N and O multi-coordinated vanadium single atom with enhanced oxygen reduction activity

被引:29
作者
Cheng, Ling [1 ]
Huang, Hao [1 ]
Lin, Zhiyu [1 ]
Yang, Yang [1 ]
Yuan, Qing [1 ]
Hu, Lin [2 ]
Wang, Changlai [1 ,3 ]
Chen, Qianwang [1 ,2 ]
机构
[1] Univ Sci & Technol China, Dept Mat Sci & Engn, Jinzhai Rd 96, Hefei 230026, Anhui, Peoples R China
[2] Chinese Acad Sci, Hefei Inst Phys Sci, Anhui High Magnet Field Lab, Hefei 230031, Anhui, Peoples R China
[3] City Univ Hong Kong, Ctr Super Diamond & Adv Films COSDAF, Dept Mat Sci & Engn, Kowloon, Tat Chee Ave, Hong Kong, Peoples R China
基金
国家重点研发计划;
关键词
Vanadium single atom; N; O co-coordination; Electrocatalyst; Electronic structure; Oxygen reduction reaction; METAL-FREE ELECTROCATALYSTS; DOPED MESOPOROUS CARBON; SPECTROSCOPIC CHARACTERIZATION; EFFICIENT ELECTROCATALYST; MECHANISTIC INSIGHTS; COMPLEXES; NITROGEN; CATALYSTS; GLYCINE; SITES;
D O I
10.1016/j.jcis.2021.03.074
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
Recently, atomically dispersed transition-metal single atom in nitrogen-doped carbon matrix as electro-catalysts has aroused general interest. However, there is no report about vanadium single atom for ORR in the literature. According to d-band center theory for transition-metals, the performance of catalysts is regulated by the electronic structure of the catalytic center which determines the intermediate adsorption kinetics. Indeed, the valence of vanadium is variable, its electron structure could be modulated by an appropriate coordination structure. Here, a novel method is developed to prepare the N and O co-coordinated vanadium single atom (V-N1O4) embedded in the carbon matrix. The catalyst displays a half-wave potential of 865 mV in base solution which surpasses 20% Pt/C, and also shows a high power density of 180 mW/cm(2) in Zn-air batteries. DFT calculations reveal that the N and O coordination configuration could regulate the electron structure and geometry of vanadium to boost the electrocatalytic activity. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:466 / 473
页数:8
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