In-situ anion exchange preparation of Ag2S/Ag2CrO4 core–shell heterojunction with enhanced visible-light photocatalytic activity

IF 2.4 3区 化学 Q4 CHEMISTRY, PHYSICAL Chemical Physics Pub Date : 2025-03-01 Epub Date: 2025-01-07 DOI:10.1016/j.chemphys.2025.112606
Yusong Pan , Shuhuan He , Linjie Ou , Shihui Zang , Run Huang
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Abstract

Photocatalytic technology is one of the most promising technologies for wastewater treatment. In this paper, Ag2S/Ag2CrO4 core–shell heterojunction were prepared using in-situ anion exchange method. The structure, morphology, and optical properties of the prepared samples were characterized by XRD, SEM, TEM, XPS, and DRS technologies. The photo-degradation results verified that the 2 %-Ag2S/Ag2CrO4 heterojunction exhibited excellent photocatalytic activity for degradation of organic dyes and antibiotics under visible light irradiation. The removal efficiency for RhB was 95 % in 15 min, which was obviously superior to that of pure Ag2CrO4 (∼73 %) and Ag2S (∼7%) photocatalysts. The enhanced photocatalytic performance of the Ag2S/Ag2CrO4 was mainly attributed to the Z-scheme core–shell heterojunction structure of the photocatalyst that facilitated excellent charge carriers separation and migration. Meanwhile, the results of trapping experiments for active species demonstrated that both the holes (h+) and superoxide radical (O2) played an important role for degradation of organic pollutants.

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增强可见光催化活性的Ag2S/Ag2CrO4核壳异质结原位阴离子交换制备
光催化技术是目前最有前途的污水处理技术之一。本文采用原位阴离子交换法制备了Ag2S/Ag2CrO4核壳异质结。采用XRD、SEM、TEM、XPS和DRS等技术对制备的样品进行了结构、形貌和光学性能表征。光降解结果证实,在可见光照射下,2% -Ag2S/Ag2CrO4异质结具有良好的光催化降解有机染料和抗生素的活性。在15 min内对RhB的去除率为95%,明显优于纯Ag2CrO4(~ 73%)和Ag2S(~ 7%)光催化剂。Ag2S/Ag2CrO4光催化性能的增强主要是由于光催化剂的z型核壳异质结结构促进了载流子的分离和迁移。同时,活性物质的捕获实验结果表明,空穴(h+)和超氧自由基(O2−)对有机污染物的降解都起着重要作用。
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来源期刊
Chemical Physics
Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
4.60
自引率
4.30%
发文量
278
审稿时长
39 days
期刊介绍: Chemical Physics publishes experimental and theoretical papers on all aspects of chemical physics. In this journal, experiments are related to theory, and in turn theoretical papers are related to present or future experiments. Subjects covered include: spectroscopy and molecular structure, interacting systems, relaxation phenomena, biological systems, materials, fundamental problems in molecular reactivity, molecular quantum theory and statistical mechanics. Computational chemistry studies of routine character are not appropriate for this journal.
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