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Recent Progress of Metal Carbides Encapsulated in Carbon‐Based Materials for Electrocatalysis of Oxygen Reduction Reaction
Author(s) -
Yan XiangHui,
Prabhu P.,
Xu Hao,
Meng Ziwei,
Xue Tong,
Lee JongMin
Publication year - 2020
Publication title -
small methods
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.66
H-Index - 46
ISSN - 2366-9608
DOI - 10.1002/smtd.201900575
Subject(s) - catalysis , electrocatalyst , carbon fibers , carbide , materials science , oxygen reduction reaction , metal , nanotechnology , chemical engineering , chemistry , composite number , electrode , metallurgy , organic chemistry , electrochemistry , composite material , engineering
Fuel cells represent the most suitable energy conversion, capable of addressing energy crises and environmental pollution. Recently, as one of nonprecious metal catalysts (NPMCs), the MC@N‐C (M = Fe, Co, Ni, Mo, W) catalysts, especially for Fe 3 C encased in carbon layer (denoted as Fe 3 C@N‐C) have emerged as promising replacements for costly Pt‐based catalysts for oxygen reduction reaction (ORR). This review highlights the synthetic strategies undertaken such as hard template, soft template, and template‐free methods for deriving enhancements in electrocatalytic activity and durability. It also provides a comparison on the synthetic methods and catalytic performance and points out issues in the ORR measurements and activity comparison. In addition, understanding of the proposed active sites and corresponding mechanisms for ORR are covered. The recent advances shed light on contributions of morphology, hierarchical pore structures, density and dispersion of active sites, and synergistic effects of multiple active sites, which endow Fe 3 C@N‐C electrocatalysts with enhanced ORR performance. These interesting effects are attained as a result of increased exposure and accessibility of the active sites to O 2 molecules, faster charge and mass transfer, and finally, protection of active sites by carbon shells. Finally, the challenges and perspectives to further improve performance of Fe 3 C@N‐C are discussed.