Enhanced photocatalytic nitrogen fixation of Ag/B-doped g-C3N4 nanosheets by one-step in-situ decomposition-thermal polymerization method

被引:85
作者
Yao, Xiaxi [1 ]
Zhang, Wenjun [1 ,2 ]
Huang, Jialei [1 ,2 ]
Du, Zhongwei [1 ]
Hong, Xuekun [1 ]
Chen, Xuefeng [3 ]
Hu, Xiuli [1 ]
Wang, Xuhong [1 ,2 ]
机构
[1] Changshu Inst Technol, Sch Mat Engn, Suzhou Key Lab Funct Ceram Mat, Changshu 215500, Jiangsu, Peoples R China
[2] Changzhou Univ, Sch Mat Sci & Engn, Changzhou 213164, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Ceram, Key Lab Inorgan Funct Mat & Devices, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Nitrogen fixation; B-doped g-C3N4; Ag; Decomposition-thermal polymerization; GRAPHITIC CARBON NITRIDE; HYDROGEN-PRODUCTION; FACILE SYNTHESIS; REDUCTION; FABRICATION; ROUTE; WATER; CO2; CU;
D O I
10.1016/j.apcata.2020.117647
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
Photocatalytic nitrogen fixation is considered as a promising strategy for ammonia production. In this study, non-metallic boron and noble metal silver modified graphitic carbon nitride were prepared by a direct in-situ decomposition-thermal polymerization method with dicyandiamide, boric acid and silver nitrate as the precursors. It was shown that Ag/B-doped g-C3N4 composites with optimal mass ratio exhibited improved photocatalytic ammonia production under simulated sunlight illumination by a factor of 5.5 and 1.5 times compared with the pristine g-C3N4 and B-doped g-C3N4, respectively. The superior photocatalytic property was attributed to the decreased band gap and formation of mesopores after boron doping, which enlarged the specific surface area and created abundant reactive sites on the g-C3N4 nanosheets. In addition, the loaded silver nanoparticles greatly inhibited the recombination of photogenerated charge carriers through heterojunction interface. This work provided new deep insights into the reasonable structure of g-C3N4 composite system for photocatalytic nitrogen fixation reactions.
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页数:7
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