Face-to-face BiOCl/BiO2-x heterojunction composites with highly efficient charge separation and photocatalytic activity

2020 ◽  
Vol 832 ◽  
pp. 153771 ◽  
Author(s):  
ZhangSheng Liu ◽  
JinXiang Wang
Crystals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 717
Author(s):  
Hassan Algadi ◽  
Ahmad Umar ◽  
Hasan Albargi ◽  
Turki Alsuwian ◽  
Sotirios Baskoutas

A low-cost and simple drop-casting method was used to fabricate a carbon nanodot (C-dot)/all-inorganic perovskite (CsPbBr3) nanosheet bilayer heterojunction photodetector on a SiO2/Si substrate. The C-dot/perovskite bilayer heterojunction photodetector shows a high performance with a responsivity (R) of 1.09 A/W, almost five times higher than that of a CsPbBr3-based photodetector (0.21 A/W). In addition, the hybrid photodetector exhibits a fast response speed of 1.318/1.342 µs and a highly stable photocurrent of 6.97 µA at 10 V bias voltage. These figures of merits are comparable with, or much better than, most reported perovskite heterojunction photodetectors. UV–Vis absorption and photoluminescent spectra measurements reveal that the C-dot/perovskite bilayer heterojunction has a band gap similar to the pure perovskite layer, confirming that the absorption and emission in the bilayer heterojunction is dominated by the top layer of the perovskite. Moreover, the emission intensity of the C-dot/perovskite bilayer heterojunction is less than that of the pure perovskite layer, indicating that a significant number of charges were extracted by the C-dot layer. The studied band alignment of the C-dots and perovskites in the dark and under emission reveals that the photodetector has a highly efficient charge separation mechanism at the C-dot/perovskite interface, where the recombination rate between photogenerated electrons and holes is significantly reduced. This highly efficient charge separation mechanism is the main reason behind the enhanced performance of the C-dot/perovskite bilayer heterojunction photodetector.


2017 ◽  
Vol 7 (23) ◽  
pp. 5594-5601 ◽  
Author(s):  
Baoying Dai ◽  
Hengming Huang ◽  
Wei Wang ◽  
Yukai Chen ◽  
Chunhua Lu ◽  
...  

Efficient charge separation accelerated by a spatial electric field is a vital factor for semiconductor photocatalysts to achieve high photocatalytic activity.


2013 ◽  
Vol 15 (24) ◽  
pp. 9562 ◽  
Author(s):  
Jens Niklas ◽  
Kristy L. Mardis ◽  
Brian P. Banks ◽  
Gregory M. Grooms ◽  
Andreas Sperlich ◽  
...  

2019 ◽  
Vol 12 (01) ◽  
pp. 1850110 ◽  
Author(s):  
Mengjun Liang ◽  
Lu Chen ◽  
Zhiyuan Yang ◽  
Zhen Zeng ◽  
Shuijin Yang

ZnO/Bi4V2O[Formula: see text] nanocomposites were prepared via a facile hydrothermal method by loading different amounts of ZnO onto the surface of Bi4V2O[Formula: see text]. The resulting ZnO/Bi4V2O[Formula: see text] composites showed excellent photocatalytic activity than that of pure ZnO under visible light irradiation. When the ratio of ZnO to Bi4V2O[Formula: see text] was 1:1 (ZB2), the photocatalytic activity was best, which could degrade RhB almost completely within 30[Formula: see text]min. The enhanced photocatalytic activity of ZnO/Bi4V2O[Formula: see text] composites could be mainly ascribed to the efficient charge separation and the increased specific surface area. Based on the experimental and bandgap calculations, a possible photocatalytic mechanism was proposed.


RSC Advances ◽  
2016 ◽  
Vol 6 (68) ◽  
pp. 63984-63990 ◽  
Author(s):  
Lu Ma ◽  
Hong Han ◽  
Lun Pan ◽  
Muhammad Tahir ◽  
Li Wang ◽  
...  

Ag3PO4 QDs sensitized and Ti3+-doped TiO2 nanosheets were fabricated, and exhibit high charge-separation efficiency and high photocatalytic activity.


2019 ◽  
Vol 174 ◽  
pp. 237-245 ◽  
Author(s):  
M. Hannula ◽  
H. Ali-Löytty ◽  
K. Lahtonen ◽  
J. Saari ◽  
A. Tukiainen ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (91) ◽  
pp. 74174-74179 ◽  
Author(s):  
Yaoguang Yu ◽  
Gang Chen ◽  
Xu Wang ◽  
Dechang Jia ◽  
Pengxiao Tang ◽  
...  

A series of BiOI/Bi5O7I composite photocatalysts with heterostructures was successfully synthetized through a facile hydrothermal method.


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