3D self-standing grass-like cobalt phosphide vesicles-decorated nanocones grown on Ni-foam as an efficient electrocatalyst for hydrogen evolution reaction

被引:14
作者
Ge, Kang [1 ]
Zeng, Yanwei [1 ]
Dong, Guodian [1 ]
Zhao, Longfei [1 ]
Wang, Zhentao [1 ]
Huang, Ming [1 ]
机构
[1] Nanjing Tech Univ, Sch Mat Sci & Engn, Nanjing 210009, Jiangsu, Peoples R China
关键词
Cobalt phosphide; Nanocones; Mini-vesicles; Hydrogen evolution reaction; Electrocatalyst; HIGH-PERFORMANCE ELECTROCATALYSTS; BIFUNCTIONAL ELECTROCATALYST; HIGHLY EFFICIENT; NANOWIRE ARRAY; NANONEEDLE ARRAYS; COP NANOCRYSTALS; LARGE-SCALE; NANOSHEETS; NANOPARTICLES; CATALYST;
D O I
10.1016/j.ijhydene.2019.04.030
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
The growing hydrogen consumption has greatly promoted the development of efficient, stable and low-cost electrocatalysts for the hydrogen evolution reaction (HER). Constructing functional nanostructures is an efficacious strategy to optimize catalytic performance. Herein, we present a feasible route to fabricate distinctive 3D grass-like cobalt phosphide nanocones clad with mini-vesicles on the hierarchically porous Ni foam, which can directly serve as a binder-free electrocatalyst with superior catalytic activity and durability in HER. Thanks to its distinctive 3D microstructure featured with favourable pore-size distribution, abundant active sites provided by mini-vesicles and rapid electron transfer with the assistance of Ni foam, the as-grown grass-like CoP/NF electrocatalyst has shown a favourable overpotential in an acidic solution with an onset overpotential of similar to 35 mV, an overpotential of 71 mV at a current density of 10 mA cm(-2), reduced by 60 mV in comparison with that realized by urchin-like CoP/NF nanoprickles. Moreover, it has exhibited an excellent HER activity in the alkaline medium, with an overpotential of 117 mV at 10 mA cm(-2), a Tafel slope of 63.0 mV dec(-1) and a long-term electrochemical durability. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13490 / 13501
页数:12
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