Abstract
Three five-coordinate transition metal complexes [2,6-(PhNCMe) 2C5H3NMCl2·CH3CN] (M = Zn, Cd, Hg) (named M1) have been assembled onto a nanocrystalline TiO 2 film to prepare transition metal complex/N719 co-sensitized photoelectrodes for dye-sensitized solar cell applications. The metal center is chelated in a tridentate manner by the ligand and further coordinated by two chlorine atoms, resulting in distorted trigonal bipyramidal geometry. In the tandem structure of the TiO2/M1/dye electrode, the M1 undergoes a re-organization of energy levels due to its single-crystal structure, which is advantageous to electron injection and hole recovery. The co-sensitized structure is proved to have a superior ability, when compared to a single N719 dye's influence on TiO2. Therefore, co-sensitized solar cells based on TiO2/M1/N719 electrodes yield a remarkably high photocurrent density (Jsc), open circuit voltage (Voc) and energy conversion efficiency under standard global AM1.5 solar irradiation conditions, which are relatively higher than those for DSSCs using single organic sensitizers.
| Original language | English |
|---|---|
| Pages (from-to) | 2599-2604 |
| Number of pages | 6 |
| Journal | New Journal of Chemistry |
| Volume | 34 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 2010 |
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