Using a polymer-masking approach, we have developed metal-free 2D carbon electrocatalysts based on single-layer graphene with and without punched holes and/or N-doping. A combined experimental and theoretical study on the resultant 2D graphene electrodes revealed that a single-layer graphene sheet exhibited a significantly higher electrocatalytic activity at its edge than that over the surface of its basal plane. Furthermore, the electrocatalytic activity of a single-layer 2D graphene sheet was significantly enhanced by simply punching microholes through the graphene electrode due to the increased edge population for the hole-punched graphene electrode. In a good consistency with the experimental observations, our density function theory calculations confirmed that the introduction of holes into a graphene sheet generated additional positive charge along the edge of the punched holes and hence the creation of more highly active sites for the oxygen reduction reaction. The demonstrated concept for less graphene material to be more electrocatalytically active shed light on the rational design of low-cost, but efficient electrocatalysts from 2D graphene for various potential applications ranging from electrochemical sensing to energy conversion and storage.
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21 August 2020
Research Article|
August 17 2020
Hole-punching for enhancing electrocatalytic activities of 2D graphene electrodes: Less is more Available to Purchase
Special Collection:
2D Materials
Yunxiang Gao;
Yunxiang Gao
1
Department of Macromolecular Science and Engineering, Case Western Reserve University
, 10900 Euclid Avenue, Cleveland, Ohio 44106, USA
2
Department of Chemistry, Prairie View A&M University
, Prairie View, Texas 77446, USA
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Lipeng Zhang;
Lipeng Zhang
3
State Key Laboratory of Organic–Inorganic Composites, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Chemical Engineering, Beijing University of Chemical Technology
, Beijing, China
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Zhenhai Xia;
Zhenhai Xia
4
Department of Materials Science and Engineering, Department of Chemistry, University of North Texas
, Denton, Texas 76203, USA
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Chang Ming Li
;
Chang Ming Li
a)
5
Institute for Advanced Cross-field Sciences, Qingdao University
, 308 Ningxia Road, Qingdao, Shandong, China
a)Author to whom correspondence should be addressed: [email protected]
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Liming Dai
Liming Dai
a)
1
Department of Macromolecular Science and Engineering, Case Western Reserve University
, 10900 Euclid Avenue, Cleveland, Ohio 44106, USA
6
UNSW-CWRU International Joint Laboratory, School of Chemical Engineering, University of New South Wales
, Sydney, NSW 2052, Australia
a)Author to whom correspondence should be addressed: [email protected]
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Yunxiang Gao
1,2
Lipeng Zhang
3
Zhenhai Xia
4
Chang Ming Li
5,a)
Liming Dai
1,6,a)
1
Department of Macromolecular Science and Engineering, Case Western Reserve University
, 10900 Euclid Avenue, Cleveland, Ohio 44106, USA
2
Department of Chemistry, Prairie View A&M University
, Prairie View, Texas 77446, USA
3
State Key Laboratory of Organic–Inorganic Composites, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Chemical Engineering, Beijing University of Chemical Technology
, Beijing, China
4
Department of Materials Science and Engineering, Department of Chemistry, University of North Texas
, Denton, Texas 76203, USA
5
Institute for Advanced Cross-field Sciences, Qingdao University
, 308 Ningxia Road, Qingdao, Shandong, China
6
UNSW-CWRU International Joint Laboratory, School of Chemical Engineering, University of New South Wales
, Sydney, NSW 2052, Australia
a)Author to whom correspondence should be addressed: [email protected]
Note: This paper is part of the JCP Special Topic on 2D Materials.
J. Chem. Phys. 153, 074701 (2020)
Article history
Received:
May 04 2020
Accepted:
July 27 2020
Citation
Yunxiang Gao, Lipeng Zhang, Zhenhai Xia, Chang Ming Li, Liming Dai; Hole-punching for enhancing electrocatalytic activities of 2D graphene electrodes: Less is more. J. Chem. Phys. 21 August 2020; 153 (7): 074701. https://doi.org/10.1063/5.0012709
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