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通过静电自组装构建WO/CsPbBr S型异质结用于高效长周期光催化CO还原

Construction of WO/CsPbBr S-scheme heterojunction via electrostatic Self-assembly for efficient and Long-Period photocatalytic CO reduction.

作者信息

Chen Qiao, Lan Xuefang, Chen Keshuai, Ren Qianqian, Shi Jinsheng

机构信息

Department of Chemistry and Pharmaceutical Science, Qingdao Agricultural University, Qingdao 266109, People's Republic of China.

School of Management, Tongmyong University, Pusan 48520, Pusan, Korea.

出版信息

J Colloid Interface Sci. 2022 Jun 15;616:253-260. doi: 10.1016/j.jcis.2022.02.044. Epub 2022 Feb 14.

DOI:10.1016/j.jcis.2022.02.044
PMID:35217241
Abstract

Owing to the severe photogenerated carriers recombination and low oxidation ability, the photocatalytic performance of pristine CsPbBr is still unsatisfactory. Herein, melamine foam supported S-scheme WO/CsPbBr heterojunction is successfully synthesized by electrostatic self-assembly. Because of the appropriate energy level positions, an S-scheme charge migration route between CsPbBr and WO is constructed. Under solar light irradiation, melamine foam assisted WO/CsPbBr exhibits significantly enhanced photocatalytic CO reduction performance under liquid HO medium, and the electron consumption rate (R) reaches to 1225.50 μmolgh, which is 1.49- and 13.7-fold of CsPbBr and WO, respectively, ascribing to the boosted charges transfer and the strengthened redox ability. Furthermore, S-scheme WO/CsPbBr heterojunction also exhibits strong durability, with no noticeable reduction of product yields after four 8-h cycles.

摘要

由于严重的光生载流子复合和较低的氧化能力,原始的CsPbBr的光催化性能仍然不尽人意。在此,通过静电自组装成功合成了三聚氰胺泡沫负载的S型WO/CsPbBr异质结。由于合适的能级位置,在CsPbBr和WO之间构建了一条S型电荷迁移路径。在太阳光照射下,三聚氰胺泡沫辅助的WO/CsPbBr在液态HO介质中表现出显著增强的光催化CO还原性能,电子消耗速率(R)达到1225.50 μmolgh,分别是CsPbBr和WO的1.49倍和13.7倍,这归因于电荷转移的增强和氧化还原能力的增强。此外,S型WO/CsPbBr异质结还表现出很强的耐久性,在四个8小时循环后产物产率没有明显降低。

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