Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118358
DC FieldValueLanguage
dc.contributorDepartment of Mechanical Engineeringen_US
dc.contributorResearch Institute for Advanced Manufacturingen_US
dc.creatorGong, Sen_US
dc.creatorHan, Xen_US
dc.creatorLi, Wen_US
dc.creatorZhao, Gen_US
dc.creatorZhai, Yen_US
dc.creatorWang, Wen_US
dc.creatorXia, Qen_US
dc.creatorWang, Xen_US
dc.creatorWu, Jen_US
dc.creatorWu, Cen_US
dc.creatorLv, Xen_US
dc.creatorZhang, Xen_US
dc.date.accessioned2026-04-09T03:44:36Z-
dc.date.available2026-04-09T03:44:36Z-
dc.identifier.issn1385-8947en_US
dc.identifier.urihttp://hdl.handle.net/10397/118358-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectBifunctional electrocatalysten_US
dc.subjectElectrocatalytic CO2 reductionen_US
dc.subjectElectrochemical sulfur oxidationen_US
dc.subjectMembrane electrode assembly electrolyzeren_US
dc.titlePaired electrolysis for efficient coproduction of CO and S₈ with techno-economic analysisen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume507en_US
dc.identifier.doi10.1016/j.cej.2025.160286en_US
dcterms.abstractElectrochemical CO<inf>2</inf> reduction (CO<inf>2</inf>RR) to carbon monoxide (CO) offers significant economic and commercial potential. However, industrial-scale implementation of CO<inf>2</inf>RR for CO is presently impeded by high energy consumption, e.g., cell voltage >2.0 V at currents densities of 100 mA cm−2, due to the low efficiency of existing catalysts, the high potential required for the anode reaction and the electrode/cell design. Herein, we developed a biomimetic bifunctional catalyst consisting of cobalt polyphthalocyanine-coated porous nitrogen-doped carbon aerogels (CoPPc/PNCA), featuring with a “coral-like” structure and stable single-molecular sites, which could drive CO<inf>2</inf>RR coupling with electrochemical sulfur oxidation reaction (SOR). Applied in the self-designed cathode gas electrode (CGE), the bifunctional catalyst achieves nearly 100 % Faradaic efficiency for CO production, and the stable SOR operation at the current density of ∼100 mA cm−2 in traditional H-cell. Furthermore, a CGE/flow membrane electrode assembly (CGE/FMA) electrolyzer was constructed with CoPPc/PNCA as the cathode and anode catalyst, achieving the industrial-level CO current density of 210 ± 16 mA cm−2 in an energy-saving CO<inf>2</inf>RR//SOR system at a cell voltage of −1.8 V, significantly reducing the energy consumption. Techno-economic analysis based on the CO<inf>2</inf>RR//SOR coupling system indicates profitability with the production cost of CO estimated to be $0.204 kg−1 at ∼110 mA cm−2.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationChemical engineering journal, 1 Mar. 2025, v. 507, 160286en_US
dcterms.isPartOfChemical engineering journalen_US
dcterms.issued2025-03-01-
dc.identifier.scopus2-s2.0-85217384970-
dc.identifier.eissn1873-3212en_US
dc.identifier.artn160286en_US
dc.description.validate202604 bchyen_US
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG001440/2026-03-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe authors thank the following funding agencies for supporting this work: National Natural Science Foundation of China ( 22205187 ), Hong Kong Polytechnic University ( CD9B , WZ4Q , CDBZ ), Shenzhen Municipal Science and Technology Innovation Commission ( JCYJ20230807140402006 ), and Department of Science and Technology of Guangdong Province ( 2023A1515110123 , 2024A1515012390 ), Zhenjiang Key Research and Development Program ( GY2021004 ), Jiangsu Funding Program for Excellent Postdoctoral Talent ( 2024ZB736 ), and China Postdoctoral Science Foundation ( GZC20240614 ). The authors would like to thank Shiyanjia Lab (www.shiyanjia.com) for the support of XPS and TEM analysis.en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2027-03-01en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2027-03-01
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