光探测
响应度
金红石
锐钛矿
析氧
材料科学
异质结
载流子
化学工程
光电子学
纳米技术
化学
光电探测器
物理化学
光催化
电化学
催化作用
工程类
生物化学
电极
作者
Yueying Ma,Yuewu Huang,Ju Huang,Zewu Xu,Yanbin Yang,Changmiao Xie,Bingke Zhang,Guanghong Ao,Zhendong Fu,Aimin Li,Dongbo Wang,Liancheng Zhao
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-06-28
卷期号:29 (13): 3096-3096
被引量:1
标识
DOI:10.3390/molecules29133096
摘要
Self-powered photoelectrochemical (PEC) ultraviolet photodetectors (UVPDs) are promising for next-generation energy-saving and highly integrated optoelectronic systems. Constructing a heterojunction is an effective strategy to increase the photodetection performance of PEC UVPDs because it can promote the separation and transfer of photogenerated carriers. However, both crystal defects and lattice mismatch lead to deteriorated device performance. Here, we introduce a structural regulation strategy to prepare TiO2 anatase-rutile heterophase homojunctions (A-R HHs) with oxygen vacancies (OVs) photoanodes through an in situ topological transformation of titanium metal–organic framework (Ti-MOF) by pyrolysis treatment. The cooperative interaction between A-R HHs and OVs suppresses carrier recombination and accelerates carrier transport, thereby significantly enhancing the photodetection performance of PEC UVPDs. The obtained device realizes a high on/off ratio of 10,752, a remarkable responsivity of 24.15 mA W−1, an impressive detectivity of 3.28 × 1011 Jones, and excellent cycling stability. More importantly, under 365 nm light illumination, a high-resolution image of “HUST” (the abbreviation of Harbin University of Science and Technology) was obtained perfectly, confirming the excellent optical imaging capability of the device. This research not only presents an advanced methodology for constructing TiO2-based PEC UVPDs, but also provides strategic guidance for enhancing their performance and practical applications.
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