掺杂剂
氨生产
硼
催化作用
材料科学
光催化
光化学
氨
密度泛函理论
析氧
氮气
氧气
兴奋剂
化学工程
化学
电化学
物理化学
计算化学
光电子学
有机化学
电极
工程类
作者
Yanting Zhang,Lei Ran,Yanxue Zhang,Panlong Zhai,Yunzhen Wu,Junfeng Gao,Zhuwei Li,Bo Zhang,Chen Wang,Zhaozhong Fan,Xiaomeng Zhang,Jiaqi Cao,Dingfeng Jin,Licheng Sun,Jungang Hou
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-10-28
卷期号:15 (11): 17820-17830
被引量:35
标识
DOI:10.1021/acsnano.1c06017
摘要
Direct nitrogen photofixation is a feasible solution toward sustainable production of ammonia under mild conditions. However, the generation of active sites for solar-dirven nitrogen fixation not only limits the fundamental understanding of the relationship among light absorption, charge transfer, and catalytic efficiency but also influences the photocatalytic activity. Herein, we report two-dimensional boron-doped niobic acid nanosheets with oxygen vacancies (B-Vo-HNbO3 NSs) for efficient N2 photofixation in the absence of any scavengers and cocatalysts. Impressively, B-Vo-HNbO3 NS as a model catalyst achieves the enhanced ammonia evolution rate of 170 μmol gcat-1 h-1 in pure water under visible-light irradiation. The doublet coupling representing 15NH4+ in an isotopic labeling experiment and in situ infrared spectra confirm the reliable ammonia generation. The experimental analysis and density functional theory (DFT) calculations indicate that the strong synergy of boron dopant and oxygen vacancy regulates band structure of niobic acid, facilitates photogenerated charge transfer, reduces free energy barriers, accelerates reaction kinetics, and promotes the high rates of ammonia evolution. This work provides a general strategy to design active photocatalysts toward solar N2 conversion.
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