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Article: Energy-Saving Hydrogen Production by Seawater Splitting Coupled with PET Plastic Upcycling

TitleEnergy-Saving Hydrogen Production by Seawater Splitting Coupled with PET Plastic Upcycling
Authors
KeywordsChlorine resistance
Cooperative catalyst
Hydrogen evolution
PET waste upcycling
Seawater splitting
Issue Date8-Feb-2024
PublisherWiley
Citation
Advanced Energy Materials, 2024, v. 14, n. 17 How to Cite?
Abstract

Direct seawater electrolysis presents a promising route for grid-scale green hydrogen (H2) production without reliance on scarce freshwater. However, it is severely hampered by high energy consumption (> 4.3–5.73 kWh m−3 H2) and harmful chlorine corrosion. Herein, an energy-saving and chlorine-free H2 production system by coupling seawater splitting and upcycling of polyethylene terephthalate (PET) waste into value-added glycolic acid (GA) over a Pd─CuCo2O4 catalyst is reported. An ultra-low potential of 1.15 V versus RHE is required to achieve an industry-level current density of 600 mA cm−2, which reduces electricity cost to 2.45 kWh m−3 H2. Notably, this system maintains 1.6 A for longer than 100 h, demonstrating excellent stability. Experimental and theoretical results unveil that 1) the specific adsorption of PET-derived ethylene glycol (EG) on Pd enhances the catalytic performance, and the downshifted d-band center of Pd accelerates the desorption of GA to prevent over-oxidation; 2) the strong adsorption of OH− on CuCo2O4 synergistically promotes EG electrooxidation (EGOR) and forms a negative charge layer that effectively repels Cl− by electrostatic repulsion, thus preventing chlorine corrosion. This work may provide new opportunities for H2 production and value-added GA from vast marine resources and PET waste.


Persistent Identifierhttp://hdl.handle.net/10722/347363
ISSN
2023 Impact Factor: 24.4
2023 SCImago Journal Rankings: 8.748

 

DC FieldValueLanguage
dc.contributor.authorLiu, Kesheng-
dc.contributor.authorGao, Xutao-
dc.contributor.authorLiu, Chu Xuan-
dc.contributor.authorShi, Rui-
dc.contributor.authorTse, Edmund C.M.-
dc.contributor.authorLiu, Fulai-
dc.contributor.authorChen, Yong-
dc.date.accessioned2024-09-21T00:31:31Z-
dc.date.available2024-09-21T00:31:31Z-
dc.date.issued2024-02-08-
dc.identifier.citationAdvanced Energy Materials, 2024, v. 14, n. 17-
dc.identifier.issn1614-6832-
dc.identifier.urihttp://hdl.handle.net/10722/347363-
dc.description.abstract<p>Direct seawater electrolysis presents a promising route for grid-scale green hydrogen (H2) production without reliance on scarce freshwater. However, it is severely hampered by high energy consumption (> 4.3–5.73 kWh m−3 H2) and harmful chlorine corrosion. Herein, an energy-saving and chlorine-free H2 production system by coupling seawater splitting and upcycling of polyethylene terephthalate (PET) waste into value-added glycolic acid (GA) over a Pd─CuCo2O4 catalyst is reported. An ultra-low potential of 1.15 V versus RHE is required to achieve an industry-level current density of 600 mA cm−2, which reduces electricity cost to 2.45 kWh m−3 H2. Notably, this system maintains 1.6 A for longer than 100 h, demonstrating excellent stability. Experimental and theoretical results unveil that 1) the specific adsorption of PET-derived ethylene glycol (EG) on Pd enhances the catalytic performance, and the downshifted d-band center of Pd accelerates the desorption of GA to prevent over-oxidation; 2) the strong adsorption of OH− on CuCo2O4 synergistically promotes EG electrooxidation (EGOR) and forms a negative charge layer that effectively repels Cl− by electrostatic repulsion, thus preventing chlorine corrosion. This work may provide new opportunities for H2 production and value-added GA from vast marine resources and PET waste.</p>-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofAdvanced Energy Materials-
dc.subjectChlorine resistance-
dc.subjectCooperative catalyst-
dc.subjectHydrogen evolution-
dc.subjectPET waste upcycling-
dc.subjectSeawater splitting-
dc.titleEnergy-Saving Hydrogen Production by Seawater Splitting Coupled with PET Plastic Upcycling-
dc.typeArticle-
dc.identifier.doi10.1002/aenm.202304065-
dc.identifier.scopuseid_2-s2.0-85184420513-
dc.identifier.volume14-
dc.identifier.issue17-
dc.identifier.eissn1614-6840-
dc.identifier.issnl1614-6832-

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