Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/95220
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorZhang, Den_US
dc.creatorShi, Yen_US
dc.creatorZhao, Hen_US
dc.creatorQi, Wen_US
dc.creatorChen, Xen_US
dc.creatorZhan, Ten_US
dc.creatorLi, Sen_US
dc.creatorYang, Ben_US
dc.creatorSun, Men_US
dc.creatorLai, Jen_US
dc.creatorHuang, Ben_US
dc.creatorWang, Len_US
dc.date.accessioned2022-09-14T08:32:44Z-
dc.date.available2022-09-14T08:32:44Z-
dc.identifier.issn2050-7488en_US
dc.identifier.urihttp://hdl.handle.net/10397/95220-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © The Royal Society of Chemistry 2021en_US
dc.rightsThe following publication Zhang, D., Shi, Y., Zhao, H., Qi, W., Chen, X., Zhan, T., Li, S., Yang, B., Sun, M., Lai, J., Huang, B., & Wang, L. (2021). The facile oil-phase synthesis of a multi-site synergistic high-entropy alloy to promote the alkaline hydrogen evolution reaction. Journal of Materials Chemistry A, 9(2), 889–893. is available at https://doi.org/10.1039/D0TA10574K.en_US
dc.titleThe facile oil-phase synthesis of a multi-site synergistic high-entropy alloy to promote the alkaline hydrogen evolution reactionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage889en_US
dc.identifier.epage893en_US
dc.identifier.volume9en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1039/d0ta10574ken_US
dcterms.abstractAlthough intensive efforts have been made and great progress has been achieved relating to the electrocatalytic hydrogen evolution reaction (HER), an advanced synthesis strategy for an efficient electrocatalyst is still the most significant goal. In this paper, we introduce PdFeCoNiCu high-entropy alloy (HEA) nanoparticles as an efficient electrocatalyst for the HER, which has been prepared in an oil phase under facile conditions for the first time. PdFeCoNiCu/C shows excellent alkaline HER catalytic performance with an overpotential of only 18 mV and a Tafel slope of 39 mV dec-1. Meanwhile, we achieved the highest mass activity (6.51 A mgPd-1 at -0.07 V vs. RHE) in the alkaline HER among all non-Pt electrocatalysts. PdFeCoNiCu/C also shows surprisingly stable catalytic properties for over 15 days without notable decay. Based on theoretical calculations, the HEA surface demonstrates the optimization of electronic structures based on a synergistic effect between all metals. Pd and Co are confirmed to be the dominant electroactive sites for both H2 formation and initial water splitting, which are assisted by Ni, Fe, and Cu promotion, enhancing electron transfer and optimizing the binding energies of hydrogen intermediates. This work has supplied significant insight into the design of an efficient electrocatalyst based on HEA materials.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of materials chemistry A, 14 Jan. 2021, v. 9, no. 2, p. 889-893en_US
dcterms.isPartOfJournal of materials chemistry Aen_US
dcterms.issued2021-01-14-
dc.identifier.scopus2-s2.0-85099547518-
dc.identifier.eissn2050-7496en_US
dc.description.validate202209 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberRGC-B2-1331, ABCT-0171en_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Taishan Scholars Program; Natural Science Foundation of Shandong Province, China; Youth Innovation of Shandong Higher Education Institutions, China; Outstanding Youth Foundation of Shandong Province, China; Taishan Scholar Project of Shandong Provinceen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS50659381en_US
dc.description.oaCategoryGreen (AAM)en_US
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