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dc.contributor.authorZhao, Damingen_US
dc.contributor.authorChen, Jieen_US
dc.contributor.authorDong, Chung-Lien_US
dc.contributor.authorZhou, Wuen_US
dc.contributor.authorHuang, Yu-Chengen_US
dc.contributor.authorMao, Samuel S.en_US
dc.contributor.authorGuo, Liejinen_US
dc.contributor.authorShen, Shaohuaen_US
dc.date.accessioned2018-08-21T05:54:27Z-
dc.date.available2018-08-21T05:54:27Z-
dc.date.issued2017-08-01en_US
dc.identifier.issn0021-9517en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.jcat.2017.06.020en_US
dc.identifier.urihttp://hdl.handle.net/11536/145965-
dc.description.abstractTwo-dimensional graphitic carbon nitride (g-C3N4) nanosheets (CNNS) have attracted intense interest in photocatalysis, given their small thickness and high specific surface area favoring charge transfer and surface reactions. Herein, a facile strategy of breaking and following repolymerizing the heptazine units in bulk g-C3N4 (BCN) is developed to synthesize ultrathin CNNS with thickness of 1 nm in relatively high product yield (similar to 24%). The as-prepared 1 nm-thick CNNS show significantly enhanced photocatalytic performance for hydrogen evolution than BCN and even the 3 nm-thick CNNS acquired by thermal oxidation etching of BCN. It is evidenced that the disordered layer structure of the obtained ultrathin CNNS causes strong interlayer C-N interaction, tunneling electron transport between the C-N layers. Meanwhile, the broken in-plane C-N bonds create more unsaturated N sites in the 1 nm-thick CNNS, facilitating the electron excitation from the occupied states in g-C3N4 to its unoccupied states for water reduction reaction. (C) 2017 Elsevier Inc. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectUltrathin nanosheetsen_US
dc.subjectGraphitic carbon nitrideen_US
dc.subjectElectron transporten_US
dc.subjectSolar hydrogen conversionen_US
dc.titleInterlayer interaction in ultrathin nanosheets of graphitic carbon nitride for efficient photocatalytic hydrogen evolutionen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jcat.2017.06.020en_US
dc.identifier.journalJOURNAL OF CATALYSISen_US
dc.citation.volume352en_US
dc.citation.spage491en_US
dc.citation.epage497en_US
dc.contributor.department電機學院zh_TW
dc.contributor.departmentCollege of Electrical and Computer Engineeringen_US
dc.identifier.wosnumberWOS:000408299600050en_US
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