Showing 3 results for Sno2
Arian Heidar Alaghband, Azam Moosavi, Saeid Baghshahi, Ali Khorsandzak,
Volume 18, Issue 3 (9-2021)
Abstract
Porous nanostructured SnO2 with a sheet-like morphology was synthesized through a simple green substrate-free gelatin-assisted calcination process using Tin tetracholoride pentahydrate as the SnO2 precursor and porcine gelatin as the template. Crystalline phase, morphology, microstructure, and optical characteristics of the as-prepared material were also investigated at different calcination temperatures using X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), UV-visible absorption, and Photoluminescence spectroscopy (PL), respectively. XRD patterns of all the samples revealed the presence of a tetragonal crystalline structure with no other crystalline phases. Moreover, the synthesized hierarchical sheets assembled with nanoparticles displayed a large surface area and porous nanostructure. The calculated optical band gap energy varied from 2.62 to 2.87 eV depending on the calcination temperature. Finally, photoluminescence spectra indicated that the nanostructured SnO2 could exhibit an intensive UV-violet luminescence emission at 396 nm, with shoulders at 374, violet emission peaks at 405 and 414 nm, blue-green emission peak at 486 nm, green emission peak at 534 nm and orange emission peak at 628 nm.
Mohammad Reza Zamani Meymian, Razieh Keshtmand,
Volume 18, Issue 4 (12-2021)
Abstract
Tin oxide (SnO2) is used as an electron transport layer (ETL) in perovskite solar cells with a planar
structure due to its good transparency and energy level alignment with the perovskite layer. The modification
interface of the electron transport layer and the perovskite absorber layer plays an important role in the efficient
charge extraction process at the interface. In this study, planar perovskite solar cells with configuration
(FTO/SnO2/mixed-cation perovskite/CuInS2/Au) were prepared to investigate the effect of UV-Ozone (UVO) treated
SnO2 as ETL on the performance of devices. ETL treatment was performed at different times (0 to 60 min). It is
shown that surface wetting was improved by UVO treating the SnO2 films prior to deposition of the perovskite layer.
The latter improves the contact between the ETL and the perovskite layer, allowing more efficient electron transport
at the interface. Contact angle, SEM, photoluminescence spectra, and the current density-voltage tests were
conducted to characterize the photovoltaic of the cells. The best PSC performance with a power conversion
efficiency of 10.96% was achieved using UVO-treated SnO2 ETL for 30 min, whereas the power conversion
efficiency of the perovskite solar cells with SnO2 ETL without UVO treatment was only 4.34%.
Eswaran Kamaraj, Kavitha Balasubramani,
Volume 21, Issue 2 (6-2024)
Abstract
Heterostructure photocatalyst of CuWO4 modified SnO2 (CuWO4/SnO2) was fabricated by in simple wet-impregnation process and evaluated via degradation of rose Bengal (RB) under visible light irradiation. The samples had been completely characterized by Ultraviolet-visible diffuse reflectance spectroscopy (UV-vis-DRS), X-ray diffraction (XRD), Scanning electron microscopy (SEM) combined with energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), High-resolution TEM (HR-TEM), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett and Teller surface analysis (BET). The result divulged that amongst the catalysts, CuWO4/SnO2 displayed higher photocatalytic activity than CuWO4 or SnO2. The enhanced photocatalytic efficiencies are attributed to the charge transfer from SnO2 to CuWO4 nanoparticles, which efficiently decrease electron-hole recombination energy level. The time required for maximum degradation of rosebengal (RB) under visible light over CuWO4/SnO2 was 180 min. The other parameters such as pH (pH=8), photocatalyst dosage (0.2 g/L) and dye concentration (20 µM) were optimized to achieve high degradation efficiency (98.5%). The excellent photocatalytic activity of CuWO4/SnO2 is due to efficient separation of photogenerated electron-hole pairs. The holes (h+) and superoxide radicals (O2•-) are the reactive species involved in photocatalytic mechanism for gdegradation of RB.
