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Single-Atom Catalysts for Selective Oxygen Reduction: Transition Metals in Uniform Carbon Nanospheres with High Loadings
[Image: see text] Transition metal single-atom catalysts (SACs) in uniform carbon nanospheres have gained tremendous interest as electrocatalysts owing to their low cost, high activity, and excellent selectivity. However, their preparation typically involves complicated multistep processes that are...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685421/ https://www.ncbi.nlm.nih.gov/pubmed/38034958 http://dx.doi.org/10.1021/jacsau.3c00557 |
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author | Jeskey, Jacob Ding, Yong Chen, Yidan Hood, Zachary D. Sterbinsky, George E. Jaroniec, Mietek Xia, Younan |
author_facet | Jeskey, Jacob Ding, Yong Chen, Yidan Hood, Zachary D. Sterbinsky, George E. Jaroniec, Mietek Xia, Younan |
author_sort | Jeskey, Jacob |
collection | PubMed |
description | [Image: see text] Transition metal single-atom catalysts (SACs) in uniform carbon nanospheres have gained tremendous interest as electrocatalysts owing to their low cost, high activity, and excellent selectivity. However, their preparation typically involves complicated multistep processes that are not practical for industrial use. Herein, we report a facile one-pot method to produce atomically isolated metal atoms with high loadings in uniform carbon nanospheres without any templates or postsynthesis modifications. Specifically, we use a chemical confinement strategy to suppress the formation of metal nanoparticles by introducing ethylenediaminetetraacetic acid (EDTA) as a molecular barrier to spatially isolate the metal atoms and thus generate SACs. To demonstrate the versatility of this synthetic method, we produced SACs from multiple transition metals, including Fe, Co, Cu, and Ni, with loadings as high as 3.87 wt %. Among these catalytic materials, the Fe-based SACs showed remarkable catalytic activity toward the oxygen reduction reaction (ORR), achieving an onset and half-wave potential of 1.00 and 0.831 V(RHE), respectively, comparable to that of commercial 20 wt % Pt/C. Significantly, we were able to steer the ORR selectivity toward either energy generation or hydrogen peroxide production by simply changing the transition metal in the EDTA-based precursor. |
format | Online Article Text |
id | pubmed-10685421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106854212023-11-30 Single-Atom Catalysts for Selective Oxygen Reduction: Transition Metals in Uniform Carbon Nanospheres with High Loadings Jeskey, Jacob Ding, Yong Chen, Yidan Hood, Zachary D. Sterbinsky, George E. Jaroniec, Mietek Xia, Younan JACS Au [Image: see text] Transition metal single-atom catalysts (SACs) in uniform carbon nanospheres have gained tremendous interest as electrocatalysts owing to their low cost, high activity, and excellent selectivity. However, their preparation typically involves complicated multistep processes that are not practical for industrial use. Herein, we report a facile one-pot method to produce atomically isolated metal atoms with high loadings in uniform carbon nanospheres without any templates or postsynthesis modifications. Specifically, we use a chemical confinement strategy to suppress the formation of metal nanoparticles by introducing ethylenediaminetetraacetic acid (EDTA) as a molecular barrier to spatially isolate the metal atoms and thus generate SACs. To demonstrate the versatility of this synthetic method, we produced SACs from multiple transition metals, including Fe, Co, Cu, and Ni, with loadings as high as 3.87 wt %. Among these catalytic materials, the Fe-based SACs showed remarkable catalytic activity toward the oxygen reduction reaction (ORR), achieving an onset and half-wave potential of 1.00 and 0.831 V(RHE), respectively, comparable to that of commercial 20 wt % Pt/C. Significantly, we were able to steer the ORR selectivity toward either energy generation or hydrogen peroxide production by simply changing the transition metal in the EDTA-based precursor. American Chemical Society 2023-10-19 /pmc/articles/PMC10685421/ /pubmed/38034958 http://dx.doi.org/10.1021/jacsau.3c00557 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Jeskey, Jacob Ding, Yong Chen, Yidan Hood, Zachary D. Sterbinsky, George E. Jaroniec, Mietek Xia, Younan Single-Atom Catalysts for Selective Oxygen Reduction: Transition Metals in Uniform Carbon Nanospheres with High Loadings |
title | Single-Atom Catalysts
for Selective Oxygen Reduction:
Transition Metals in Uniform Carbon Nanospheres with High Loadings |
title_full | Single-Atom Catalysts
for Selective Oxygen Reduction:
Transition Metals in Uniform Carbon Nanospheres with High Loadings |
title_fullStr | Single-Atom Catalysts
for Selective Oxygen Reduction:
Transition Metals in Uniform Carbon Nanospheres with High Loadings |
title_full_unstemmed | Single-Atom Catalysts
for Selective Oxygen Reduction:
Transition Metals in Uniform Carbon Nanospheres with High Loadings |
title_short | Single-Atom Catalysts
for Selective Oxygen Reduction:
Transition Metals in Uniform Carbon Nanospheres with High Loadings |
title_sort | single-atom catalysts
for selective oxygen reduction:
transition metals in uniform carbon nanospheres with high loadings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685421/ https://www.ncbi.nlm.nih.gov/pubmed/38034958 http://dx.doi.org/10.1021/jacsau.3c00557 |
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