Journal
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 165, Issue 16, Pages F1286-F1291Publisher
ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.0131816jes
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Funding
- National Natural Science Foundation of China [91534122, 91534202]
- Social Development Program of Shanghai [17DZ1200900]
- Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning
- Shanghai Scientific and Technological Innovation Project [18JC1410600]
- Fundamental Research Funds for the Central Universities [222201718002]
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Developing efficient non-noble metal electrocatalysts for hydrogen evolution reaction (HER) in alkaline media is still a significant challenge. Sluggish kinetics of the Volmer step of water dissociation is a major cause. Herein, we demonstrate that the kinetics can be boosted by constructing abundant heterogeneous interfaces between nickel phosphide and cobalt phosphide nanocrystals. A nickel phosphide nanoparticles coated on cobalt phosphide nanoarrays nanostructure derived from metal-organic framework is rationally designed and synthesized on carbon cloth (Ni2P-CoP/CC). Electrochemical tests reveal that even under extremely alkaline concentration (1 M KOH), the Ni2P-CoP/CC exhibits excellent HER activity, with overpotentials of 74 and 120 mV at 10 and 100 mA cm(-2) respectively, and excellent stability of continuously working for more than 20 h. The electrochemical performance is better than most of cobalt phosphide-based catalysts and comparable to noble-metal benchmarks. This work opens up a new avenue for designing efficient alkaline HER electrocatalysts. (C) 2018 The Electrochemical Society.
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