| Literature DB >> 28371425 |
Huanlei Lin1, Wenbiao Zhang1, Zhangping Shi2, Minwei Che1, Xiang Yu1,3, Yi Tang2, Qingsheng Gao1.
Abstract
Heterostructured electrocatalysts with multiple active components are expected to synchronously address the two elementary steps in the hydrogen evolution reaction (HER), which require varied hydrogen-binding strength on the catalyst surface. Herein, electrospinning followed by a pyrolysis is introduced to design Fe3 C-Mo2 C/nitrogen-doped carbon (Fe3 C-Mo2 C/NC) hetero-nanofibers (HNFs) with tunable composition, leading to abundant Fe3 C-Mo2 C hetero-interfaces for synergy in electrocatalysis. Owing to the strong hydrogen binding on Mo2 C and the relatively weak one on Fe3 C, the hetero-interfaces of Fe3 C-Mo2 C remarkably promote HER kinetics and intrinsic activity. Additionally, the loose and porous N-doped carbon matrix, as a result of Fe-catalyzed carbonization, ensures the fast transport of electrolytes and electrons, thus minimizing diffusion limitation. As expected, the optimized Fe3 C-Mo2 C/NC HNFs afforded a low overpotential of 116 mV at a current density of -10 mA cm-2 and striking kinetics metrics (onset overpotential: 42 mV, Tafel slope: 43 mV dec-1 ) in 0.5 m H2 SO4 , outperforming most recently reported noble-metal-free electrocatalysts.Entities:
Keywords: electrocatalysts; heterostructures; hydrogen evolution reaction; metal carbides; synergic enhancement
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Year: 2017 PMID: 28371425 DOI: 10.1002/cssc.201700207
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928