Literature DB >> 16853176

Mechanisms of electron injection from retinoic acid and carotenoic acids to TiO2 nanoparticles and charge recombination via the T1 state as determined by subpicosecond to microsecond time-resolved absorption spectroscopy: dependence on the conjugation length.

Junfeng Xiang1, Ferdy S Rondonuwu, Yoshinori Kakitani, Ritsuko Fujii, Yasutaka Watanabe, Yasushi Koyama, Hiroyoshi Nagae, Yumiko Yamano, Masayoshi Ito.   

Abstract

To examine the mechanisms of electron injection to TiO2 in retinoic acid (RA) and carotenoic acids (CAs), including RA5, CA6, CA7, CA8, CA9, and CA11 having the number of conjugated double bonds n = 5, 6, 7, 8, 9, and 11, respectively, their subpicosecond time-resolved absorption spectra were recorded free in solution and bound to TiO2 nanoparticles in suspension. The time-resolved spectra were analyzed by singular-value decomposition (SVD) followed by global fitting based on an energy diagram consisting of the 3A(g)(-), 1B(u)(-), 1B(u)(+), and 2A(g)(-) singlet excited states, whose energies had been determined as functions of 1/(2n + 1) by the use of carotenoids with n = 9-13. It was found that electron injection took place from both the 1B(u)(+) and 2A(g)(-) states in RA5, CA6, CA7, and CA8, whereas only from the 1B(u)(+) state in CA9 and CA11. The electron-injection efficiencies were determined, by the use of the relevant time constants determined by the SVD and global-fitting analyses, to be in the following order: RA5 approximately CA6 < CA7 > CA8 > CA9 > CA11. To determine the mechanism of charge recombination via the T(1) state, submicrosecond time-resolved absorption spectra of RA5, CA6, CA7, and CA8 bound to TiO2 nanoparticles in suspension were recorded. The SVD and global-fitting analyses lead us to a new scheme, which includes the formation of the D(0)(*+) - T(1) complex followed by transformation to both the D(0)(*+) and T(1) states. On the other hand, their one-electron oxidation potentials were determined, and their singlet and triplet levels were scaled to the conduction band edge (CBE) of TiO2. The T(1) level was lower than, but closest to, the CBE in RA5, and it became lower in the order RA5, CA6, CA7, and CA8. Consistent with the energy gap between the CBE and the T(1) levels, the generation of the T(1) state (or in other words, charge recombination) decreased in the order RA5 > CA6 > CA7 > CA8.

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Year:  2005        PMID: 16853176     DOI: 10.1021/jp051480p

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  3 in total

Review 1.  Mechanisms of suppression and enhancement of photocurrent/conversion efficiency in dye-sensitized solar-cells using carotenoid and chlorophyll derivatives as sensitizers.

Authors:  Yasushi Koyama; Yoshinori Kakitani; Hiroyoshi Nagae
Journal:  Molecules       Date:  2012-02-22       Impact factor: 4.411

Review 2.  Dye-sensitized solar cells based on the principles and materials of photosynthesis: mechanisms of suppression and enhancement of photocurrent and conversion efficiency.

Authors:  Yasushi Koyama; Takeshi Miki; Xiao-Feng Wang; Hiroyoshi Nagae
Journal:  Int J Mol Sci       Date:  2009-10-27       Impact factor: 6.208

3.  Near field enhanced photocurrent generation in p-type dye-sensitized solar cells.

Authors:  Xiaobao Xu; Jin Cui; Junbo Han; Junpei Zhang; Yibo Zhang; Lin Luan; Getachew Alemu; Zhong Wang; Yan Shen; Dehua Xiong; Wei Chen; Zhanhua Wei; Shihe Yang; Bin Hu; Yibing Cheng; Mingkui Wang
Journal:  Sci Rep       Date:  2014-02-04       Impact factor: 4.379

  3 in total

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