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《化学世界》2016,(8)
利用气相沉积法在碳纸表面生长聚(3,4-乙烯二氧噻吩)(PEDOT)纳米颗粒,通过控制单体用量,制备了一系列PEDOT/碳纸复合材料,通过场发射扫描电镜、傅里叶红外光谱、X射线衍射、拉曼光谱、X射线光电子能谱分析了不同复合材料的形貌与结构,同时利用循环伏安、恒流充放电、交流阻抗方法对所制备的复合材料进行了电化学性能的测试。结果表明,PEDOT呈纳米短棒状均匀生长于碳纸上,且当单体用量为20μL时,所得PEDOT/碳纸复合材料显示了较好的电化学性能,在0.1mA/cm2充放电电流下,面积比电容达到138.75mF/cm2,经过4 000次循环测试后其面积比电容仍可保留原来的72.6%,以碳纸为基材大大缩短了离子传输和电荷转移路径,从而使得复合材料呈现良好的电化学性能。 相似文献
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以樟脑磺酸(HCSA)为掺杂剂,FeCl3为氧化剂,通过化学氧化聚合合成了聚(3,4-乙撑二氧噻吩)/樟脑磺酸(PEDOT/HCSA)复合材料;采用FTIR和SEM对其结构和形貌进行了表征;探讨了掺杂剂与单体摩尔比、氧化剂用量和反应时间对产品导电性能的影响;分析了产品的电化学性能。结果表明,当n〔3,4-乙撑二氧噻吩(EDOT)〕:n(樟脑磺酸):n(氯化铁)=2:1:40,反应时间41 h时,复合材料具有良好的导电性能和电化学性能,电导率为10.4 S/cm,经150次充放电老化后比容量可保持在140 F/g左右,是一种潜在的超级电容器电极材料。 相似文献
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聚3,4-乙撑二氧噻吩具有导电率高、热稳定性好、成膜性好的特点。在光伏电池、抗静电与电磁屏蔽等领域具有良好的用途。由于传统的3,4-乙撑二氧噻吩单体合成过程繁杂,导致3,4-乙撑二氧噻吩单体收率低、价格昂贵,至今未得到良好应用。本文介绍了合成3,4-乙撑二氧噻吩单体的最新研究进展,着重讨论了以价廉易得的氯乙酸乙酯为原料,经亲核取代、酯缩合、烷基化、水解与脱羧合成3,4-乙撑二氧噻吩的新"五步法"合成路线。通过对3,4-乙撑二氧噻吩新"五步法"合成路线的分析,总结了各步最优合成方法与条件,为3,4-乙撑二氧噻吩研究开发提供了借鉴。 相似文献
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本论文围绕制备导电聚合物PEDOT(聚3,4-二氧乙基噻吩)与无机氧化物及金属纳米复合材料的研究,探索了不同复合材料所表现的独特的电学、光学和结构等方面性质,并建立了一种无模板制备有机/无机一维纳微米结构复合材料的一步合成新方法,制备了具有core-shell结构的PEDOT/PSS-ZnO,PEDOT/PSS-Au复合纳米线,取得了以下创新性结果. 相似文献
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《塑料》2014,(2)
通过3,4-乙撑二氧噻吩(EDOT)在多壁碳纳米管(MWNTs)表面的原位氧化聚合,得到聚苯乙烯磺酸钠(PSSNa)掺杂聚(3,4-乙撑二氧噻吩)(PEDOT)/多壁碳纳米管导电复合材料。复合材料中PEDOT-PSSNa包覆在MWNTs表面,形成MWNTs为核、PEDOT-PSSNa为壳的纳米复合结构,PEDOT与MWNTs间存在较强的π-π*共轭效应。复合材料的热失重受PEDOT分子骨架热降解和MWNTs热分解的双重控制,在300~500℃的热稳定性较PEDOT-PSSNa明显提高。聚合得到的核(MWNTs)-壳(PEDOT-PSSNa)结构能均匀分散在水中,形成具有良好透光性的水溶性复合分散体系。将水溶性复合材料涂覆于PET薄膜表面,室温电导率比PEDOT-PSSNa提高2个数量级。 相似文献
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Esma Sezer A.H. Sezai Saraç Elif Altürk Parlak 《Journal of Applied Electrochemistry》2003,33(12):1223-1231
3,6 bis(3,4-ethylenedioxythiophenyl)-9-Ethylcarbazole (EDOT-ECZ-EDOT or EEE) films are coated electrochemically onto carbon fiber micro-electrodes. Deposition conditions on the electroactivity of the resulting polymers are studied. Structural studies of the polymers have been conducted using different techniques such as cyclic voltammetry, ATR-FTIR, scanning electron microscopy and four-point probe conductivity. 相似文献
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单体配比对聚苯硫醚低聚物合成的影响 总被引:2,自引:0,他引:2
以六甲基磷酸酰三胺为溶剂,脱硫化钠和对二氯苯为单体,常压下研究了聚苯硫醚(PPS)低聚物的合成反应。研究了单体配比对聚合反应及低聚物结构的影响,用红外光谱、激光拉曼光谱、X-射线衍射等分析手段对低聚物的结构进行了初步表征。结果表明,在硫化钠过量条件下制备的PPS低聚物具有较低的熔点和结晶度,在极性有机溶剂中的溶解性较好;在对二氯苯过量条件下制备的PPS低聚物的熔点较高,结晶性较好,但在有机溶剂中的 相似文献
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Murat Ates Alpay Garip Ozan Yörük Yuksel Bayrak Ozge Kuzgun Murat Yildirim 《塑料、橡胶和复合材料》2013,42(4):168-184
ABSTRACTSupercapacitor properties of rGO, CuO, PEDOT and rGO/CuO at [rGO]o/[CuO]o?=?1:1; 1:1.5; 1:2 and rGO/CuO/PEDOT nanocomposite at [rGO]o/[CuO]o/[EDOT]o?=?1:1:1; 1:1:3; 1:1:5 were investigated using chemical reduction of GO and in-situ polymerisation process. SEM-EDX, HRTEM, BET surface area analysis confirm the nanocomposite formations. Nanocomposite materials are also analysed through FTIR-ATR, Raman, TGA-DTA, GCD, CV and EIS. The highest specific capacitance of C sp?=?156.7 F/g at 2?mV/s is determined as rGO/CuO/PEDOT at [rGO]o/[CuO]o/[EDOT]o?=?1:1:5. In addition, two-electrode supercapacitor device for rGO/CuO/PEDOT at [rGO]o/[CuO]o/[EDOT]o?=?1:1:5 are found to provide a maximum specific energy (E?=?14.15 Wh/kg at 20?mA) and specific power (P?=?24730 W/kg at 50?mA), electrical serial resistance (ESR?=?13.33 Ω) with good capacity retention after 3000 cycles. An equivalent circuit model of LR1(CR2)(QR3) is proposed to interpret the EIS data. The supercapacitor performance of the rGO/CuO/PEDOT nanocomposite electrode indicates the synergistic effect of hybrid supercapacitors. 相似文献
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通过改性二氧化锰和氧化石墨烯片之间的静电自组装制备了层状的rGO/MnO2复合纳米材料。通过XRD分析材料的晶体结构,用扫描电镜观察材料的微观表面形貌。这种材料用来研究其电化学电容性能,结果表明这种纳米复合材料显示出很好的电容性能(在0.2 A/g的电流密度下可达246 F/g)。此外,在2 A/g的电流密度下循环1000次后容量保持率为91%。材料的性能提升是因为复合材料中二氧化锰纳米棒和石墨烯片层很好的贴合,而石墨烯片的加入也大大提高了材料的导电性。 相似文献
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V.S. Vasantha 《Electrochimica acta》2005,51(2):347-355
The poly(3,4-ethylenedioxy thiophene) (PEDOT)/ferricyanide (FCN) film was synthesized by a potentiostatic and also using potentiodynamic methods namely cyclic voltammetric and chronoamperometric techniques. The EQCM technique was used to study the mechanism of the incorporation of ferricyanide ions on the PEDOT film. The UV-vis absorption results too confirmed the presence of ferricyanide with the PEDOT film. The electrocatalytic oxidation of ascorbic acid was carried out on a glassy carbon electrode modified with the PEDOT/FCN film through cyclic voltammetry, chronoamperometry and rotating disk electrode (RDE) voltammetry as diagnostic techniques. It was found that the catalytic current depended on the concentration of ascorbic acid. The number of electron transfer involved in the rate-determining step was found to be 1 and transfer coefficient (α) equal to 0.476. The diffusion coefficient of ascorbic acid was also estimated through the chrono amperometric and rotating disk electrode methods. The D values of ascorbic acid obtained by through the cyclic and chronoamperometric methods were found to be 4.4103 × 10−6 and 4.9595 × 10−6 cm2 s−1, respectively. This modified electrode was also used for the simultaneous determination of ascorbic acid and dopamine. 相似文献
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Compounding polyaniline (PANI) and reduced graphite oxide (rGO) is a fascinating cost-effective way to combine the high energy density of faradic material and high power density of carbonaceous material. In this study, in-situ polymerization of dopamine was used to reduce graphite oxide and to modify the rGO product with polydopamine (PDA) simultaneously. This modification prevented restacking of rGO, and enhanced the interactions between PANI and rGO. The partial reduction of GO during the polymerization of dopamine was proven by X-ray diffraction, Fourier transform infrared attenuated total reflectance, and UV–vis spectroscopy. Surprisingly, the electrochemical performance of the composites depends strongly on the preparation sequence. PANI/(rGO-PDA) composites obtained by the synthesis of PANI in the presence of rGO-PDA show better electrochemical performance than (PANI/rGO)-PDA composites, which were produced by polymerizing dopamine in the presence of PANI/GO composite. At a given scan rate of 20 mV s−1, the highest specific capacity of PANI/(rGO-PDA) composites was 230.7 F g−1, which was higher than those of all (PANI/rGO)-PDA composites. This phenomenon is tightly related to the differences in morphologies, conductivities and specific surface areas of the two types of composites. 相似文献
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合成了阳离子单体甲基丙烯酰氧乙基三甲基氯化铵(DMC)引入量不同的聚羧酸减水剂,采用傅里叶红外光谱进行了结构确证.通过水泥净浆流动度、凝结时间、净浆和胶砂抗压强度测试,研究了阳离子单体不同引入量对聚羧酸减水剂分散性、凝结时间和早强性能的影响.通过XRD、TG对作用机理进行了分析.结果表明:DMC引入量占大单体4%时,净浆流动度达到最大值;引入DMC后,净浆凝结时间缩短,净浆和胶砂试件早期抗压期强度明显提高;当引入量占大单体12%时早强性能最好.由XRD和TG分析可知,引入DMC促进了C3S的早期水化,生成较多的水化硅酸钙和氢氧化钙. 相似文献
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采用一步水热法制备具有海胆状纳米/微米结构的MnO_2和MnO_2/rGO复合电极材料。用扫描电子显微镜(SEM)和透射电子显微镜(TEM)表征分析其微观形貌,X射线衍射(XRD)对其成分进行分析,结果表明:rGO,MnO_2成功复合在一起。rGO包覆在海胆型MnO_2表面,有效增大了MnO_2导电率。MnO_2∶rGO=1∶1的复合材料在电流密度为0.5 A·g~(-1)时比电容可达200.13 F·g~(-1)。经过5000次循环充放电后,其比电容保持率为92%。 相似文献
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单体和预聚物对UV喷墨油墨性能的影响 总被引:1,自引:0,他引:1
单体和预聚物对UV喷墨油墨的性能有很大的影响,本论文通过改变预聚物的种类和颜基比,制备色浆,测试了粒度及其分布,探讨了不同的预聚物和颜基比对UV喷墨油墨色浆分散性的影响,实验结果表明,用预聚物V100在颜基比为2:1时所制备的色浆具有良好的分散性;通过考察单一单体对UV喷墨油墨性能的影响,利用NPGDA、EOEOEA、DPGDA组成的混合单体稀释色浆制备成UV喷墨油墨样品,采用配方试验方法,得到UV喷墨油墨样品各项性能参数最佳的混合单体的比例为3:30:20。 相似文献