Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100127
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorBu, Len_US
dc.creatorHuang, Ben_US
dc.creatorZhu, Yen_US
dc.creatorNing, Fen_US
dc.creatorZhou, Xen_US
dc.creatorHuang, Xen_US
dc.date.accessioned2023-08-08T01:52:24Z-
dc.date.available2023-08-08T01:52:24Z-
dc.identifier.urihttp://hdl.handle.net/10397/100127-
dc.language.isoenen_US
dc.publisherChinese Chemical Societyen_US
dc.rights© 2020 Chinese Chemical Societyen_US
dc.rightsArticles at the CCS Chemistry are published under a Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC 3.0) (https://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.rightsThe following publication Bu, L., Huang, B., Zhu, Y., Ning, F., Zhou, X., & Huang, X. (2020). Highly distorted platinum nanorods for high-efficiency fuel cell catalysis. CCS Chemistry, 2(5), 401-412 is available at https://doi.org/10.31635/ccschem.020.201900123.en_US
dc.subjectDistortionen_US
dc.subjectFuel cell catalysisen_US
dc.subjectNanoroden_US
dc.subjectOxygen reduction reactionen_US
dc.subjectPlatinumen_US
dc.titleHighly distorted platinum nanorods for high-efficiency fuel cell catalysisen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage401en_US
dc.identifier.epage412en_US
dc.identifier.volume2en_US
dc.identifier.issue5en_US
dc.identifier.doi10.31635/ccschem.020.201900123en_US
dcterms.abstractDifferent from studies where less defective platinum (Pt)-based nanomaterials have been widely used to improve the catalysis of the oxygen reduction reaction (ORR) for proton-exchange membrane fuel cells (PEMFCs), herein we have demonstrated that a new class of Pt nanorods (NRs) with a highly distorted configuration can be applied as an advanced, high-efficiency fuel cell catalyst, as transformed from spongy Pt-tellurium NRs (PtTe2 NRs) through sequential chemical and electrochemical aging procedures. The resulting highly distorted Pt NRs exhibit excellent ORR-specific and mass activities of 4.70mA cm-2 and 2.77 A mg-1 Pt at 0.90 V versus the reversible hydrogen electrode (RHE), which are 18.8 and 16.3 times higher than those of commercial Pt/C catalyst, and the mass activity is 6.3 times higher than 2020 U.S. Department of Energy target. Additionally, negligible activity decays were observed after 30,000 cycles. The high ORR performance endows these unique Pt NRs with enhanced activity and lifetimes for practical fuel cell catalysis in comparison with commercial Pt/C, which is consistent with the experimental results. It has been demonstrated that the anomaly of strong electron-lattice coupling suppresses Coulombic repulsion for barrier-free electron transfer while concurrently exposing a large number of active sites, which is a key to superior high-performance fuel cell reactions.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationCCS chemistry, Oct. 2020, v. 2, no. 5, p. 401-412en_US
dcterms.isPartOfCCS chemistryen_US
dcterms.issued2020-10-
dc.identifier.scopus2-s2.0-85102384786-
dc.identifier.eissn2096-5745en_US
dc.description.validate202308 bckwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberABCT-0206-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextMinistry of Science and Technology of China; National Natural Science Foundation of China; Young Thousand Talented Program; Natural Science Foundation of Jiangsu Higher Education Institutions; Special Funded Project of China Postdoctoral Science Foundation; Project of scientific and technologic infrastructure of Suzhou; Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD); Start-up support from Soochow Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS55723133-
dc.description.oaCategoryCCen_US
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