Plasmon Resonant Enhancement of Photocatalytic Water Splitting Under Visible Illumination

被引:926
作者
Liu, Zuwei [2 ]
Hou, Wenbo [3 ]
Pavaskar, Prathamesh [1 ]
Aykol, Mehmet [1 ]
Cronin, Stephen B. [1 ,2 ,3 ]
机构
[1] Univ So Calif, Dept Elect Engn, Los Angeles, CA 90089 USA
[2] Univ So Calif, Dept Phys, Los Angeles, CA 90089 USA
[3] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
关键词
Plasmonic; photocatalytic; photocatalysis; water splitting; anodic titanium oxide; enhancement; FDTD; CHEMICAL-VAPOR-DEPOSITION; ELECTROMAGNETIC-FIELDS; OPTICAL-PROPERTIES; LIGHT IRRADIATION; TITANIUM-DIOXIDE; RAMAN-SCATTERING; TIO2; FILMS; THIN-FILMS; NANOPARTICLES; SEMICONDUCTOR;
D O I
10.1021/nl104005n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We demonstrate plasmonic enhancement of photocatalytic water splitting under visible illumination by integrating strongly plasmonic Au nanoparticles with strongly catalytic TiO2. Under visible illumination, we observe enhancements of up to 66x in the photocatalytic splitting of water in TiO2 with the addition of Au nanoparticles. Above the plasmon resonance, under ultraviolet radiation we observe a 4-fold reduction in the photocatalytic activity. Electromagnetic simulations indicate that the improvement of photocatalytic activity in the visible range is caused by the local electric field enhancement near the TiO2 surface, rather than by the direct transfer of charge between the two materials. Here, the near-field optical enhancement increases the electron-hole pair generation rate at the surface of the TiO2, thus increasing the amount of photogenerated charge contributing to catalysis. This mechanism of enhancement is particularly effective because of the relatively short exciton diffusion length (or minority carrier diffusion length), which otherwise limits the photocatalytic performance. Our results suggest that enhancement factors many times larger than this are possible if this mechanism can be optimized.
引用
收藏
页码:1111 / 1116
页数:6
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