Synergistic Degradation of 2,4,4′-Trihydroxybenzophenone Using Carbon Quantum Dots, Ferrate, and Visible Light Irradiation: Insights into Electron Generation/Consumption Mechanism

光致发光 电子顺磁共振 光化学 化学 激进的 猝灭(荧光) 降级(电信) 反应机理 催化作用 光催化 密度泛函理论 羟基化 材料科学 计算化学 荧光 有机化学 核磁共振 物理 电信 酶 量子力学 光电子学 计算机科学
作者
Afzal Ahmed Dar,Muhammad Usman,Wei Zhang,Qiuhui Zhu,Bao Pan,Atif Sial,Chuanyi Wang
出处
期刊:ACS ES&T engineering [American Chemical Society]
卷期号:2 (10): 1942-1952 被引量:13
标识
DOI:10.1021/acsestengg.2c00118
摘要

In this study, we reported a unique single-step synthesis of photocatalytic carbon quantum dots (CQDs) with high electron density, efficient aggregation-induced emission, and improved surface chemistry properties. As-synthesized CQDs were applied with ferrate (a reactive and green oxidant) to synergistically degrade 2,4,4′-trihydroxybenzophenone (2,4,4′-HBP). The restriction of molecular rotation, vibration in the crystal structure, modification of the surface chemistry, and the aggregation/quenching of CQDs were highlighted by comprehensive characterization. Newly synthesized CQDs’ generated electrons were consumed by ferrate, and this mechanism was highlighted by photoluminescence analyses. It was found that the photoluminescence intensity of CQDs was reduced by more than 96% when ferrate was introduced into the CQDs reaction system. The reaction kinetics of 2,4,4′-HBP degradation was inspected at different pH values (7.0, 8.0 and 9.0) using ferrate in a single dose and multiple-dose (sequential) additions. The CQDs + ferrate + visible light (Vis) was proven to be the best reaction system with a 99.9% degradation efficiency, as compared to CQDs alone (63%) and ferrate single dose (85%) and multiple-dose (96%) methods. In addition, 10 reaction intermediates were identified, implying that C–C cleavage, hydroxylation, self, cross, and end linkage were involved in the potential reaction mechanism. Besides, hydroxyl radicals were found to be the primary reactive species in electron paramagnetic resonance (EPR) analyses. The computational analyses including density functional theory and molecular orbital distribution elucidated the reaction sites of CQDs and 2,4,4′-HBP. These findings have important implications in understanding electron generation and consumption mechanisms with the synergetic contribution of CQDs and ferrate to degrade organic pollutants such as 2,4,4′-HBP.
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