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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributor.advisorLo, Benedict (ABCT)en_US
dc.creatorLin, Biyun-
dc.identifier.urihttps://theses.lib.polyu.edu.hk/handle/200/14420-
dc.languageEnglishen_US
dc.publisherHong Kong Polytechnic Universityen_US
dc.rightsAll rights reserveden_US
dc.titleEngineering dual active metal sites on metal-organic frameworks for photocatalytic CO2 reductionen_US
dcterms.abstractPhotocatalytic CO₂ reduction (CO₂RR) presents a promising strategy for addressing the global challenges of CO₂ emissions and renewable energy utilization. Metal-organic frameworks (MOFs) have received extensive research attention for their applications in CO₂RR due to their superior CO₂ capture capabilities, photochemical properties, and structural tunability. In this thesis, we investigated the atomic-level engineering of the dual metal active sites on metal-organic frameworks to optimize photocatalytic CO₂RR performance. We systemically evaluated how dual-atom catalysts (DACs), metal loading density, and bimetallic combinations (electronic structure tuning) influence the selectivity and efficiency of CO₂ conversion, particularly towards high-value multi-carbon (C₂+) products. Combining experimental results with theoretical modeling, we established structure-activity relationships and developed rational design principles for optimizing MOF-based photocatalysts with tailored dual metal site. Advanced characterization techniques, including transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), X-ray absorption fine structure (XAFS) analysis, and photoluminescence (PL) were employed to probe the coordination environment and photoinduced charge transfer capability of catalysts.en_US
dcterms.extentvii, 241 pages : color illustrationsen_US
dcterms.isPartOfPolyU Electronic Thesesen_US
dcterms.issued2026en_US
dcterms.educationalLevelPh.D.en_US
dcterms.educationalLevelAll Doctorateen_US
dcterms.accessRightsopen accessen_US

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