Templated synthesis of cobalt subnanoclusters dispersed N/C nanocages from COFs for highly-efficient oxygen reduction reaction

被引:68
作者
Chen, Hao [1 ,3 ]
Li, Qiao-Hong [1 ]
Yan, Wensheng [2 ]
Gu, Zhi-Gang [1 ,3 ]
Zhang, Jian [1 ,3 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[2] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Covalent organic frameworks; Templated synthesis; Subnanoclusters; Nanocages; Electrocatalysis; COVALENT ORGANIC FRAMEWORK; DOPED CARBON SPHERES; DENSITY-FUNCTIONAL THEORY; BIFUNCTIONAL ELECTROCATALYSTS; HIGH-PERFORMANCE; POROUS CARBON; AIR; NANOPARTICLES; CATALYSTS; DESIGN;
D O I
10.1016/j.cej.2020.126149
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Development of nonprecious metal-based electrocatalysts with highly efficient oxygen reduction reaction (ORR) has increasingly attracted wide attention in energy conversion and storage systems. In this work, we stepwise grow cobalt chelated COF TpBpy (Co-TpBpy) on silica nanospheres to form core-shell SiO2@Co-TpBpy nanospheres. After calcination high temperatures and removing silica template, cobalt subnanoclusters dispersed in N-doped carbon (N/C) nanocages are obtained for ORR. As a result, the Co-TpBpy-800 nanocages exhibit highly efficient activity on electrocatalytic ORR with 0.831 V of half-wave potential and high stability. Moreover, DFT calculation verifies the resulting unique nanocages reveal an unconventional five-step ORR process in which it skips the intermediate OOH* because the oxygen dissociation and adsorption directly occur on the catalyst surface. The present work will help the development of highly-efficient nonprecious metal-based catalysts for various energy applications.
引用
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页数:9
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