Ultra-fast sintered TiO2 films in dye-sensitized solar cells: phase variation, electron transport and recombination

被引:34
作者
Carnie, Matthew J. [1 ]
Charbonneau, Cecile [1 ]
Barnes, Piers R. F. [2 ]
Davies, Matthew L. [3 ]
Mabbett, Ian [1 ]
Watson, Trystan M. [1 ]
O'Regan, Brian C. [4 ]
Worsley, David A. [1 ]
机构
[1] Swansea Univ, Coll Engn, Baglan Bay Innovat & Knowledge Ctr, SPECIFIC, Swansea SA12 7AX, W Glam, Wales
[2] Imperial Coll London, Dept Phys, London, England
[3] Bangor Univ, Sch Chem, Bangor, Gwynedd, Wales
[4] Imperial Coll London, Dept Chem, London, England
基金
英国工程与自然科学研究理事会;
关键词
LONG-TERM STABILITY; EFFICIENCY; FABRICATION; RUTILE;
D O I
10.1039/c2ta01005d
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
With the application of near-infrared radiation (NIR), TiO2 films for dye-sensitized solar cells (DSCs) on metallic substrates can be sintered in just 12.5 seconds. The photovoltaic performance of devices made with NIR sintered films match those devices made with conventionally sintered films prepared by heating for 1800 seconds. Here we characterise the electron transport, electron lifetime and phase-morphological properties of ultrafast NIR sintered films, using impedance spectroscopy, transient photovoltage decay and X-ray diffraction measurements. An important factor in NIR processing of TiO2 films is the peak metal temperature (PMT) and we show that during the 12.5 second heat treatment, a PMT of around 635 degrees C gives near identical electron transport, electron lifetime and morphological properties, as well comparable photovoltaic performance to a conventionally sintered (500 degrees C, 30 min) film. We demonstrate that the rapid heating of the TiO2 (to temperatures of up to 785 degrees C) does not lead to a large scale rutile phase transition. As such photovoltaic performance of resultant DSC devices is maintained since the heating period is insufficient to induce a significant transition from anatase to rutile or morphology changes which result in a loss of photocurrent.
引用
收藏
页码:2225 / 2230
页数:6
相关论文
共 26 条
[11]  
Ito S., 2010, DYE SENSITIZED SOLAR
[12]   Fabrication of thin film dye sensitized solar cells with solar to electric power conversion efficiency over 10% [J].
Ito, Seigo ;
Murakami, Takurou N. ;
Comte, Pascal ;
Liska, Paul ;
Graetzel, Carole ;
Nazeeruddin, Mohammad K. ;
Graetzel, Michael .
THIN SOLID FILMS, 2008, 516 (14) :4613-4619
[13]   High-efficiency (7.2%) flexible dye-sensitized solar cells with Ti-metal substrate for nanocrystalline-TiO2 photoanode [J].
Ito, Seigo ;
Ha, Ngoc-Le Cevey ;
Rothenberger, Guido ;
Liska, Paul ;
Comte, Pascal ;
Zakeeruddin, Shaik M. ;
Pechy, Peter ;
Nazeeruddin, Mohammad Khaja ;
Graetzel, Michael .
CHEMICAL COMMUNICATIONS, 2006, (38) :4004-4006
[14]   A new method to make dye-sensitized nanocrystalline solar cells at room temperature [J].
Lindström, H ;
Holmberg, A ;
Magnusson, E ;
Malmqvist, L ;
Hagfeldt, A .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2001, 145 (1-2) :107-112
[15]   WATER-PURIFICATION BY SEMICONDUCTOR PHOTOCATALYSIS [J].
MILLS, A ;
DAVIES, RH ;
WORSLEY, D .
CHEMICAL SOCIETY REVIEWS, 1993, 22 (06) :417-425
[16]   Laser-Sintered TiO2 Films for Dye Solar Cell Fabrication: An Electrical, Morphological, and Electron Lifetime Investigation [J].
Mincuzzi, Girolamo ;
Vesce, Luigi ;
Liberatore, Massimiliano ;
Reale, Andrea ;
Di Carlo, Aldo ;
Brown, Thomas M. .
IEEE TRANSACTIONS ON ELECTRON DEVICES, 2011, 58 (09) :3179-3188
[17]   A LOW-COST, HIGH-EFFICIENCY SOLAR-CELL BASED ON DYE-SENSITIZED COLLOIDAL TIO2 FILMS [J].
OREGAN, B ;
GRATZEL, M .
NATURE, 1991, 353 (6346) :737-740
[18]   Comparison of dye-sensitized rutile- and anatase-based TiO2 solar cells [J].
Park, NG ;
van de Lagemaat, J ;
Frank, AJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (38) :8989-8994
[19]   The Scherrer formula for x-ray particle size determination [J].
Patterson, AL .
PHYSICAL REVIEW, 1939, 56 (10) :978-982
[20]   Influence of a TiCl4 post-treatment on nanocrystalline TiO2 films in dye-sensitized solar cells [J].
Sommeling, P. M. ;
O'Regan, B. C. ;
Haswell, R. R. ;
Smit, H. J. P. ;
Bakker, N. J. ;
Smits, J. J. T. ;
Kroon, J. M. ;
van Roosmalen, J. A. M. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (39) :19191-19197