Hollow mesoporous SiO2-BiOBr nanophotocatalyst: Synthesis, characterization and application in photodegradation of organic dyes under visible-light irradiation
writer：W. Li, X. Jia, P. Li, B. Zhang, H. Zhang, W. Geng, Q. Zhang
keywords：Hollow silica, Rhodamine B, Electron?hole pair, Photocatalyst, Quantization
source：期刊
specific source：https://pubs.acs.org/doi/pdf/10.1021/acssuschemeng.5b00033
Issue time：2015年
In this paper, a novel visible-light-driven hollow mSiO2-BiOBr (H-mSiO2-BiOBr) nanophotocatalyst was successfully synthesized by a facile three-step method. First, the hollow mesoporous silica submicrospheres with orderly mesoporous opening structure and an independent internal cavity were synthesized by combining Sto?ber hydrolysis and chemical etching. Second, the hollow mesoporous silica submicrospheres were functionalized by 3-triethoxysilylpropylamine (APTES), then the amino-groups were successfully introduced into the surface of this material. Third, the BiOBr nanophotocatalyst with size of about 8-15 nm was successfully synthesized on the surface of the aforementioned amino-functionalized hollow mesoporous silica submicrospheres by solvothermal synthesis with the aid of the oriented function of the surface amino-groups. After several characterizations of the materials, the photocatalytic degradation of RhB by this HmSiO2-BiOBr nanophotocatalyst under visible-light irradiation was investigated. The experimental results revealed that the photocatalytic activity of the H-mSiO2-BiOBr nanophotocatalyst was higher than that of the core-shell SiO2@mSiO2-BiOBr nanophotocatalyst under visible-light irradiation. More importantly, the nanoscale BiOBr photocatalyst, which was synthesized by controlling the addition amounts of the bismuth source, would lead to an increased band gap (1.47 eV), and it would further lead to the effective restraint for the recombination of the photoexcited electron-hole pairs. However, the rapid migration of the interface charges would enhance the photoactivity of this novel supported nanophotocatalyst significantly. Furthermore, the existence of the internal cavities of this novel nanophotocatalyst would lead to the multiple reflections of the irradiated light and effectively prolong its action time, which is also very conducive to the enhancement of the photoactivity of this supported nanophotocatalyst. Beyond that, the orderly mesoporous opening structure and the independent internal cavities can effectively facilitate the transfer of reactant molecules. This would lead to the enhanced photocatalytic performance of this novel supported BiOBr nanophotocatalyst.
ACS Sustainable Chem. Eng. 2015, 3, 1101?1110