TY - JOUR
T1 - An Ion-Imprinting Derived Strategy to Synthesize Single-Atom Iron Electrocatalysts for Oxygen Reduction
AU - Ding, Shichao
AU - Lyu, Zhaoyuan
AU - Zhong, Hong
AU - Liu, Dong
AU - Sarnello, Erik
AU - Fang, Lingzhe
AU - Xu, Mingjie
AU - Engelhard, Mark H.
AU - Tian, Hangyu
AU - Li, Tao
AU - Pan, Xiaoqing
AU - Beckman, Scott P.
AU - Feng, Shuo
AU - Du, Dan
AU - Li, Jin Cheng
AU - Shao, Minhua
AU - Lin, Yuehe
N1 - Publisher Copyright:
© 2020 Wiley-VCH GmbH
PY - 2021/4/22
Y1 - 2021/4/22
N2 - 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–N4–Cx) moiety covalently binds oxygen atoms in Si-based molecular sieve frameworks. Such a feature makes Me–N4–Cx 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 FeN4 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.
AB - 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–N4–Cx) moiety covalently binds oxygen atoms in Si-based molecular sieve frameworks. Such a feature makes Me–N4–Cx 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 FeN4 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.
KW - Fe–N–C
KW - ion imprinting
KW - oxygen reduction reaction
KW - single-atom catalyst
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000597415100001
UR - https://openalex.org/W3111671656
UR - https://www.scopus.com/pages/publications/85097383137
U2 - 10.1002/smll.202004454
DO - 10.1002/smll.202004454
M3 - Journal Article
C2 - 33306278
SN - 1613-6810
VL - 17
JO - Small
JF - Small
IS - 16
M1 - 2004454
ER -