光催化
甲基橙
可见光谱
纳米颗粒
水溶液
材料科学
分解
电子转移
光化学
化学工程
纳米技术
催化作用
化学
物理化学
光电子学
有机化学
工程类
作者
Cuiling Zhang,Hua Hao,Jianlin Liu,Xiangyu Han,Qipeng Liu,Zidong Wei,Shao Cheng-bin,Chenguo Hu
标识
DOI:10.1007/s40820-017-0150-8
摘要
Ag–AgX(X = Cl, Br)@TiO2 nanoparticle-aggregated spheres with different mass ratio of R = TiO2/Ag(X) from 35:1 to 5:1 were synthesized by a facile sol–gel technique with post-photoreduction. The photocatalytic activities of both Ag–AgCl@TiO2 and Ag–AgBr@TiO2 under visible light are effectively improved by ~3 times relative to TiO2 NPAS under the simulated sunlight for the decomposition of methyl orange (MO). Ag–AgBr@TiO2 showed 30% improvement and less stable in photocatalytic activity than that of AgCl@TiO2. The role of Ag and AgX nanoparticles on the surface of Ag–AgX(X = Cl, Br)@TiO2 was discussed. Ag on these samples not only can efficiently harvest visible light especially for AgCl, but also efficiently separate excited electrons and holes via the fast electron transfer from AgX(X = Cl, Br) to metal Ag nanoparticles and then to TiO2-aggregated spheres on the surface of heterostructure. On the basis of their efficient and stable photocatalytic activities under visible-light irradiation, these photocatalysts could be widely used for degradation of organic pollutants in aqueous solution.
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