Visible-light-driven photocatalytic oxidation of furfural to furoic acid over Ag/g-C3N4

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2024-08-31 DOI:10.1016/j.jphotochem.2024.115998
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Abstract

Furoic acid (FA) is a useful bio-chemicals, which can be used in the production of pharmaceuticals, food additives, flavors, industrial chemicals, biofuels, etc. Oxidation of furfural to FA has been carried out by a thermal catalytic method, but photocatalytic oxidation protocol has not been reported yet. Here, g-C3N4-supported Ag nanoparticles (Ag NPs) catalysts with different Ag loading were synthesized and used for the photocatalytic oxidation of furfural to FA under visible light irradiation. The physicochemical and photoelectrochemical properties of the catalysts were systematically investigated by XRD, TEM, XPS, UV–Vis diffuse reflectance spectroscopy (UV–Vis DRS), photoluminescence, etc. Compared with the pristine g-C3N4, Ag-CN(N2 + H2) was found to have better photocatalytic performances in the aerobic oxidation of furfural under visible light irradiation, and the conversion can reach 82 % with a FA yield of 30 %. Importantly, the loading of Ag NPs has a significant effect on the photoelectrochemical properties. Specifically, 0.5 % Ag NPs loading maximized the photocurrent response, indicating that the loading of Ag NPs enhances charge separation and migration under visible light excitation. The introduction of Ag NPs also led to a significant decrease in electrochemical impedance, which promoted the rate of electron transfer at the interface, further confirming the improved photocatalytic efficiency. The addition of Ag NPs broadens the solar absorption and promotes the separation/transport of photo-generated carriers to form “hot electrons”, and provides the active species for furfural oxidation. The reasonable reaction mechanism of the photocatalytic oxidation of furfural to FA was elucidated. This work offers a novel method for the oxidation of furfural to FA in a mild and green way.

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Ag/g-C3N4 在可见光驱动下光催化氧化糠醛生成糠酸
糠酸是一种有用的生物化学品,可用于生产药品、食品添加剂、香精、工业化学品和生物燃料等。糠醛氧化成 FA 的过程已通过热催化法进行,但光催化氧化方案尚未见报道。本文合成了不同Ag负载量的g-C3N4支撑的Ag纳米颗粒(Ag NPs)催化剂,并将其用于可见光照射下糠醛到FA的光催化氧化。通过 XRD、TEM、XPS、紫外可见光漫反射光谱(UV-Vis DRS)、光致发光等方法对催化剂的物理化学和光电化学性质进行了系统研究。与原始 g-C3N4 相比,Ag-CN(N2 + H2) 在可见光照射下的糠醛有氧氧化中具有更好的光催化性能,转化率可达 82%,糠醛产率为 30%。重要的是,Ag NPs 的负载量对光电化学特性有显著影响。具体来说,0.5% 的 Ag NPs 负载可使光电流响应最大化,这表明在可见光激发下,Ag NPs 负载可增强电荷分离和迁移。Ag NPs 的引入还导致电化学阻抗显著下降,从而促进了界面上的电子转移速度,进一步证实了光催化效率的提高。Ag NPs 的加入拓宽了太阳能吸收范围,促进了光生载流子的分离/传输,形成 "热电子",为糠醛氧化提供了活性物种。阐明了光催化氧化糠醛的合理反应机理。这项研究为温和、绿色地将糠醛氧化成脂肪酸提供了一种新方法。
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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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