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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...

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Autores principales: Jeskey, Jacob, Ding, Yong, Chen, Yidan, Hood, Zachary D., Sterbinsky, George E., Jaroniec, Mietek, Xia, Younan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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