Implication of device functioning due to back reaction of electrons via the conducting glass substrate in dye sensitized solar cells

被引:55
作者
Hore, S
Kern, R
机构
[1] Freiburg Mat Res Ctr, D-79104 Freiberg, Germany
[2] Fraunhofer Inst Solar Energy Syst, D-79110 Freiberg, Germany
关键词
D O I
10.1063/1.2149215
中图分类号
O59 [应用物理学];
学科分类号
摘要
Enhanced efficiency of dye sensitized solar cells requires minimization of all electron losses in the device. In addition to the loss via the nanoparticles of TiO2, the loss via the surface of the conducting glass substrate (TCO) needs to be contained. This additional electron recombination pathway at the TCO becomes increasingly pronounced at low light intensities. Hence, the determination of the lifetime of electrons within the nanoparticles of TiO2 requires a resistive layer at the surface of the TCO. Lowering the electron loss at the TCO/electrolyte interface increases the shunt resistance, thereby increasing the fill factor by over 10%.
引用
收藏
页码:1 / 3
页数:3
相关论文
共 17 条
[1]   Solid-state dye-sensitized mesoporous TiO2 solar cells with high photon-to-electron conversion efficiencies [J].
Bach, U ;
Lupo, D ;
Comte, P ;
Moser, JE ;
Weissörtel, F ;
Salbeck, J ;
Spreitzer, H ;
Grätzel, M .
NATURE, 1998, 395 (6702) :583-585
[2]  
Barbe CJ, 1997, J AM CERAM SOC, V80, P3157, DOI 10.1111/j.1151-2916.1997.tb03245.x
[3]   How does back-reaction at the conducting glass substrate influence the dynamic photovoltage response of nanocrystalline dye-sensitized solar cells? [J].
Cameron, PJ ;
Peter, LM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (15) :7392-7398
[4]   How important is the back reaction of electrons via the substrate in dye-sensitized nanocrystalline solar cells? [J].
Cameron, PJ ;
Peter, LM ;
Hore, S .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (02) :930-936
[5]   Characterization of titanium dioxide blocking layers in dye-sensitized nanocrystalline solar cells [J].
Cameron, PJ ;
Peter, LM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (51) :14394-14400
[6]   Intensity dependence of the back reaction and transport of electrons in dye-sensitized nanacrystalline TiO2 solar cells [J].
Fisher, AC ;
Peter, LM ;
Ponomarev, EA ;
Walker, AB ;
Wijayantha, KGU .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (05) :949-958
[7]   Diffusion in the electrolyte and charge-transfer reaction at the platinum electrode in dye-sensitized solar cells [J].
Hauch, A ;
Georg, A .
ELECTROCHIMICA ACTA, 2001, 46 (22) :3457-3466
[8]   Long-term stability of dye-sensitised solar cells [J].
Hinsch, A ;
Kroon, JM ;
Kern, R ;
Uhlendorf, I ;
Holzbock, J ;
Meyer, A ;
Ferber, J .
PROGRESS IN PHOTOVOLTAICS, 2001, 9 (06) :425-438
[9]   Acid versus base peptization of mesoporous nanocrystalline TiO2 films:: functional studies in dye sensitized solar cellst [J].
Hore, S ;
Palomares, E ;
Smit, H ;
Bakker, NJ ;
Comte, P ;
Liska, P ;
Thampi, KR ;
Kroon, JM ;
Hinsch, A ;
Durrant, JR .
JOURNAL OF MATERIALS CHEMISTRY, 2005, 15 (03) :412-418
[10]   Modeling and interpretation of electrical impedance spectra of dye solar cells operated under open-circuit conditions [J].
Kern, R ;
Sastrawan, R ;
Ferber, J ;
Stangl, R ;
Luther, J .
ELECTROCHIMICA ACTA, 2002, 47 (26) :4213-4225