Boosting electrocatalytic N2 reduction by MnO2 with oxygen vacancies

被引:127
|
作者
Zhang, Ling [1 ]
Xie, Xiao-Ying [2 ]
Wang, Huanbo [3 ]
Ji, Lei [1 ]
Zhang, Ya [1 ]
Chen, Hongyu [1 ,4 ]
Li, Tingshuai [5 ]
Luo, Yonglan [4 ]
Cui, Ganglong [2 ]
Sun, Xuping [1 ]
机构
[1] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Sichuan, Peoples R China
[2] Beijing Normal Univ, Coll Chem, Beijing 100875, Peoples R China
[3] Southwest Univ Sci & Technol, Sch Environm & Resource, Mianyang 621010, Sichuan, Peoples R China
[4] China West Normal Univ, Sch Chem & Chem Engn, Chem Synth & Pollut Control Key Lab Sichuan Prov, Nanchang 637002, Sichuan, Peoples R China
[5] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
ATMOSPHERIC-PRESSURE; MANGANESE OXIDES; NITROGEN; AMMONIA; NH3; WATER; TEMPERATURE; ALPHA-MNO2; CONVERSION; EVOLUTION;
D O I
10.1039/c9cc00936a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here, we demonstrate the experimental verification of utilizing a MnO2 with oxygen vacancies (MnOx) nanowire array for high-performance and durable electrocatalytic reduction at neutral pH. Such MnOx nanoarray obtains a high rate of NH3 formation (1.63 x 10(-10) mol cm(-2) s(-1)) and a high Faradaic efficiency of 11.40%, which are much higher than those of its pristine MnO2 counterpart (2.3 x 10(-11) mol cm(-2) s(-1); 1.96%). Density functional theory calculations demonstrate that the enhancement of N-2 adsorption on the MnOx surface is due to stronger electronic interaction between the N-2 molecule and the Mn-6c atoms as a result of the oxygen vacancy. This work opens up a new avenue to explore oxygen nonstoichiometry toward the rational design of N-2-fixing electrocatalysts with boosted performance for applications.
引用
收藏
页码:4627 / 4630
页数:4
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