4.6 Article

Superior Electron Transport and Photocatalytic Abilities of Metal-Nanoparticle-Loaded TiO2 Superstructures

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 116, 期 48, 页码 25444-25453

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jp309683f

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资金

  1. Ministry of Education, Science and Technology through the National Research Foundation of Korea [R31-2011-000-10035-0]
  2. JSPS [P11041]
  3. Renovation Center of Instruments for Science Education and Technology, Osaka University
  4. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of the Japanese Government [22245022]
  5. Kansai Research Foundation (KRF) for technology promotion
  6. National Research Foundation of Korea [R31-2012-000-10035-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. Grants-in-Aid for Scientific Research [11F01041, 22245022, 23655009] Funding Source: KAKEN

向作者/读者索取更多资源

Metal-semiconductor nanocomposites have been widely employed for designing efficient optoelectronic devices and catalysts. The performance of such nanocomposites is significantly influenced by both the method of preparation and the electronic and morphological structures of metals and semiconductors. Here, we have synthesized novel nanocomposites containing plate-like anatase TiO2 mesocrystal superstructures and noble metal (Au, Pt) nanoparticles. These metal nanoparticles were preferentially photodeposited on the edge of TiO2, mesocrystals. The electron transport and photocatalytic properties of the novel nanocomposites were subsequently studied. Single-molecule fluorescence spectroscopy measurements on a single particle directly revealed that most of the photogenerated electrons could migrate from the dominant surface to the edge of the TiO2 mesocrystal with the reduction reactions mainly occurring at its lateral surfaces containing {101} facets. The loading of metal nanoparticles on the superstructure of TiO2 was found to greatly improve the photogenerated charge separation efficiency allowing significant (more than 1 order of magnitude) enhancement of the photocatalytic reaction rate in organic degradation reactions. These outstanding features allowed significantly reduced consumption (ca. 10% of that of typical TiO2 nanocrystal samples) of the Au or Pt loading on the TiO2 mesocrystal while maintaining the same photocatalytic activity.

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