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    請使用永久網址來引用或連結此文件: https://ir.lib.ncu.edu.tw/handle/987654321/101927


    題名: Plasmonically Enhanced Photocatalytic Hydrogen Production from Water: The Critical Role of Tunable Surface Plasmon Resonance from Gold-Silver Nanoshells
    作者: 李岱洲;Li, Chien-Hung;Li, Min-Chih;Liu, Si-Ping;Jamison, Andrew C;Lee, Dahye;Lee, T. Randall;Lee, Tai-Chou
    貢獻者: 工學院化學工程與材料工程學系
    關鍵詞: absorption;diameter;electrons;hydrogen;hydrogen production;indium;microwave treatment;photocatalysts;silica;sulfides;surface plasmon resonance;zinc
    日期: 2016-04-27
    上傳時間: 2026-04-21 14:51:15 (UTC+8)
    出版者: American Chemical Society;United States: American Chemical Society
    摘要: 摘要: Gold–silver nanoshells (GS-NSs) having a tunable surface plasmon resonance (SPR) were employed to facilitate charge separation of photoexcited carriers in the photocalytic production of hydrogen from water. Zinc indium sulfide (ZnIn2S4; ZIS), a visible-light-active photocatalyst, where the band gap varies with the [Zn]/[In] ratio, was used as a model ZIS system (E g = 2.25 eV) to investigate the mechanisms of plasmonic enhancement associated with the nanoshells. Three types of GS-NS cores with intense absorptions centered roughly at 500, 700, and 900 nm were used as seeds for preparing GS-NSZIS core–shell structures via a microwave-assisted hydrothermal reaction, yielding core–shell particles with composite diameters of ∼200 nm. Notably, an interlayer of dielectric silica (SiO2) between the GS-NSs and the ZIS photocatalyst provided another parameter to enhance the production of hydrogen and to distinguish the charge-transfer mechanisms. In particular, the direct transfer of hot electrons from the GS-NSs to the ZIS photocatalyst was blocked by this layer. Of the 10 particle samples examined in this study, the greatest hydrogen gas evolution rate was observed for GS-NSs having a SiO2 interlayer thickness of ∼17 nm and an SPR absorption centered at ∼700 nm, yielding a rate 2.6 times higher than that of the ZIS without GS-NSs. The apparent quantum efficiencies for these core–shell particles were recorded and compared to the absorption spectra. Analyses of the charge-transfer mechanisms were evaluated and are discussed based on the experimental findings.
    其他題名: ACS Appl. Mater. Interfaces
    出版者: United States: American Chemical Society
    出版日期: 2016-04-13
    出處: ACS applied materials & interfaces, 2016-04, Vol.8 (14), p.9152-9161
    資源來源: American Chemical Society Journals
    版權: Copyright © 2016 American Chemical Society
    識別號: ISSN: 1944-8244
    識別號: ISSN: 1944-8252
    識別號: EISSN: 1944-8252
    識別號: DOI: 10.1021/acsami.6b01197
    識別號: PMID: 26973998
    顯示於類別:[化學工程與材料工程學系 ] 期刊論文

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