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 Fe C-Mo C/nitrogen-doped carbon (Fe C-Mo C/NC) hetero-nanofibers (HNFs) with tunable composition, leading to abundant Fe C-Mo C hetero-interfaces for synergy in electrocatalysis. Owing to the strong hydrogen binding on Mo C and the relatively weak one on Fe C, the hetero-interfaces of Fe C-Mo 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 Fe C-Mo C/NC HNFs afforded a low overpotential of 116 mV at a current density of -10 mA cm and striking kinetics metrics (onset overpotential: 42 mV, Tafel slope: 43 mV dec ) in 0.5 m H SO , outperforming most recently reported noble-metal-free electrocatalysts.
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http://dx.doi.org/10.1002/cssc.201700207 | DOI Listing |
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