In this work, pure BiFeO3 and samples doped with different concentrations of chromium were synthesized to improve the optical properties and efficiency of solar cells based on BiFeO3. The sol-gel method was used for synthesis due to its ability to produce nanostructured materials with high purity and good homogeneity, as well as the possibility of controlling the size and shape of the resulting particles. The samples were characterized by different analytical techniques. Thermal analysis results indicate that the dopant increases the weight loss of the sample from 61 to 81%, with an increase in the exothermal in the nucleation and crystallization temperature range. The X-ray diffraction patterns and UV-visible spectra show a dependence of the crystallite size and bandgap with respect to the amount of Cr dopant, decreasing from 168 to 73 nm and from 2.14 to 1.92 eV, respectively. Scanning electron microscopy images display a decreasing grain size as a result of an increasing amount of dopant. The I-V analysis results show a 1% Cr-doped BiFeO3 photovoltaic device exhibits enhanced photovoltaic performance with higher photocurrent and 4.17 times greater energy conversion efficiency compared with a pure BiFeO3 photovoltaic device. For their behavior, Cr-doped BiFeO3-based photoelectrodes are very promising materials for photovoltaic devices.
This study investigates the effects of chromium (Cr3+) doping on BaTiO3 nanoparticles synthesized via the sol–gel route. X-ray diffraction confirms a Cr-induced cubic-to-tetragonal phase transition, with lattice parameters and crystallite size varying systematically with Cr3+ content. UV–visible spectroscopy reveals a monotonic decrease in bandgap energy from 3.168 eV (pure BaTiO3) to 2.604 eV (5% Cr3+-doped BaTiO3). Raman and FTIR spectroscopy elucidate structural distortions and vibrational mode alterations caused by Cr3+ incorporation. Transmission electron microscopy and energy-dispersive X-ray spectroscopy verify nanoscale morphology and successful Cr3+ doping (up to 1.64 atom%). Antioxidant activity, evaluated using the DPPH assay, shows stable radical scavenging for pure BaTiO3 (40.70–43.33%), with decreased activity at higher Cr3+ doping levels. Antibacterial efficacy against Escherichia coli peaks at 0.5% Cr3+ doping (10.569 mm inhibition zone at 1.5 mg/mL), decreasing at higher concentrations. This study demonstrates the tunability of structural, optical, and bioactive properties in Cr3+-doped BaTiO3 nanoparticles, highlighting their potential as multifunctional materials for electronics, photocatalysis, and biomedical applications.
Dye-sensitized solar cells (DSSCs) have attracted renewed research interest as a potential low-cost substitute for conventional silicon photovoltaics. This work aims to improve the photovoltaic performance of the DSSCs by incorporating multi-walled carbon nanotubes (MWCNTs) into the BaTiO3 photoelectrode. The pure BaTiO3 and BaTiO3/MWCNT nanocomposites were sensitized with N719 dye and fabricated into solar cell devices for testing. The structural characterization confirmed the successful formation of the nanocomposite with an optimal dispersion at 6% of MWCNT incorporation, beyond which agglomeration effects manifested. The optical analysis verified the modulation of defect states and bandgap engineering induced by the MWCNT network. The morphological studies revealed irregular nanoparticle clusters with embedded nanotubes. Solar cell testing under AM1.5G-simulated sunlight demonstrated a peak power conversion efficiency of 4.044% for 6% of MWCNT doping, constituting a 6-fold increment versus pure BaTiO3 (0.693%). It originated from the simultaneous enhancements in the open-circuit voltage and short-circuit current enabled by the favorable band structure alterations and percolation-assisted charge transport. However, further increasing MWCNT content deteriorated the device metrics, owing to emerging limitations like trapping. The rational integration of multi-walled carbon nanotubes with lead-free ferroelectric metal oxides can contribute to the development of emerging organic-inorganic hybrid solar platforms.