Carbon nanofiber-supported PdNi alloy nanoparticles as highly efficient bifunctional catalysts for hydrogen and oxygen evolution reactions

被引:69
作者
Chen, Jiawei [1 ]
Chen, Jiadong [1 ]
Yu, Danni [1 ]
Zhang, Ming [1 ]
Zhu, Han [1 ]
Du, Mingliang [1 ]
机构
[1] Zhejiang Sci Tech Univ, Coll Mat & Text, Hangzhou 310018, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
PdNi alloy nanoparticles; carbon nanofibers; bifunctional electrocatalysts; hydrogen and oxygen evolution reactions; COBALT; WATER; ELECTROCATALYST; PERFORMANCE; PHOSPHATE; GRAPHENE; NICKEL;
D O I
10.1016/j.electacta.2017.06.047
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Efficient bifunctional electrocatalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) must be developed to realize an inexpensive water-splitting system for large-scale applications. Herein, a novel PdNi carbon nanofiber (PdNi/CNF) catalyst was synthesized by facile electrospinning and carbonization processes. The size and homogeneity of the Pd-Ni alloy nanoparticles (NPs) could be effectively tuned by controlling the molar feed ratio of metal precursors. The morphology and structure of the PdNi/CNFs were characterized, and the working electrodes fabricated from the prepared catalyst mats were directly employed in the HER and OER. The PdNi/CNFs-1:2 catalyst exhibits high catalytic activity in the HER with a low overpotential of 55 mV at a current density of 10 mA cm(-2) in an acidic solution. Moreover, under 1 M KOH electrolyte, an overpotential of 187 mV is required in the HER over the catalyst to arrive 10 mA cm(-2) and an overpotential of 289 mV is achieved in the OER at the same current density. The superior HER and OER activities of the PdNi/CNFs are attributed to the synergistic effects of the PdNi alloy nanoparticles (NPs) assembled on the CNFs. This work provides a simple route for synthesizing highly efficient bifunctional electrocatalysts from 3d transition metals and a small amount of noble metals for hydrogen and oxygen evolution reactions. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:17 / 26
页数:10
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