High performance metal-semiconductor-metal ultraviolet photodetector based on mixed-dimensional TiO2/CsPbBr3 heterostructures

被引:2
|
作者
Zhang, Tao [1 ]
Cai, Siyu [1 ]
Liang, Nina [1 ]
Gao, Yalei [1 ]
Li, Yuanpeng [1 ]
Liu, Fuchi [1 ]
Long, Lizhen [1 ,2 ]
Liu, Jun [1 ,2 ]
机构
[1] Guangxi Normal Univ, Sch Phys Sci & Technol, Guilin 541004, Peoples R China
[2] Guangxi Normal Univ, Guangxi Key Lab Nucl Phys & Technol, Guilin 541004, Peoples R China
关键词
ultraviolet photodetector; mixed-dimension; metal-semiconductor-metal (MSM) structure; charge transfer; COMPOSITE-BASED PHOTODETECTORS; QUANTUM DOTS; GRAPHENE;
D O I
10.1088/1402-4896/ad166a
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Zero-dimensional (0D) and one-dimensional (1D) mixed heterostructure semiconductors can bring superior electrical and optoelectronic performances due to the synergistic advantages of different dimensionalities. Here, a metal-semiconductor-metal (MSM) ultraviolet (UV) photodetector based on 1D-0D TiO2/CsPbBr3 heterostructure semiconductor is constructed, which exhibits excellent photodetection performance. A back-to-back Schottky contact is formed in the MSM (Au/TiO2/Au) structure due to the large band-energy bending resulted from the abundant surface-states at 1D-TiO2 surface. Under an applied voltage, a small saturation current flows through the device. Benefiting from the decoration of CsPbBr3 QDs, the dark current of MSM photodetectors can be further suppressed, and producing the improved on/off ratio (I-light/I-dark), photoresponsivity (R-lambda), and detectivity (D*). PL properties study suggested that an energy transfer is occurred between the 0D-CsPbBr3 and 1D-TiO2. The TiO2/CsPbBr3 heterojunctions are beneficial for photo-induced charge transfer in hetero-interface because of the type-II energy-band alignment, but not non-radiative energy transfer from 0D-CsPbBr3 to 1D-TiO2. On the whole, this study depicts a fascinating coupling architecture of mixed-dimensional materials toward implementing low-cost and high-performance optoelectronic devices.
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页数:11
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