Synthesis and characterization of the doped/co‐doped SnO2 nanoparticles by the sol–gel method

Tin oxide (SnO2) is one of the important semiconductors used in the application of solar cells because of its chemical–mechanical stability and wide band gap. These properties are very important for the performance development and photoanode optimization of a dye‐sensitized solar cell (DSSC). However, the low conduction band value of SnO2 reduces the photovoltaic efficiency, which limits the application of DSSC. Therefore, the doping strategy was used to increase the sensitivity to the visible light spectrum and change the light absorption properties of SnO2. In this paper, pure SnO2, Ag/SnO2, Pt/SnO2, and Pt/Ag/SnO2 nanoparticles were synthesized at the nanoscale by a simple chemical sol–gel method. To characterize the structure, morphological/chemical properties, optical properties, and surface properties of the synthesized SnO2 nanoparticles, X‐Ray Diffraction (XRD), ultraviolet–visible, Brunauer–Emmett–Teller, Scanning Electron Microscopy (SEM)/Energy Dispersive X‐Ray Spectroscopy (EDX), Transmission Electron Microscopy (TEM), and particle size analysis were respectively used. XRD results showed that the crystal sizes varied between 8.8 and 12.2 nm depending on the doping. Doping processes resulted in reductions in particle sizes. Optical studies resulted in decreases in the band gap with the doping process. The conclusions obtained have shown that Ag doping, and Pt–Ag co‐doping can be promising for use as photoanode materials in semiconductor technology and especially in DSSC applications. • Doped/co‐doped SnO2 compounds with different element combinations were synthesized using the sol–gel method. • Pure and doped SnO2 samples were produced in the nanoscale. • With doping, changes in pore volume–pore width, energy differences in the optical band gap, and variety in microstructures were observed. • In addition, doped SnO2 samples are compatible with each other in terms of particle size, surface area, and crystal structure.