Towards understanding the doping mechanism of organic semiconductors by Lewis acids

被引:169
|
作者
Yurash, Brett [1 ]
Cao, David Xi [1 ]
Brus, Viktor V. [1 ]
Leifert, Dirk [1 ]
Wang, Ming [2 ]
Dixon, Alana [1 ]
Seifrid, Martin [1 ]
Mansour, Ahmed E. [3 ,4 ]
Lungwitz, Dominique [3 ,4 ]
Liu, Tuo [5 ]
Santiago, Peter J. [1 ]
Graham, Kenneth R. [5 ]
Koch, Norbert [3 ,4 ]
Bazan, Guillermo C. [1 ]
Thuc-Quyen Nguyen [1 ]
机构
[1] Univ Calif Santa Barbara, Ctr Polymers & Organ Solids, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Donghua Univ, Ctr Adv Low Dimens Mat, Shanghai, Peoples R China
[3] Humboldt Univ, Inst Phys, Berlin, Germany
[4] Humboldt Univ, IRIS Adlershof, Berlin, Germany
[5] Univ Kentucky, Dept Chem, Lexington, KY USA
基金
美国国家科学基金会;
关键词
CONJUGATED POLYMERS; TRIS(PENTAFLUOROPHENYL)BORANE; CHEMISTRY; TRANSPORT; WATER; PHTHALOCYANINE; AGGREGATION; GENERATION; REACTIVITY; COMPLEXES;
D O I
10.1038/s41563-019-0479-0
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
Precise doping of organic semiconductors allows control over the conductivity of these materials, an essential parameter in electronic applications. Although Lewis acids have recently shown promise as dopants for solution-processed polymers, their doping mechanism is not yet fully understood. In this study, we found that B(C6F5)(3) is a superior dopant to the other Lewis acids investigated (BF3, BBr3 and AlCl3). Experiments indicate that Lewis acid-base adduct formation with polymers inhibits the doping process. Electron-nuclear double-resonance and nuclear magnetic resonance experiments, together with density functional theory, show that p-type doping occurs by generation of a water-Lewis acid complex with substantial Bronsted acidity, followed by protonation of the polymer backbone and electron transfer from a neutral chain segment to a positively charged, protonated one. This study provides insight into a potential path for protonic acid doping and shows how trace levels of water can transform Lewis acids into powerful Bronsted acids.
引用
收藏
页码:1327 / +
页数:9
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