Structure-Function Relationship of Organic Semiconductors: Detailed Insights From Time-Resolved EPR Spectroscopy

被引:46
作者
Biskup, Till [1 ]
机构
[1] Univ Freiburg, Inst Phys Chem, Freiburg, Germany
关键词
organic semiconductors; EPR (electron paramagnetic resonance); triplet state; structure-function relationship; electronic structure; morphology; ELECTRON-PARAMAGNETIC-RESONANCE; HETEROJUNCTION SOLAR-CELLS; CORRELATED RADICAL PAIRS; TRIPLET-STATE DELOCALIZATION; SPIN TRANSIENT NUTATION; CHARGE SEPARATION; HIGH-PERFORMANCE; CONJUGATED POLYMERS; HIGH-MOBILITY; POLARON DELOCALIZATION;
D O I
10.3389/fchem.2019.00010
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic photovoltaics (OPV) is a promising technology to account for the increasing demand for energy in formof electricity. Whereas the last decades have seen tremendous progress in the field witnessed by the steady increase in efficiency of OPV devices, we still lack proper understanding of fundamental aspects of light-energy conversion, demanding for systematic investigation on a fundamental level. A detailed understanding of the electronic structure of semiconducting polymers and their building blocks is essential to develop efficient materials for organic electronics. Illuminating conjugated polymers not only leads to excited states, but sheds light on some of the most important aspects of device efficiency in organic electronics as well. The interplay between electronic structure, morphology, flexibility, and local ordering, while at the heart of structure-function relationship of organic electronic materials, is still barely understood. (Time-resolved) electron paramagnetic resonance (EPR) spectroscopy is particularly suited to address these questions, allowing one to directly detect paramagnetic states and to reveal their spin-multiplicity, besides its clearly superior spectral resolution compared to optical methods. This article aims at giving a non-specialist audience an overview of what EPR spectroscopy and particularly its time-resolved variant (TREPR) can contribute to unraveling aspects of structure-function relationship in organic semiconductors.
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页数:22
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共 207 条
[1]  
Abragam A., 1983, PRINCIPLES NUCL MAGN
[2]   Multifrequency EPR analysis of the positive polaron in I2-doped poly(3-hexylthiophene) and in poly[2-methoxy-5-(3,7-dimethyloctyloxy)]-1,4-phenylenevinylene [J].
Aguirre, Aranzazu ;
Gast, Peter ;
Orlinskii, Sergey ;
Akimoto, Ikuko ;
Groenen, Edgar J. J. ;
El Mkami, Hassane ;
Goovaerts, Etienne ;
Van Doorslaer, Sabine .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (47) :7129-7138
[3]   An electron-accepting molecular unit exhibiting an orientational preference favorable for organic photovoltaic applications [J].
Akaike, Kouki ;
Andoa, Shinji ;
Enozawa, Hideo ;
Kosaka, Atsuko ;
Kajitani, Takashi ;
Fukushima, Takanori .
THIN SOLID FILMS, 2015, 583 :34-39
[4]  
[Anonymous], P INT S AM U BELR LE
[5]  
[Anonymous], 1993, Principles of electron spin resonance
[6]  
[Anonymous], THESIS
[7]  
[Anonymous], 1963, Principles of magnetic resonance: with examples from solid state physics
[8]  
[Anonymous], 1991, PRINCIPLES PULSE ELE
[9]   Initial photooxidation mechanism leading to reactive radical formation of polythiophene derivatives [J].
Aoyama, Yoshinori ;
Yamanari, Toshihiro ;
Murakami, Takurou N. ;
Nagamori, Tatsuya ;
Marumoto, Kazuhiro ;
Tachikawa, Hiroto ;
Mizukado, Junji ;
Suda, Hiroyuki ;
Yoshida, Yuji .
POLYMER JOURNAL, 2015, 47 (01) :26-30
[10]   ELECTRON-SPIN TRANSIENT NUTATION - A NEW APPROACH TO SIMPLIFY THE INTERPRETATION OF ESR-SPECTRA [J].
ASTASHKIN, AV ;
SCHWEIGER, A .
CHEMICAL PHYSICS LETTERS, 1990, 174 (06) :595-602