Research Progress of Non-Fullerene Small-Molecule Acceptor Materials for Organic Solar Cells

被引:21
作者
Fu Yu [1 ]
Wang Fang [1 ]
Zhang Yan [1 ]
Fang Xu [1 ]
Lai Wenyong [1 ]
Huang Wei [1 ]
机构
[1] Nanjing Univ Posts & Telecommun, IAM, KLOEID, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
n-type small-molecular acceptors; wide spectral absorption; solution processing; organic photovoltaics; OPEN-CIRCUIT VOLTAGE; STARBURST MACROMOLECULAR MATERIALS; POWER-CONVERSION EFFICIENCY; ELECTRON-ACCEPTOR; PHOTOVOLTAIC CELLS; NAPHTHALENE DIIMIDES; CONJUGATED POLYMERS; PERYLENE BISIMIDE; DERIVATIVES; DESIGN;
D O I
10.6023/A13111142
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bulk heterojunction organic photovoltaics have been the subject of intensive academic interest over the past two decades. Numerous recent efforts have been directed towards this area with the vision of developing next-generation low-cost solar cells. In the field of bulk heterojunction organic photovoltaics, fullerene and its derivatives are an important class of n-type electron acceptor materials. However, their disadvantages such as narrow wavelength absorption, high affinity, poor solubility, have severely limited their wide application as electron acceptors for organic solar cells and have largely hampered further improvement of the device performance. Recently, a number of research efforts have been focused on the development of novel non-fullerene n-type small-molecule acceptors. Various design rules and interesting new materials have been explored. The non-fullerene n-type small-molecule acceptors usually appear to possess lots of attractive advantages, such as adjustable energy levels, facile synthesis, good solubility, low processing cost. More important, when compared to the fullerene and its derivatives, this kind of small-molecule acceptors has wider spectral absorption that allows to absorb more sunlight to generate electricity. Recent breakthroughs rely mostly on the development of novel high-performance acceptor materials and optimization of the device structures. The up-to-date power conversion efficiencies exceeding 4% with using non-fullerene small-molecule acceptor materials in bulk heterojunction organic solar cells have been achieved. In this review, recent advances of non-fullerene small-molecule n-type acceptor materials for organic solar cells are reviewed, including rylene diimide-based acceptors, pentacene-based acceptors, benzothiadiazole-based acceptors, 1,4-diketopyrrolo-[3,4-c]-pyrrole (DPP)-based acceptors, fluorene-based acceptors, fluoranthene-fused imide-based acceptors and so on. Meanwhile, the future trends on material design and development have also been discussed. This review on illustrating the influence of the molecular structures and corresponding photovoltaic properties would thus be helpful to further unravel the role of electron acceptors and shed light on exploring efficient n-type electron acceptor materials for high performance organic photovoltaic devices.
引用
收藏
页码:158 / 170
页数:13
相关论文
共 73 条
[1]   Design of New Electron Acceptor Materials for Organic Photovoltaics: Synthesis, Electron Transport, Photophysics, and Photovoltaic Properties of Oligothiophene-Functionalized Naphthalene Diimides [J].
Ahmed, Eilaf ;
Ren, Guoqiang ;
Kim, Felix S. ;
Hollenbeck, Emily C. ;
Jenekhe, Samson A. .
CHEMISTRY OF MATERIALS, 2011, 23 (20) :4563-4577
[2]   n-Type Organic Semiconductors in Organic Electronics [J].
Anthony, John E. ;
Facchetti, Antonio ;
Heeney, Martin ;
Marder, Seth R. ;
Zhan, Xiaowei .
ADVANCED MATERIALS, 2010, 22 (34) :3876-3892
[3]   Oligothiophene-S,S-dioxides:: a new class of thiophene-based materials [J].
Barbarella, G ;
Pudova, O ;
Arbizzani, C ;
Mastragostino, M ;
Bongini, A .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (05) :1742-1745
[4]   Oligothiophene S,S-dioxides.: Synthesis and electronic properties in relation to the parent oligothiophenes [J].
Barbarella, G ;
Favaretto, L ;
Sotgiu, G ;
Zambianchi, M ;
Antolini, L ;
Pudova, O ;
Bongini, A .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (16) :5497-5506
[5]   Chemistry of naphthalene diimides [J].
Bhosale, Sheshanath V. ;
Jani, Chintan H. ;
Langford, Steven J. .
CHEMICAL SOCIETY REVIEWS, 2008, 37 (02) :331-342
[6]   Branched thiophene-based oligomers as electron acceptors for organic photovoltaics [J].
Camaioni, N ;
Ridolfi, G ;
Fattori, V ;
Favaretto, L ;
Barbarella, G .
JOURNAL OF MATERIALS CHEMISTRY, 2005, 15 (22) :2220-2225
[7]   Oligothiophene-S,S-dioxides as a class of electron-acceptor materials for organic photovoltaics [J].
Camaioni, N ;
Ridolfi, G ;
Fattori, V ;
Favaretto, L ;
Barbarella, G .
APPLIED PHYSICS LETTERS, 2004, 84 (11) :1901-1903
[8]   ORGANIC SOLAR-CELLS - A REVIEW [J].
CHAMBERLAIN, GA .
SOLAR CELLS, 1983, 8 (01) :47-83
[9]   Novel Urea-Functionalized Quinacridone Derivatives: Ultrasound and Thermo Effects on Supramolecular Organogels [J].
Dou, Chuandong ;
Wang, Chenguang ;
Zhang, Hongyu ;
Gao, Hongze ;
Wang, Yue .
CHEMISTRY-A EUROPEAN JOURNAL, 2010, 16 (35) :10744-10751
[10]   A Narrow Optical Gap Small Molecule Acceptor for Organic Solar Cells [J].
Fang, Yuan ;
Pandey, Ajay K. ;
Nardes, Alexandre M. ;
Kopidakis, Nikos ;
Burn, Paul L. ;
Meredith, Paul .
ADVANCED ENERGY MATERIALS, 2013, 3 (01) :54-59