Improved Performance of Polymer:Polymer Solar Cells by Doping Electron-Accepting Polymers with an Organosulfonic Acid

被引:42
|
作者
Nam, Sungho [1 ]
Shin, Minjung [1 ,5 ]
Kim, Hwajeong [1 ]
Ha, Chang-Sik [2 ]
Ree, Moonhor [3 ,4 ]
Kim, Youngkyoo [1 ]
机构
[1] Kyungpook Natl Univ, Dept Chem Engn, Organ Nanoelect Lab, Taegu 702701, South Korea
[2] Pusan Natl Univ, Dept Polymer Sci & Engn, Pusan 609735, South Korea
[3] Pohang Univ Sci & Technol POSTECH, Div Adv Mat Sci, Ctr Electrophoto Behav Adv Mol Syst, Dept Chem,BK Sch Mol Sci, Pohang 790784, South Korea
[4] Pohang Univ Sci & Technol POSTECH, Polymer Res Inst, Pohang 790784, South Korea
[5] LG Innotek, Solar Cell Business Team, Gyeonggi Do 447705, South Korea
基金
新加坡国家研究基金会;
关键词
Polymer Solar Cells; Electron-Accepting Polymers; Organosulfonic Acids; Doping; Electron Mobility; RAY PHOTOELECTRON-SPECTROSCOPY; PHOTOVOLTAIC DEVICES; CONJUGATED POLYMERS; FILMS; MORPHOLOGY;
D O I
10.1002/adfm.201101215
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The performance of polymer:polymer solar cells that are made using blend films of poly(3-hexylthiophene) (P3HT) and poly(9,9-dioctylfluorene-co- benzothiadiazole (F8BT) is improved by doping the F8BT polymer with an organosulfonic acid [4-ethylbezenesulfonic acid (EBSA)]. The EBSA doping of F8BT, to form F8BT-EBSA, is performed by means of a two-stage reaction at room temperature and 60 degrees C with various EBSA weight ratios. The X-ray photoelectron spectroscopy measurement reveals that both sulfur and nitrogen atoms in the F8BT polymer are affected by the EBSA doping. The F8BT-EBSA films exhibit huge photoluminescence quenching, ionization potential shift toward lower energy, and greatly enhanced electron mobility. The short-circuit current density of solar cells is improved by ca. twofold (10 wt.% EBSA doping), while the open-circuit voltage increases by ca. 0.4 V. Consequently, the power conversion efficiency was improved by ca. threefold, even though the optical density of the P3HT:F8BT-EBSA blend film is reduced by 10 wt.% EBSA doping due to the nanostructure and surface morphology change.
引用
收藏
页码:4527 / 4534
页数:8
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