A high-cyano groups-content amorphous-crystalline carbon nitride isotype heterojunction photocatalyst for high-quantum-yield H2 production and enhanced CO2 reduction

被引:99
作者
Cheng, Cheng [1 ,2 ]
Mao, Liuhao [1 ]
Kang, Xing [1 ]
Dong, Chung-Li [3 ]
Huang, Yu-Cheng [3 ]
Shen, Shaohua [1 ]
Shi, Jinwen [1 ,4 ]
Guo, Liejin [1 ]
机构
[1] Xian Jiaotong Univ XJTU, Int Res Ctr Renewable Energy IRCRE, State Key Lab Multiphase Flow Power Engn MFPE, 28 West Xianning Rd, Xian 710049, Peoples R China
[2] Xian Jiaotong Univ XJTU, Sch Chem Engn & Technol, 28 West Xianning Rd, Xian 710049, Peoples R China
[3] Tamkang Univ, Dept Phys, 151 Yingzhuan Rd, Tamsui 25137, Taiwan
[4] Sichuan Digital Econ Ind Dev Res Inst, Integrated Energy Inst, 88 Jiefang Rd, Chengdu 610036, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dioxide; Crystallinity; Hydrogen; Eutectic salt; Solar energy; HYDROGEN-PRODUCTION; EVOLUTION; NANOSHEETS; MODULATION; WATER;
D O I
10.1016/j.apcatb.2023.122733
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
Polymeric carbon nitride suffers terrible recombination of photo-generated carriers and thus usually results in limited photocatalytic activity. Improving crystallinity and creating novel structure can effectively alleviate the aforementioned problem. Herein, a high-cyano groups-content and amorphous-crystalline carbon nitride isotype heterojunction (BCN-NaK) was obtain via a post treatment strategy in eutectic salt. The cyano groups acted as electron acceptors, and the intimate isotype heterojunction constructed by amorphous carbon nitride and crystalline poly-heptazine-imide built interfacial electric field. Both synergistically enabled BCN-NaK more efficient charge transfer than other amorphous and crystalline carbon nitrides. Comprehensive and systematic analysis demonstrated that the promoted charge transfer made the predominant contribution to the ultrahigh photocatalytic H-2-production activity of BCN-NaK with an excellent apparent quantum yield of 68.9 % at 405 nm. In addition, BCN-NaK exhibited a good photocatalytic CO2-to-CO conversion rate of 22.8 mu mol h(-1) g(cat) (-1) without adding sacrificial agent or loading metal under visible light.
引用
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页数:10
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