Influence of solution heating on the properties of PEDOT:PSS colloidal solutions and impact on the device performance of polymer solar cells

被引:37
作者
Friedel, Bettina [1 ,2 ]
Brenner, Thomas J. K. [2 ]
McNeill, Christopher R. [2 ]
Steiner, Ullrich [2 ]
Greenham, Neil C. [2 ]
机构
[1] Graz Univ Technol, Inst Solid State Phys, A-8010 Graz, Austria
[2] Univ Cambridge, Cavendish Lab, Dept Phys, Cambridge CB3 0HE, England
基金
英国工程与自然科学研究理事会;
关键词
Organic solar cell; PEDOT:PSS; Phase transition; Particle size; INDIUM-TIN-OXIDE; PHOTOELECTRON-SPECTROSCOPY; THIN-FILMS; POLY(STYRENE SULFONATE); WORK FUNCTION; PSS; CONDUCTIVITY; STABILITY; LAYER; POLYELECTROLYTES;
D O I
10.1016/j.orgel.2011.07.003
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We have investigated the effects of temperature variation on colloidal solutions of the electrode polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) (PEDOT:PSS) and its consequences for photovoltaic devices using conjugated polymer blends as the photoactive material. By variation of the PEDOT:PSS solution temperature between 20 and 90 degrees C we observed reversible temperature-dependent change in size of the PEDOT:PSS particles. This process is associated with temperature and concentration dependent phase transitions of the PSS electrolyte chains. We found optimum device performance, in particular high quantum efficiency and power conversion efficiency for solar cells, with PEDOT:PSS layers produced from 70 degrees C solutions. After consideration of film morphology, particle size, conductivity and work function, we conclude that improved device performance originates from enhanced conductivity in films deposited from heated solutions. While film conductivity increases mo\notonically with solution temperature, devices produced using solution temperatures greater than 70 degrees C suffer from the increased work function of the PEDOT:PSS layer. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1736 / 1745
页数:10
相关论文
共 45 条
[1]   Nonequilibrium Polymer Rheology in Spin-Cast Films [J].
Barbero, David R. ;
Steiner, Ullrich .
PHYSICAL REVIEW LETTERS, 2009, 102 (24)
[2]   Conformation of poly(styrene sulfonate) layers physisorbed from high salt solution studied by force measurements on two different length scales [J].
Block, Stephan ;
Helm, Christiane A. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (31) :9318-9327
[3]   Device physics of inverted all-polymer solar cells [J].
Brenner, Thomas J. K. ;
Hwang, Inchan ;
Greenham, Neil C. ;
McNeill, Christopher R. .
JOURNAL OF APPLIED PHYSICS, 2010, 107 (11)
[4]   Detailed Molecular Dynamics Simulations of a Model NaPSS in Water [J].
Carrillo, Jan-Michael Y. ;
Dobrynin, Andrey V. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2010, 114 (29) :9391-9399
[5]   Effect of ionization potential change in poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid) on the performance of polymer light emitting diodes due to its reaction with indium tin oxide [J].
Chang, Chih-Hao ;
Chen, Show-An .
APPLIED PHYSICS LETTERS, 2007, 91 (10)
[6]   Polymer solar cells with enhanced open-circuit voltage and efficiency [J].
Chen, Hsiang-Yu ;
Hou, Jianhui ;
Zhang, Shaoqing ;
Liang, Yongye ;
Yang, Guanwen ;
Yang, Yang ;
Yu, Luping ;
Wu, Yue ;
Li, Gang .
NATURE PHOTONICS, 2009, 3 (11) :649-653
[7]   Conductivity, morphology, interfacial chemistry, and stability of poly(3,4-ethylene dioxythiophene)-poly(styrene sulfonate): A photoelectron spectroscopy study [J].
Crispin, X ;
Marciniak, S ;
Osikowicz, W ;
Zotti, G ;
Van der Gon, AWD ;
Louwet, F ;
Fahlman, M ;
Groenendaal, L ;
De Schryver, F ;
Salaneck, WR .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2003, 41 (21) :2561-2583
[8]   Stability of the interface between indium-tin-oxide and poly(3,4-ethylenedioxythiophene)/poly(styrenesulfonate) in polymer light-emitting diodes [J].
de Jong, MP ;
van IJzendoorn, LJ ;
de Voigt, MJA .
APPLIED PHYSICS LETTERS, 2000, 77 (14) :2255-2257
[9]   Theory of polyelectrolytes in solutions and at surfaces [J].
Dobrynin, AV ;
Rubinstein, M .
PROGRESS IN POLYMER SCIENCE, 2005, 30 (11) :1049-1118
[10]   Innovative applications of controlled particle interactions [J].
Franks, GV .
CHEMICAL ENGINEERING RESEARCH & DESIGN, 2005, 83 (A7) :937-945