z-logo
Premium
The Proportion of Fe‐N X , N Doping Species and Fe 3 C to Oxygen Catalytic Activity in Core‐Shell Fe‐N/C Electrocatalyst
Author(s) -
Liu Yanyan,
Zhu Yihua,
Jiang Hongliang,
Shen Jianhua,
Li Chunzhong
Publication year - 2020
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201901571
Subject(s) - electrocatalyst , bifunctional , catalysis , oxygen , x ray photoelectron spectroscopy , materials science , doping , carbon fibers , inorganic chemistry , zinc , x ray absorption spectroscopy , xanes , chemistry , electrode , absorption spectroscopy , chemical engineering , spectroscopy , electrochemistry , metallurgy , physics , organic chemistry , composite material , quantum mechanics , composite number , engineering , biochemistry , optoelectronics
A bifunctional oxygen electrocatalyst composed of iron carbide (Fe 3 C) nanoparticles encapsulated by nitrogen doped carbon sheets is reported. X‐ray photoelectron spectroscopy and X‐ray absorption near edge structure revealed the presence of several kinds of active sites (Fe−N x sites, N doping sites) and the modulated electron structure of nitrogen doped carbon sheets. Fe 3 C@ N ‐CSs shows excellent oxygen evolution and oxygen reduction catalytic activity owing to the modulated electron structure by encapsulated Fe 3 C core via biphasic interfaces electron interaction, which can lower the free energy of intermediate, strengthen the bonding strength and enhance conductivity. Meanwhile, the contribution of the Fe−N x sites, N doping sites and the effect of Fe 3 C core for the electrocatalytic oxygen reaction is originally revealed. The Fe 3 C@ N ‐CSs air electrode‐based zinc‐air battery demonstrates a high open circuit potential of 1.47 V, superior charge‐discharge performance and long lifetime, which outperforms the noble metal‐based zinc‐air battery.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here