Carbon hybrid with 3D nano-forest architecture in-situ catalytically constructed by CoFe alloy as advanced multifunctional electrocatalysts for Zn-air batteries-driven water splitting

被引:52
|
作者
Wang, Shuguang [1 ]
Wang, Jie [1 ]
Wang, Xin [1 ]
Li, Long [1 ]
Qin, Jinwen [1 ]
Cao, Minhua [1 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Minist Educ China, Lab Cluster Sci, Beijing 100081, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Carbon nanotubes; Grafted growth; Multifunctional electrocatalysts; Water splitting; Zinc-air batteries; OXYGEN-EVOLUTION ELECTROCATALYSTS; DOPED GRAPHENE; REDUCTION REACTION; HYDROGEN; TEMPLATE; IRON; NANOFIBERS; CATALYSTS; NANOTUBES; OXIDATION;
D O I
10.1016/j.jechem.2020.07.045
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Rational design and facile synthesis of non-noble materials as the effective multifunctional electrocatalysts are still challenging. Herein, a self-catalytically grafted growth approach is developed to construct carbon hybrid with three-dimensional (3D) nano-forest architecture via controlled pyrolysis of metal polymer nanofiber precursor and melamine. The metal-polymer nanofibers act as the matrix, and melamine is used as the initiator for orientated growth of one-dimensional (1D) N-doped carbon nanotubes (N-CNTs) on carbon nanofibers. The as-prepared CoFe-N-CNTs/CNFs-900 possesses unique structure and component advantages in terms of 3D structure, special synapse-like structure, porous feature, high-level N doping and bimetallic active components, which endow the material with structural stability, high mass/electron transport ability and large active sur-/interfaces. Benefiting from the integrated effects of all the above factors, CoFe-N-CNTs/CNFs were successfully applied to overall water splitting and Zn-air batteries. It is believed that this integrated design methodology can be extended to prepare other M-N-C materials for energy-related electrochemical reactions. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
引用
收藏
页码:422 / 432
页数:11
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