Li Guisheng, Jiang Bo, Xiao Shuning, Lian Zichao, Zhang Dieqing, Yu Jimmy C, Li Hexing
Department of Chemistry, Key Laboratory of Resource Chemistry of Ministry of Education and Shanghai Key Laboratory of Rare Earth Functional Materials, Shanghai Normal University, Shanghai 200234, China.
Environ Sci Process Impacts. 2014 Aug;16(8):1975-80. doi: 10.1039/c4em00196f.
A photosensitized BiOCl catalyst was found to be effective for photocatalytic water purification and air remediation under visible light irradiation (λ > 420 nm). Prepared by a solvothermal method, the BiOCl crystals possessed a 3D hierarchical spherical structure with the highly active facets exposed. When sensitized by Rhodamine B (RhB), the photocatalyst system was more active than N-doped TiO2 for breaking down 4-chlorophenol (4-CP, 200 ppm) and nitric monoxide (NO, 500 ppb). The high activity could be attributed to the hierarchical structure (supplying feasible reaction tunnels for adsorption and transition of reactants or products) and the efficient exposure of the {001} facets. The former provides an enriched oxygen atom density that promotes adsorption of cationic dye RhB, and creates an oxygen vacancy state. The HO˙ and ˙O2(-) radicals produced from the injected electrons from the excited dye molecule (RhB*) into the conduction band of BiOCl were responsible for the excellent photocatalytic performance of the RhB-BiOCl system.
研究发现,一种光敏化的BiOCl催化剂在可见光照射(λ > 420 nm)下对光催化水净化和空气修复有效。通过溶剂热法制备的BiOCl晶体具有三维分级球形结构,暴露出高活性晶面。当用罗丹明B(RhB)敏化时,该光催化剂体系在分解4-氯苯酚(4-CP,200 ppm)和一氧化氮(NO,500 ppb)方面比氮掺杂TiO2更具活性。高活性可归因于分级结构(为反应物或产物的吸附和转移提供可行的反应通道)以及{001}晶面的有效暴露。前者提供了富集的氧原子密度,促进阳离子染料RhB的吸附,并产生氧空位状态。从激发的染料分子(RhB*)注入到BiOCl导带中的电子产生的HO˙和˙O2(-)自由基是RhB-BiOCl体系优异光催化性能的原因。