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Enhancing O2 adsorption and activation over porous S-doped g-C3N4 rod toward efficient photocatalytic rhodamine-B degradation

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dc.contributor.authorXie, Zhuohong-
dc.contributor.authorLin, Jianbin-
dc.contributor.authorZhang, Weibin-
dc.contributor.authorZhang, Chi-
dc.contributor.authorYang, Woochul-
dc.date.accessioned2024-09-26T21:00:44Z-
dc.date.available2024-09-26T21:00:44Z-
dc.date.issued2024-01-
dc.identifier.issn0925-9635-
dc.identifier.issn1879-0062-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/26255-
dc.description.abstractPhotocatalytic oxygen molecular (O2) activation to generate reactive oxygen species (ROS) is a promising strategy for the oxidative degradation of organic pollutants. Herein, a porous S-doped g-C3N4 rod (S-g-CN-rod) was synthesized and applied to photocatalytic superoxide radicals (.O2- ) evolution and rhodamine-B (RhB) degradation. The morphological, structural, and optical properties of all samples were investigated. DFT calculation demonstrated that the carbon site adjacent to S was energetically favorable for O2 adsorption, which was conducive to .O2- evolution. The porous S-g-CN-rod exhibited an excellent photocatalytic .O2- evolution rate of 268.2 mu mol L-1 h-1, which was the main active species to degrade RhB. Conceivably, the porous S-g-CN-rod demonstrated exceptionally high efficiency of photocatalytic RhB degradation and achieved almost complete disposal of RhB (99.7 %) in only 30 min, which was higher than most reported photocatalysts. The experimental results and theoretical calculations demonstrated that the preeminent photocatalytic activities were ascribed to enhanced light-harvesting, improved migration and separation of photo-induced electrons, and the superior O2 adsorption and activation induced by S doping.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleEnhancing O2 adsorption and activation over porous S-doped g-C3N4 rod toward efficient photocatalytic rhodamine-B degradation-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.1016/j.diamond.2023.110658-
dc.identifier.scopusid2-s2.0-85178338422-
dc.identifier.wosid001127987000001-
dc.identifier.bibliographicCitationDiamond and Related Materials, v.141, pp 1 - 10-
dc.citation.titleDiamond and Related Materials-
dc.citation.volume141-
dc.citation.startPage1-
dc.citation.endPage10-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryMaterials Science, Coatings & Films-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.subject.keywordPlusCARBON NITRIDE-
dc.subject.keywordPlusOXYGEN REDUCTION-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusNANOTUBES-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusCHARGE-
dc.subject.keywordAuthorOxygen adsorption-
dc.subject.keywordAuthorSuperoxide radical evolution-
dc.subject.keywordAuthorPhotocatalytic degradation-
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