Grain morphology and trapping effects on electron transport in dye-sensitized nanocrystalline solar cells

被引:89
作者
Cass, MJ
Walker, AB [1 ]
Martinez, D
Peter, LM
机构
[1] Univ Bath, Dept Phys, Bath BA2 7AY, Avon, England
[2] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1021/jp047073f
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
We have examined the combined effects of grain morphology and electron trapping on the transient response of photoelectrons moving through the TiO2 grains in a dye-sensitized nanocrystalline solar cell using a multitime-scale random walk Monte Carlo model. Our use of a multi-time-scale approach enables us to simulate transport for electrons moving through spherical connected grains in a three-dimensional (3D) voided network and look at the effect of the size of interparticle boundaries on carrier dynamics. We can also address similar times to those over which measurements are taken, namely, 0.1 ins. These times are long because of deep traps in the TiO2 grains. The grains have 2-fold connectivity in one dimension (linear chains) or 4-fold or 6-fold connectivity in three dimensions and traps with an exponential distribution of energies. Photoelectrons are generated by a light pulse of short duration. The spatial distribution of the photogenerated electron density from this pulse either has a uniform profile or is peaked on the electrolyte side. We show that the constrictions at the grain necks slow the electrons, making trapping more likely and hence further delaying their passage to the extracting electrode. By comparing our results for 4-fold and 6-fold coordinated particles on a cubic lattice with 2-fold coordinated particles on linear chains, we show that transport is slowed in the former case due to the additional paths available to the electrons in the 3D network. We also find that the charge and current transients cannot be fit to an analytical solution of the continuum equations with an effective diffusion coefficient even at long times. Therefore, caution must be exercised when attempting to fit experimental transient data with an effective diffusion coefficient.
引用
收藏
页码:5100 / 5107
页数:8
相关论文
共 29 条
  • [1] Charge transport model for disordered materials:: Application to sensitized TiO2 -: art. no. 125324
    Anta, JA
    Nelson, J
    Quirke, N
    [J]. PHYSICAL REVIEW B, 2002, 65 (12): : 1 - 10
  • [2] Benkstein KD, 2003, J PHYS CHEM B, V107, P7759, DOI [10.1021/jp022681l, 10.1021/jp0226811]
  • [3] Electron transport in porous nanocrystalline TiO2 photoelectrochemical cells
    Cao, F
    Oskam, G
    Meyer, GJ
    Searson, PC
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (42) : 17021 - 17027
  • [4] Influence of grain morphology on electron transport in dye sensitized nanocrystalline solar cells
    Cass, MJ
    Qiu, FL
    Walker, AB
    Fisher, AC
    Peter, LM
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (01) : 113 - 119
  • [5] CASS MJ, 2003, THESIS U BATH
  • [6] Dynamic response of dye-sensitized nanocrystalline solar cells: Characterization by intensity-modulated photocurrent spectroscopy
    Dloczik, L
    Ileperuma, O
    Lauermann, I
    Peter, LM
    Ponomarev, EA
    Redmond, G
    Shaw, NJ
    Uhlendorf, I
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (49): : 10281 - 10289
  • [7] Characterisation of electron transport and back reaction in dye-sensitised nanocrystalline solar cells by small amplitude laser pulse excitation
    Duffy, NW
    Peter, LM
    Wijayantha, KGU
    [J]. ELECTROCHEMISTRY COMMUNICATIONS, 2000, 2 (04) : 262 - 266
  • [8] A novel charge extraction method for the study of electron transport and interfacial transfer in dye sensitised nanocrystalline solar cells
    Duffy, NW
    Peter, LM
    Rajapakse, RMG
    Wijayantha, KGU
    [J]. ELECTROCHEMISTRY COMMUNICATIONS, 2000, 2 (09) : 658 - 662
  • [9] DUFFY NW, 2001, P PHOT 2001 10 WASH
  • [10] Spectroscopic determination of electron and mole effective masses in a nanocrystalline semiconductor film
    Enright, B
    Fitzmaurice, D
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (03) : 1027 - 1035