Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/116910
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dc.contributorDepartment of Applied Physics-
dc.creatorZhang, Hen_US
dc.creatorDuan, Men_US
dc.creatorGuo, Sen_US
dc.creatorLeeflang, Ren_US
dc.creatorSzalay, Den_US
dc.creatorLi, Jen_US
dc.creatorTseng, JCen_US
dc.creatorWu, Sen_US
dc.creatorCai, Sen_US
dc.creatorPrabhakaran, Den_US
dc.creatorTaylor, RAen_US
dc.creatorLi, Yen_US
dc.creatorTsang, SCEen_US
dc.date.accessioned2026-01-21T03:53:55Z-
dc.date.available2026-01-21T03:53:55Z-
dc.identifier.urihttp://hdl.handle.net/10397/116910-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2025 The Author(s). Advanced Science published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication H. Zhang, M. Duan, S. Guo, et al. “ Hydrazine-Mediated Thermally Assisted Photocatalytic Ammonia Decomposition Over Layered Protonated Perovskites.” Adv. Sci. 12, no. 42 (2025): e11212 is available at https://doi.org/10.1002/advs.202511212.en_US
dc.subjectAmmonia decompositionen_US
dc.subjectLayered perovskitesen_US
dc.subjectPhotocatalysisen_US
dc.titleHydrazine-mediated thermally assisted photocatalytic ammonia decomposition over layered protonated perovskitesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume12en_US
dc.identifier.issue42en_US
dc.identifier.doi10.1002/advs.202511212en_US
dcterms.abstractPhotocatalytic ammonia decomposition offers a sustainable route for hydrogen production, but its development is limited by low catalytic efficiency and poorly understood mechanisms. Here, a protonated layered perovskite, HPrNb2O7 (HPNO), is reported as an efficient catalyst for ammonia decomposition under mild photo-thermal conditions. Upon exposure to NH3 at elevated temperatures, HPNO promotes the in situ formation and intercalation of hydrazine intermediates within its interlayer galleries, enabled by thermally generated oxygen vacancies and hydrogen bonding. Advanced characterization techniques have been applied to confirm the formation and stabilization of hydrazine. It is also shown that thermal energy prolongs charge carrier lifetimes and enhances oxygen vacancy formation, contributing to a strong photo-thermal synergy. The stabilization of hydrazine intermediate promotes the associative mechanism, lowering the activation barrier, thus leading to an enhanced hydrogen evolution rate of 1311.2 µmol·g−1·h−1 at 200 °C under simulated solar irradiation without any noble metal co-catalyst. This work reveals a distinct, hydrazine-mediated reaction pathway and positions layered protonated perovskites as promising materials for efficient, solar-driven ammonia decomposition and sustainable hydrogen generation.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced science, 13 Nov. 2025, v. 12, no. 42, e11212en_US
dcterms.isPartOfAdvanced scienceen_US
dcterms.issued2025-11-13-
dc.identifier.scopus2-s2.0-105014604645-
dc.identifier.pmid40879150-
dc.identifier.eissn2198-3844en_US
dc.identifier.artne11212en_US
dc.description.validate202601 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextH.Z. acknowledges the financial support from the Chinese Scholarship Council of the People's Republic of China. M.D. acknowledges the financial support from EPSRC Doctoral Training Partnership (DTP). D.P. acknowledges the EPSRC (UK grant number EP/R024278/1) and the Oxford-ShanghaiTech collaboration project for financial support. All NPD data in this work were collected at the WISH beamline at the ISIS Neutron and Muon Source. The assistance from Dr. Fabio Orlandi and Dr. Pascal Manuel for setting up the NPD experiments is greatly acknowledged. All XPDF data were collected at beamline BL08W at SPring-8, Japan.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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