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Size controllable synthesis of single-crystal ferroelectric Bi4Ti3O12 nanosheet dominated with {0 0 1} facets toward enhanced visible-light-driven photocatalytic activities

光催化 材料科学 光降解 罗丹明B 钛酸铋 熔盐 纳米片 介电谱 可见光谱 表面光电压 光电子学 动力学 化学工程 分析化学(期刊) 铁电性 纳米技术 电化学 化学 光谱学 电极 催化作用 物理化学 有机化学 冶金 电介质 量子力学 工程类 物理
作者
Hongquan He,Jiao Yin,Yingxuan Li,Ying Zhang,Hengshan Qiu,Jinbao Xu,Tao Xu,Chuanyi Wang
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:156-157: 35-43 被引量:177
标识
DOI:10.1016/j.apcatb.2014.03.003
摘要

• Size and facet controlling of Bi 4 Ti 3 O 12 (BTO) is achieved by varying the amount of added salts (NaCl and KCl). • BTO-50 (molten salt synthesis) shows an activity about 8.65 times higher than that of BTO-0 obtained by solid-state reaction method in photodegradation of rhodamine B under visible-light irradiation. • Effect of the ferroelectric nature of BTO on the photocatalytic activities is well illustrated by Kevin probe force microscopy and electrochemical measurement for the first time. Highly crystallized single crystal Bi 4 Ti 3 O 12 nanosheets with dominant {0 0 1} facets were synthesized by heating a stoichiometric composition of α-Bi 2 O 3 and TiO 2 in molten NaCl–KCl at 800 °C for 2 h. Effects of the amount of the added molten salts (their mole ratio ( M ) to nominal Bi 4 Ti 3 O 12 varied from 4 to 60 and the samples were denoted as BTO- M ) on the size distribution and photoactivity of the resulting products were systematically evaluated. The side length of as-prepared Bi 4 Ti 3 O 12 gradually decreases by increasing the addition of molten salts, and the minimal side length is achieved in the sample BTO-50. As a result, the sample BTO-50 shows the best photocatalytic kinetics in photodegradation of rhodamine B (RhB) under visible-light irradiation, which is about 8.65 times faster than that of the sample BTO-0 obtained by a traditional solid-state reaction method, demonstrating the superiority of the present molten salts synthesis for bismuth titanate. The improved photocatalytic kinetics of BTO- M is a concert of several factors including the highly faceted surfaces, thin flakes that shorten the charge transport distance to the surface, as well as the internal electric fields produced by the spontaneous polarization in the BTO-50 sample that facilitate the separation of photoinduced charges as evidenced by Kelvin probe force microscopy. Electrochemical impedance spectroscopy further reveals that under visible-light, the electron transfer resistance of the BTO-50 decreases to nearly 50% of that of the BTO-0 sample.
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