4-Nitrophenol (4-NP) is reported to originate disadvantageous effects on the human body collected from industrial pollutants; therefore, the detoxification of 4-NP in aqueous contamination is strongly recommended. In this study, the heterojunction mesoporous α-Fe2O3/TiO2 modulated with diverse Ag percentages has been constructed via a sol–gel route in the occurrence of a soft template P123. The formation of biphasic crystalline TiO2 anatase and brookite phases has been successfully achieved with the average 10 nm particle sizes. The photo/-catalytic reduction of 4-NP has been performed utilizing NaBH4 as a reducing agent with and without visible illumination. All Ag/Fe2O3/TiO2 nanocomposites exhibited significantly higher photo/-catalytic reduction efficiency than pure Fe2O3, TiO2 NPs, and Fe2O3/TiO2 nanocomposite. 2.5% Ag/Fe2O3/TiO2 nanocomposite was considered the highest and superior photocatalytic reduction efficiency, and it almost achieved 98% after 9 min. Interestingly, the photocatalytic reduction of 4-NP was accelerated 9 times higher than the catalytic reduction over 2.5% Ag/Fe2O3/TiO2; its rate constant value was 709 and 706 times larger than pure TiO2 and Fe2O3 NPs, respectively. The enhanced photocatalytic reduction ability of Ag/Fe2O3/TiO2 nanocomposite might be referred to as significantly providing visible light absorption and a large surface area, and it can upgrade the effective separation and mobility of electron holes. The stability of the synthesized catalysts exhibited that the obtained catalysts can undergo a slight decrease in reduction efficiency after five successive cycles. This approach highlights a novel route for constructing ternary nanocomposite systems with high photo/-catalytic ability.
Research Abstract
Research Date
Research Department
Research Journal
Environmental Science and Pollution Research
Research Member
Research Publisher
Springer Berlin Heidelberg
Research Rank
Q1
Research Vol
30
Research Website
https://link.springer.com/article/10.1007/s11356-023-25228-w
Research Year
2023
Research Pages
41405-41418