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Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction
Carbon‐based metal‐free catalysts for the hydrogen evolution reaction (HER) are essential for the development of a sustainable hydrogen society. Identification of the active sites in heterogeneous catalysis is key for the rational design of low‐cost and efficient catalysts. Here, by fabricating hole...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524082/ https://www.ncbi.nlm.nih.gov/pubmed/31131204 http://dx.doi.org/10.1002/advs.201900119 |
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author | Kumatani, Akichika Miura, Chiho Kuramochi, Hirotaka Ohto, Tatsuhiko Wakisaka, Mitsuru Nagata, Yuki Ida, Hiroki Takahashi, Yasufumi Hu, Kailong Jeong, Samuel Fujita, Jun‐ichi Matsue, Tomokazu Ito, Yoshikazu |
author_facet | Kumatani, Akichika Miura, Chiho Kuramochi, Hirotaka Ohto, Tatsuhiko Wakisaka, Mitsuru Nagata, Yuki Ida, Hiroki Takahashi, Yasufumi Hu, Kailong Jeong, Samuel Fujita, Jun‐ichi Matsue, Tomokazu Ito, Yoshikazu |
author_sort | Kumatani, Akichika |
collection | PubMed |
description | Carbon‐based metal‐free catalysts for the hydrogen evolution reaction (HER) are essential for the development of a sustainable hydrogen society. Identification of the active sites in heterogeneous catalysis is key for the rational design of low‐cost and efficient catalysts. Here, by fabricating holey graphene with chemically dopants, the atomic‐level mechanism for accelerating HER by chemical dopants is unveiled, through elemental mapping with atomistic characterizations, scanning electrochemical cell microscopy (SECCM), and density functional theory (DFT) calculations. It is found that the synergetic effects of two important factors—edge structure of graphene and nitrogen/phosphorous codoping—enhance HER activity. SECCM evidences that graphene edges with chemical dopants are electrochemically very active. Indeed, DFT calculation suggests that the pyridinic nitrogen atom could be the catalytically active sites. The HER activity is enhanced due to phosphorus dopants, because phosphorus dopants promote the charge accumulations on the catalytically active nitrogen atoms. These findings pave a path for engineering the edge structure of graphene in graphene‐based catalysts. |
format | Online Article Text |
id | pubmed-6524082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65240822019-05-24 Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction Kumatani, Akichika Miura, Chiho Kuramochi, Hirotaka Ohto, Tatsuhiko Wakisaka, Mitsuru Nagata, Yuki Ida, Hiroki Takahashi, Yasufumi Hu, Kailong Jeong, Samuel Fujita, Jun‐ichi Matsue, Tomokazu Ito, Yoshikazu Adv Sci (Weinh) Communications Carbon‐based metal‐free catalysts for the hydrogen evolution reaction (HER) are essential for the development of a sustainable hydrogen society. Identification of the active sites in heterogeneous catalysis is key for the rational design of low‐cost and efficient catalysts. Here, by fabricating holey graphene with chemically dopants, the atomic‐level mechanism for accelerating HER by chemical dopants is unveiled, through elemental mapping with atomistic characterizations, scanning electrochemical cell microscopy (SECCM), and density functional theory (DFT) calculations. It is found that the synergetic effects of two important factors—edge structure of graphene and nitrogen/phosphorous codoping—enhance HER activity. SECCM evidences that graphene edges with chemical dopants are electrochemically very active. Indeed, DFT calculation suggests that the pyridinic nitrogen atom could be the catalytically active sites. The HER activity is enhanced due to phosphorus dopants, because phosphorus dopants promote the charge accumulations on the catalytically active nitrogen atoms. These findings pave a path for engineering the edge structure of graphene in graphene‐based catalysts. John Wiley and Sons Inc. 2019-04-01 /pmc/articles/PMC6524082/ /pubmed/31131204 http://dx.doi.org/10.1002/advs.201900119 Text en © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Kumatani, Akichika Miura, Chiho Kuramochi, Hirotaka Ohto, Tatsuhiko Wakisaka, Mitsuru Nagata, Yuki Ida, Hiroki Takahashi, Yasufumi Hu, Kailong Jeong, Samuel Fujita, Jun‐ichi Matsue, Tomokazu Ito, Yoshikazu Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction |
title | Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction |
title_full | Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction |
title_fullStr | Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction |
title_full_unstemmed | Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction |
title_short | Chemical Dopants on Edge of Holey Graphene Accelerate Electrochemical Hydrogen Evolution Reaction |
title_sort | chemical dopants on edge of holey graphene accelerate electrochemical hydrogen evolution reaction |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524082/ https://www.ncbi.nlm.nih.gov/pubmed/31131204 http://dx.doi.org/10.1002/advs.201900119 |
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