Parameters influencing charge separation in solid-state dye-sensitized solar cells using novel hole conductors

被引:167
作者
Kroeze, Jessica E.
Hirata, Narukuni
Schmidt-Mende, Lukas
Orizu, Charles
Ogier, Simon D.
Carr, Kathryn
Graetzel, Michael
Durrant, James R.
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Elect Mat & Devices, London SW7 2AY, England
[2] Swiss Fed Inst Technol, Inst Chem Sci & Engn, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[3] Merck Chem Ltd, Manchester Tech Ctr, Manchester M9 8ZS, Lancs, England
关键词
D O I
10.1002/adfm.200500748
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state dye-sensitized solar cells employing a solid organic hole-transport material (HTM) are currently under intensive investigation, since they offer a number of practical advantages over liquid-electrolyte junction devices. Of particular importance to the design of such devices is the control of interfacial charge transfer. In this paper, the factors that determine the yield of hole transfer at the dye/HTM interface and its correlation with solid-state-cell performance are identified. To this end, a series of novel triarylamine type oligomers, varying in molecular weight and mobility, are studied. Transient absorption spectroscopy is used to determine hole-transfer yields and pore-penetration characteristics. No correlation between hole mobility and cell performance is observed. However, it is found that the photocurrent is directly proportional to the hole-transfer yield. This hole-transfer yield depends on the extent of pore penetration in the dye-sensitized film as well as on the thermodynamic driving force Delta G(dye-HTM) for interfacial charge transfer. Future design of alternative solid-state HTMs should focus on the optimization of pore-filling properties and the control of interfacial energetics rather than on increasing material hole mobilities.
引用
收藏
页码:1832 / 1838
页数:7
相关论文
共 41 条
[31]   EFFECT OF SURFACE CHELATION ON THE ENERGY OF AN INTRABAND SURFACE-STATE OF A NANOCRYSTALLINE TIO2 FILM [J].
REDMOND, G ;
FITZMAURICE, D ;
GRAETZEL, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (27) :6951-6954
[32]   Solid state dye sensitized solar cells using in situ polymerized PEDOTs as hole conductor [J].
Saito, Y ;
Fukuri, N ;
Senadeera, R ;
Kitamura, T ;
Wada, Y ;
Yanagida, S .
ELECTROCHEMISTRY COMMUNICATIONS, 2004, 6 (01) :71-74
[33]   Band edge movement and recombination kinetics in dye-sensitized nanocrystalline TiO2 solar cells: A study by intensity modulated photovoltage spectroscopy [J].
Schlichthorl, G ;
Huang, SY ;
Sprague, J ;
Frank, AJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (41) :8141-8155
[34]   Effect of hydrocarbon chain length of amphiphilic ruthenium dyes on solid-state dye-sensitized photovoltaics [J].
Schmidt-Mende, L ;
Kroeze, JE ;
Durrant, JR ;
Nazeeruddin, MK ;
Grätzel, M .
NANO LETTERS, 2005, 5 (07) :1315-1320
[35]   TiO2 pore-filling and its effect on the efficiency of solid-state dye-sensitized solar cells [J].
Schmidt-Mende, L ;
Grätzel, M .
THIN SOLID FILMS, 2006, 500 (1-2) :296-301
[36]   Efficiency improvement in solid-state-dye-sensitized photovoltaics with an amphiphilic Ruthenium-dye -: art. no. 013504 [J].
Schmidt-Mende, L ;
Zakeeruddin, SM ;
Grätzel, M .
APPLIED PHYSICS LETTERS, 2005, 86 (01) :013504-1
[37]   Poly(4-undecyl-2,2′-bithiophene) as a hole conductor in solid state dye sensitized titanium dioxide solar cells [J].
Spiekermann, S ;
Smestad, G ;
Kowalik, J ;
Tolbert, LM ;
Grätzel, M .
SYNTHETIC METALS, 2001, 121 (1-3) :1603-1604
[38]   Low-k insulators as the choice of dielectrics in organic field-effect transistors [J].
Veres, J ;
Ogier, SD ;
Leeming, SW ;
Cupertino, DC ;
Khaffaf, SM .
ADVANCED FUNCTIONAL MATERIALS, 2003, 13 (03) :199-204
[39]   A stable quasi-solid-state dye-sensitized solar cell with an amphiphilic ruthenium sensitizer and polymer gel electrolyte [J].
Wang, P ;
Zakeeruddin, SM ;
Moser, JE ;
Nazeeruddin, MK ;
Sekiguchi, T ;
Grätzel, M .
NATURE MATERIALS, 2003, 2 (06) :402-407
[40]   Electric potential distribution and short-range screening in nanoporous TiO2 electrodes [J].
Zaban, A ;
Meier, A ;
Gregg, BA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (40) :7985-7990