Influence of position of auxiliary acceptor in D–A–π–A photosensitizes on photovoltaic performances of dye-sensitized solar cells
详细信息    查看全文
  • 作者:Pei Yu ; Fengying Zhang ; Ming Li ; Rongxing He
  • 刊名:Journal of Materials Science
  • 出版年:2015
  • 出版时间:November 2015
  • 年:2015
  • 卷:50
  • 期:22
  • 页码:7333-7342
  • 全文大小:801 KB
  • 参考文献:1.Yella A, Lee H-W, Tsao HN, Yi C, Chandiran AK, Nazeeruddin MK, Diau EW-G, Yeh C-Y, Zakeeruddin SM, Gr?tzel M (2011) Porphyrin-sensitized solar cells with cobalt (II/III)—based redox electrolyte exceed 12 percent efficiency. Science 334(6056):629-34CrossRef
    2.Yu G, Gao J, Hummelen J, Wudl F, Heeger A (1995) Polymer photovoltaic cells: enhanced efficiencies via a network of internal donor-acceptor heterojunctions. Science 270(5243):1789-790CrossRef
    3.Lee MM, Teuscher J, Miyasaka T, Murakami TN, Snaith HJ (2012) Efficient hybrid solar cells based on meso-superstructured organometal halide perovskites. Science 338(6107):643-47CrossRef
    4.Jung J, Pang X, Feng C, Lin Z (2013) Semiconducting conjugated polymer–inorganic tetrapod nanocomposites. Langmuir 29(25):8086-092CrossRef
    5.Pang X, Zhao L, Feng C, Lin Z (2011) Novel amphiphilic multiarm, starlike coil-rod diblock copolymers via a combination of click chemistry with living polymerization. Macromolecules 44(18):7176-183CrossRef
    6.O’regan B, Grfitzeli M (1991) A low-cost, high-efficiency solar cell based on dye-sensitized. Nature 353:737-40CrossRef
    7.Mathew S, Yella A, Gao P, Humphry-Baker R, Curchod BF, Ashari-Astani N, Tavernelli I, Rothlisberger U, Nazeeruddin MK, Gr?tzel M (2014) Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers. Nature Chem 6(3):242-47CrossRef
    8.Holliman PJ, Al-Salihi KJ, Connell A, Davies ML, Jones EW, Worsley DA (2014) Development of selective, ultra-fast multiple co-sensitization to control dye loading in dye-sensitized solar cells. RSC Adv 4(5):2515-522CrossRef
    9.Piatkowski P, Martin C, di Nunzio MR, Cohen B, Pandey SS, Hayase S, Douhal A (2014) Complete photodynamics of the efficient YD2-o-C8-Based Solar Cell. J Phys Chem C 118(51):29674-9687CrossRef
    10.Chaitanya K, Ju X-H, Heron BM (2014) Theoretical study on the light harvesting efficiency of zinc porphyrin sensitizers for DSSCs. RSC Adv 4(51):26621-6634CrossRef
    11.Zhang J-Z, Zhang J, Li H-B, Wu Y, Xu H-L, Zhang M, Geng Y, Su Z-M (2014) Modulation on charge recombination and light harvesting toward high-performance benzothiadiazole-based sensitizers in dye-sensitized solar cells: a theoretical investigation. J Power Sources 267:300-08CrossRef
    12.Perera IR, Daeneke T, Makuta S, Yu Z, Tachibana Y, Mishra A, B?uerle P, Ohlin CA, Bach U, Spiccia L (2015) Application of the tris (acetylacetonato) iron (III)/(II) redox couple in p-type dye-sensitized solar cells. Angew Chem Int Ed 54(12):3758-762CrossRef
    13.Li M, Kou L, Diao L, Zhang Q, Li Z, Wu Q, Lu W, Pan D (2015) Theoretical study of acene
    idged dyes for dye-sensitized solar cells. J Phys Chem A 119(13):3299-309CrossRef
    14.Yuan W, Zhao H, Baker GL (2014) Low glass transition temperature hole transport material in enhanced-performance solid-state dye-sensitized solar cell. Org Electron 15(11):3362-369CrossRef
    15.Yuan W, Zhao H, Hu H, Wang S, Baker GL (2013) Synthesis and characterization of the hole-conducting silica/polymer nanocomposites and application in solid-state dye-sensitized solar cell. ACS Appl Mater Interfaces 5(10):4155-161
    16.Hagfeldt A, Boschloo G, Sun L, Kloo L, Pettersson H (2010) Dye-sensitized solar cells. Chem Rev 110(11):6595-663CrossRef
    17.Sánchez-de-Armas R, San-Miguel MA, Oviedo J, Sanz JF (2012) Molecular modification of coumarin dyes for more efficient dye sensitized solar cells. J Chem Phys 136(19):194702CrossRef
    18.Koops SE, Barnes PR, O’Regan BC, Durrant JR (2010) Kinetic competition in a coumarin dye-sensitized solar cell: injection and recombination limitations upon device performance. J Phys Chem C 114(17):8054-061CrossRef
    19.Wang J, Li M, Qi D, Shen W, He R, Lin SH (2014) Exploring photophysical properties of metal-free coumarin sensitizers: an efficient strategy to improve the performance of dye-sensitized solar cells. RSC Adv 4(96):53927-3938CrossRef
    20.Liu B, Wang B, Wang R, Gao L, Huo S, Liu Q, Li X, Zhu W (2014) Influence of conjugated π-linker in D-D–π–A indoline dyes: towards long-term stable and efficient dye-sensitized solar cells with high photovoltage. J Mater Chem A 2(3):804-12CrossRef
    21.Kuang D, Uchida S, Humphry-Baker R, Zakeeruddin SM, Gr?tzel M (2008) Organic dye-sensitized ionic liquid based solar cells: remarkable enhancement in performance through molecular design of indoline sensitizers. Angew Chem Int Ed 47(10):1923-927CrossRef
    22.Huang J-F, Liu J-M, Tan L-L, Chen Y-F, Shen Y, Xiao L-M, Kuang D-B, Su C-Y (2015) Novel carbazole based sensitizers for efficient dye-sensitized solar cells: role of the hexyl chain. Dyes Pigm 114:18-3CrossRef
    23.Koumura N, Wang Z-S, Miyashita M, Uemura Y, Sekiguchi H, Cui Y, Mori A, Mori S, Hara K (2009) Substituted carbazole dyes for efficient molecular photovoltaics: long electron lifetime and high open circuit voltage performance. J Mater Chem 19(27):4829-836CrossRef
    24.Ki
  • 作者单位:Pei Yu (1)
    Fengying Zhang (1)
    Ming Li (1)
    Rongxing He (1)

    1. Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Materials Science
    Characterization and Evaluation Materials
    Polymer Sciences
    Continuum Mechanics and Mechanics of Materials
    Crystallography
    Mechanics
  • 出版者:Springer Netherlands
  • ISSN:1573-4803
文摘
Several novel indoline dyes configured with donor–acceptor–bridge–acceptor (D–A–π–A) structures were designed and applied to organic dye-sensitized solar cells. These D–A–π–A dye molecules are composed of indoline (electron donating group), benzothiadiazole (BDT) (auxiliary acceptor), two furan rings (π-conjugated group), and 2-cyanoacrylic acid (electron accepting group). The influence of position of auxiliary acceptor in D–A–π–A organic sensitizer on the performance of photosensitize is investigated in detail. Calculated results show that the sensitizer could achieve a red-shifted absorption in long-wavelength region and a stronger absorption in short-wavelength region when the position of auxiliary acceptor changes from the donor to the acceptor. Moreover, among these dyes, WS-12, whose auxiliary acceptor nearing the 2-cyanoacrylic acid, possesses the better performance in terms of the charge transfer characteristics, lifetime of excited state as well as the vertical dipole moment when compared with WS-1 and WS-11. We hope that the present results could provide theoretical guidance for designing photosensitizes with higher efficiencies. Electronic supplementary materialThe online version of this article (doi:10.-007/?s10853-015-9290-8) contains supplementary material, which is available to authorized users.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700