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An Ion‐Imprinting Derived Strategy to Synthesize Single‐Atom Iron Electrocatalysts for Oxygen Reduction
Author(s) -
Ding Shichao,
Lyu Zhaoyuan,
Zhong Hong,
Liu Dong,
Sarnello Erik,
Fang Lingzhe,
Xu Mingjie,
Engelhard Mark H.,
Tian Hangyu,
Li Tao,
Pan Xiaoqing,
Beckman Scott P.,
Feng Shuo,
Du Dan,
Li JinCheng,
Shao Minhua,
Lin Yuehe
Publication year - 2021
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.202004454
Subject(s) - catalysis , moiety , metal , covalent bond , nanoparticle , materials science , oxygen , carbon fibers , molecular sieve , atom (system on chip) , chemical engineering , inorganic chemistry , nanotechnology , photochemistry , combinatorial chemistry , chemistry , organic chemistry , composite number , computer science , engineering , composite material , embedded system , metallurgy
Carbon‐based single‐atom catalysts (CSACs) have recently received extensive attention in catalysis research. However, the preparation process of CSACs involves a high‐temperature treatment, during which metal atoms are mobile and aggregated into nanoparticles, detrimental to the catalytic performance. Herein, an ion‐imprinting derived strategy is proposed to synthesize CSACs, in which isolated metal–nitrogen–carbon (Me–N 4 –C x ) moiety covalently binds oxygen atoms in Si‐based molecular sieve frameworks. Such a feature makes Me–N 4 –C x moiety well protected/confined during the heat treatment, resulting in the final material enriched with single‐atom metal active sites. As a proof of concept, a single‐atom Fe–N–C catalyst is synthesized by using this ion‐imprinting derived strategy. Experimental results and theoretical calculations demonstrate high concentration of single FeN 4 active sites distributed in this catalyst, resulting in an outstanding oxygen reduction reaction (ORR) performance with a half‐wave potential of 0.908 V in alkaline media.