{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1360002215850233984.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1016/j.ccr.2012.04.018"}},{"identifier":{"@type":"URI","@value":"https://api.elsevier.com/content/article/PII:S0010854512001002?httpAccept=text/xml"}},{"identifier":{"@type":"URI","@value":"https://api.elsevier.com/content/article/PII:S0010854512001002?httpAccept=text/plain"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Recent advances in the photocatalytic conversion of carbon dioxide to fuels with water and/or hydrogen using solar energy and beyond"}],"description":[{"notation":[{"@value":"Abstract   Photocatalytic reduction of carbon dioxide to fuels using solar energy is an attractive option for simultaneously capturing this major greenhouse gas and solving the shortage of sustainable energy. Efforts to demonstrate the photocatalytic reduction of CO2 are reviewed herein. Although the photocatalytic results depended on the reaction conditions, such as the incident/absorbing light intensity from the sun or a simulated solar light source, the performance of different systems is compared. When the reactants included CO2 and water, it was necessary to determine whether the products were derived from CO2 and not from impurities that accumulated on/in the catalysts as a result of washing, calcination, or pretreatment in a moist environment. Isotope labeling of 13CO2 was effective for this evaluation using Fourier-transform infrared (FTIR) spectroscopy and mass spectrometry (MS). Comparisons are limited to reports in which the reaction route was verified spectroscopically, the C source was traced isotopically, or sufficient kinetic analyses were performed to verify the photocatalytic events. TiO2 photocatalytically produced methane at the rate of ∼0.1 μmol h−1 gcat−1. In aqueous solutions, formic acid, formaldehyde, and methanol were also produced. When TiO2 was atomically dispersed in zeolites or ordered mesoporous SiO2 and doped with Pt, Cu, N, I, CdSe, or PbS, the methane and CO formation rates were greater, reaching 1–10 μmol h−1 gcat−1. As for semiconductors other than TiO2, CdS, SiC, InNbO4, HNb3O8, Bi2WO6, promoted NaNbO3, and promoted Zn2GeO4 produced methane or methanol at rates of 1–10 μmol h−1 gcat−1, and promoted AIILa4Ti4O15 produced CO at a rate greater than 10 μmol h−1 gcat−1, in addition to the historically known ZnO and GaP (formaldehyde and methanol formation). The photocatalytic reduction of CO2 was also surveyed with hydrogen, because hydrogen can be obtained from water photosplitting by utilizing natural light. CO was formed at a rate of ∼1 μmol h−1 gcat−1 using TiO2, ZrO2, MgO, and Ga2O3, whereas both CO and methanol were formed at a rate of 0.1–1 μmol h−1 gcat−1 using layered-double hydroxides consisting of Zn, Cu, Al, and Ga. When hydrogen is used, in addition to identifying the origin of the carbon, it is critical to confirm that the products are photocatalytically formed, not thermally produced via CO2 hydrogenation. The feasibility of the strategy involving the recycling of a sacrificial electron donor and the direct supply of protons and electrons released from water oxidation catalysts to photocatalysts for the reduction of CO2 to fuels has been demonstrated. However, based on the results obtained to date, it is clear that the practical use of the photocatalytic reduction of CO2 as one possible solution for global warming and the world's energy problems requires the development of more efficient photocatalysts."}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1420564276185896064","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"50251666"},{"@type":"NRID","@value":"1000050251666"},{"@type":"NRID","@value":"9000000824672"},{"@type":"NRID","@value":"9000001819431"},{"@type":"NRID","@value":"9000016657022"},{"@type":"NRID","@value":"9000256011260"},{"@type":"NRID","@value":"9000256019723"},{"@type":"NRID","@value":"9000283903049"},{"@type":"NRID","@value":"9000253648882"},{"@type":"NRID","@value":"9000000238111"},{"@type":"NRID","@value":"9000018731227"},{"@type":"NRID","@value":"9000242710690"},{"@type":"NRID","@value":"9000000827099"},{"@type":"NRID","@value":"9000257712379"},{"@type":"NRID","@value":"9000255702345"},{"@type":"NRID","@value":"9000256020862"},{"@type":"NRID","@value":"9000413587287"},{"@type":"NRID","@value":"9000000257395"},{"@type":"NRID","@value":"9000257726040"},{"@type":"NRID","@value":"9000404620537"},{"@type":"NRID","@value":"9000007894865"},{"@type":"NRID","@value":"9000413373315"},{"@type":"NRID","@value":"9000256019929"},{"@type":"NRID","@value":"9000281370549"},{"@type":"NRID","@value":"9000014200448"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/yasuoizumi"}],"foaf:name":[{"@value":"Yasuo Izumi"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00108545"}],"prism:publicationName":[{"@value":"Coordination Chemistry Reviews"}],"dc:publisher":[{"@value":"Elsevier BV"}],"prism:publicationDate":"2013-01","prism:volume":"257","prism:number":"1","prism:startingPage":"171","prism:endingPage":"186"},"reviewed":"false","dcterms:accessRights":"http://purl.org/coar/access_right/c_abf2","dc:rights":["https://www.elsevier.com/tdm/userlicense/1.0/","https://www.elsevier.com/legal/tdmrep-license","http://www.elsevier.com/open-access/userlicense/1.0/"],"url":[{"@id":"https://api.elsevier.com/content/article/PII:S0010854512001002?httpAccept=text/xml"},{"@id":"https://api.elsevier.com/content/article/PII:S0010854512001002?httpAccept=text/plain"}],"createdAt":"2012-04-21","modifiedAt":"2025-09-14","foaf:topic":[{"@id":"https://cir.nii.ac.jp/all?q=Chemistry(all)","dc:title":"Chemistry(all)"}],"project":[{"@id":"https://cir.nii.ac.jp/crid/1040282257097106432","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"22550117"},{"@type":"JGN","@value":"JP22550117"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-22550117/"}],"notation":[{"@language":"ja","@value":"CO2還元およびCO選択酸化用光触媒の開発と選択分光による作用機構追跡"},{"@language":"en","@value":"Development of Photocatalysts for CO2 Reduction and Selective CO Oxidation and Monitoring of the Mechanism by Selective Spectroscopy"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360001114003565568","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Photocatalytic conversion of carbon dioxide into methanol using zinc–copper–M(III) (M=aluminum, gallium) layered double hydroxides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360001114156363392","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Minimizing Graphene Defects Enhances Titania Nanocomposite-Based Photocatalytic Reduction of CO<sub>2</sub> for Improved Solar Fuel Production"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002216660170112","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Photocatalytic Reduction of Low Concentration of 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