Molten-salt-chemistry-assisted synthesis of heterostructured g-C3N4/BiOI nanocomposites with enhanced sunlight absorption properties for efficient solar-to-chemical energy conversion

被引:3
作者
Deng, Xinyue [1 ]
Luo, Rui [1 ]
Zhu, Gang [1 ]
Shi, Xiangyang [1 ]
Hao, Weiju [1 ]
Fan, Jinchen [1 ]
Bi, Qingyuan [1 ]
Li, Guisheng [1 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Mat & Chem, Shanghai 200093, Peoples R China
基金
中国国家自然科学基金;
关键词
G-C3N4; nanosheets; BiOI; Heterojunction structure; Photocatalytic dye degradation; Solar-to-chemical energy conversion; REDUCTION; PHOTOCATALYSIS;
D O I
10.1016/j.jallcom.2024.176910
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
The g-C3N4 nanosheets coupled BiOI (g-C3N4/BiOI) nanocomposites with unique heterojunction structure and excellent wide-spectrum sunlight absorption properties have been developed via molten-salt-chemistry-assisted strategy. The heterostructured g-C3N4/BiOI shows enhanced solar to the thermal effect, improved electron mobility and carrier lifetime for efficient photocatalytic dye degradation. The engineered g-C3N4/BiOI catalyst exhibits outstanding photocatalytic activity for methyl orange (MO) removal with 100 % degradation conversion and excellent stability under solar light irradiation, which is respectively 2.69 and 1.27 times higher than those of g-C3N4 and BiOI counterparts. The broad scope toward other dyes degraded by g-C3N4/BiOI and the generality of the molten-salt-chemistry-assisted strategy for synthesizing g-C3N4/BiOCl and g-C3N4/BiOBr with considerable photodegradation efficiency are proved. The analysis of kinetic behaviors, electron spin resonance, and nanosecond transient absorption spectra for structure-activity relationship, key intermediate of center dot O-2(-) species, and excited state lifetime of g-C3N4/BiOI heterojunction material in the photocatalytic MO degradation processes are also demonstrated.
引用
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页数:12
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