Hydrogen-bonded diketopyrrolopyrrole (DPP) pigments as organic semiconductors

被引:96
|
作者
Glowacki, Eric Daniel [1 ]
Coskun, Halime [1 ]
Blood-Forsythe, Martin A. [2 ]
Monkowius, Uwe [3 ]
Leonat, Lucia [1 ]
Grzybowski, Marek [4 ]
Gryko, Daniel [4 ]
White, Matthew Schuette [1 ]
Aspuru-Guzik, Alan [2 ]
Sariciftci, Niyazi Serdar [1 ]
机构
[1] Johannes Kepler Univ Linz, Linz Inst Organ Solar Cells LIOS, A-4040 Linz, Austria
[2] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[3] Johannes Kepler Univ Linz, Inst Inorgan Chem, A-4040 Linz, Austria
[4] Polish Acad Sci, Inst Organ Chem, Warsaw, Poland
关键词
Organic pigments; Organic field-effect transistors; Diketopyrrolopyrrole; Hydrogen-bonding; DFT calculations; FIELD-EFFECT TRANSISTORS; CONJUGATED POLYMERS; CHARGE-TRANSPORT; CRYSTAL; DESIGN; THERMOCHEMISTRY; ALUMINUM; ELECTRON; SPECTRA; INDIGO;
D O I
10.1016/j.orgel.2014.09.038
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Diketopyrrolopyrroles (DPPs) have recently gained attention as building-blocks for organic semiconducting polymers and small molecules, however the semiconducting properties of their hydrogen-bonded (H-bonded) pigment forms have not been explored. Herein we report on the performance of three archetypical H-bonded DPP pigments, which show ambipolar carrier mobilities in the range 0.01-0.06 cm(2)/V s in organic field-effect transistors. Their semiconducting properties are correlated with crystal structure, where an H-bonded crystal lattice supports close and relatively cofacial pi-pi stacking. To better understand transport in these systems, density functional theory calculations were carried out, indicating theoretical maximum ambipolar mobility values of similar to 0.3 cm(2)/V s. Based on these experimental and theoretical results, H-bonded DPPs represent a viable alternative to more established DPP-containing polymers and small molecules where H-bonding is blocked by N-alkylation. (C) 2014 The Authors. Published by Elsevier B.V.
引用
收藏
页码:3521 / 3528
页数:8
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