Adsorption–photocatalysis synergistic degradation of ethylene by Ag2S–TiO2–Bi2WO6 immobilized on starch/reduced graphene oxide aerogels under full-spectrum light

IF 4.1 3区 化学 Q2 CHEMISTRY, PHYSICAL
Yi Yi , Rui Wang , Jiawen Xie , Junying Peng , Wenbei Situ , Xianliang Song
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引用次数: 0

Abstract

To address the low quantum efficiency and poor dispersion of powdered photocatalysts in fruit and vegetable preservation, a multifunctional composite aerogel was developed by immobilizing a Z-scheme Ag2S–TiO2–Bi2WO6 heterojunction onto a three-dimensional starch/reduced graphene oxide (rGO) matrix. Ag2S quantum dots (QDs), synthesized via γ-ray irradiation reduction, were deposited onto TiO2–Bi2WO6 (TB) to construct the ternary heterojunction. The introduction of Ag2S QDs extended light absorption into the near-infrared region and facilitated efficient charge separation via the Z-scheme pathway, significantly suppressing high-energy electron–hole recombination and enhancing quantum efficiency. Photocatalytic characterization showed that Ag2S–TB exhibited reduced electrochemical impedance and lower photoluminescence than TiO2, Bi2WO6, and TB. Under visible light, the ethylene degradation rate constant of Ag2S–TB reached 9.54 × 10−4 min−1, representing improvements of 591.30 %, 211.75 %, and 44.11 % over TiO2, Bi2WO6, and TB, respectively. To further improve dispersion and gas–solid contact, Ag2S–TB was immobilized onto a starch/rGO aerogel. The π–π interactions of rGO enhanced ethylene adsorption, while the porous starch network facilitated ethylene diffusion toward catalytic sites. At optimal loading (3.0 % internal doping, 1.5 % surface), the aerogel achieved a synergistic degradation efficiency of 33.08 % under visible light and 40.75 % under full-spectrum light. This work presents a sustainable, high-performance platform for ethylene removal via combined adsorption and photocatalysis.
全光谱下淀粉/还原氧化石墨烯气凝胶固定化Ag2S-TiO2-Bi2WO6吸附-光催化协同降解乙烯
为了解决粉末光催化剂在果蔬保鲜中量子效率低、分散性差的问题,将Z-scheme Ag2S-TiO2-Bi2WO6异质结固定在三维淀粉/还原氧化石墨烯(rGO)基体上,制备了一种多功能复合气凝胶。将γ射线辐照还原合成的Ag2S量子点(QDs)沉积在TiO2-Bi2WO6 (TB)上,形成三元异质结。Ag2S量子点的引入将光吸收扩展到近红外区域,并通过z方案途径促进了有效的电荷分离,显著抑制了高能电子-空穴复合,提高了量子效率。光催化表征表明,与TiO2、Bi2WO6和TB相比,Ag2S-TB具有更低的电化学阻抗和更低的光致发光。在可见光下,Ag2S-TB的乙烯降解速率常数达到9.54 × 10−4 min−1,比TiO2、Bi2WO6和TB分别提高了591.30%、211.75%和44.11%。为了进一步改善分散和气固接触,将Ag2S-TB固定在淀粉/还原氧化石墨烯气凝胶上。还原氧化石墨烯的π -π相互作用增强了乙烯的吸附,而多孔淀粉网络促进了乙烯向催化位点的扩散。在最佳负载(3.0%内掺杂,1.5%表面掺杂)下,气凝胶在可见光下的协同降解效率为33.08%,在全光谱下的协同降解效率为40.75%。这项工作提出了一个可持续的、高性能的平台,通过联合吸附和光催化去除乙烯。
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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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