鳞片
纳米复合材料
材料科学
光催化
碳纳米管
纳米管
异质结
化学工程
纳米技术
复合材料
化学
有机化学
催化作用
光电子学
工程类
作者
Weiwei Tie,Zhaoyu Du,Hongwei Yue,Surjya Sarathi Bhattacharyya,Zhi Zheng,Weiwei He,Seung Hee Lee
标识
DOI:10.1016/j.jcis.2020.06.088
摘要
A self-assembled nanocomposite of lamellar BiOBr covalently bonded with conductive network of dispersive one-dimensional carbon nanotubes (1D CNT) and two-dimensional reduced graphitic-like flakes (2D GF) had been in situ constructed using one-pot facile solvothermal technique. Through self-assembly, BiOBr/CNT/GF (BiOBr/CG) displayed three-dimensional architectures in which a strong interfacial contact interaction and covalent banding between BiOBr nanostructures and CNT/GF network appeared. Furthermore, visible-light-driven catalytic activity of BiOBr/CG for RhB dye degradation was superior to that of pure BiOBr or BiOBr/C. Interestingly, the photodegradation activity of the BiOBr/CG nanocomposite could be improved further by subsequent facile annealing treatment, in which the annealed BiOBr/CG-DS had degraded almost 97.9% of RhB dye within only 100 min of visible-light irradiation. Moreover, analysis of the photodegradation mechanism revealed that the repression of electron-hole recombination in the nanocomposites, with sufficient covalent interfacial contact with CNT/GF as effective electron collecting and transferring system, were responsible for the outstanding photocatalytic performance. This effect, in turn, led to the continuous generation of O2- and OH reactive oxygen species for the degradation of RhB dye, which was verified by active species trapping and ESR spectra.
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