Abstract

Different structures of anatase TiO2 from nanoparticles-based spheres to aggregated nanoparticles have been successfully fabricated by a simple refluxing method using a prepared titanium glycolate precursor. Variations in crystal phase, morphology, and size of TiO2 nanostructures were investigated by powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), Raman spectroscopy, and the Brunauer–Emmett–Teller method. It was found that the size of the prepared titanium glycolate precursor plays an important role in the formation of different anatase TiO2 aggregated spheres with high specific surface area (≈260 m2 g−1). Different TiO2 structures show a significant effect on the photovoltaic performance of dye-sensitized solar cells (DSSCs). The aggregated anatase TiO2 nanoparticles photoanode-based DSSC presents an overall light-to-electricity conversion efficiency of 4.2% accompanying a short-circuit current density of 13.63 mA cm−2, which is higher than those of closely packed TiO2 sphere (3.4%) and loosely packed TiO2 sphere (3.7%) photoanodes. The higher short-circuit current density and conversion efficiency for the aggregated nanoparticles-based DSSCs may be attributed to the high surface areas, which lead to larger dye loading and less resistance to electron transfer, and the high charge transfer at the interface of photoanode (TiO2/dye) and electrolyte layer.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.