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Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light
Published on: September 12, 2014
Tailored Sr-Bi4Ti3O12/Co3O4 S-scheme heterojunction for highly efficient solar-light photodegradation of crystal
Rasmirekha Pattanaik1, Suresh Kumar Dash1, Rishabh Kamal1
1Department of Chemistry, ITER, Siksha 'O' Anusandhan (Deemed to be University) Bhubaneswar Odisha 751030 India sureshdash@soa.ac.in.
Abstract:
The development of efficient photocatalysts for wastewater treatment is crucial for mitigating organic pollution. In this work, a Sr-doped Bi4Ti3O12/Co3O4 S-scheme heterojunction was synthesized via a facile solid-state and precipitation method and evaluated for the solar-light-driven photodegradation of crystal violet (CV) dye. X-ray diffraction (XRD) confirmed the orthorhombic phase of Bi4Ti3O12 with successful Sr incorporation along with spinel Co3O4. FTIR spectra displayed characteristic metal oxygen vibrations, validating composite formation. UVDRS analysis revealed extended solar light absorption with a significantly reduced band gap of 1.6 eV compared to pristine Bi4Ti3O12 (2.8 eV). Photoluminescence studies showed suppressed charge recombination, indicating efficient charge carrier separation. Under solar -light irradiation, the Sr-doped Bi4Ti3O12/Co3O4 composite achieved ∼95% degradation of CV within 55 min, following pseudo-first-order kinetics (k = 0.035 min-1). Furthermore, the photocatalyst exhibited excellent stability and reusability over multiple cycles. These findings highlight the synergistic role of Sr doping and S-scheme heterojunction formation in enhancing photocatalytic performance, offering a promising pathway for the design of advanced materials for wastewater remediation.

