Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/92097
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorYu, H-
dc.creatorXue, Y-
dc.creatorHui, L-
dc.creatorZhang, C-
dc.creatorFang, Y-
dc.creatorLiu, Y-
dc.creatorChen, X-
dc.creatorZhang, D-
dc.creatorHuang, B-
dc.creatorLi, Y-
dc.date.accessioned2022-02-07T07:06:07Z-
dc.date.available2022-02-07T07:06:07Z-
dc.identifier.issn2095-5138-
dc.identifier.urihttp://hdl.handle.net/10397/92097-
dc.language.isoenen_US
dc.publisherOxford University Pressen_US
dc.rights© The Author(s) 2020. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd.en_US
dc.rightsThis is an Open Access article distributed under the terms of the CreativeCommons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the originalwork is properly cited.en_US
dc.rightsThe following publication Yu, H., Xue, Y., Hui, L., Zhang, C., Fang, Y., Liu, Y., ... & Li, Y. (2021). Graphdiyne-based metal atomic catalysts for synthesizing ammonia. National science review, 8(8), nwaa213 is available at https://doi.org/10.1093/nsr/nwaa213en_US
dc.subjectGraphdiyneen_US
dc.subjectAtomic catalysten_US
dc.subjectTwo-dimensional carbon materialen_US
dc.subjectAmmoniaen_US
dc.subjectNitrogen reduction reactionen_US
dc.titleGraphdiyne-based metal atomic catalysts for synthesizing ammoniaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume8-
dc.identifier.issue8-
dc.identifier.doi10.1093/nsr/nwaa213-
dcterms.abstractDevelopment of novel catalysts for nitrogen reduction at ambient pressures and temperatures with ultrahigh ammonia (NH3) yield and selectivity is challenging. In this work, an atomic catalyst with separated Pd atoms on graphdiyne (Pd-GDY) was synthesized, which shows fascinating electrocatalytic properties for nitrogen reduction. The catalyst has the highest average NH3 yield of 4.45 +/- 0.30 mg(NH3) mg(Pd)(-1) h(-1), almost tens of orders larger than for previously reported catalysts, and 100% reaction selectivity in neutral media. Pd-GDY exhibits almost no decreases in NH3 yield and Faradaic efficiency. Density functional theory calculations show that the reaction pathway prefers to perform at the (Pd, C1, C2) active area because of the strongly coupled (Pd, C1, C2), which elevates the selectivity via enhanced electron transfer. By adjusting the p-d coupling accurately, reduction of self-activated nitrogen is promoted by anchoring atom selection, and side effects are minimized.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNational science review, Aug. 2021, v. 8, no. 8, nwaa213-
dcterms.isPartOfNational science review-
dcterms.issued2021-08-
dc.identifier.isiWOS:000692594900002-
dc.identifier.eissn2053-714X-
dc.identifier.artnnwaa213-
dc.description.validate202202 bchy-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by the National Natural Science Foundation of China (21790050, 21790051 and 21771156), the National Key Research and Development Project of China (2016YFA0200104 and 2018YFA0703501), the Key Program of the Chinese Academy of Sciences (QYZDY-SSW-SLH015) and the EarlyCareer Scheme (ECS) Fund (PolyU 253026/16P) from the Research Grant Council (RGC) in Hong Kong.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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