Base Metal Catalyst
US-2015360178-A1 · Dec 17, 2015 · US
US2021316290A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2021316290-A1 |
| Application number | US-201917266333-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 6, 2019 |
| Priority date | Aug 6, 2018 |
| Publication date | Oct 14, 2021 |
| Grant date | — |
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Carbon-based single metal atom or bimetallic, trimetallic, or multimetallic alloy transition metal-containing catalysts derived from exoelectrogen bacteria and their methods of making and using thereof are described. The method comprising the steps of: (a) preparing a solution medium comprising at least an electron donor and an electron acceptor comprised of one or more salts of a transition metal; (b) providing exoelectrogen bacterial cells and mixing the exoelectrogen bacterial cells into the solution medium of step (a); (c) incubating the solution medium of step (b); (d) isolating the exoelectrogen bacterial cells from the incubated solution medium of step (c); and (e) pyrolyzing the exoelectrogen bacterial cells resulting in formation of the catalyst. The electron donor can be formate, acetate, or hydrogen.
Opening claim text (preview).
1 . A single atom or bimetallic alloy catalyst comprising: a carbonaceous support; a plurality of at least one type of zero-valent transition metal dispersed on the carbonaceous support. 2 . The catalyst of claim 1 , wherein the at least one zero-valent transition metal is a formed of a single atom of the zero-valent transition metal. 3 . The catalyst of claim 1 , wherein the at least one zero-valent transition metal is selected from the group consisting of Pt, Fe, Ag, Au, Pd, Rh, Ru, Ir, Co, Ni, Cu, and combinations thereof. 4 . The catalyst of claim 1 , wherein the at least one zero-valent transition metal is a bimetallic alloy of at least two transition metals. 5 . The catalyst of claim 4 , wherein the bimetallic alloy is selected from the group consisting of NiCo, NiCu, PtNi, IrNi, RhCo, PtCo, PtIr, PtRh, and combinations thereof. 6 . The catalyst of claim 1 , wherein the plurality of the at least one type of zero-valent transition metal is uniformly dispersed on surfaces of the carbonaceous support. 7 . The catalyst of claim 1 , wherein the plurality of the at least one type of zero-valent transition metal is formed of isolated single atoms of the zero-valent transition metal which are dispersed on the carbonaceous support. 8 . The catalyst of claim 4 , wherein the bimetallic alloy is uniformly dispersed on one or more surfaces of the carbonaceous support. 9 . The catalyst of claim 1 , wherein the catalyst does not comprise aggregates and/or clusters of zero-valent metals. 10 . The catalyst of claim 1 , wherein the carbonaceous support is a graphitized carbon. 11 . The catalyst of claim 1 , wherein the carbonaceous support is mesoporous. 12 . The catalyst of claim 11 , wherein the mesoporous carbonaceous support comprises mesopores having a volume ranging from about 0.1 to 0.8 cm 3 g −1 , about 0.1 to 0.7 cm 3 g −1 , about 0.1 to 0.6 cm 3 g −1 , about 0.1 to 0.5 cm 3 g −1 , about 0.1 to 0.4 cm 3 g −1 , about 0.1 to 0.3 cm 3 g −1 , or about 0.1 to 0.2 cm 3 g −1 . 13 . The catalyst of claim 1 , wherein the carbonaceous support has a surface area, as measured by Brunauer-Emmett-Teller method, ranging from about 100 to 700 m 2 g −1 , about 100 to 650 m 2 g −1 , about 100 to 600 m 2 g −1 , or about 100 to 500 m 2 g −1 . 14 . The catalyst of claim 1 , wherein the carbonaceous support is a graphitized carbon comprising heteroatom doping; wherein the heteroatoms are selected from nitrogen, oxygen, hydrogen, sulfur, phosphorus, and combinations thereof. 15 . The catalyst of claim 14 , wherein the heteroatoms present in the carbonaceous support originate from exoelectrogen bacteria. selected from the group consisting of Geobacter sulfurreducens, Desulfuromonas acetexigens, Geobacter metallireducens, Shewanella oneidensis MR-1, Shewanella putrefaciens IR-1, Clostridium butyricum, Rhodoferax ferrireducens, Aeromonas hydrophilia (A3), Desulfobulbus propionicus, Shewanella oneidensis DSP10 , Rhodoseudomonas palustris, Geothrix fermentans, Geopsychrobacter electrodiphilus , and combinations thereof. 16 . The catalyst of claim 1 , wherein the catalyst is an electrocatalyst or a photocatalyst. 17 . A method of preparing a single atom or bimetallic alloy catalyst of claim 1 , the method comprising the steps of: (a) preparing a solution medium comprising at least an electron donor and an electron acceptor comprised of one or more salts of a transition metal; (b) providing exoelectrogen bacterial cells and mixing the exoelectrogen bacterial cells into the solution medium of step (a); (c) incubating the solution medium of step (b); (d) isolating the exoelectrogen bacterial cells from the incubated solution medium of step (c); and (e) pyrolyzing the exoelectrogen bacterial cells resulting in formation of the catalyst. 18 . The method of claim 17 , wherein the electron donor is formate, acetate, or hydrogen. 19 . The method of claim 17 , wherein the transition metal of the one or more salts forms a soluble Mn + metal ion where n is 1, 2, or 3 and M is selected from the group consisting of Pt, Fe, Ag, Au, Pd, Rh, Ru, Ir, Co, Ni, and Cu. 20 . The method of claim 17 , wherein exoelectrogen bacterial cells are selected from the group consisting of Geobacter sulfurreducens, Desulfuromonas acetexigens, Geobacter metallireducens, Shewanella oneidensis MR-1, Shewanella putrefaciens IR-1, Clostridium butyricum, Rhodoferax ferrireducens, Aeromonas hydrophilia (A3), Desulfobulbus propionicus, Shewanella oneidensis DSP10 , Rhodoseudomonas palustris, Geothrix fermentans, Geopsychrobacter electrodiphilus , and combinations thereof.
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