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Updated: Jun 13, 2026
Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light
Published on: September 12, 2014
Remarkably efficient photocurrent generation based on a [60]fullerene-triosmium cluster/Zn-porphyrin/boron-dipyrrin
Chang Yeon Lee1, Jae Kwon Jang, Chul Hoon Kim
1Department of Chemistry and School of Molecular Science, Korea Advanced Institute of Science and Technology, Daejeon, 305-701 Korea.
Abstract:
A new artificial photosynthetic triad array, a [60]fullerene-triosmium cluster/zinc-porphyrin/boron-dipyrrin complex (1, Os(3)C(60)/ZnP/Bodipy), has been prepared by decarbonylation of Os(3)(CO)(8)(CN(CH(2))(3)Si(OEt)(3))(mu(3)-eta(2):eta(2):eta(2)-C(60)) (6) with Me(3)NO/MeCN and subsequent reaction with the isocyanide ligand CNZnP/Bodipy (5) containing zinc porphyrin (ZnP) and boron dipyrrin (Bodipy) moieties. Triad 1 has been characterized by various spectroscopic methods (MS, NMR, IR, UV/Vis, photoluminescence, and transient absorption spectroscopy). The electrochemical properties of 1 in chlorobenzene (CB) have been examined by cyclic voltammetry; the general feature of the cyclic voltammogram of 1 is nine reversible one-electron redox couples, that is, the sum of those of 5 and 6. DFT has been applied to study the molecular and electronic structures of 1. On the basis of fluorescence-lifetime measurements and transient absorption spectroscopic data, 1 undergoes an efficient energy transfer from Bodipy to ZnP and a fast electron transfer from ZnP to C(60); the detailed kinetics involved in both events have been elucidated. The SAM of triad 1 (1/ITO; ITO=indium-tin oxide) has been prepared by immersion of an ITO electrode in a CB solution of 1 and diazabicyclo-octane (2:1 equiv), and characterized by UV/Vis absorption spectroscopy, water contact angle, X-ray photoelectron spectroscopy, and cyclic voltammetry. The photoelectrochemical properties of 1/ITO have been investigated by a standard three-electrode system in the presence of an ascorbic acid sacrificial electron donor. The quantum yield of the photoelectrochemical cell has been estimated to be 29 % based on the number of photons absorbed by the chromophores. Our triad 1 is unique when compared to previously reported photoinduced electron-transfer arrays, in that C(60) is linked by pi bonding with little perturbation of the C(60) electron delocalization.
