; d is ≧1; and e is ≧2. A method of forming the macroporous sodium transition metal silicate material includes mixing one or more transition metal precursor materials in a solvent to form a transition metal mixture; adding one or more silicate precursors to the transition metal mixture to form a precursor mixture; raising the pH of the precursor mixture to form a precipitate; stirring the mixture; aging and drying the mixture; washing the mixture; and drying.

First claim

1 . A method of forming a macroporous sodium transition metal silicate material comprising a composition represented by Chemical Formula (1):
A a M 1 b M 2 c X d O e   (1)
wherein A is sodium or a mixture of sodium with lithium and/or potassium; M 1 is one or more transition metals; M 2 is one or more metals and/or metalloids; X is silicon or a mixture containing silicon and one or more elements selected from phosphorus, boron and aluminium; a is >0; b is >0; c is ≧0; d is ≧1; and e is ≧2, the method comprising: mixing one or more transition metal precursor materials in a solvent to form a transition metal mixture; adding one or more silicate precursors to the transition metal mixture to form a precursor mixture; adjusting the pH of the precursor mixture to form a mixture of a precipitate of a silicate and a metal cation; stirring the mixture including the precipitate; aging the stirred mixture including the precipitate; drying the aged mixture including the precipitate to remove the solvent therefrom, the drying forming one or more secondary salts; washing the mixture including the precipitate and the one or more secondary salts with an additional solvent to remove the secondary salt; and drying the washed mixture.

2 . The method of claim 1 , further comprising annealing the aged and dried mixture including the precipitate and the one or more secondary salts prior to washing.

3 . The method of claim 2 , wherein the annealing is performed at a temperature of 120° C. to 1000° C. for a time of 10 minutes to 12 hours.

4 . The method of claim 1 , wherein the one or more transition metal precursors comprises one or more of chloride, fluoride, iodide, sulfate, nitrate, and carbonate.

5 . The method of claim 1 , wherein the solvent comprises one or more of water, ethanol, ethylene glycol, methanol, isopropyl alcohol, ether, acetonitrile and hexanol.

6 . The method of claim 1 , wherein the one or more silicate precursors comprises one or more of tetra ethylene orthosilicate, sodium metasilicate, and sodium orthosilicate.

7 . The method of claim 6 , wherein the one or more silicate precursors is dissolved in a silicate precursor solvent prior to addition to the transition metal mixture, the silicate precursor solvent comprising one or more of tetra ethylene orthosilicate, sodium metasilicate, and sodium orthosilicate.

8 . The method of claim 1 , wherein the aging is performed at a temperature of 25° C. to 80° C. for a time of 2 hours to 14 days.

9 . The method of claim 1 , wherein the drying is performed at a temperature of 100° C. to 150° C. in vacuum oven for a time of 2 hours to 24 hours.

10 . The method of claim 1 , wherein A is 100% sodium.

11 . The method of claim 1 , wherein M 1 is one or more of titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, yttrium, zirconium, niobium, molybdenum, rhodium, palladium, silver, cadmium, hafnium, tantalum, tungsten, osmium, platinum, and gold.

12 . The method of claim 1 , wherein M 2 is one or more of magnesium, zinc, calcium, beryllium, strontium, barium, aluminium and boron.

13 . A macroporous sodium transition metal silicate material comprising a composition represented by Chemical Formula (1):
A a M 1 b M 2 c X d O e   (1)
wherein A is sodium or a mixture of sodium with lithium and/or potassium; M 1 is one or more transition metals; M 2 is one or more metals and/or metalloids; X is silicon or a mixture containing silicon and one or more elements selected from phosphorus, boron and aluminium; a is >0; b is >0; c is ≧0; d is ≧1; and e is ≧2.

14 . The macroporous sodium transition metal silicate material of claim 13 , wherein an average pore size of the material ≧50 nm.

15 . The macroporous sodium transition metal silicate material of claim 13 , wherein the material comprises primary particles comprising the composition represented by Chemical Formula (1) and having an average size of equal to or less than 300 nm.

16 . The macroporous sodium transition metal silicate material of claim 15 , further comprising secondary particles comprising the composition represented by Chemical Formula (1), the secondary particles comprising an agglomeration of the primary particles, the secondary particles having an average size of 10 μm to 100 μm.

17 . The macroporous sodium transition metal silicate material of claim 13 , wherein the material has a surface area of ≧2 m 2 /g.

18 . The macroporous sodium transition metal silicate material of claim 13 , wherein A is 100% sodium.

19 . The macroporous sodium transition metal silicate material of claim 13 , wherein M 1 is one or more of titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, yttrium, zirconium, niobium, molybdenum, rhodium, palladium, silver, cadmium, hafnium, tantalum, tungsten, osmium, platinum, and gold.

20 . The macroporous sodium transition metal silicate material of claim 13 , wherein M 2 is one or more of magnesium, zinc, calcium, beryllium, strontium, barium, aluminium and boron.

Assignees

• Sharp Kk

Inventors

• Kendrick Emma
• Treacher Joshua Charles

Classifications

• B01J2235/15

  X-ray diffraction · CPC title

• B01J2235/30

  Scanning electron microscopy; Transmission electron microscopy · CPC title

• C01P2006/16

  Pore diameter · CPC title

• C01P2004/62

  Submicrometer sized, i.e. from 0.1-1 micrometer · CPC title

• H01M2004/028

  Positive electrodes · CPC title