Turning the coordination environment of atomic Fe-N4 center by peripheral nitrogen species for boosted catalytic performance

被引:16
作者
Cao, Fengliang [1 ]
Zhao, Qingshan [1 ]
Kong, Debin [1 ]
Tan, Xiaojie [1 ]
Li, Xinxin [2 ]
Liu, Tengfei [1 ]
Zhi, Linjie [1 ]
Wu, Mingbo [1 ]
机构
[1] China Univ Petr East China, Coll Chem & Chem Engn, Coll New Energy, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] Qingdao Inst Bioenergy & Bioproc Technol, Chinese Acad Sci, Qingdao Key Lab Funct Membrane Mat & Membrane Tech, Qingdao 266101, Peoples R China
基金
中国国家自然科学基金;
关键词
Single-atom catalyst; Fe-N4; Nitrogen dopant; Coordination environment regulation; Nitroarene reduction; SINGLE; EFFICIENT; REDUCTION; HYDROGENATION; NITROARENES; GRAPHENE;
D O I
10.1016/j.cej.2023.145181
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Atomically dispersed metal-nitrogen-carbon (M-N-C) catalysts show great potential for heterogeneous catalysis. However, recognizing and engineering the microenvironment of M-N-x sites to achieve satisfactory catalytic performance remains challenging. Herein, we propose a facile g-C3N4-assisted template strategy to anchor atomic Fe-N-4 sites on highly nitrogen-doped carbon nanosheets. Through regulating the ratio and type of peripheral nitrogen species by carbonization temperature, the optimal Fe-N-C-800 catalyst showed significantly boosted catalytic activities (overall turnover frequency of 13.43 min(-1) and activation energy of 19.44 kJ mol(-1)) for nitroarene reduction with extremely low reductant dosage, exceeding most reported metal catalysts. Experimental and theoretical results reveal appropriate graphitic- and pyrrolic-N dopants surrounding the Fe-N-4 center can tailor the local electronic structure and contribute to obvious upshift of the d-band center, which dramatically promotes the adsorption and conversion of reactant substrates, eventually delivering the unprecedented catalytic performance. This work provides a guide for rational coordination environment regulation of single-atom catalysts for efficient chemical transformations.
引用
收藏
页数:10
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