Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117744
DC FieldValueLanguage
dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.contributorResearch Centre for Resources Engineering towards Carbon Neutralityen_US
dc.creatorDeng, Xen_US
dc.creatorSu, Qen_US
dc.creatorZhang, Hen_US
dc.creatorHe, Yen_US
dc.creatorXie, Hen_US
dc.creatorLu, JXen_US
dc.creatorPoon, CSen_US
dc.creatorCui, Xen_US
dc.date.accessioned2026-03-05T01:51:55Z-
dc.date.available2026-03-05T01:51:55Z-
dc.identifier.issn1616-301Xen_US
dc.identifier.urihttp://hdl.handle.net/10397/117744-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.subjectGeopolymer zeoliteen_US
dc.subjectGraphene and CNTen_US
dc.subjectPhotocatalysisen_US
dc.subjectPhotothermal conversionen_US
dc.subjectSolar-driven interfacial evaporationen_US
dc.titleConstruction of geopolymer zeolite-graphene/carbon nanotube interface for strong metal−support interaction (SMSI) effect to achieve efficient solar evaporation and highly selective synergistic catalytic reduction of CO₂en_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume36en_US
dc.identifier.issue32en_US
dc.identifier.doi10.1002/adfm.202520177en_US
dcterms.abstractThe challenges of CO₂ energy conversion and the shortage of clean water resources have become critical global issues. Photocatalytic CO₂ reduction and solar-driven evaporation technology are promising solutions to address these challenges. In this study, a dual-functional biomimetic, mushroom-shaped 3D geopolymer zeolite-nickel@carbon nanotube-graphene composite material (3DGZ-Ni@CNTG) solar evaporator was developed, which integrates high photothermal evaporation with excellent CO₂ photocatalytic reduction performance. It precisely combines the zeolite water transport layer, carbon nanotube-graphene (CNTG) photothermal layer, and metallic nickel catalyst, with each component's functions working synergistically. Under 1-sun intensity, the evaporator achieves an evaporation efficiency of 151% and an evaporation rate of 2.84 kg·m⁻²·h⁻¹, significantly outperforming similar devices. Additionally, it maintains high operational stability over 14 days of continuous evaporation in simulated seawater salinity without any salt accumulation on the surface. Moreover, the 3DGZ-Ni@CNTG material efficiently photocatalyzes CO₂ reduction to produce CO at relatively low temperatures, with high selectivity. The H₂O (water vapor) generated by the solar-driven photothermal evaporation process, along with CO produced from CO₂ reduction, can serve as key components of the water-gas shift reaction (mainly CO and H₂O), a key process in the synthetic chemical industry. This provides a new idea for the integrated use of “solar energy-freshwater-carbon-based chemicals,” creating a closed-loop material cycle.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationAdvanced functional materials, 20 Apr. 2026, v. 36, no. 32, e20177en_US
dcterms.isPartOfAdvanced functional materialsen_US
dcterms.issued2026-04-20-
dc.identifier.scopus2-s2.0-105026490151-
dc.identifier.eissn1616-3028en_US
dc.identifier.artne20177en_US
dc.description.validate202603 bcjzen_US
dc.description.oaNot applicableen_US
dc.identifier.SubFormIDG001065/2026-02-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by the National Natural Science Foundation of China (Grant Nos. 51772055, 52302019, and 52308275), the Hong Kong Innovation and Technology Funds (P0051376, P0050447), the Guangdong Basic and Applied Basic Research Foundation Fund (2024A1515240013), and the Innovation Project of Guangxi Graduate Education (Grant No. YCBZ2022052).en_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2027-04-20en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
Open Access Information
Status embargoed access
Embargo End Date 2027-04-20
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.