Abstract
TiO2-Ag hetero-nanocrystals (HNCs) with controllable Ag particle numbers and domain size were synthesized by in situ reduction of silver acetate and further growth of Ag on TiO2 nanorods. The nucleation of Ag on TiO2 as well as the tuning of Ag number and size can be explained by the electrostatic attraction between Ag precursor and TiO2 nanorods as well as further deposition of Ag onto initially formed Ag domains. The formation of hetero-nanostructures was verified by XRD patterns and UV-Vis absorbance. The reported synthesis provides an effective method to produce ultra-small (1-2 nm) nanocatalysts, as the hetero-nanostructures are intrinsic advantageous in forming nanocrystals due to the confinement of nano-size supporting materials, which present improved catalytic activities than most isolated Ag nanocrystals in nanoscale.
| Original language | English |
|---|---|
| Pages (from-to) | 7230-7235 |
| Number of pages | 6 |
| Journal | CrystEngComm |
| Volume | 15 |
| Issue number | 36 |
| DOIs | |
| State | Published - 28 Sep 2013 |