Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118483
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.contributorResearch Institute for Smart Energyen_US
dc.contributorMainland Development Officeen_US
dc.creatorBodedla, GBen_US
dc.creatorPiradi, Ven_US
dc.creatorImran, Men_US
dc.creatorZhao, Jen_US
dc.creatorZhu, Xen_US
dc.creatorWong, WYen_US
dc.date.accessioned2026-04-17T03:30:42Z-
dc.date.available2026-04-17T03:30:42Z-
dc.identifier.urihttp://hdl.handle.net/10397/118483-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © The Royal Society of Chemistry and the Chinese Chemical Society 2026en_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (http://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.rightsThe following publication Bodedla, G. B., Piradi, V., Imran, M., Zhao, J., Zhu, X., & Wong, W.-Y. (2026). Design and synthesis of a fused porphyrin dimer for enhanced visible-to-near-infrared-driven photocatalytic hydrogen evolution. Materials Chemistry Frontiers, 10(9), 1497–1509 is available at https://doi.org/10.1039/D5QM00920K.en_US
dc.titleDesign and synthesis of a fused porphyrin dimer for enhanced visible-to-near-infrared-driven photocatalytic hydrogen evolutionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1497en_US
dc.identifier.epage1509en_US
dc.identifier.volume10en_US
dc.identifier.issue9en_US
dc.identifier.doi10.1039/D5QM00920Ken_US
dcterms.abstractA new acceptor–linker–donor–linker–acceptor (A–π–D–π–A) structured porphyrin dimer, F-C19ZnP, was designed and synthesized as a visible-to-near-infrared (Vis-NIR) light-harvesting photosensitizer for photocatalytic hydrogen evolution (PHE). F-C19ZnP features a bimetallic Zn(II)-coordinated fused porphyrin dimer as the donor, a phenylene–ethynylene π-linker, and a 3-ethylrhodanine acceptor. Its photophysical, electrochemical, thermal, and morphological properties, as well as photocurrent response, water contact angle, and PHE performance, were systematically investigated and compared with those of C19ZnP, a structurally similar monometallic porphyrin. Density functional theory calculations provided further insight into the optoelectronic and charge separation characteristics of both porphyrins. F-C19ZnP exhibited markedly broader light absorption (400–1100 nm) and stronger Vis-NIR light-harvesting ability than C19ZnP. F-C19ZnP also exhibits a higher surface area and a larger pore size than C19ZnP, providing more accessible channels for electron transport. It also showed a longer photoexcited electron lifetime (4.9 ns vs. 2.1 ns), enabling more efficient electron transfer to water and resulting in enhanced PHE performance. F-C19ZnP demonstrated a higher photocurrent response, signifying improved charge separation and transport. Its lower water contact angle, attributed to its well-dispersed 300 nm nanosphere morphology, enabled better interfacial interaction with water. Under optimized PHE conditions, F-C19ZnP achieved a PHE rate (ηH2) of 7.93 mmol g−1 h−1, which is eight times higher than that of C19ZnP (1.01 mmol g−1 h−1), and outperformed C19ZnP at all tested irradiation wavelengths (420, 630, and 810 nm). Furthermore, F-C19ZnP displayed excellent photostability and reusability. As the first Vis-NIR fused porphyrin dimer for efficient PHE, F-C19ZnP paves a promising path for the development of advanced porphyrin-based photosensitizers.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMaterials chemistry frontiers, 5 May 2026, v. 10, no. 9, p. 1497-1509en_US
dcterms.isPartOfMaterials chemistry frontiersen_US
dcterms.issued2026-05-05-
dc.identifier.eissn2052-1537en_US
dc.description.validate202604 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera4384a-
dc.identifier.SubFormID52671-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextG. B. B. acknowledges the financial support from the Start-up Fund for RAPs under the Strategic Hiring Scheme (P0048725) of the Hong Kong Polytechnic University. W. -Y. W. acknowledges the financial support from the RGC Senior Research Fellowship Scheme (SRFS2021-5S01), the Research Centre for Carbon-Strategic Catalysis (CE01 and CE41), the Hong Kong Polytechnic University (YXA2), the Research Institute for Smart Energy (CDAQ) and Ms Clarea Au for the Endowed Professorship in Energy (847S). X. Z. acknowledges the funding from the General Research Fund (HKBU12304320), the NSFC/RGC Joint Research Scheme (N_HKBU213/22), and the Initiation Grant for Faculty Niche Research Areas (IG-FNRA) (2020/21)-RC-FNRA-IG/20-21/SCI/06 from Hong Kong Baptist University.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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