Real time studies of thiophene-based conjugated oligomer solidification

被引:7
|
作者
Mikayelyan, Eduard [1 ]
Bakirov, Artem V. [2 ,3 ]
Shcherbina, Maxim A. [2 ,4 ]
Chvalun, Sergei N. [4 ]
Ponomarenko, Sergei A. [2 ,3 ,5 ]
Grigorian, Souren [1 ]
机构
[1] Univ Siegen, Fachbereich Phys, D-57068 Siegen, Germany
[2] Russian Acad Sci, Enikolopov Inst Synthet Polymer Mat, Moscow 117393, Russia
[3] Sci & Res Ctr Kurchatov Inst, Moscow 123182, Russia
[4] Moscow Inst Phys & Technol, Dolgoprudnyi 141700, Russia
[5] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia
关键词
ORGANIC SEMICONDUCTORS; OLIGOTHIOPHENES; MONOLAYERS; BEHAVIOR; ALPHA;
D O I
10.1039/c4ra13109f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The understanding of the charge transport depending on crystalline structure in organic semiconductors is an important aspect of their functionality in different organic electronic applications. For this reason we performed in situ grazing incidence X-ray diffraction (GIXD) studies to trace the solidification. Simultaneously applying the voltage to the thiophene-based oligomer system the current response was measured. The complex behaviour of the solidification process was monitored from the structure and electrical performance and the highest current was observed for the final solid film. Real time studies revealed that for the oligomers the high crystallinity is a key factor for the improvement of the charge transport.
引用
收藏
页码:1319 / 1322
页数:4
相关论文
共 50 条
  • [1] Thiophene-based branched conjugated polymers.
    Sankaran, B
    Vaia, RA
    Tan, LS
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2001, 221 : U310 - U310
  • [2] Selenophene and Thiophene-Based Conjugated Polymer Gels
    Li, Sheng
    He, Keqiang
    Prince, Elisabeth
    Li, Yuning
    Seferos, Dwight S.
    ACS MATERIALS LETTERS, 2020, 2 (12): : 1617 - 1623
  • [3] Amplified spontaneous emission from a soluble thiophene-based oligomer
    Anni, M
    Gigli, G
    Cingolani, R
    Zavelani-Rossi, M
    Gadermaier, C
    Lanzani, G
    Barbarella, G
    Favaretto, L
    APPLIED PHYSICS LETTERS, 2001, 78 (18) : 2679 - 2681
  • [4] New thiophene-based conjugated macrocycles for optoelectronic applications
    dos Santos, John Marques
    Jagadamma, Lethy Krishnan
    Cameron, Joseph
    Wiles, Alan A.
    Wilson, Claire
    Skabara, Peter J.
    Samuel, Ifor D. W.
    Cooke, Graeme
    JOURNAL OF MATERIALS CHEMISTRY C, 2021, 9 (45) : 16257 - 16271
  • [5] A Conjugated Thiophene-Based Rotaxane: Synthesis, Spectroscopy, and Modeling
    Zalewski, Leszek
    Wykes, Michael
    Brovelli, Sergio
    Bonini, Massimo
    Breiner, Thomas
    Kastler, Marcel
    Doetz, Florian
    Beljonne, David
    Anderson, Harry L.
    Cacialli, Franco
    Samori, Paolo
    CHEMISTRY-A EUROPEAN JOURNAL, 2010, 16 (13) : 3933 - 3941
  • [6] Thiophene-based conjugated oligomers for organic solar cells
    Zhang, Fan
    Wu, Dongqing
    Xu, Youyong
    Feng, Xinliang
    JOURNAL OF MATERIALS CHEMISTRY, 2011, 21 (44) : 17590 - 17600
  • [7] Interactions of a zwitterionic thiophene-based conjugated polymer with surfactants
    Costa, Telma
    de Azevedo, Diego
    Stewart, Beverly
    Knaapila, Matti
    Valente, Artur J. M.
    Kraft, Mario
    Scherf, Ullrich
    Burrows, Hugh D.
    POLYMER CHEMISTRY, 2015, 6 (46) : 8036 - 8046
  • [8] Synthesis of a benzothiadiazole/thiophene-based oligomer for bulk heterojunction photovoltaic cells
    Li, Ji-Cheng
    Lee, Hye-Young
    Lee, Soo-Hyoung
    Zong, Kyukwan
    Jin, Sung-Ho
    Lee, Youn-Sik
    SYNTHETIC METALS, 2009, 159 (3-4) : 201 - 208
  • [9] Synthesis of New Thiophene-Based π-Conjugated Organic Compounds and Polymer
    Usui, Motoaki
    Fukumoto, Hiroki
    Yamamoto, Takakazu
    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2010, 83 (11) : 1397 - 1399
  • [10] Thiophene-Based Conjugated Polymers with Photolabile Solubilizing Side Chains
    Smith, Zachary C.
    Meyer, Dianne M.
    Simon, Marc G.
    Staii, Cristian
    Shukla, Deepak
    Thomas, Samuel W., III
    MACROMOLECULES, 2015, 48 (04) : 959 - 966