An Ion-Imprinting Derived Strategy to Synthesize Single-Atom Iron Electrocatalysts for Oxygen Reduction

被引:68
作者
Ding, Shichao [1 ]
Lyu, Zhaoyuan [1 ]
Zhong, Hong [1 ]
Liu, Dong [1 ]
Sarnello, Erik [2 ]
Fang, Lingzhe [2 ]
Xu, Mingjie [3 ,4 ]
Engelhard, Mark H. [5 ]
Tian, Hangyu [1 ]
Li, Tao [2 ,6 ]
Pan, Xiaoqing [3 ]
Beckman, Scott P. [1 ]
Feng, Shuo [1 ]
Du, Dan [1 ]
Li, Jin-Cheng [1 ,4 ]
Shao, Minhua [4 ]
Lin, Yuehe [1 ]
机构
[1] Washington State Univ, Sch Mech & Mat Engn, Pullman, WA 99164 USA
[2] Northern Illinois Univ, Dept Chem & Biochem, De Kalb, IL 60115 USA
[3] Univ Calif Irvine, Irvine Mat Res Inst IMRI, Irvine, CA 92697 USA
[4] Hong Kong Univ Sci & Technol, Fok Ying Tung Res Inst, Guangzhou 511458, Peoples R China
[5] Pacific Northwest Natl Lab, Environm Mol Sci Lab, 902 Battelle Blvd, Richland, WA 99354 USA
[6] Argonne Natl Lab, Xray Sci Div, Lemont, IL 60439 USA
基金
中国博士后科学基金;
关键词
Fe– N– C; ion imprinting; oxygen reduction reaction; single‐ atom catalyst; DOPED CARBON; CATALYSTS; NITROGEN; SITES; HYDROGEN; COPPER; MEDIA;
D O I
10.1002/smll.202004454
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 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.
引用
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页数:8
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