The efficient electron transport layer (ETL) plays a critical role in the performance of perovskites solar cells (PSCs). Ideally, an unobstructed network with smooth channels for electron flow is required, which is lacking in the pristine TiO2-based ETL. As a potential solution, here we tuned the structure of TiO2 via optimized heteroatom doping of Al. Different concentrations (1, 2, and 3 wt%) of Al were doped in TiO2 and were successfully applied as an ETL in PSC using spin coating. A significant difference in the structural, opto-electronic, chemical, and electrical characteristics was observed in Al-doped TiO2 structures. The opto-electronic properties revealed that Al doping shifted the absorption spectra toward the visible range. Pure titania possesses a bandgap of 3.38 eV; however, after 1, 2, and 3% Al doping, the bandgap was linearly reduced to 3.29, 3.25, and 3.18 eV, respectively. In addition, higher light transmission was observed for Al-doped TiO2, which was due to the scattering effects of the interconnected porous morphology of doped-TiO2. Al-doped titania shows higher thermal stability and a 28% lower weight loss and can be operated at higher temperatures compared to undoped titania (weight loss 30%) due to the formation of stable states after Al doping. In addition, Al-doped TiO2 showed significantly high conductivity, which provides smooth paths for electron transport. Thanks to the effective tuning of band structure and morphology of Al-doped TiO2, a significant improvement in current densities, fill factor, and efficiency was observed in PSCs. The combined effect of better Jsc and FF renders higher efficiencies in Al-doped TiO2, as 1, 2, and 3% Al-doped TiO2 showed 12.5, 14.1, and 13.6% efficiency, respectively. Compared to undoped TiO2 with an efficiency of 10.3%, the optimized 2% Al doping increased the efficiency up to 14.1%. In addition, Al-doped TiO2 also showed improvements in antibacterial effects, required for photoactive textiles.
Using of nano-inclusion to reinforce polymeric materials has emerged as a potential technique to achieve an upper extreme of specific strength. Despite the significant improvement of mechanical properties via nano-reinforcements, the commercial application of such nano-composites is still restricted, due to high cost and unwanted aggregation of nanoparticles in the polymer matrix. To address these issues, here we proposed a scalable and economical synthesis of TiO2 at low temperatures, resulting in self-dispersed nanoparticles, without any surfactant. As lower energy is consumed in the synthesis and processing of such nanoparticles, so their facile gram-scale synthesis is possible. The defect-rich surface of such nanoparticles accommodates excessive dangling bonds, serving as a center for the functional groups on the surface. Functional surface enables high dispersion stability of room temperature synthesized TiO2 particles. With this motivation, we optimized the processing conditions and concentration of as-synthesized nano-particles for better mechanical properties of unsaturated polyester (UP) resin. The composite structure (UP-TiO2) showed nearly two folds higher tensile, flexural, and impact strength, with 4% content of nanoparticles. Characterization tools show that these better mechanical properties are attributed to a strong interface and superior dispersion of nanoparticles, which facilitate better stress distribution in the composite structure. In addition, the crack generation and propagation are restricted at a much smaller scale in nanocomposites, therefore significant improvement in mechanical properties was observed.
ZnO and TiO2 are both well-known electron transport materials; however, an exact comparison of their performance, when fabricated under the same synthesis conditions, is missing in the literature. Considering this, we introduced a viable electrospinning route for the development of highly polycrystalline TiO2 and ZnO nanofibers for an electron transport material (ETM) of perovskite solar cells and photocatalysts for textiles. Thanks to the effective tuning of band structure and morphology of TiO2, a significant improvement in performance as compared to ZnO was observed when both were used as photoanodes and photocatalysts. X-ray diffraction detected polycrystalline structural properties and showed that peaks are highly corresponding to TiO2 and ZnO. Morphological analysis was carried out with a scanning electron microscope, which revealed that nanofibers are long, uniform, and polycrystalline, having diameter in the nano regime. TiO2 nanofibers are more aligned and electron-supportive for conduction as compared to ZnO nanofibers, which are dense and agglomerated at some points. Optoelectronic properties showed that TiO2 and ZnO show absorption values in the range of ultraviolet, and visible range and band gap values for TiO2 and ZnO were 3.3 and 3.2 eV, respectively. The TiO2 band gap and semiconductor nature was more compatible for ETL as compared to ZnO. Electrical studies revealed that TiO2 nanofibers have enhanced values of conductivity and sheet carrier mobility as compared to ZnO nanofibers. Therefore, a higher photovoltaic conversion efficiency and antibacterial activity was achieved for TiO2 nanofibers (10.33%), as compared to ZnO (8.48%). In addition, the antibacterial activity of TiO2 was also recorded as better than ZnO. Similarly, compared to ZnO nanofibers, TiO2 nanofibers possess enhanced photoactivity for antimicrobial and dye degradation effects when applied to fabrics.
Ca-doped TiO2 films were synthesized by the modified sol-gel method and employed as the electron transport material of perovskite solar cells (PSCs). Morphological, optoelectronic, thermal, and electrical studies of thin films were investigated through XRD, RAMAN, SEM, AFM, UV- Vis, FTIR, and IV characteristics. Ca doping was detected with the help of structural properties while morphological analysis revealed that thin films based on Ca-doped titania are crack-free, homogenous, and uniformly distributed. Further optoelectronic properties have shown a promising conversion efficiency of 9.79% for 2% Ca-doped titania followed by 1% Ca-doped titania, while 3% have shown the lowest conversion efficiency among these prepared samples. The 2% an optimized doping of Ca has shown an almost two-fold increase in conversion efficiency in comparison to pristine TiO2, along with an increase in current density from 15 mA cm−2 to 19.3 mA⋅cm−2. Improved energy efficiency and higher current density are attributed to faster electron transportation; moreover, the optimized percentage of Ca doping seems to be an effective approach to improve the PSCs’ performance.
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