TY - JOUR
T1 - Photoinduced electron transfer of platinum(ii) bipyridine diacetylides linked by triphenylamine- and naphthaleneimide-derivatives and their application to photoelectric conversion systems
AU - Suzuki, Shuichi
AU - Matsumoto, Yuma
AU - Tsubamoto, Mai
AU - Sugimura, Ryoji
AU - Kozaki, Masatoshi
AU - Kimoto, Kenshi
AU - Iwamura, Munetaka
AU - Nozaki, Koichi
AU - Senju, Naoki
AU - Uragami, Chiasa
AU - Hashimoto, Hideki
AU - Muramatsu, Yohei
AU - Konno, Akinori
AU - Okada, Keiji
PY - 2013/6/7
Y1 - 2013/6/7
N2 - The recently reported efficient charge-separated system based on bipyridine-diacetylide platinum(ii) complexes was applied to photoelectric conversion systems herein, based on the design and synthesis of two triads: MTA-Pt-NDISAc (3, MTA: dimethoxytriphenylamine, Pt: platinum(ii) complex, NDISAc: thioacetate derivative linked to naphthalenediimide) and MTA-Pt-MNICOOH (4, MNICOOH: naphthaleneimide-4-carboxylic acid). The charge-separated (CS) states of triads 3 and 5 (MOM-protected 4) were effectively generated by photo-induced electron transfer in both THF and toluene, although the rate of formation of the CS state from 5 was relatively slow in toluene. The lifetimes of these CS states were determined to be 730 ns in toluene and 61 ns (70%) and 170 ns (30%) as a double exponential decay in THF for 3, and 600 ns in toluene and 170 ns in THF for 5. The acetylthio group of triad 3 was exploited in the preparation of a self-assembled monolayer (SAM) on a gold surface. Photocurrent was detected upon irradiation of an electrochemical cell comprising Au/3/Na ascorbate/Pt, which was ascribed to the platinum(ii) complex based on the action spectrum. The carboxylic acid group of triad 4 facilitated adsorption on the TiO2 surface, and a dye-sensitized solar cell constructed based on FTO/TiO2/4/electrolyte (LiI-I2)/Pt exhibited a poor energy conversion efficiency (η = 0.20%) based on the incident photon-to-current conversion efficiency spectrum and the I-V curve. This poor efficiency may be derived from the bent molecular shape of 4, or may be due to a possible high energy barrier in the electron injection process through the adsorption site.
AB - The recently reported efficient charge-separated system based on bipyridine-diacetylide platinum(ii) complexes was applied to photoelectric conversion systems herein, based on the design and synthesis of two triads: MTA-Pt-NDISAc (3, MTA: dimethoxytriphenylamine, Pt: platinum(ii) complex, NDISAc: thioacetate derivative linked to naphthalenediimide) and MTA-Pt-MNICOOH (4, MNICOOH: naphthaleneimide-4-carboxylic acid). The charge-separated (CS) states of triads 3 and 5 (MOM-protected 4) were effectively generated by photo-induced electron transfer in both THF and toluene, although the rate of formation of the CS state from 5 was relatively slow in toluene. The lifetimes of these CS states were determined to be 730 ns in toluene and 61 ns (70%) and 170 ns (30%) as a double exponential decay in THF for 3, and 600 ns in toluene and 170 ns in THF for 5. The acetylthio group of triad 3 was exploited in the preparation of a self-assembled monolayer (SAM) on a gold surface. Photocurrent was detected upon irradiation of an electrochemical cell comprising Au/3/Na ascorbate/Pt, which was ascribed to the platinum(ii) complex based on the action spectrum. The carboxylic acid group of triad 4 facilitated adsorption on the TiO2 surface, and a dye-sensitized solar cell constructed based on FTO/TiO2/4/electrolyte (LiI-I2)/Pt exhibited a poor energy conversion efficiency (η = 0.20%) based on the incident photon-to-current conversion efficiency spectrum and the I-V curve. This poor efficiency may be derived from the bent molecular shape of 4, or may be due to a possible high energy barrier in the electron injection process through the adsorption site.
UR - http://www.scopus.com/inward/record.url?scp=84877691108&partnerID=8YFLogxK
U2 - 10.1039/c3cp50182e
DO - 10.1039/c3cp50182e
M3 - 学術論文
C2 - 23532104
AN - SCOPUS:84877691108
SN - 1463-9076
VL - 15
SP - 8088
EP - 8094
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 21
ER -