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Enhanced UV Photoresponse Performances of TiO2/Bi2Se3 Heterostructure‐Based Photoelectrochemical Photodetector.

Authors :
Yang, Jinhai
Ye, Yanhong
Yu, Ruiyang
Yang, Han
Qiao, Hui
Huang, Zongyu
Qi, Xiang
Source :
Physica Status Solidi. A: Applications & Materials Science. Dec2024, Vol. 221 Issue 23, p1-8. 8p.
Publication Year :
2024

Abstract

Bi2Se3 has a unique surface state and excellent electron transport performance, but because of its narrow band gap, Bi2Se3‐based photodetectors are difficult to achieve high response to ultraviolet (UV) light. In this paper, the TiO2/Bi2Se3 heterostructure was constructed by spin‐coating TiO2 on Bi2Se3 film, and TiO2/Bi2Se3 heterostructure‐based photoelectrochemical (PEC) photodetector was constructed, and a series of measurements were carried out. The measure results showed that the photoresponse performance of TiO2/Bi2Se3 heterostructure‐based photodetector was improved in the visible region, and the performance in the UV was further improved. This is because the type ii band alignment between TiO2 and Bi2Se3 is beneficial for the effective separation and transfer of photogenerated electron‐hole pairs, reducing recombination losses and enhancing the overall photoresponse. In addition, under the action of the built‐in electric field formed by the heterostructure, the photogenerated electrons and holes are easier to separate, which reduces the recombination probability of the photogenerated electron‐hole pair and improves the photoelectric conversion efficiency. In the UV, TiO2/Bi2Se3 heterostructure can make more efficient use of the light absorption characteristics of TiO2 and absorb more photons, resulting in a larger photocurrent. These results indicate that TiO2/Bi2Se3 heterostructure‐based photodetector has great application potential in the UV. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18626300
Volume :
221
Issue :
23
Database :
Academic Search Index
Journal :
Physica Status Solidi. A: Applications & Materials Science
Publication Type :
Academic Journal
Accession number :
181439736
Full Text :
https://doi.org/10.1002/pssa.202400522