用户名: 密码: 验证码:
Molecular-Scale Transition Metal Oxide Nanocluster Surface-Modified Titanium Dioxide as Solar-Activated Environmental Catalysts
详细信息    查看全文
  • 作者:Hiroaki Tada ; Qiliang Jin ; Anna Iwaszuk ; Michael Nolan
  • 刊名:Journal of Physical Chemistry C
  • 出版年:2014
  • 出版时间:June 12, 2014
  • 年:2014
  • 卷:118
  • 期:23
  • 页码:12077-12086
  • 全文大小:606K
  • 年卷期:v.118,no.23(June 12, 2014)
  • ISSN:1932-7455
文摘
The development of environmental catalysts is an urgent subject to be tackled by scientists and engineers all over the world due to the borderless nature of environmental pollution. We named the catalyst enabling the decomposition of the pollutants by effectively utilizing the solar energy from ultraviolet to infrared as 鈥渟olar environmental catalysts鈥? This Feature Article reviews the recent studies on a novel class of solar environmental catalysts consisting of TiO2 and molecular scale oxides of 3d metals and for comparison d10 (Sn) on the surface (MOs/TiO2). The TiO2 surface modification with MO clusters by the chemisorption鈥揷alcination cycle (CCC) technique presents novel band engineering for finely tuning the top of the valence band, while the unique physicochemical and electronic properties of MOs/TiO2 give rise to the outstanding photo- and thermocatalytic activities for the decomposition of organic pollutants. In the first part following the Introduction, the CCC technique for forming extremely small MO clusters on TiO2, the structures, physicochemical properties, and electronic structures of MOs/TiO2 are described. The second part deals with their thermo- and photocatalytic activities for the degradation of model organic pollutants and the essential action mechanisms of the MO clusters. The combination of experiments and first-principles density functional theory simulations shows that Co2O3/TiO2 can be a prototype of the solar environmental catalyst with high levels of photo(UV and visible)- and thermocatalytic activities.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700