Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/110601
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dc.contributorDepartment of Applied Physics-
dc.contributorResearch Institute for Smart Energy-
dc.creatorShe, X-
dc.creatorZhai, L-
dc.creatorWang, Y-
dc.creatorXiong, P-
dc.creatorLi, MMJ-
dc.creatorWu, TS-
dc.creatorWong, MC-
dc.creatorGuo, X-
dc.creatorXu, Z-
dc.creatorLi, H-
dc.creatorXu, H-
dc.creatorZhu, Y-
dc.creatorTsang, SCE-
dc.creatorLau, SP-
dc.date.accessioned2024-12-27T06:26:47Z-
dc.date.available2024-12-27T06:26:47Z-
dc.identifier.urihttp://hdl.handle.net/10397/110601-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rights© The Author(s) 2024en_US
dc.rightsThe following publication She, X., Zhai, L., Wang, Y. et al. Pure-water-fed, electrocatalytic CO2 reduction to ethylene beyond 1,000 h stability at 10 A. Nat Energy 9, 81–91 (2024) is available at https://doi.org/10.1038/s41560-023-01415-4.en_US
dc.titlePure-water-fed, electrocatalytic CO₂ reduction to ethylene beyond 1,000 h stability at 10 Aen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage81-
dc.identifier.epage91-
dc.identifier.volume9-
dc.identifier.doi10.1038/s41560-023-01415-4-
dcterms.abstractElectrocatalytic CO2 reduction at near-ambient temperatures requires a complex inventory of protons, hydroxyls, carbonate ions and alkali-metal ions at the cathode and anode to be managed, necessitating the use of ion-selective membranes to regulate pH. Anion-exchange membranes provide an alkaline environment, allowing CO2 reduction at low cell voltages and suppression of hydrogen evolution while maintaining high conversion efficiencies. However, the local alkaline conditions and the presence of alkali cations lead to problematic carbonate formation and even precipitation. Here we report a pure-water-fed (alkali-cation-free) membrane–electrode–assembly system for CO2 reduction to ethylene by integrating an anion-exchange membrane and a proton-exchange membrane at the cathode and anode side, respectively, under forward bias. This system effectively suppresses carbonate formation and prevents salt precipitation. A scaled-up electrolyser stack achieved over 1,000 h stability without CO2 and electrolyte losses and with 50% Faradaic efficiency towards ethylene at a total current of 10 A.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNature energy, 2024, v. 9, p. 81-91-
dcterms.isPartOfNature energy-
dcterms.issued2024-
dc.identifier.scopus2-s2.0-85181476735-
dc.identifier.eissn2058-7546-
dc.description.validate202412 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextHong Kong Polytechnic University; National Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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