Influence of iodide source on the performance of liquid and silica nanoparticle-loaded quasi-solid electrolyte-based dye-sensitized solar cells

被引:2
作者
Mohanty, Shyama Prasad [1 ]
Bhargava, Parag [1 ]
机构
[1] Indian Inst Technol, Dept Met Engn & Mat Sci, Bombay 400076, Maharashtra, India
关键词
Dye-sensitized solar cell; Gel electrolyte; Zeta potential; Adsorption; Cation; NANOCRYSTALLINE TIO2;
D O I
10.1007/s11581-014-1237-6
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
Presence of cations from iodide source in liquid electrolyte has strong influence on photoelectrochemical characteristics of dye-sensitized solar cells (DSSCs). The present work shows the effect of different cations in liquid and silica-loaded gel electrolyte on the photovoltaic properties of DSSCs. Zeta potential measurements have been carried out to probe into the adsorption behavior of ions. It has been found out that lithium ions being smaller in size as compared to 1-methyl-3-propylimidazolium and tetrabutylammonium ions effectively get adsorbed onto the surface of silica nanopowder. Liquid and gel electrolytes were characterized by cyclic voltammetry and electrochemical impedance spectroscopy. In DSSCs, it was found that silica nanopowder addition to lithium ions-based liquid electrolyte significantly increases the open-circuit voltage as compared to the other two ions used in the study. This is due to adsorption of lithium ions onto silica surface which retards such ions to intercalate into or adsorb onto titania.
引用
收藏
页码:849 / 854
页数:6
相关论文
共 9 条
  • [1] Ionic liquid-based electrolyte solidified with SiO2 nanoparticles for dye-sensitized solar cells
    Berginc, M.
    Hocevar, M.
    Krasovec, U. Opara
    Hinsch, A.
    Sastrawan, R.
    Topic, M.
    [J]. THIN SOLID FILMS, 2008, 516 (14) : 4645 - 4650
  • [2] Influence of electrolytes on the photovoltaic performance of organic dye-sensitized nanocrystalline TiO2 solar cells
    Hara, K
    Horiguchi, T
    Kinoshita, T
    Sayama, K
    Arakawa, H
    [J]. SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2001, 70 (02) : 151 - 161
  • [3] Improved exchange reaction in an ionic liquid electrolyte of a quasi-solid-state dye-sensitized solar cell by using 15-crown-5-functionalized MWCNT
    Huang, Kuan-Chieh
    Chang, Yu-Hsun
    Chen, Chia-Yuan
    Liu, Chen-Yu
    Lin, Lu-Yin
    Vittal, R.
    Wu, Chun-Guey
    Lin, King-Fu
    Ho, Kuo-Chuan
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2011, 21 (45) : 18467 - 18474
  • [4] Influence of Different Iodide Salts on the Performance of Dye-Sensitized Solar Cells Containing Phosphazene-Based Nonvolatile Electrolytes
    Lee, Seung-Hyun Anna
    Jackson, Anne-Martine S.
    Hess, Andrew
    Fei, Shih-To
    Pursel, Sean M.
    Basham, James
    Grimes, Craig A.
    Horn, Mark W.
    Allcock, Harry R.
    Mallouk, Thomas E.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (35) : 15234 - 15242
  • [5] Investigation of influence of redox species on the interfacial energetics of a dye-sensitized nanoporous TiO2 solar cell
    Liu, Y
    Hagfeldt, A
    Xiao, XR
    Lindquist, SE
    [J]. SOLAR ENERGY MATERIALS AND SOLAR CELLS, 1998, 55 (03) : 267 - 281
  • [6] A LOW-COST, HIGH-EFFICIENCY SOLAR-CELL BASED ON DYE-SENSITIZED COLLOIDAL TIO2 FILMS
    OREGAN, B
    GRATZEL, M
    [J]. NATURE, 1991, 353 (6346) : 737 - 740
  • [7] Cooperative effect of adsorbed cations and iodide on the interception of back electron transfer in the dye sensitization of nanocrystalline TiO2
    Pelet, S
    Moser, JE
    Grätzel, M
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (08) : 1791 - 1795
  • [8] Quasi-solid-state dye-sensitized solar cells based on gel electrolytes containing different alkali metal iodide salts
    Shen, Xiaolin
    Xu, Weilin
    Xu, Jie
    Liang, Guijie
    Yang, Hongjun
    Yao, Mu
    [J]. SOLID STATE IONICS, 2008, 179 (35-36) : 2027 - 2030
  • [9] Influence of Electrolyte Cations on Electron Transport and Electron Transfer in Dye-Sensitized Solar Cells
    Wang, Hongxia
    Peter, Laurence M.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (19) : 10468 - 10475