Plasmon-Enhanced Self-Powered UV Photodetectors Assembled by Incorporating Ag@SiO<sub>2</sub> Core–Shell Nanoparticles into TiO<sub>2</sub> Nanocube Photoanodes

et al. 2019

Crystals

Self Cite

The dye-sensitized solar cell (DSSC) is one candidate among the third-generation solar cells. The performance of most DSSCs based on TiO2 photoanode was limited by the low electron mobility within TiO2. To produce a much higher power conversion efficiency, Sn-doped TiO2 nanowire arrays were successfully prepared using a simple hydrothermal process. It was found that Sn doping augments electron mobility well and raises the flat band potential to improve the performance of DSSCs. The power conversion efficiency (η) of a DSSC based on the reasonable Sn-doped TiO2, N719 dye, platinized counter electrode and iodide/triiodide electrolyte reaches 8.75%. Furthermore, with an anatase TiO2 light scattering layer, a DSSC based on the Sn-doped TiO2 NWAs exhibits a remarkable power conversion efficiency of 9.43%, which is especially useful in weak light conditions.

Section: Resultssupporting

confidence: 92%

Modification of TiO2 Nanowire Arrays with Sn Doping as Photoanode for Highly Efficient Dye-Sensitized Solar Cells

Guo

et al. 2019

Crystals

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“…The TiO 2 MSs were synthesized under hydrothermal conditions as previously reported [ 33 ]. NaBH 4 and TiO 2 powders were mixed in an equal ratio, and the mixture was ground for 20 min completely.…”

Section: Methodsmentioning

confidence: 99%

Efficient Photocatalytic Hydrogen Evolution over TiO2-X Mesoporous Spheres-ZnO Nanorods Heterojunction

Zhang

et al. 2020

Nanomaterials

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Photocatalytic water splitting into hydrogen is regarded as one of the key solutions to the deterioration of the global environment and energy. Due to the significantly reduced grain boundaries, ZnO nanorods facilitate a fast electron transfer through their smooth tunnels and are well suited as a photocatalyst. However, the photocatalytic hydrogen evolution performance of pristine ZnO nanorods is still low due to the high recombination rate of photogenerated electron-hole pairs and the less light absorption. Here, a novel structure about black ZnO nanorods (NRs)/TiO2-X mesoporous spheres (MSs) heterojunction has been prepared and the photocatalytic hydrogen evolution performance has been explored. The photocatalytic activity test results showed that ZnO NRs/TiO2-X MSs exhibited higher catalytic activity than ZnO NRs for hydrogen production. Compared to the pure ZnO NRs photoanode, the photocurrent of ZnO NRs/TiO2-X MSs heterojunction photoanode could reach 0.41 mA/cm2 in view of the expanding spectral response region and effective inhibition of e−/h+ recombination at the same condition. Using a relatively integrated experimental investigation and mechanism analysis, we scrutinized that after being treated with NaBH4, TiO2 MSs introduce oxygen vacancies expanding the photocatalytic activity of pure TiO2, and improving conductivity and charge transport capabilities through coating on ZnO NRs. More importantly, the results provide a promising approach in the NRs/MSs composite structure serving as photoanodes for photocatalytic hydrogen production.

“…Due to important application in environmental monitoring and surveillance, missile warning, chemical and physiology analyses, fire detection, and secure communication, the precise detection of ultraviolet (UV) radiation is desperately in demand [1]. Semiconductor UV photodetectors (UVPDs) can be categorized into two types: photoconductive and photovoltaic.…”

Section: Introductionmentioning

confidence: 99%

Optimal Sr-Doped Free TiO2@SrTiO3 Heterostructured Nanowire Arrays for High-Efficiency Self-Powered Photoelectrochemical UV Photodetector Applications

Guo

et al. 2019

Crystals

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Due to their high performance, photoelectrochemical ultraviolet (UV) photodetectors have attracted much attention, but the recombination of photogenerated electrons at the interface of photoanode/electrolyte limited further improvement of photoelectrochemical UV photodetectors (PEC UVPDs). Modification of TiO2 photoanode by SrTiO3 could improve the performance of UVPD, because the energy barrier that is established at the TiO2–SrTiO3 interface could accelerate the separation of the photogenerated electrons-holes pair. However, the recombination center that is caused by the preparation of TiO2@SrTiO3 core-shell heterostructured nanostructure decreases the performance of PEC UVPDs, which is still an important problem that hindered its application in PEC UVPDs. In this paper, we presented a Sr-doped free TiO2@SrTiO3 core-shell heterostructured nanowire arrays as a photoanode for the self-powered PEC UVPD. This will not only accelerate the separation of the photogenerated electrons-holes pair, but it will also reduce the recombination of photogenerated electron-hole pairs in the photoanode. The intrinsic effect of SrTiO3 reaction time on the J variations of UVPDs is investigated in detail. An impressive responsivity of 0.358 A W−1 was achieved at 360 nm for the UVPD based on TiO2@SrTiO3 core-shell heterostructured nanowire arrays, which heretofore is a considerably high photoresponsivity for self-powered photoelectrochemical UVPDs. Additionally, this UVPD also exhibits a high on/off ratio, fast response time, excellent visible-blind characteristic, and linear optical signal response.