Photocatalytic Dinitrogen Fixation with Water on Bismuth Oxychloride in Chloride Solutions for Solar-to-Chemical Energy Conversion

被引:168
作者
Shiraishi, Yasuhiro [1 ,2 ]
Hashimoto, Masaki [1 ,2 ]
Chishiro, Kiyomichi [1 ,2 ]
Moriyama, Kenta [1 ,2 ]
Tanaka, Shunsuke [3 ]
Hirai, Takayuki [1 ,2 ]
机构
[1] Osaka Univ, Res Ctr Solar Energy Chem, Grad Sch Engn Sci, Toyonaka, Osaka 5608531, Japan
[2] Osaka Univ, Div Chem Engn, Grad Sch Engn Sci, Toyonaka, Osaka 5608531, Japan
[3] Kansai Univ, Dept Chem Energy & Environm Engn, Suita, Osaka 5648680, Japan
基金
日本科学技术振兴机构;
关键词
DRIVEN NITROGEN-FIXATION; METAL-FREE PHOTOCATALYSTS; HYDROGEN-PEROXIDE; OXYGEN VACANCIES; AMMONIA-SYNTHESIS; ELECTRON-TRANSFER; BIOBR NANOSHEETS; EFFICIENT; CARBON; NANOPARTICLES;
D O I
10.1021/jacs.0c01683
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ammonia is an indispensable chemical. Photocatalytic NH3 production via dinitrogen fixation using water by sunlight illumination under ambient conditions is a promising strategy, although previously reported catalysts show insufficient activity. Herein, we showed that ultraviolet light irradiation of a semiconductor, bismuth oxychloride with surface oxygen vacancies (BiOCl-OVs), in water containing chloride anions (Cl-) under N-2 flow efficiently produces NH3. The surface OVs behave as the N-2 reduction sites by the photoformed conduction band electrons. The valence band holes are consumed by self-oxidation of interlayer Cl- on the catalyst. The hypochloric acid (HClO) formed absorbs ultraviolet light and undergoes photodecomposition into O-2 and Cl-. These consecutive photoreactions produce NH3 with water as the electron donor. The Cl- in solution compensates for the removed interlayer Cl- and inhibits catalyst deactivation. Simulated sunlight illumination of the catalyst in seawater stably generates NH3 with 0.05% solar-to-chemical conversion efficiency, thus exhibiting significant potential of the seawater system for artificial photosynthesis.
引用
收藏
页码:7574 / 7583
页数:10
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