Journal
NANO ENERGY
Volume 30, Issue -, Pages 858-866Publisher
ELSEVIER
DOI: 10.1016/j.nanoen.2016.09.005
Keywords
Graphdiyne; 2D carbon structure; Self-catalyzed growth; Electrocatalysts; Hydrogen evolution reaction
Categories
Funding
- National Basic Research 973 Program of China [2012CB932901]
- NSFC-DFG [21261130581]
- Strategic Priority Research Program of the Chinese Academy of Sciences [XDA09020302, XDB12010300]
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Here we show that a high efficient hydrogen evolution reaction which was carried out on the in-situ growth of self-supported core-shell nanowires array consisting of graphdiyne as the shell and Cu as the core on Cu foams (Cu@GD NA/CF). Subject to potential cycling treatment in 0.5 M H2SO4, the Cu@GD NA/CF exhibits highly catalytic activity for hydrogen evolution reaction with an onset overpotential of 52 mV and a Tafel slope of 69 mV dec(-1). Our findings suggest that synergetic interaction between GD and Cu is crucial for the catalytic performance of the electrode. This electrode needs only overpotentials of 79 and 162 mV to achieve catalytic current densities of 10 and 100 mA cm(-2), respectively, and maintains its catalytic activity for almost 20 h. The attractive performances of such array make it promising candidate as a future high-performance catalyst for applications. Summary: The first GD based 3D carbon nanoarchitectures with well-defined porous network structures working as a highly active hydrogen evolution cathode is developed. Its excellent electrocatalytic activities, combined with low-cost, convenient and scale-up preparation process, make it promising candidate for practical and efficient energy applications. (C) 2016 Elsevier Ltd. All rights reserved.
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