Improved catalysts for hydrogen evolution reaction in alkaline solutions through the electrochemical formation of nickel-reduced graphene oxide interface

被引:47
作者
Gutic, Sanjin J. [1 ]
Dobrota, Ana S. [2 ]
Leetmaa, Mikael [3 ]
Skorodumova, Natalia V. [3 ,4 ]
Mentus, Slavko V. [2 ,5 ]
Pasti, Igor A. [2 ]
机构
[1] Univ Sarajevo, Fac Sci, Dept Chem, Zmaja & Bosne 33-35, Sarajevo 71000, Bosnia & Herceg
[2] Univ Belgrade, Fac Phys Chem, Studentski Trg 12-16, Belgrade 11158, Serbia
[3] KTH Royal Inst Technol, Dept Mat Sci & Engn, Brinellvagen 23, S-10044 Stockholm, Sweden
[4] Uppsala Univ, Dept Phys & Astron, Box 516, S-75120 Uppsala, Sweden
[5] Serbian Acad Arts & Sci, Knez Mihajlova 35, Belgrade 11000, Serbia
基金
瑞典研究理事会;
关键词
EFFICIENT; PERFORMANCE; REDUCTION; SPILLOVER; CARBON; MOS2; ELECTROCATALYSTS; DOPANTS; STORAGE; COBALT;
D O I
10.1039/c7cp01237c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
H-2 production via water electrolysis plays an important role in hydrogen economy. Hence, novel cheap electrocatalysts for the hydrogen evolution reaction ( HER) are constantly needed. Here, we describe a simple method for the preparation of composite catalysts for H-2 evolution, consisting in simultaneous reduction of the graphene oxide film, and electrochemical deposition of Ni on its surface. The obtained composites (Ni@rGO), compared to pure electrodeposited Ni, show an improved electrocatalytic activity towards HER in alkaline media. We found that the activity of the Ni@rGO catalysts depends on the surface composition ( Ni vs. C mole ratio) and on the level of structural disorder of the rGO support. We suggest that HER activity is improved via H-ads spillover from the Ni particles to the rGO support, where quick recombination to molecular hydrogen is favored. A deeper insight into such a mechanism of H-2 production was achieved by kinetic Monte-Carlo simulations. These simulations enabled the reproduction of experimentally observed trends under the assumption that the support can act as a Hads acceptor. We expect that the proposed procedure for the production of novel HER catalysts could be generalized and lead to the development of a new generation of HER catalysts by tailoring the catalyst/support interface.
引用
收藏
页码:13281 / 13293
页数:13
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