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dc.contributor.authorShoji, Shusakuen_US
dc.contributor.authorPeng, Xiaoboen_US
dc.contributor.authorYamaguchi, Akiraen_US
dc.contributor.authorWatanabe, Ryoen_US
dc.contributor.authorFukuhara, Chojien_US
dc.contributor.authorCho, Yoheien_US
dc.contributor.authorYamamoto, Tomokazuen_US
dc.contributor.authorMatsumura, Syoen_US
dc.contributor.authorYu, Min-Wenen_US
dc.contributor.authorIshii, Satoshien_US
dc.contributor.authorFujita, Takeshien_US
dc.contributor.authorAbe, Hidekien_US
dc.contributor.authorMiyauchi, Masahiroen_US
dc.date.accessioned2020-03-02T03:23:30Z-
dc.date.available2020-03-02T03:23:30Z-
dc.date.issued1970-01-01en_US
dc.identifier.issn2520-1158en_US
dc.identifier.urihttp://dx.doi.org/10.1038/s41929-019-0419-zen_US
dc.identifier.urihttp://hdl.handle.net/11536/153773-
dc.description.abstractDry reforming of methane is one of the key reactions to exploit natural gas feedstocks by their catalytic conversion to synthesis gas (CH4 + CO2 -> 2H(2) + 2CO), which is used in the production of transportable liquid fuel. However, this reaction suffers from thermodynamic conversion limits and high thermal energy requirements. Herein we report that a SrTiO3-supported rhodium (Rh/STO) catalyst efficiently promotes methane reforming under ultraviolet light irradiation without heat supply at low temperatures, which cannot be achieved by conventional thermal catalysis. The photoexcited holes and electrons are used for CH4 oxidation over STO and CO2 reduction over rhodium, respectively. Isotope analysis clarified that the lattice oxygens (O2-) act as mediator to drive dry reforming of methane. The materials design of Rh/STO can be extended in principle to diverse uphill reactions that utilize photon energy to obtain valued products from different carbon resources.en_US
dc.language.isoen_USen_US
dc.titlePhotocatalytic uphill conversion of natural gas beyond the limitation of thermal reaction systemsen_US
dc.typeArticleen_US
dc.identifier.doi10.1038/s41929-019-0419-zen_US
dc.identifier.journalNATURE CATALYSISen_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.identifier.wosnumberWOS:000509653400001en_US
dc.citation.woscount0en_US
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