Doping effect of dodecyl benzene sulphonic acid in poly(3-hexylthiophene)-P3HT-films

被引:14
作者
Alveroglu, Esra [1 ]
机构
[1] Istanbul Tech Univ, Fac Sci & Letters, Dept Engn Phys, TR-34469 Istanbul, Turkey
关键词
Organic semiconductor; Doping; P3HT; Protonation; Sulphonic acid; SOLAR-CELLS; POLYMER;
D O I
10.1016/j.molstruc.2015.01.006
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
We demonstrated that how dodecyl benzene sulphonic acid (DBSA) as a small-molecular dopant, affects the spectroscopic, electronic and structural properties of poly(3-hexylthiophene) (P3HT). The DBSA volume ratio was varied from 0.001 mu L to 30 mu L per 1 mL P3HT solvent in p-xylene. DBSA doping reaction was confirmed by the emerging huge absorption peak at the wavelength of similar to 800 nm while the ionization potential and nanostructure of P3HT films were highly affected. Additionally, conductivity of P3HT films increased nearly 1000 times at 30 mu L DBSA. The crystallinity, as well as the conductivity and the UV-Vis absorption changed with the presence of P3HT. P3HT grain sized crystals seems to be disturbed by the addition of DBSA, but still remained even more DBSA was introduced. DBSA doping has interesting properties when incorporated in OFTs, OPVs and bioelectronics applications, so addition of DBSA can open new pathways for structural, spectroscopic and electronic control of organic semiconductor's blends. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:86 / 92
页数:7
相关论文
共 17 条
[1]   Effects of solvent and annealing on the improved performance of solar cells based on poly(3-hexylthiophene): Fullerene [J].
Al-Ibrahim, M ;
Ambacher, O ;
Sensfuss, S ;
Gobsch, G .
APPLIED PHYSICS LETTERS, 2005, 86 (20) :1-3
[2]   Effect of interchain interactions on the absorption and emission of poly(3-hexylthiophene) -: art. no. 064203 [J].
Brown, PJ ;
Thomas, DS ;
Köhler, A ;
Wilson, JS ;
Kim, JS ;
Ramsdale, CM ;
Sirringhaus, H ;
Friend, RH .
PHYSICAL REVIEW B, 2003, 67 (06)
[3]   Influence of nanomorphology on the photovoltaic action of polymer-fullerene composites [J].
Chirvase, D ;
Parisi, J ;
Hummelen, JC ;
Dyakonov, V .
NANOTECHNOLOGY, 2004, 15 (09) :1317-1323
[4]   A new route to synthesize high degree polythiophene in a room temperature melt medium [J].
Geetha, S ;
Trivedi, DC .
SYNTHETIC METALS, 2005, 155 (01) :232-239
[5]   Efficient tandem polymer solar cells fabricated by all-solution processing [J].
Kim, Jin Young ;
Lee, Kwanghee ;
Coates, Nelson E. ;
Moses, Daniel ;
Nguyen, Thuc-Quyen ;
Dante, Mark ;
Heeger, Alan J. .
SCIENCE, 2007, 317 (5835) :222-225
[6]   Air stable polymer photovoltaics based on a process free from vacuum steps and fullerenes [J].
Krebs, Frederik C. .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2008, 92 (07) :715-726
[7]   All solution roll-to-roll processed polymer solar cells free from indium-tin-oxide and vacuum coating steps [J].
Krebs, Frederik C. .
ORGANIC ELECTRONICS, 2009, 10 (05) :761-768
[8]  
Lee J.H., 2014, ORGAN ELECT, V15
[9]   Synthesis and photovoltaic properties of oligothiophene derivatives [J].
Liu, P ;
Wang, XB ;
Zhang, YM ;
Zhou, XP ;
Deng, WH .
SYNTHETIC METALS, 2005, 155 (03) :565-568
[10]   Doping of organic semiconductors [J].
Luessem, B. ;
Riede, M. ;
Leo, K. .
PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE, 2013, 210 (01) :9-43