Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/109612
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorWang, Yen_US
dc.creatorSun, Men_US
dc.creatorZhou, Jen_US
dc.creatorXiong, Yen_US
dc.creatorZhang, Qen_US
dc.creatorYe, Cen_US
dc.creatorWang, Xen_US
dc.creatorLu, Pen_US
dc.creatorFeng, Ten_US
dc.creatorHao, Fen_US
dc.creatorLiu, Fen_US
dc.creatorWang, Jen_US
dc.creatorMa, Yen_US
dc.creatorYin, Jen_US
dc.creatorChu, Sen_US
dc.creatorGu, Len_US
dc.creatorHuang, Ben_US
dc.creatorFan, Zen_US
dc.date.accessioned2024-11-08T06:10:27Z-
dc.date.available2024-11-08T06:10:27Z-
dc.identifier.issn0027-8424en_US
dc.identifier.urihttp://hdl.handle.net/10397/109612-
dc.language.isoenen_US
dc.publisherNational Academy of Sciencesen_US
dc.rightsCopyright © 2023 the Author(s). Published by PNAS. This article is distributed under Creative CommonsAttribution-NonCommercial- NoDerivatives License 4.0(CC BY-NC- ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Y. Wang, M. Sun, J. Zhou, Y. Xiong, Q. Zhang, C. Ye, X. Wang, P. Lu, T. Feng, F. Hao, F. Liu, J. Wang, Y. Ma, J. Yin, S. Chu, L. Gu, B. Huang, Z. Fan, Atomic coordination environment engineering of bimetallic alloy nanostructures for efficient ammonia electrosynthesis from nitrate, Proc. Natl. Acad. Sci. U.S.A. 120 (32) e2306461120 is available at https://doi.org/10.1073/pnas.2306461120.en_US
dc.subjectAmmonia synthesisen_US
dc.subjectAtomic coordination environmenten_US
dc.subjectElectrochemical nitrate reduction reactionen_US
dc.subjectNitrogen cycleen_US
dc.subjectUltrathin metal nanostructuresen_US
dc.titleAtomic coordination environment engineering of bimetallic alloy nanostructures for efficient ammonia electrosynthesis from nitrateen_US
dc.typeConference Paperen_US
dc.identifier.volume120en_US
dc.identifier.issue32en_US
dc.identifier.doi10.1073/pnas.2306461120en_US
dcterms.abstractElectrochemical nitrate reduction reaction (NO3RR) to ammonia has been regarded as a promising strategy to balance the global nitrogen cycle. However, it still suffers from poor Faradaic efficiency (FE) and limited yield rate for ammonia production on heterogeneous electrocatalysts, especially in neutral solutions. Herein, we report one-pot synthesis of ultrathin nanosheet-assembled RuFe nanoflowers with low-coordinated Ru sites to enhance NO3RR performances in neutral electrolyte. Significantly, RuFe nanoflowers exhibit outstanding ammonia FE of 92.9% and yield rate of 38.68 mg h−1 mgcat−1 (64.47 mg h−1 mgRu−1) at −0.30 and −0.65 V (vs. reversible hydrogen electrode), respectively. Experimental studies and theoretical calculations reveal that RuFe nanoflowers with low-coordinated Ru sites are highly electroactive with an increased d-band center to guarantee efficient electron transfer, leading to low energy barriers of nitrate reduction. The demonstration of rechargeable zinc-nitrate batteries with large-specific capacity using RuFe nanoflowers indicates their great potential in next-generation electrochemical energy systems.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationProceedings of the National Academy of Sciences of the United States of America, 8 Aug. 2023, v. 120, no. 32, e2306461120en_US
dcterms.isPartOfProceedings of the National Academy of Sciences of the United States of Americaen_US
dcterms.issued2023-08-08-
dc.identifier.scopus2-s2.0-85167815108-
dc.identifier.pmid37523530-
dc.identifier.eissn1091-6490en_US
dc.identifier.artne2306461120en_US
dc.description.validate202411 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Shenzhen Science and Technology Program; Beijing Natural Science Foundation; ITC via Hong Kong Branch of National Precious Metals Material Engineering Research Center; City University of Hong Kongen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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