{"title":"Synthesis, characterization, photocatalytic activity of selenium vacancy in BiSeX and BiSeX/GO (X = Cl、Br、I) photocatalysts","authors":"Yu-Yun Lin, Hong-Han Huang, Shiuh-Tsuen Huang, Fu-Yu Liu, Jia-Hao Lin, Chiing-Chang Chen","doi":"10.1016/j.jphotochem.2025.116330","DOIUrl":null,"url":null,"abstract":"<div><div>BiSeX (X = Cl, Br, I) belongs to the V–VI–VII compounds, known for their high dielectric constants, ferroelectric properties, excellent photoconductivity, and well-suited valence bands. In this study, we successfully synthesized a series of BiSeX compounds through a simple hydrothermal method. We then combined varying amounts of graphene oxide (GO) with BiSeX in an autoclave, heating the mixture at 100 °C for 4 h to create the binary composite photocatalyst BiSeX/GO. The resulting products were extensively characterized using XRD, SEM-EDS, DR-UV, GC, BET, PL, UV–Vis-NIR, and HR-XPS techniques. To assess the photocatalytic efficiency of BiSeX and BiSeX/GO, these catalysts were tested for the degradation of the organic pollutant crystal violet (CV), yielding significant outcomes. BiSeCl/GO-25 wt% demonstrated exceptional effectiveness in degrading CV dyes, achieving a maximum reaction rate constant (<em>k</em>) of 0.0465 h<sup>−1</sup>. Additionally, the photocatalytic conversion of carbon dioxide into chemical fuels offers a promising strategy to tackle escalating environmental issues and holds potential for renewable energy development. Our research revealed that selenium vacancies in BiSeX act as adsorption sites, significantly enhancing electron transfer at the interface, resulting in high activity and selectivity for the carbon dioxide reduction reaction.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"464 ","pages":"Article 116330"},"PeriodicalIF":4.1000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Photochemistry and Photobiology A-chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S101060302500070X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
BiSeX (X = Cl, Br, I) belongs to the V–VI–VII compounds, known for their high dielectric constants, ferroelectric properties, excellent photoconductivity, and well-suited valence bands. In this study, we successfully synthesized a series of BiSeX compounds through a simple hydrothermal method. We then combined varying amounts of graphene oxide (GO) with BiSeX in an autoclave, heating the mixture at 100 °C for 4 h to create the binary composite photocatalyst BiSeX/GO. The resulting products were extensively characterized using XRD, SEM-EDS, DR-UV, GC, BET, PL, UV–Vis-NIR, and HR-XPS techniques. To assess the photocatalytic efficiency of BiSeX and BiSeX/GO, these catalysts were tested for the degradation of the organic pollutant crystal violet (CV), yielding significant outcomes. BiSeCl/GO-25 wt% demonstrated exceptional effectiveness in degrading CV dyes, achieving a maximum reaction rate constant (k) of 0.0465 h−1. Additionally, the photocatalytic conversion of carbon dioxide into chemical fuels offers a promising strategy to tackle escalating environmental issues and holds potential for renewable energy development. Our research revealed that selenium vacancies in BiSeX act as adsorption sites, significantly enhancing electron transfer at the interface, resulting in high activity and selectivity for the carbon dioxide reduction reaction.
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.