Direct conversion mechanism from BiOCl nanosheets to BiOF, Bi7F11O5 and BiF3 in the presence of a fluorine resource

作者：Kan, Yandong; Teng, Fei^*; Yang, Yang; Xu, Juan; Yang, Liming

来源：RSC Advances, 2016, 6(68): 63347-63357.

DOI：10.1039/c6ra11877a

• DRIVEN PHOTOCATALYTIC ACTIVITY
• IN-SITU SYNTHESIS
• TIO2
• SEMICONDUCTORS
• ARCHITECTURES
• ADSORPTION
• OXIDATION
• STRATEGY
• REMOVAL
• BI2O3

In this work, we report the facile conversion from BiOCl nanosheets to BiOF, Bi7F11O5 and BiF3 by a novel ion exchange approach, in which the effects of fluorine source, F/Bi molar ratio and reaction medium (ethanol/water) on the products are mainly investigated. A plausible conversion mechanism is proposed to illustrate the formation of BiOF, Bi7F11O5 and BiF3. Furthermore, the photocatalytic activities of the samples are also investigated. It is amazing that under ultraviolet light irradiation (lambda <= 420 nm), the activity of the as-formed Bi7F11O5/BiOCl sample is 3.28 times higher than that of BiOCl for the degradation of methyl orange (MO). It is demonstrated that the improved activity is mainly attributed to the formation of Bi7F11O5/BiOCl heterojunction, which has significantly improved the separation and transfer efficiency of charges. It is important that this study provides an initiative post-synthesis strategy to develop new, efficient photocatalysts.

• 出版日期2016
• 单位南京信息工程大学