Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113626
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dc.contributorDepartment of Industrial and Systems Engineeringen_US
dc.creatorLi, Ren_US
dc.creatorLiu, Xen_US
dc.creatorLiu, Wen_US
dc.creatorLi, Zen_US
dc.creatorChan, KCen_US
dc.creatorLu, Zen_US
dc.date.accessioned2025-06-16T00:36:56Z-
dc.date.available2025-06-16T00:36:56Z-
dc.identifier.urihttp://hdl.handle.net/10397/113626-
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbH & Co. KGaAen_US
dc.rights© 2022 The Authors. 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 R. Li, X. Liu, W. Liu, Z. Li, K. C. Chan, Z. Lu, Design of Hierarchical Porosity Via Manipulating Chemical and Microstructural Complexities in High-Entropy Alloys for Efficient Water Electrolysis. Adv. Sci. 2022, 9, 2105808 is available at https://doi.org/10.1002/advs.202105808.en_US
dc.subjectHierarchical poreen_US
dc.subjectHigh-entropy alloyen_US
dc.subjectPhase separationen_US
dc.subjectSpinodal decompositionen_US
dc.subjectWater electrolysisen_US
dc.titleDesign of hierarchical porosity via manipulating chemical and microstructural complexities in high-entropy alloys for efficient water electrolysisen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume9en_US
dc.identifier.issue12en_US
dc.identifier.doi10.1002/advs.202105808en_US
dcterms.abstractAchieving a porous architecture with multiple-length scales and utilizing the synergetic effects of multicomponent chemicals bring up new opportunities for further improving the electrocatalytic performance of nanocatalysts. Herein, the synthesis of a self-supported hierarchical porous electrocatalyst based on a high-entropy alloy (HEA) containing multiple transitional metals via physical metallurgy and dealloying strategies is reported. Microscale phase separation and nanoscale spinodal decomposition are modulated in a highly concentrated FeCoNiCu HEA, which makes it possible to obtain a porous structure with different length scales, i.e., relatively large porous channels formed by removing one separated phase and ultrafine mesopores obtained from leaching out one decomposition phase. The resultant hierarchical porous HEA exhibits superior water splitting performance, which takes full advantage of the enlarged surface area offered by the bi-continuous mesoporous structure with the exceptional intrinsic reactivity originating from the synergetic electronic effects of the different components in alloying. Moreover, the microscale porous structure plays an important role in the significantly improved mass transportation, as well as the durability during electrocatalysis. This effective strategy that simultaneously utilizes the chemical and microstructural advantages of HEAs opens up a new avenue for developing HEA-based, high-performance porous electrocatalysts for various energy conversion/store applications.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAdvanced science, 25 Apr. 2022, v. 9, no. 12, 2105808en_US
dcterms.isPartOfAdvanced scienceen_US
dcterms.issued2022-04-25-
dc.identifier.scopus2-s2.0-85125133693-
dc.identifier.eissn2198-3844en_US
dc.identifier.artn2105808en_US
dc.description.validate202506 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera3700-
dc.identifier.SubFormID50756-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China (Nos. 52101202, 52071024, 11790293, 51961160729); the Funds for Creative Research Groups of China (No. 51921001); the Gusu Leading Talents Program (No. ZXL2021206); the Basic Research Programs of Taicang (No. TC2021JC03); the Fundamental Research Funds for the Central Universities (No. G2021KY05102); the Natural Science Foundation of Shanxi Province of China (No. 2021JQ-080)en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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