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dc.contributor.authorWu, Hung-Yuen_US
dc.contributor.authorNhat Huy Nguyenen_US
dc.contributor.authorBai, Hsunlingen_US
dc.contributor.authorChang, Sue-minen_US
dc.contributor.authorWu, Jeffrey C. S.en_US
dc.date.accessioned2019-04-03T06:40:20Z-
dc.date.available2019-04-03T06:40:20Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5ra10408den_US
dc.identifier.urihttp://hdl.handle.net/11536/128102-
dc.description.abstractIn this study, the photocatalytic reduction of CO2 in a monoethanolamine solution to form valuable energy sources was investigated using Mo-doped TNTs photocatalysts for the first time. The results revealed that the structure of Mo-doped TNTs changed with the increase of calcination temperature. For Mo-doped TNTs calcined at 500 degrees C, the partial corruption of titanate nanotubes into anatase particles caused the reduction of Mo species from Mo6+ to Mo5+ and produced oxygen vacancies, which resulted in the highest CO2 reduction ability. The yield rates of CH4, CO and total combustible organic compounds were 0.52, 10.41 and 13.53 mu mol g(cat)(-1), respectively, under UVA (8 W, 63 mu W cm(-2)) irradiation. The photoreduction quantum efficiencies of CH4 and CO were achieved at 0.036% and 0.180%, respectively. It was found that the molybdenum structure and oxygen vacancies could be the key factors controlling the photocatalytic reduction efficiency of CO2. A possible structure transformation of Mo-doped TNTs at different calcination temperatures was inferred and the reaction mechanism for photocatalytic CO2 reduction with oxygen vacancy sites of Mo-doped TNTs was proposed.en_US
dc.language.isoen_USen_US
dc.titlePhotocatalytic reduction of CO2 using molybdenum-doped titanate nanotubes in a MEA solutionen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5ra10408den_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume5en_US
dc.citation.issue78en_US
dc.citation.spage63142en_US
dc.citation.epage63151en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000358734800001en_US
dc.citation.woscount6en_US
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