铁电性
材料科学
光激发
载流子
四方晶系
光致发光
偶极子
光催化
光电子学
电介质
可见光谱
相(物质)
激发态
催化作用
原子物理学
化学
有机化学
物理
作者
Yongfei Cui,Huanhuan Sun,Joe Briscoe,Rory M. Wilson,Nadezda V. Tarakina,Steve Dunn,Yongping Pu
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2019-02-27
卷期号:30 (25): 255702-255702
被引量:31
标识
DOI:10.1088/1361-6528/ab0b00
摘要
Using BaTiO3 as a model ferroelectric material we investigated the influence of the ferroelectric dipole on the photocatalytic activity of a heterogeneous BaTiO3/α-Fe2O3 photocatalyst. Two distinct BaTiO3 samples were used: BTO and BTO-A. The latter consists more ferroelectric tetragonal phase and thus stronger ferroelectricity. It was found that under identical experimental conditions, the photodecolourisation rate of a target dye using BTO-A/α-Fe2O3 under visible light was 1.3 times that of BTO/α-Fe2O3. Photoelectrochemical and photoluminescence analysis confirmed a more effective charge carrier separation in BTO-A/α-Fe2O3. Considering solely the photoexcitation of α-Fe2O3 in the composite photocatalysts under visible light and the similar microstructures of the two catalysts, we propose that the enhanced decolourisation rate when using BTO-A/α-Fe2O3 is due to the improved charge carrier separation and extended charge carrier lifetime arising from an interaction between the ferroelectric dipole and the carriers in α-Fe2O3. Our results demonstrate a new process to use a ferroelectric dipole to manipulate the charge carrier transport, overcome recombination, and extend the charge carrier lifetime of the surface material in a heterogeneous catalyst system.
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