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dc.contributor.authorOshikiri, Tomoyaen_US
dc.contributor.authorShi, Xuen_US
dc.contributor.authorMisawa, Hiroakien_US
dc.date.accessioned2020-03-02T03:23:32Z-
dc.date.available2020-03-02T03:23:32Z-
dc.date.issued1970-01-01en_US
dc.identifier.issn1434-1948en_US
dc.identifier.urihttp://dx.doi.org/10.1002/ejic.201901260en_US
dc.identifier.urihttp://hdl.handle.net/11536/153800-
dc.description.abstractThe production of ammonia from atmospheric nitrogen and water using sunlight is an important way to obtain ammonia as an energy carrier and is a new paradigm for achieving a low-carbon and sustainable-energy society. In this study, we attempted to enhance the ammonia photosynthesis efficiency both by increasing the electron supply using a novel photoanode composed of Au film, TiO2, and Au-NPs (ATA) with hybrid energy states due to modal strong coupling and by increasing the surface area of the Zr cathode. We investigated the key properties of this hybrid mode-assisted NH3 photosynthesis using two-electrode systems combining photoanodes and cathodes by performing photoelectrochemical measurements and product analysis. We found that the ATA structure has high absorptivity and enhances the quantum efficiency of ammonia photosynthesis and the surface area available to adsorb N-2 on the Zr cathode is a critical factor for enhancing the reaction rate.en_US
dc.language.isoen_USen_US
dc.subjectNitrogen fixationen_US
dc.subjectArtificial photosynthesisen_US
dc.subjectModal strong couplingen_US
dc.subjectLocalized surface plasmon resonanceen_US
dc.subjectElectrochemistryen_US
dc.subjectAmmoniaen_US
dc.titleEnhancement of Selective Fixation of Dinitrogen to Ammonia Under Modal Strong Coupling Conditionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ejic.201901260en_US
dc.identifier.journalEUROPEAN JOURNAL OF INORGANIC CHEMISTRYen_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:000510496400001en_US
dc.citation.woscount0en_US
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