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Electrospinning Hetero‐Nanofibers of Fe 3 C‐Mo 2 C/Nitrogen‐Doped‐Carbon as Efficient Electrocatalysts for Hydrogen Evolution
Author(s) -
Lin Huanlei,
Zhang Wenbiao,
Shi Zhangping,
Che Minwei,
Yu Xiang,
Tang Yi,
Gao Qingsheng
Publication year - 2017
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201700207
Subject(s) - overpotential , tafel equation , electrocatalyst , materials science , catalysis , exchange current density , carbon fibers , chemical engineering , carbon nanofiber , hydrogen , inorganic chemistry , nanotechnology , electrochemistry , chemistry , carbon nanotube , electrode , organic chemistry , composite material , composite number , engineering
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 3 C‐Mo 2 C/nitrogen‐doped carbon (Fe 3 C‐Mo 2 C/NC) hetero‐nanofibers (HNFs) with tunable composition, leading to abundant Fe 3 C‐Mo 2 C hetero‐interfaces for synergy in electrocatalysis. Owing to the strong hydrogen binding on Mo 2 C and the relatively weak one on Fe 3 C, the hetero‐interfaces of Fe 3 C‐Mo 2 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 3 C‐Mo 2 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 H 2 SO 4 , outperforming most recently reported noble‐metal‐free electrocatalysts.