Mixed-dimensional heterostructures of hydrophobic/hydrophilic graphene foam for tunable hydrogen evolution reaction

被引:33
作者
Aslam, Sehrish [1 ]
Sagar, Rizwan Ur Rehman [2 ]
Kumar, Hitanshu [3 ]
Zhang, Gaowei [1 ]
Nosheen, Farhat [4 ]
Namvari, Mina [5 ]
Mahmood, Nasir [6 ]
Zhang, Min [2 ]
Qiu, Yejun [1 ]
机构
[1] Harbin Inst Technol, Shenzhen Engn Lab Flexible Transparent Conduct Fi, Sch Mat Sci & Engn, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
[3] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen 518055, Peoples R China
[4] Univ Educ, Div Sci & Technol, Dept Chem, Lahore, Pakistan
[5] Palacky Univ Olomouc, Dept Phys Chem, Reg Ctr Adv Technol & Mat, Fac Sci, 17 Listopadu 1192-12, Olomouc 77146, Czech Republic
[6] RMIT Univ, Sch Engn, 124 La Trobe St, Melbourne, Vic 3001, Australia
关键词
Graphene oxide; Graphene foam; Hydrogen evolution reaction; Hydrophobic/hydrophilic interface; Heterostructure; ELECTRODE; MECHANISM; FILMS;
D O I
10.1016/j.chemosphere.2019.125607
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The synergetic effect of hydrophilic and hydrophobic carbon can be used to obtain tunable hydrogen evolution reaction (HER) at the interface. Herein, graphene oxide (GO-Hummers method) was coated on graphene foam (GF) synthesized via chemical vapor deposition to develop mixed-dimensional heterostructure for the observation of HER. The porosity of GF not only provides an optimized diffusion co-efficient for better mass transport but also modified surface chemistry (GF/GO-hydrophobic/hydrophilic interface), which results in an onset potential 50 mV and overpotential of 450 mV to achieve the current density 10 mA/cm(2). The surface analysis shows that inherent functional groups at the surface played a key role in tuning the activity of hybrid, providing a pathway to introduce non-corrosive electrodes for water splitting. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:8
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