4.4 Article

A novel Sillen-structured Bi-based oxybromide: CdBiO2Br ultrathin nanosheets for enhanced photocatalytic activity

期刊

ENVIRONMENTAL TECHNOLOGY
卷 44, 期 28, 页码 4394-4408

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TAYLOR & FRANCIS LTD
DOI: 10.1080/09593330.2022.2093651

关键词

CdBiO2Br; BiOBr; Sillen-structured bimetallic oxyhalide; photocatalytic activity; pollutant degradation

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The Sillen-structured bimetallic oxyhalide CdBiO2Br was successfully synthesized using a simple solvothermal method in the presence of a reactive ionic liquid. The introduction of CdBiO2Br shortened the distance between layers, facilitating the migration and separation of photogenerated carriers and promoting the generation of reactive oxygen species. This study provides a feasible scheme for the research and development of new layered photocatalytic materials.
According to the typical Sillen-structured BiOBr, a simple solvothermal method was used to successfully synthesise Sillen-structured bimetallic oxyhalide CdBiO2Br with the existence of 1-hexadecyl-3-methylimidazolium bromide ([C(16)mim]Br), a kind of reactive ionic liquid. The introduction of the metal cadmium, which can form Sillen-structured bimetallic oxyhalide, made the alternating structure of BiOBr originally [Bi2O2](2+) and bilayer Br- modified to that of [CdBiO2](+) and monolayer Br-. So that the distance between layer and layer is greatly shortened, which facilitates the migration and separation of photogenerated carriers and promotes the generation of more reactive oxygen species. After modification, the band positions of CdBiO2Br materials can make more full use of visible light and more favourable utilisation of solar resources. As confirmed by radical trapping analysis and ESR analysis, superoxide radical (center dot O-2(-)) and hole (h(+)) acted the major part during photocatalysis. The possible intermediate products that appeared during the degradation progress were analyzed by LC-MS. Moreover, the generation of superoxide ions was quantitatively analyzed by nitroblue tetrazolium chloride (NBT). In this paper, we present an ultra-thin layered material for visible light catalysis, which enlightens a feasible scheme for the research and development of new layered photocatalytic materials.

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