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Synergistic effect in heterojunction TiO2/SnO2 nanofibers: boosting photocatalytic performance for methylene blue
Jiaqi Xu1, Feng Ye1, Yeqian Ge1,2,3,4
1School of Textile Science and Engineering, Shaoxing University Shaoxing Zhejiang 312000 China geyeqian@163.com.
Abstract:
Titanium dioxide (TiO2) is widely applied in water treatment, air purification, self-cleaning surfaces, and other fields owing to its strong oxidizing capacity, excellent chemical stability, low cost, and non-toxicity. However, its practical application as a photocatalyst is severely limited by the extremely low solar light utilization efficiency. To address this defect and enhance the photocatalytic performance of TiO2 under ultraviolet (UV) and nature light irradiation, TiO2/SnO2 composite nanofibers were fabricated via electrospinning combined with calcination processes. SnO2 possesses high electron mobility as well as stable chemical and thermal properties, the construction of a heterojunction between TiO2 and SnO2 is conducive to improving the separation efficiency of photogenerated electron-hole pairs, thereby enhancing the overall photocatalytic activity. The morphology, crystal structure, and photocatalytic properties of the prepared composite nanofibers were systematically characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and photocatalytic degradation experiments with methylene blue (MB) as the target pollutant. The results demonstrated that the TiO2/SnO2 nanofibers prepared at a TiO2 : SnO2 molar ratio of 10 : 1 and a calcination temperature of 450 °C exhibited the optimal photocatalytic activity under UV light, achieving a MB degradation rate of 99% within 60 min. Additionally, the photocatalytic performance of TiO2/SnO2 nanofibers under nature light was significantly improved with the calcination temperature of 650 °C: the MB degradation rates after 3 h of irradiation were 42.39%, 66.15%, and 74.06% at 450 °C, 550 °C, and 650 °C, respectively, which represented increments of 12.26%, 36.02%, and 43.93% compared with pure TiO2. This work provides a feasible strategy for the modification of TiO2-based photocatalysts and offers technical support for the efficient treatment of dyeing and printing wastewater.
