CdS/CdSe co-sensitized brookite H:TiO2 nanostructures: Charge carrier dynamics and photoelectrochemical hydrogen generation

被引:125
作者
Chang, Yung-Shan [1 ]
Choi, Mingi [2 ]
Baek, Minki [2 ]
Hsieh, Ping-Yen [1 ]
Yong, Kijung [2 ]
Hsu, Yung-Jung [1 ]
机构
[1] Natl Chiao Tung Univ, Dept Mat Sci & Engn, Hsinchu 30010, Taiwan
[2] Pohang Univ Sci & Technol POSTECH, Surface Chem Lab Elect Mat, Dept Chem Engn, Pohang 790784, South Korea
基金
新加坡国家研究基金会;
关键词
Brookite TiO2; Hydrogen doping; Sensitization; Interfacial charge dynamics; PEC hydrogen production; NANOWIRE ARRAYS; QUANTUM DOTS; WATER; NANOHETEROSTRUCTURES; PHOTOCATALYST; NANOCRYSTALS; PHOTOANODE; DEPOSITION; CELL; CDS;
D O I
10.1016/j.apcatb.2017.11.063
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we have synthesized CdS/CdSe co-sensitized brookite TiO2 nanostructures with hydrogen doping (H:TiO2/CdS/CdSe) in a facile solution reaction and studied their PEC performances. Compared to undoped brookite TiO2, the H:TiO2/CdS/CdSe composites exhibit much enhanced photocurrent generation, which originates from the improved charge transfer kinetics endowed by hydrogen doping and sensitization. Time-resolved photoluminescence (PL) and electrochemical impendence spectroscopy (EIS) are employed to explore the charge transfer dynamics between sensitizers and TiO2 and charge carrier kinetics at the semiconductor/electrolyte interface. According to the analytical results, sensitizations of TiO2 are found to enhance the charge separation efficiency. Besides, the hydrogen doping into TiO2 generates oxygen vacancy states, providing additional charge transfer pathway and prohibiting charge recombination, beneficial for enhancing the PEC performances as well. Based on the charge dynamics data, we further develop charge transfer models for TiO2/CdS/CdSe and H:TiO2/CdS/CdSe. The findings from this work can help understanding the charge transfer dynamics in brookite TiO(2)based composite systems as well as designing versatile photoelectrodes for solar energy conversion.
引用
收藏
页码:379 / 385
页数:7
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