Abstract

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 0.5M H2SO4, the Cu@GD NA/CF exhibits highly catalytic activity for hydrogen evolution reaction with an onset overpotential of 52mV and a Tafel slope of 69mVdec−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 162mV to achieve catalytic current densities of 10 and 100mAcm–2, respectively, and maintains its catalytic activity for almost 20h. The attractive performances of such array make it promising candidate as a future high-performance catalyst for applications. SummaryThe 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.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.