MXene boosted metal-organic framework-derived Fe-N-C as an efficient electrocatalyst for oxygen reduction reactions

被引:32
作者
Gu, Wenling [1 ]
Wu, Maochun [1 ,2 ,3 ]
Xu, Jianbo [1 ,2 ,3 ]
Zhao, Tianshou [1 ,2 ,3 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, HKUST Energy Inst, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[3] Guangzhou HKUST Fok Ying Tung Res Inst, Hong Kong 511458, Peoples R China
关键词
Fe-N-C catalysts; Oxygen reduction reaction; MXene; Electronic interaction; Metal-organic framework; ACTIVE-SITES; FREE CATALYSTS; CARBON; HYBRIDS; IRON;
D O I
10.1016/j.ijhydene.2022.03.229
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Iron-nitrogen-carbon (Fe-N-C) electrocatalysts offer great promise to replace their noble metal-based counterparts for oxygen reduction reactions (ORR). However, the practical applications of this type of catalyst are hindered by insufficient accessible active sies, low electrical conductivity, and poor durability. Here, we report a Ti3C2 MXene supported metal-organic framework (MOF)-derived Fe-N-C (Fe-Nx/N/Ti3C2) catalyst to simultaneously address the issues. Owing to the negatively charged characteristics, NH2-MIL53(Fe) is firmly anchored on Ti3C2 MXene, which not only serves as a conductive substrate to alleviate the collapse and agglomeration of MOFs during the pyrolysis, but also modulates the electronic properties of active FeNx sites to improve the electrocatalytic activity and stability. As a result, the as-prepared Fe-Nx/N/Ti3C2 catalyst exhibits superb ORR activity and long-term stability in both alkaline and acidic electrolytes. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:17224 / 17232
页数:9
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