A molecular tetrad allowing efficient energy storage for 1.6 s at 163 K

被引:171
作者
Guldi, DM [1 ]
Imahori, H
Tamaki, K
Kashiwagi, Y
Yamada, H
Sakata, Y
Fukuzumi, S
机构
[1] Univ Notre Dame, Radiat Lab, Notre Dame, IN 46556 USA
[2] Kyoto Univ, PRESTO, JST, Grad Sch Engn,Dept Mol Engn,Nishikyo Ku, Kyoto 6158510, Japan
[3] Kyoto Univ, Fukui Inst Fundamental Chem, Sakyo Ku, Kyoto 6068103, Japan
[4] Osaka Univ, Inst Sci & Ind Res, Osaka 5670047, Japan
[5] Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, CREST,JST, Suita, Osaka 5650871, Japan
基金
美国国家航空航天局; 美国国家卫生研究院;
关键词
D O I
10.1021/jp036382n
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In a novel molecular ferrocene-zinc porphyrin-zinc porphyrin-fullerene (Fc-ZnP-ZnP-C-60) tetrad, the longest lifetime of a charge-separated state ever reported in an artificial photosynthetic reaction center (1.6 s in DMF at 163 K) has been attained. This lifetime is comparable, for example, to the lifetime (similar to1 s) of the bacteriochlorophyll dimer radical cation ((Bchl)(2)(.+))-secondary quinone radical anion (Q(B)(.-)) ion pair in the bacterial photosynthetic reaction centers. The present far distant radical ion pair is formed with a quantum yield of 34%. The radical ion pair Fc(+)-ZnP-ZnP-C-60(.-) produced by photoinduced electron transfer was detected by means of transient absorption spectra as well as ESR spectra. Both the lifetime and the quantum yield of the final charge-separated state are improved in Fc-ZnP-ZnP-C-60 relative to the corresponding ferrocene-zinc porphyrin-free base porphyrin-fullerene (Fc-ZnP-H2P-C-60) tetrad.
引用
收藏
页码:541 / 548
页数:8
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