完整後設資料紀錄
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dc.contributor.authorChung, Ming-Yanen_US
dc.contributor.authorChen, Guan-Rueien_US
dc.contributor.authorLee, Chi-Shenen_US
dc.date.accessioned2019-12-13T01:10:03Z-
dc.date.available2019-12-13T01:10:03Z-
dc.date.issued2019-09-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://dx.doi.org/10.1002/jccs.201900174en_US
dc.identifier.urihttp://hdl.handle.net/11536/153107-
dc.description.abstractTwo new quaternary polyselenides, Ba4TMSbSe12 (TM = Nb, Ta), are synthesized using a solid state reaction. They crystallize in a new structural type with a P-1 triclinic space group, characterized according to single-crystal X-ray diffraction. The structure is alternately stacked using isolated NbSe95- and SbSe33-, which are separated by Ba2+. The structure contains the NbSe95- unit with a bipentagonal pyramidal shape coordinated with Se2- and Se-2(2-) in monodenteate and bidentate modes. The vibrational property of the diselenide Se-2(2-) unit was studied using Raman spectrum analysis. ultraviolet-visible diffused reflectance and temperature-dependent resistivity measurements indicate semiconductor behaviors. Calculations of electronic structures indicate the presence of a band gap and strong Se-Se interactions in the diselenide group, which experimentally supports the measured physical properties.en_US
dc.language.isoen_USen_US
dc.subjectcrystal structureen_US
dc.subjectquaternary selenideen_US
dc.subjectSe-Se bonden_US
dc.titleSynthesis and characterization of new quaternary polyselenide Ba4TMSbSe12 (TM = Nb, Ta)en_US
dc.typeArticleen_US
dc.identifier.doi10.1002/jccs.201900174en_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume66en_US
dc.citation.issue9en_US
dc.citation.spage1072en_US
dc.citation.epage1077en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000488854000013en_US
dc.citation.woscount0en_US
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