光催化
异质结
罗丹明B
带偏移量
材料科学
介电谱
光电子学
半导体
带隙
电化学
光化学
电极
化学
价带
催化作用
生物化学
物理化学
作者
Lianwei Shan,Yuteng Liu,Jingjing Bi,Jagadeesh Suriyaprakash,Zhidong Han
标识
DOI:10.1016/j.jallcom.2017.06.041
摘要
Abstract One of the current key issues in the photocatalysis is to obtain the band alignment of coupled semiconductor experimentally, which is the most significant aspect for understanding the efficient photocatalytic activity precisely. In this article, a BiVO 4 /BiOI{001} heterojunction was detected by the transmission electron microscopy (TEM). The results of electrochemical impedance spectroscopy (EIS) reveal that a higher efficiency of charge immigration across the electrode/electrolyte interface for the BiVO 4 /BiOI{001}. In addition, the electron lifetime was investigated by the Bode phase plots, which are responsible for the observed photocatalytic behaviors. As a result, the photocatalytic activities for rhodamine B (RhB) degradation and iodine ion oxidation are remarkably increased compared to the individual BiVO 4 and BiOI{001}. In fact, a direct band alignment in the BiVO 4 /BiOI{001} does not give well a logical interpreting on its photocatalytic behavior. However, through the valence-band offset formula, we demonstrated the exact band alignment of corresponding components in the BiVO 4 /BiOI{001}. This band alignment was further confirmed by the PL spectra, which CM2 with photo-oxidation (Mn 2+ ) is red shift and CM2 with photo-reduction (Ag + ) is blue shift compared with CM2.
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