Photocatalytic degradation of naproxen by Bi2MoO6/g-C3N4 heterojunction photocatalyst under visible light: Mechanisms, degradation pathway, and DFT calculation

IF 4.7 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2021-05-01 DOI:10.1016/j.jphotochem.2021.113235
Kun Fu , Yishuai Pan , Chao Ding , Jun Shi , Huiping Deng
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引用次数: 37

Abstract

In this research, a 2D/2D Bi2MoO6/g-C3N4 heterojunction photocatalyst, which can be driven by visible light, was fabricated through a hydrothermal coprecipitation method. Naproxen was used as the target organic contaminant to evaluate the photocatalytic performance of Bi2MoO6/g-C3N4. The composite photocatalyst showed promoted photocatalytic activity, among which BMO/CN50−50 with a mass ratio 50/50 exhibited the fastest degradation rate, the degradation rate was 3.9 and 2.5 times higher than that of g-C3N4 and Bi2MoO6, respectively. Scavenger experiments and EPR measurements demonstrated that hole (h+) and superoxide radical (O2) play a leading role in the degradation reactions. Moreover, the degradation pathway was suggested in the light of identified intermediates by Liquid Chromatography-Mass Spectrometry (LC–MS/MS) and DFT analysis. Furthermore, the Quantitative Structure-Activity Relationship (QSAR) analysis was used to evaluate the toxicity of identified degradation intermediates.

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Bi2MoO6/g-C3N4异质结光催化剂在可见光下光催化降解萘普生:机理、降解途径及DFT计算
本研究采用水热共沉淀法制备了2D/2D Bi2MoO6/g-C3N4异质结光催化剂,该催化剂可由可见光驱动。以萘普生为目标有机污染物,评价Bi2MoO6/g-C3N4的光催化性能。复合光催化剂具有较好的光催化活性,其中质量比为50/50的BMO/CN50−50的降解速率最快,降解速率分别是g-C3N4和Bi2MoO6的3.9倍和2.5倍。清道夫实验和EPR测量表明,空穴(h+)和超氧自由基(O2−)在降解反应中起主导作用。通过液相色谱-质谱联用(LC-MS /MS)和DFT分析,对鉴定的中间体进行了降解途径分析。此外,采用定量构效关系(QSAR)分析对鉴定的降解中间体的毒性进行了评价。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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