Preparation and Characterization of TiO2 Barrier Layers for Dye-Sensitized Solar Cells

被引:11
作者
Zheng, Yichen [1 ]
Klankowski, Steven [1 ]
Yang, Yiqun [1 ]
Li, Jun [1 ]
机构
[1] Kansas State Univ, Dept Chem, Manhattan, KS 66503 USA
基金
美国国家科学基金会;
关键词
TiO2 barrier layer; dye sensitized solar cells; interface; photovoltaic; electron backflow; COMPACT LAYER; BLOCKING LAYERS; BACK-REACTION; LOW-COST; DEPOSITION; EFFICIENT; DEVICE;
D O I
10.1021/am502421w
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A TiO2 barrier layer is critical in enhancing the performance of dye-sensitized solar cells (DSSCs). Two methods to prepare the TiO2 barrier layer on fluorine-doped tin dioxide (FTO) surface were systematically studied in order to minimize electron-hole recombination and electron backflow during photovoltaic processes of DSSCs. The film structure and materials properties were correlated with the photovoltaic characteristics and electrochemical properties. In the first approach, a porous TiO2 layer was deposited by wet chemical treatment of the sample with TiCl4 solution for time periods varying from 0 to 60 min. The N719 dye molecules were found to be able to insert into the porous barrier layers. The 20 min treatment formed a nonuniform but intact TiO2 layer of similar to 100-300 nm in thickness, which gave the highest open-circuit voltage V-OC, short-circuit photocurrent density J(SC), and energy conversion efficiency. But thicker TiO2 barrier layers by this method caused a decrease in J(SC), possibly limited by lower electrical conductance. In the second approach, a compact TiO2 barrier layer was created by sputter-coating 0-15 nm Ti metal films on FTO/glass and then oxidizing them into TiO2 with thermal treatment at 500 degrees C in the air for 30 min. The dye molecules were found to only attach at the outer surface of the barrier layer and slightly increased with the layer thickness. These two kinds of barrier layer showed different characteristics and may be tailored for different DSSC studies.
引用
收藏
页码:10679 / 10686
页数:8
相关论文
共 24 条
[1]   Effects of a surfactant-templated nanoporous TiO2 interlayer on dye-sensitized solar cells [J].
Ahn, Kwang-Soon ;
Kang, Moon-Sung ;
Lee, Ji-Won ;
Kang, Yong Soo .
JOURNAL OF APPLIED PHYSICS, 2007, 101 (08)
[2]   Electron Lifetime in Dye-Sensitized Solar Cells: Theory and Interpretation of Measurements [J].
Bisquert, Juan ;
Fabregat-Santiago, Francisco ;
Mora-Sero, Ivan ;
Garcia-Belmonte, Germa ;
Gimenez, Sixto .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (40) :17278-17290
[3]   The function of a TiO2 compact layer in dye-sensitized solar cells incorporating "Planar" organic dyes [J].
Burke, Anthony ;
Ito, Seigo ;
Snaith, Henry ;
Bach, Udo ;
Kwiatkowski, Joe ;
Graetzel, Michael .
NANO LETTERS, 2008, 8 (04) :977-981
[4]   TiO2 sol-gel blocking layers for dye-sensitized solar cells [J].
Hart, Judy N. ;
Menzies, David ;
Cheng, Yi-Bing ;
Simon, George P. ;
Spiccia, Leone .
COMPTES RENDUS CHIMIE, 2006, 9 (5-6) :622-626
[5]   Carrier leakage blocking effect of high temperature sputtered TiO2film on dye-sensitized mesoporous photoelectrode [J].
Hattori, Ryo ;
Goto, Hajime .
THIN SOLID FILMS, 2007, 515 (20-21) :8045-8049
[6]   Implication of device functioning due to back reaction of electrons via the conducting glass substrate in dye sensitized solar cells [J].
Hore, S ;
Kern, R .
APPLIED PHYSICS LETTERS, 2005, 87 (26) :1-3
[7]   Control of dark current in photoelectrochemical (TiO2/I--I3-) and dye-sensitized solar cells [J].
Ito, S ;
Liska, P ;
Comte, P ;
Charvet, RL ;
Péchy, P ;
Bach, U ;
Schmidt-Mende, L ;
Zakeeruddin, SM ;
Kay, A ;
Nazeeruddin, MK ;
Grätzel, M .
CHEMICAL COMMUNICATIONS, 2005, (34) :4351-4353
[8]   HIGHLY EFFICIENT SEMICONDUCTING TIO2 PHOTOELECTRODES PREPARED BY AEROSOL PYROLYSIS [J].
KAVAN, L ;
GRATZEL, M .
ELECTROCHIMICA ACTA, 1995, 40 (05) :643-652
[10]   Charge transport and back reaction in solid-state dye-sensitized solar cells:: A study using intensity-modulated photovoltage and photocurrent spectroscopy [J].
Krüger, J ;
Plass, R ;
Grätzel, M ;
Cameron, PJ ;
Peter, LM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (31) :7536-7539