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Investigating the electron-scale adsorption mechanisms using DFT calculations and experimental studies in self-assembly magnetic biochar gel incorporated with graphene nanosheets for enhanced Sb(III) removal

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dc.contributor.authorChen, Hanbo-
dc.contributor.authorGao, Yurong-
dc.contributor.authorFang, Zheng-
dc.contributor.authorLi, Jiayi-
dc.contributor.authorPillai, Suresh C.-
dc.contributor.authorSong, Hocheol-
dc.contributor.authorSun, Chenghua-
dc.contributor.authorBolan, Nanthi-
dc.contributor.authorYang, Xing-
dc.contributor.authorVithanage, Meththika-
dc.contributor.authorShan, Shengdao-
dc.contributor.authorWang, Hailong-
dc.date.accessioned2025-11-26T08:00:51Z-
dc.date.available2025-11-26T08:00:51Z-
dc.date.issued2024-05-
dc.identifier.issn1385-8947-
dc.identifier.issn1873-3212-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/209337-
dc.description.abstractEnvironmental contamination posed by trivalent antimony [Sb(III)] in water has been globally recognized as a complex challenge, garnering considerable public concern. To enhance the adsorption efficiency of pristine biochar (BC) for Sb(III), a novel Fe/graphene-loaded biochar (FeGB) gel was synthesized through a facile in-situ self-assembly method. This study aimed to investigate the adsorption performance and elucidate the electron-scale adsorption mechanism for Sb(III) by the FeGB-gel. The Sb(III) adsorption isotherm data fitted well with the Langmuir model, and the maximum Sb(III) adsorption capacity of FeGB-gel (113.1 mg g−1) was significantly higher compared to that of BC (28.6 mg g−1). Spectroscopic investigations revealed that surface complexation and π–π stacking were the key mechanisms for Sb(III) adsorption. Electrochemical analyses confirmed an enhanced electron-accepting capacity (0.815 mmol e- g−1) of FeGB-gel, linked to the formation of Fe-related functional groups (Fe–O and Fe–O–OH), which contributed to a stronger Sb(III) oxidation capacity than BC (78.5% v.s. 49.3%). Density functional theory calculations highlighted that the presence of defects on graphene nanosheets enhanced the anchoring of FeOx on biochar, thereby elevating the Sb(III) adsorption energy of FeGB-gel to −1.96 eV. Additionally, the projected density of states profile suggested that the enhanced adsorption of FeGB-gel could be attributable to the orbital hybridization of Sb-p, O-p, and Fe-p/d orbitals (i.e., Fe–O–Sb bonding), which strengthened the electron transfer and chemical interaction during the Sb(III) removal process. The functionalization of biochar surface characteristics with Fe/graphene offers possibilities for a diverse range of biochar-based adsorbents and their application in addressing numerous environmental concerns.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleInvestigating the electron-scale adsorption mechanisms using DFT calculations and experimental studies in self-assembly magnetic biochar gel incorporated with graphene nanosheets for enhanced Sb(III) removal-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.1016/j.cej.2024.150740-
dc.identifier.scopusid2-s2.0-85189667865-
dc.identifier.wosid001221007100001-
dc.identifier.bibliographicCitationChemical Engineering Journal, v.487, pp 1 - 12-
dc.citation.titleChemical Engineering Journal-
dc.citation.volume487-
dc.citation.startPage1-
dc.citation.endPage12-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryEngineering, Environmental-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusAQUEOUS-SOLUTION-
dc.subject.keywordPlusSORPTION-
dc.subject.keywordAuthorModified biochar-
dc.subject.keywordAuthorHeavy metal-
dc.subject.keywordAuthorAdsorption-
dc.subject.keywordAuthorTheoretical calculations-
dc.subject.keywordAuthorDensity of states-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1385894724022277?via%3Dihub-
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