| Literature DB >> 33733600 |
Dong Liu1, Haoqiang Ai2, Mingpeng Chen1, Pengfei Zhou1, Bowen Li1, Di Liu1, Xinyu Du2, Kin Ho Lo2, Kar-Wei Ng1, Shuang-Peng Wang1, Shi Chen1, Guichuan Xing1, Jinsong Hu3, Hui Pan1,4.
Abstract
Hydrogen evolution reaction (HER) is a key step for electrochemical energy conversion and storage. Developing well defined nanostructures as noble-metal-free electrocatalysts for HER is promising for the application of hydrogen technology. Herein, it is reported that 3D porous hierarchical CoNiP/Cox P multi-phase heterostructure on Ni foam via an electrodeposition method followed by phosphorization exhibits ultra-highly catalytic activity for HER. The optimized CoNiP/Cox P multi-phase heterostructure achieves an excellent HER performance with an ultralow overpotential of 36 mV at 10 mA cm-2 , superior to commercial Pt/C. Importantly, the multi-phase heterostructure shows exceptional stability as confirmed by the long-term potential cycles (30,000 cycles) and extended electrocatalysis (up to 500 h) in alkaline solution and natural seawater. Experimental characterizations and DFT calculations demonstrate that the strong electronic interaction at the heterointerface of CoNiP/CoP is achieved via the electron transfer from CoNiP to the heterointerface, which directly promotes the dissociation of water at heterointerface and desorption of hydrogen on CoNiP. These findings may provide deep understanding on the HER mechanism of heterostructure electrocatalysts and guidance on the design of earth-abundant, cost-effective electrocatalysts with superior HER activity for practical applications.Entities:
Keywords: electrocatalysis; heterostructure; hydrogen generation; interface engineering; transition metal phosphide
Year: 2021 PMID: 33733600 DOI: 10.1002/smll.202007557
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281