On the Air Stability of n-Channel Organic Field-Effect Transistors: A Theoretical Study of Adiabatic Electron Affinities of Organic Semiconductors

被引:139
作者
Chang, Yu-Chang [1 ]
Kuo, Ming-Yu [2 ]
Chen, Chih-Ping [1 ]
Lu, Hsiu-Feng [1 ]
Chao, Ito [1 ]
机构
[1] Acad Sinica, Inst Chem, Taipei 11529, Taiwan
[2] Natl Chi Nan Univ, Dept Appl Chem, Nantou 545, Taiwan
关键词
THIN-FILM TRANSISTORS; POLYCYCLIC AROMATIC-HYDROCARBONS; DENSITY-FUNCTIONAL THEORY; DIIMIDE SEMICONDUCTORS; PERFORMANCE; MOBILITY; CORE; NAPHTHALENE; TRANSPORT; ANTHRACENE;
D O I
10.1021/jp1025625
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
In an air-stable n-channel organic field-effect transistor (OFET), the charge carrier (i.e., the radical anion of an organic semiconductor (OSC)) has to be stable enough against ambient oxidants such as O-2 and H2O. It has been suggested that OSCs with large enough electron affinity (EA) will possess air-stable charge carriers, but extensive correlation between air stability and EA has not been established. We have studied 47 existing n-channel OSCs with different molecular core structures and device configurations. A correlation between calculated adiabatic EA and air stability was established, and the threshold value found at the B3LYP/6-31+G*//B3LYP/6-31G** level for air stability was ca. 2.8 eV. This information provides a foundation for theoretical screening of potential n-channel OFETs before their synthesis and facilitates the discussion of the complex device degradation mechanism. Analysis of EAs of derivatives of perylenetetracarboxylic diimide (PDI) and naphthalenetetracarboxylic diimide (NDI) also sheds light on the roles of various substituents.
引用
收藏
页码:11595 / 11601
页数:7
相关论文
共 67 条
[21]   Perfluorinated Polycyclic Aromatic Hydrocarbons: Anthracene, Phenanthrene, Pyrene, Tetracene, Chrysene, and Triphenylene [J].
Feng, Xuejun ;
Li, Qianshu ;
Gu, Jiande ;
Cotton, F. Albert ;
Xie, Yaoming ;
Schaefer, Henry F., III .
JOURNAL OF PHYSICAL CHEMISTRY A, 2009, 113 (05) :887-894
[22]  
Frisch M., 2004, GAUSSIAN 03 REVISION, DOI DOI 10.1016/J.MOLSTRUC.2017.03.014
[23]   Cyclopentadiene annulated polycyclic aromatic hydrocarbons: Investigations of electron affinities [J].
Gonzales, JM ;
Barden, CJ ;
Brown, ST ;
Schleyer, PV ;
Schaefer, HF ;
Li, QS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (04) :1064-1071
[24]   A Crystal-Engineered Hydrogen-Bonded Octachloroperylene Diimide with a Twisted Core: An n-Channel Organic Semiconductor [J].
Gsaenger, Marcel ;
Oh, Joon Hak ;
Koenemann, Martin ;
Hoeffken, Hans Wolfgang ;
Krause, Ana-Maria ;
Bao, Zhenan ;
Wuerthner, Frank .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (04) :740-743
[25]   High-mobility air-stable n-type semiconductors with processing versatility:: Dicyanoperylene-3,4:9,10-bis(dicarboximides) [J].
Jones, BA ;
Ahrens, MJ ;
Yoon, MH ;
Facchetti, A ;
Marks, TJ ;
Wasielewski, MR .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (46) :6363-6366
[26]   Tuning orbital energetics in arylene diimide semiconductors. Materials design for ambient stability of n-type charge transport [J].
Jones, Brooks A. ;
Facchetti, Antonio ;
Wasielewski, Michael R. ;
Marks, Tobin J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (49) :15259-15278
[27]   Cyanonaphthalene diimide semiconductors for air-stable, flexible, and optically transparent n-channel field-effect transistors [J].
Jones, Brooks A. ;
Facchetti, Antonio ;
Marks, Tobin J. ;
Wasielewski, Michael R. .
CHEMISTRY OF MATERIALS, 2007, 19 (11) :2703-2705
[28]   Naphthalenetetracarboxylic diimide-based n-channel transistor semiconductors: Structural variation and thiol-enhanced gold contacts [J].
Katz, HE ;
Johnson, J ;
Lovinger, AJ ;
Li, WJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (32) :7787-7792
[29]   A soluble and air-stable organic semiconductor with high electron mobility [J].
Katz, HE ;
Lovinger, AJ ;
Johnson, J ;
Kloc, C ;
Siegrist, T ;
Li, W ;
Lin, YY ;
Dodabalapur, A .
NATURE, 2000, 404 (6777) :478-481
[30]  
Katz HE, 2001, CHEMPHYSCHEM, V2, P167, DOI 10.1002/1439-7641(20010316)2:3<167::AID-CPHC167>3.0.CO