PANI/Bi12TiO20 complex architectures: Controllable synthesis and enhanced visible-light photocatalytic activities

被引:64
作者
Hou, Jungang [1 ]
Cao, Rui [1 ]
Jiao, Shuqiang [1 ]
Zhu, Hongmin [1 ]
Kumar, R. V. [2 ]
机构
[1] Univ Sci & Technol Beijing, Sch Met & Ecol Engn, Beijing 100083, Peoples R China
[2] Univ Cambridge, Dept Mat Sci & Met, Cambridge CB2 3QZ, England
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
Photocatalytic activity; Bismuth titanate; Polyaniline; Degradation; BISMUTH TITANATE BI12TIO20; SEMICONDUCTOR; WATER; OXIDE; PHOTOACTIVITY; HYBRIDIZATION; IRRADIATION; DEGRADATION; BI2WO6; TIO2;
D O I
10.1016/j.apcatb.2011.02.032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Bi12TiO20 complex architectures (BiT) with flower-, spindle- and jujube-like shapes, were prepared through a facile template-free hydrothermal process, by controlling the reaction parameters, such as temperature, reagent concentration, and reaction time. Within the hydrothermal temperature range from 150 to 200 degrees C, the morphology transformed progressively from microjujube to microflowers consisted with nanospindles. A possible growth mechanism for BiT architectures was proposed to explain the transformation of nanoparticles to microflowers via an Ostwald ripening mechanism followed by self-assembly. Most importantly, much higher photocatalytic activities of BiT spindle-like structures modified with 0.5% polyaniline (PANI) via a simple chemisorption approach in comparison with unmodified BIT were obtained for the degradation of Rhodamine B (RhB) solution under visible-light irradiation (lambda > 420 nm). Furthermore, an enhanced photocatalytic performance for RhB degradation was also observed with the assistance of a small amount of H2O2. The reason could be ascribed to the synergic effect between PANI and BIT, which promoted the migration efficiency of photogenerated electron-hole on the interface of PAN! and BIT, demonstrating that PANI/BiT architecture is a promising candidate as a visible light photocatalyst. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:399 / 406
页数:8
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