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1.
Small molecule additives have been shown to increase the device efficiency of conjugated polymer (donor) and fullerene derivative (acceptor) based organic solar cells by modifying the morphology of the device active layer. In this paper we conduct a systematic study of how additives affect the donor‐acceptor morphology using molecular dynamics simulations of blends of thiophene‐based oligomers, mimicking poly(3‐dodecylthiophene) (P3DDT) or poly(2,2′:5′,2”‐3,3”‐didocyl‐terthiophene) (PTTT), and fullerene derivatives with additives of varying length and chemical functionalization, mimicking experimentally used additives like methyl ester additives, diiodooctane, and alkanedithiols. We find that functionalization of additives with end groups that are attracted to acceptor molecules are necessary to induce increased donor‐acceptor macrophase separation. In blends where acceptors intercalate between oligomer alkyl side chains, functionalized additives decrease acceptor intercalation. Functionalized additives with shorter alkyl segments increase acceptor macrophase separation more than additives with same chemical functionalization but longer alkyl segments. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1046–1057  相似文献   
2.
Proton conductivity of phosphoric acid derivative of fullerene   总被引:1,自引:0,他引:1  
The proton conductive property of methano [60] fullerene diphosphoric acid has been investigated under various humidity conditions at the temperature range between 15 and 45 °C. It shows proton conductivity as high as 10−2 S cm−1 at 25 °C under relative humidity of 95%. Thermal analyses including TG–DTA and thermal desorption mass spectroscopy (TDS) confirm that the compound is thermally stable up to 200 °C. Proton conduction of the compound depends very much on humidity or water content. The logarithmic conductivity at 25 °C is increased linearly with increasing relative humidity. The activation energy (Ea) estimated from the slope of log(σT) vs. 1/T is decreased from 1.08 to 0.52 eV, as the relative humidity is increased from 40% to 75%. The humidity dependence of conductivity is discussed in the light of the observed hydration isotherm.  相似文献   
3.
通过溶液共混及流涎成膜法制备了一系列不同C60乙醇胺含量的壳聚糖共混膜。以及含Cu(Ⅱ)的C60乙醇胺/壳聚糖共混膜。研究表明,C60乙醇胺/壳聚糖共混膜具有优异的可调紫外滤光性能,随着C60乙醇胺含量的增加,其紫外滤光波长从200nm红移至400nm左右。在该复合体系中引入Cu(Ⅱ)能有效改善膜的紫外光学性能,同时还初步探讨了这类复合材料的紫外滤光机制。  相似文献   
4.
Fullerene deuteride was obtained by the reaction of deuterium with solid palladium fulleride C60Pd4.9 under fairly mild conditions. The compound was identified by FD-MS, UV-Vis and IR spectroscopies, and TLC.Translated from Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 483–484, February, 1996  相似文献   
5.
Doping of conductive fullerene particles to the formulation of conventional holographic polymer dispersed liquid crystal‐induced dual effects of reducing both droplet coalescence and operating voltage. Fullerene induced an induction period which otherwise does not exist, followed by a gradual increase of diffraction efficiency to a saturation value being increased with increasing fullerene content. The increased diffraction efficiency was caused by the decreased droplet coalescence which was due to the hindered migration of LC by the fullerene particles. On the other hand, doped fullerene particles augmented the conductivity of polymer phase and hence the local electrical field imposed on LC droplet, which overcome the threshold for driving and reduced operating voltage and response times. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5590–5596, 2007  相似文献   
6.
介绍了19世纪存在于澳大利亚土著中的一种婚姻形式—级别婚,从群论的角度说明级别婚的三种主要形式都对应于一个对称群,从而可以用几何方法形象的表示这种婚姻形式;进而,从对称的观点说明婚姻形式从简单到复杂的演化过程,代数上对应于对称群阶数的增加,几何上则对应于对称性的加强.  相似文献   
7.
采用某些特殊的放电和提取方法,如反向放电和甲苯高温高压提取等可以有效地提高稀土富勒烯的生成效率[‘,‘’,并已先后成功高效地合成了许多含稀土富勒烯「‘’.对其提纯、表征、衍生和应用也进行了研究[‘-’j.但对影响稀土富勒烯生成的因素研究较少.在石墨律中同时填入La,Y,Sc的稀土氧化物,对其稀土富勒烯生成效率的情况进行了研究,认为稀土元素的第一电离能是影响稀土富勒烯生成的主要因素‘’,’‘.Moro等采用激光和热解吸质谱对稀土富勒烯的研究结果表明,稀土元素的氧化态是影响稀土富勒烯生成的决定性因素”’.本…  相似文献   
8.
The calixarene-fullerene interaction,which causes only a slight change in the absorptionspectra, has been substantiated by calorimetricmeasurements: the H° values arecomparable with those obtained from the associationconstants estimated by a spectroscopic method. Furthermore, we determined the association constantbetween homooxacalix[3]arene and [60]fullerenederivatives with a porphyrin moiety by fluorescencespectra.  相似文献   
9.
The combined electrochemical reduction of fullerene C60 in the presence of p-bromo-benzoyldibromomethane or bis(diisopropoxyphosphoryl)dibromomethane at a brass electrode in a mixed solvent o-dichlorobenzene-MeCN (3:1 v/v)/0.05 M Bu4NBF4 at room temperature affords 61-(p-bromobenzoyl)methano[60]fullerene or 61,61-bis(diisopropoxyphosphoryl)methano[60]fullerene, respectively, in 50% yields.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2681–2685, December, 2004.  相似文献   
10.
The use of the reverse atom transfer radical polymerization (RATRP) to end-functionalize poly(methyl methacrylate) (PMMA) with fullerenes, e.g. C60 and C70 was described in this paper. The Cl-terrninated PMMA was prepared via RATRP with designed molecular weight and narrow molecular weight distributions, and then directly used to react with fullerenes to produce C60(C70) terminated PMMA polymers in the presence of CuBr/Cu/bipy or FeCl2/bipy catalysts. The resultant polymers exhibit good solubility in some common organic solvents, e.g. THF, CHCl3 and toluene, and were well structurally characterized by a variety of physical techniques.  相似文献   
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