Shining a light on fungicide- water: enhanced photocatalytic degradation using the CoTiO3/CaTiO3 nanocomposite and experimental and theoretical viewpoints on improved intervalence charge transfer from O2- to Ti4+ and from Co2+ to Ti4+ ions and spatial charge transfer

Narendran, Moorthy Gnanasekar; Vijayakumar, Elayaperumal; Raj, Muniyandi Govinda; Preetha, Rajaraman; Alphin, Joseph John; Mahaan, Ramalingam; Neppolian, Bernaurdshaw; Bosco, Aruljothy John

Abstract

Perovskite materials are emerging as the most promising and efficient low-cost energy materials for various applications. The construction of heterojunctions has become a field of interest because of their high potential to give off a large amount of energy. Herein, a Z-scheme heterojunction was made between two perovskites (CoTiO3 and CaTiO3) in order to make a cheap material that is good at photocatalysis. Various methods were used to characterize the resulting CoTiO3/CaTiO3 (CCO 75 : 25) composite, including XRD, Raman, XPS, HRSEM, HRTEM, BET, and UV-vis. The increased photocatalytic activity of the CoTiO3/CaTiO3 (CCO) composite is attributed to the accelerated charge transfer from O2- to Ti4+ and from Co2+ to Ti4+ ions, revealing the close interfacial contact between CoTiO3 and CaTiO3, and spatial charge transfer within the CoTiO3/CaTiO3 heterojunction. A direct Z-scheme mechanism was developed, and charge transfer properties were verified by the scavenger test and ESR, PL, and EIS analyses. The enhanced degradation rate of k = 0.0373 min(-1) is achieved for the CCO 75 : 25 composite. Meanwhile, the CCO 75 : 25 composite established high photocatalytic stability when recycled for CBZ degradation. This research offers mechanistic and practical views on designing simple and cost-effective materials for pollutant removal.

Más información

Título según WOS: ID WOS:001184372900001 Not found in local WOS DB
Título de la Revista: NEW JOURNAL OF CHEMISTRY
Volumen: 48
Número: 14
Editorial: Royal Society of Chemistry
Fecha de publicación: 2024
Página de inicio: 6109
Página final: 6123
DOI:

10.1039/d3nj05399g

Notas: ISI