http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Ribierre, Jean-Charles,Li, Zhao,Liu, Xiao,Lacaze, Emmanuelle,Heinrich, Benoî,t,Mé,ry, Stephane,Sleczkowski, Piotr,Xiao, Yiming,Lafolet, Fré,dé,ric,Hashizume, Daisuke,Aoyama, Tet The Royal Society of Chemistry 2019 Journal of materials chemistry. C, Materials for o Vol.7 No.11
<P>We report on an improved melt-processing method to prepare organic semiconducting layers with large crystal size and enhanced charge carrier mobilities. The organic compound used in this work is a solution-processable oligo(<I>p</I>-phenylene vinylene) derivative substituted at both ends with pyrene moieties. Accurate control of the temperature during the recrystallization of this compound from the melt enables the formation of large single crystal monodomains in thin films. The melt-processed organic layer shows higher mobilities in transistor configuration than in spin-coated films, which can be attributed to the presence of large-size crystalline monodomains as evidenced by X-ray diffraction measurements. We also investigated the photophysical properties of this material in spin-coated and melted films and found an increase of the photoluminescence quantum yield with the size of the crystals in the organic layer. The advantage of this method over the spin coating also allowed observation of amplified spontaneous emission that was only achieved in the melted film due to its improved luminescence efficiency. Overall, this study demonstrates a simple and versatile method, which does not require the use of any solvent and vacuum, to fabricate organic layers with large crystal size, suitable for the realization of organic electronic and light-emitting devices.</P>
Charge carrier mobility study of a mesogenic thienothiophene derivative in bulk and thin films
Mazur, L.,Castiglione, A.,Ocytko, K.,Kameche, F.,Macabies, R.,Ainsebaa, A.,Kreher, D.,Heinrich, B.,Donnio, B.,Sanaur, S.,Lacaze, E.,Fave, J.L.,Matczyszyn, K.,Samoc, M.,Wu, J.W.,Attias, A.J.,Ribierre, Elsevier Science 2014 Organic electronics Vol.15 No.4
A novel mesogenic 2,5-bis-(5-octylthiophene)-thieno[3,2b]thiophene (TT) derivative has been synthesized. The fused-ring thiophene, end-capped with two octylthiophenes, exhibits ordered lamellar mesophases which were characterized by polarizing optical microscopy, differential scanning calorimetry and small-angle X-ray diffraction at various temperatures. The charge transport properties were investigated by time-of-flight technique as a function of temperature. On cooling from isotropic phase, a maximum hole mobility value of 0.07cm<SUP>2</SUP>V<SUP>-1</SUP>s<SUP>-1</SUP> was measured in the highly ordered mesophase of the bulk films. Field-effect transistor experiments on both solution and vacuum deposited thin films have also been performed. The solution-processed films exhibit charge carrier mobilities several orders of magnitude lower than values extracted from bulk time-of-flight curves and from vacuum deposited thin film transistors. This work provides evidence that the melt-processing route is an efficient alternative to commonly used solution-processing for fabrication of charge transporting layers from liquid crystalline semiconductors, with performances comparable to evaporation techniques.