Journal article
Exceptional Excited-State Lifetime of an Iron(II)-N-Heterocyclic Carbene Complex Explained
‡Wigner Research Centre for Physics, Hungarian Academy of Sciences, P.O. Box 49, H-1525 Budapest, Hungary.1
Earth-abundant transition-metal complexes are desirable for sensitizers in dye-sensitized solar cells or photocatalysts. Iron is an obvious choice, but the energy level structure of its typical polypyridyl complexes, featuring low-lying metal-centered states, has made such complexes useless as energy converters.
Recently, we synthesized a novel iron-N-heterocyclic carbene complex exhibiting a remarkable 100-fold increase of the lifetime compared to previously known iron(II) complexes. Here, we rationalize the measured excited-state dynamics with DFT and TD-DFT calculations. The calculations show that the exceptionally long excited-state lifetime (∼9 ps) is achieved for this Fe complex through a significant destabilization of both triplet and quintet metal-centered scavenger states compared to other Fe(II) complexes.
In addition, a shallow (3)MLCT potential energy surface with a low-energy transition path from the (3)MLCT to (3)MC and facile crossing from the (3)MC state to the ground state are identified as key features for the excited-state deactivation.
Language: | English |
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Year: | 2014 |
Pages: | 2066-2071 |
ISSN: | 19487185 |
Types: | Journal article |
DOI: | 10.1021/jz500829w |