Characterization of high-photovoltage CuPc-based solar cell structures

被引:41
作者
Singh, VP [1 ]
Parsarathy, B
Singh, RS
Aguilera, A
Anthony, J
Payne, M
机构
[1] Univ Kentucky, Dept Elect & Comp Engn, Lexington, KY 40506 USA
[2] Univ Kentucky, Ctr Nanoscale Sci & Engn, Lexington, KY 40506 USA
[3] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
关键词
CuPc/PTCBI solar cells; organic semiconductors; electron transport modeling;
D O I
10.1016/j.solmat.2005.04.016
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Organic solar cells of the configuration ITO/PEDOT:PSS/CuPc/PTCBI/Al (Indium Tin Oxide/poly(3,4-ethylenedioxythiophene): polystyrene sulfonic acid/Copper phthalocyanine/ 3,4,9,10-perylenetetracarboxylic bisbenzimidazole/Aluminum) were investigated. A high open circuit voltage (V-OC) of 1.15 V was obtained when the PTCBI layer was 7 nm thick. Lower V-oc values were observed for the same structure with silver, copper and gold electrodes instead of aluminum. However, short-circuit current density (J(SC)) with these electrodes was much higher (4 mA/cm(2)) than in the case of aluminum (0.12mA/cm(2)). Incorporating a 10nm thick US interlayer between PTCBI and aluminum resulted in an increase in current density to 0.3 mA/ cm(2). Results were interpreted in terms of a modified CuPc/Al Schottky diode for the thin PTCBI case and a CuPc/PTCBI heterojunction for the thick PTCBI case. Also, the formation of a thin, protective aluminum oxide layer under the aluminum electrode was postulated. For devices with silver, copper and gold electrodes, absence of this protective layer was thought to be the cause of a relatively lower V-oc and higher J(SC). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:798 / 812
页数:15
相关论文
共 16 条
[1]   Interface-limited injection in amorphous organic semiconductors [J].
Baldo, MA ;
Forrest, SR .
PHYSICAL REVIEW B, 2001, 64 (08)
[2]   THIN-FILM CDS/CDTE SOLAR-CELL WITH 15.8-PERCENT EFFICIENCY [J].
BRITT, J ;
FEREKIDES, C .
APPLIED PHYSICS LETTERS, 1993, 62 (22) :2851-2852
[3]   Stability of CdTe/CdS thin-film solar cells [J].
Dobson, KD ;
Visoly-Fisher, I ;
Hodes, G ;
Cahen, D .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2000, 62 (03) :295-325
[4]  
DWEIDEN AW, 1975, PHYS STATUS SOLIDI A, V27, P223
[5]   WORK FUNCTION MEASUREMENTS ON (100), (110) AND (111) SURFACES OF ALUMINUM [J].
EASTMENT, RM ;
MEE, CHB .
JOURNAL OF PHYSICS F-METAL PHYSICS, 1973, 3 (09) :1738-1745
[6]   Metal-dependent charge transfer and chemical interaction at interfaces between 3,4,9,10-perylenetetracarboxylic bisimidazole and gold, silver and magnesium [J].
Hill, I. G. ;
Schwartz, J. ;
Kahn, A. .
ORGANIC ELECTRONICS, 2000, 1 (01) :5-13
[7]   Chemistry and electronic properties of metal-organic semiconductor interfaces: Al, Ti, In, Sn, Ag, and Au on PTCDA [J].
Hirose, Y ;
Kahn, A ;
Aristov, V ;
Soukiassian, P ;
Bulovic, V ;
Forrest, SR .
PHYSICAL REVIEW B, 1996, 54 (19) :13748-13758
[8]   Improvement of the efficiency of phthalocyanine organic Schottky solar cells with ITO electrode treatment [J].
Kwong, CY ;
Djurisic, AB ;
Chui, PC ;
Lam, LSM ;
Chan, WK .
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 2003, 77 (3-4) :555-560
[9]   Factors limiting the efficiency of molecular photovoltaic devices [J].
Nelson, J ;
Kirkpatrick, J ;
Ravirajan, P .
PHYSICAL REVIEW B, 2004, 69 (03)
[10]   Lithium doping of semiconducting organic charge transport materials [J].
Parthasarathy, G ;
Shen, C ;
Kahn, A ;
Forrest, SR .
JOURNAL OF APPLIED PHYSICS, 2001, 89 (09) :4986-4992