One-pot co-precipitation of enhanced visible light active BiOCl based photocatalysts: Characterization, mechanism and DFT modelling
Metadatos
Mostrar el registro completo del ítemAutor
Kimbi Yaah, Velma Beri; Martinez Quimbayo, Jennyffer; Ahmadi, Sajad; Lempelto, Aku; Sliz, Rafal; Cao, Wei; Pastrana Martínez, Luisa María; Maldonado Hódar, Francisco José; Morales Torres, SergioEditorial
Elsevier
Materia
BiOCl Scavenger Heterostructures
Fecha
2025-12Referencia bibliográfica
Kimbi Yaah, V. B., Quimbayo, J. S. M., Ahmadi, S., Lempelto, A., Sliz, R., Cao, W., Pastrana-Martínez, L. M., Maldonado-Hódar, F. J., & Morales-Torres, S. (2025). One-pot co-precipitation of enhanced visible light active BiOCl based photocatalysts: Characterization, mechanism and DFT modelling. Inorganic Chemistry Communications, 182(115699), 115699. https://doi.org/10.1016/j.inoche.2025.115699
Patrocinador
MCIN/AEI/10.13039/501100011033 - ERDF “A way of making Europe” (Proyecto PID2021-126579OB-C31); European Research Council (ERC) - Union’s Horizon 2020 (grant agreement no. 101002219)Resumen
BiOCl, though being a promising photocatalyst for water pollutants degradation, its large band gap limits its
efficiency to the ultraviolet region of light. To overcome this challenge, we employed a one-step simple coprecipitation method at room temperature to synthesize visible light responsive BiOCl based nanoflakes.
Doping with biochar from pyrolyzed spruce wood led to an improvement in electronic and optical properties.
BiOCl doped with pyrolyzed wood exhibited better photocatalytic degradation of diuron on account of the slower
charge recombination, lower band gap and better charge transfer ability suggesting the formation of heterostructures in this case. Complete removal of diuron was obtained with pristine and doped BiOCl, however the
kinetics of removal was twice higher for the doped BiOCl. Scavenger experiments revealed that the O2
− • radicals
were responsible for the photocatalytic degradation. A study into the photothermal effect showed that BiOCl
pyro converted the light irradiation energy into heat slightly more than the pristine BiOCl. This heat energy could
further be utilized for the photon-heat energy and improved photocatalytic performance. Characterization of the
spent materials showed that they maintained their crystallinity and functionality. These findings provide a lowcost approach to synthesize BiOCl materials active under visible light and efficient for environmental
remediation.





