Abstract
A series of Mn 2+ doped CdS photocatalysts were prepared by a co-precipitation method and characterized by XRD, DRS, TEM, and XPS techniques. While the band gap, crystal phase and the morphology of CdS nanocrystal were not found to be affected noticeably by Mn 2+ doping, there was an optimal Mn 2+ doping content of wt 0.5% where the hydrogen production was more than doubled compared to pure CdS. Calculations of density functional theory (DFT) with plane waves and pseudopotentials were used to characterize the doping effect of Mn in cubic CdS. It is assumed that Mn 2+ serving as shallow trapping sites can separate e-/h + pairs at surface of nanosized CdS, so as to greatly reduce their surface recombination and which in turn leads to improved hydrogen yield.
| Original language | English |
|---|---|
| Pages (from-to) | 730-736 |
| Number of pages | 7 |
| Journal | International Journal of Hydrogen Energy |
| Volume | 37 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2012 |
Keywords
- Charge separation
- Co-precipitation
- Hydrogen production
- Photocatalyst