Catalytic composition for the electrochemical reduction of carbon dioxide
Abstract
The catalytic composition for the electrochemical reduction of carbon dioxide is a metal oxide supported by multi-walled carbon nanotubes. The metal oxide may be nickel oxide (NiO) or tin dioxide (SnO 2 ). The metal oxides form 20 wt % of the catalyst. In order to make the catalysts, a metal oxide precursor is first dissolved in deionized water to form a metal oxide precursor solution. The metal oxide precursor solution is then sonicated and the solution is impregnated in a support material composed of multi-walled carbon nanotubes to form a slurry. The slurry is then sonicated to form a homogeneous solid solution. Solids are removed from the homogeneous solid solution and dried in an oven for about 24 hours at a temperature of about 110° C. Drying is then followed by calcination in a tubular furnace under an argon atmosphere for about three hours at a temperature of 450° C.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A catalytic composition for the electrochemical reduction of carbon dioxide, comprising a metal oxide supported on multi-walled carbon nanotubes, wherein the metal oxide comprises about 20 wt % of the catalytic composition.
2 . The catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 1 , wherein the metal oxide comprises nickel oxide (NiO).
3 . An electrode for electrochemical reduction of carbon dioxide having the composition of claim 2 coated thereon.
4 . The catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 1 , wherein the metal oxide comprises tin dioxide (SnO 2 ).
5 . An electrode for electrochemical reduction of carbon dioxide having the composition of claim 4 coated thereon.
6 . A method of making a catalytic composition for the electrochemical reduction of carbon dioxide, comprising the steps of:
dissolving nickel nitrate hexahydrate, Ni(NO 3 ) 2 ·6H 2 O, in deionized water to form a nickel precursor solution; sonicating the nickel precursor solution; impregnating the sonicated nickel precursor solution in a support material comprising multi-walled carbon nanotubes to form a slurry; sonicating the slurry to form a homogeneous solid solution; removing solids from the homogenous solid solution; drying the solids; and calcining the dried solids to form the catalytic composition.
7 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 6 , wherein the step of sonicating the slurry comprises sonicating the slurry for about two hours.
8 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 6 , wherein the step of drying the solids comprises drying the solids at a temperature of about 110° C. for a period of about 24 hours.
9 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 6 , wherein the step of calcining the dried solids is performed in an argon atmosphere.
10 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 9 , wherein the step of calcining the dried solids comprises calcining the dried solids for about three hours at a temperature of about 450° C.
11 . A method of making a catalytic composition for the electrochemical reduction of carbon dioxide, comprising the steps of:
dissolving tin chloride (SnCl 2 ) in deionized water to form a tin precursor solution; sonicating the tin precursor solution; impregnating the sonicated tin precursor solution in a support material comprising multi-walled carbon nanotubes to form a slurry; sonicating the slurry to form a homogeneous solid solution; removing solids from the homogenous solid solution; drying the solids; and calcining the dried solids to form the catalytic composition.
12 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 11 , further comprising the step of adding hydrochloric acid (HCl) to the sonicated tin precursor solution.
13 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 11 , wherein the step of sonicating the slurry comprises sonicating the slurry for about two hours.
14 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 11 , wherein the step of drying the solids comprises drying the solids at a temperature of about 110° C. for a period of about 24 hours.
15 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 11 , wherein the step of calcining the dried solids is performed in an argon atmosphere.
16 . The method of making a catalytic composition for the electrochemical reduction of carbon dioxide as recited in claim 15 , wherein the step of calcining the dried solids comprises calcining the dried solids for about three hours at a temperature of about 450° C.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.