摘要
Iridium complexes with dicyanovinyl-grafted phenylpyridine/1-phenylisoquinoline as ligands are synthesized and their photophysical, electrochemical, and sensitization properties in DSSCs are investigated. The iridium complexes present significantly enhanced absorption from 400 to 525 nm. The 1-phenylisoquinoline-based iridium complex show bathochromic-shift emission in DMSO solution compared with their phenylpyridine-based counterpart, while their absorption response and photoluminescence peak in solid show little difference despite extension of the conjugated system. Using DSSCs, the conversion efficiency of 0.62% and open-circuit current of 1.4 m A/cm2 is achieved. The poor performance is attributed to the excited-state properties of iridium complexes according to the TD-DFT calculation.
Iridium complexes with dicyanovinyl-grafted phenylpyridine/l-phenylisoquinoline as ligands are synthesized and their photo- physical, electrochemical, and sensitization properties in DSSCs are investigated. The iridium complexes present significantly enhanced absorption from 400 to 525 nm. The 1-phenylisoquinoline-based iridium complex show bathochromic-shift emission in DMSO solution compared with their phenylpyridine-based counterpart, while their absorption response and photoluminescence peak in solid show little difference despite extension of the conjugated system. Using DSSCs, the conversion efficiency of 0.62% and open-circuit current of 1.4 mA/cm2 is achieved. The poor performance is attributed to the excited-state properties of iridium complexes according to the TD-DFT calculation.
基金
supported by the Fundamental Research Funds for the Central Universities(08143034)
the National Basic Research Program of China(2013CB328705,2013CB328706)
the National Natural Science Foundation of China(61275034,61106123)