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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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.
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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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