@article{scholars19641, title = {Synthesis of novel TiO2/CeFeO3 heterojunction using Mugwort (Artemisia vulgaris) leaves extracts with enhanced photocatalytic activity under visible light irradiation}, journal = {Applied Surface Science Advances}, publisher = {Elsevier B.V.}, note = {cited By 1}, volume = {21}, doi = {10.1016/j.apsadv.2024.100599}, year = {2024}, abstract = {TiO2 is a low-cost and biocompatible material with high oxidizing ability. However, their photocatalytic activity is limited to UV light irradiation. In this research, for the first time, a novel TiO2/CeFeO3 heterojunction was synthesized by the green synthesis method using an aqueous fraction of Artemisia vulgaris leaf extracts. TiO2/CeFeO3 shows enhanced photocatalytic performance under visible light irradiation. The vibrational, structural, optical, and compositional properties of TiO2/CeFeO3 were characterized. The as-prepared TiO2/CeFeO3 has spherical-shaped particles and shows a significantly diminished bandgap energy (3.25 eV to 2.75 eV). The photocatalytic performance of TiO2/CeFeO3 was investigated to degrade malachite green (MG) with an efficiency of up to 93.53 under its optimum dose. TiO2/CeFeO3 shows stable photocatalytic performance until the fourth cycle. The kinetics of the photodegradation of MG followed the pseudo-first-order reaction with a rate constant (ka pp) of 2.14{\~A}?10{\^a}??2 min{\^a}??1. The enhanced photocatalytic activity of TiO2/CeFeO3 was attributable to the creation of heterojunction, which suppresses the recombination rate of photogenerated electron-hole validated by the photoluminescence analysis. This work presents an eco-friendly approach to synthesizing novel heterojunction material with enhanced photocatalytic dye degradation. {\^A}{\copyright} 2024}, url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85189800336&doi=10.1016\%2fj.apsadv.2024.100599&partnerID=40&md5=341b5144f60b9f53ae9160748669806b}, issn = {26665239}, author = {Wijaya, B. and Apriandanu, D. O. B. and Surya, R. M. and Yulizar, Y. and Sambudi, N. S. and Khalil, M. and Umar, A.} }