期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 26, 期 70, 页码 16939-16946出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202003990
关键词
nanoparticles; photocatalysis; redox mediator; surface modification; water splitting
资金
- ENEOS Hydrogen Trust Fund
- JSPS KAKENHI [JP18K19086, JP17H06367, JP20H05082]
To investigate the effect of the surface structure of dye-sensitized photocatalyst nanoparticles, we prepared three types of Ru-II-photosensitizer (PS)-double-layered Pt-cocatalyst-loaded TiO2 nanoparticles with different surface structures, Zr-RuCP6-Zr-RuP6@N wt %Pt-TiO2, RuCP6-Zr-RuP6@N wt %Pt-TiO2, and RuCP2-Zr-RuP6@N wt %Pt-TiO2 (N=0.2, 1, and 5), and evaluated their photocatalytic H-2 evolution activity in the presence of redox-reversible iodide as the electron donor. Although the driving force of the electron injection from I- to the photo-oxidized Ru-III PS is comparable, the activity increased in the following order: RuCP2-Zr-RuP6@1 wt %Pt-TiO2 < RuCP6-Zr-RuP6@1 wt %Pt-TiO2 < Zr-RuCP6-Zr-RuP6@1 wt %Pt-TiO2. The apparent quantum yield of Zr-RuCP6-Zr-RuP6@1 wt %Pt-TiO2 in the first hour reached 1 %. Zeta-potential measurements suggest that the surface Zr4+-phosphate groups attracted I- anions to the nanoparticle-solution interface. Our results indicate that the surface modification of dye-sensitized photocatalysts is a promising approach to enhance photocatalytic activity with various redox mediators.
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