共查询到19条相似文献,搜索用时 62 毫秒
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化学氧化法制备聚苯胺/多壁碳纳米管复合材料(PANI/MWCNT),扫描电镜(SEM)、XRD及IR表征样品结构及形貌,电化学方法测定复合电极循环伏安曲线、恒流充放电曲线及电极交流阻抗.结果表明,PANI/MWCNT电极在1mol/L的Li2SO4溶液中具有较好电容性能,在电流密度为5mA/cm2时,比电容为412F/g.PANI/MWCNT电极较PANI电极有更好的大电流放电能力,50mA/cm2下复合电极的比电容仍达318F/g,为5mA/cm2时该电极比电容的77.2%,而PANI电极的比电容仅为其5mA/cm2时的56.2%.交流阻抗证明碳纳米管降低复合电极的电阻,显著提高大电流放电能力. 相似文献
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通过真空抽滤的方法制备碳纳米管纸,并对其进行循环伏安电化学氧化处理.以该电化学氧化处理的碳纳米管(CV-CNT)纸为基体,采用电化学聚合沉积聚苯胺(PANI),随后吸附石墨烯(GR),制备具有三明治夹心结构的碳纳米管/聚苯胺/石墨烯(CV-CNT/PANI/GR)复合纳米碳纸.该结构外层为GR,内层由PANI包裹的CNT形成网络骨架,充分发挥三者各自优势构建柔性电极材料.用场发射扫描电镜(FE-SEM)、透射电子显微镜(TEM)、拉曼光谱对其形貌与结构进行表征,并测试其电化学性能.研究发现:PANI呈纳米晶须状,并均匀包裹在CV-CNT表面;该复合碳纸具有良好的电容特性、大电流充放电特性以及良好的循环稳定性能.电流密度为0.5A·g-1时,比电容可达415F·g-1;20A·g-1时仍能保持106F·g-1的比电容.由于GR的保护作用,1000次循环之后较CV-CNT/PANI保持更高的有效比电容.该CV-CNT/PANI/GR复合碳纸展现出在高性能超级电容器柔性电极材料的潜在应用价值. 相似文献
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低温合成樟脑磺酸掺杂聚苯胺微管的电化学电容行为 总被引:1,自引:0,他引:1
在低温条件下合成了长约为2-3 μm, 外径约为300-400 nm 的樟脑磺酸掺杂聚苯胺微管. 扫描电镜(SEM)和透射电镜(TEM)显示, 生成的聚苯胺微管管径受樟脑磺酸浓度的影响, 高浓度的掺杂剂有利于管状聚苯胺的形成. 采用交流阻抗、循环伏安、恒流充放电等测试技术对不同产物的电化学电容行为进行了研究, 结果表明, 苯胺单体与樟脑磺酸的摩尔比为1:1时所得掺杂态聚苯胺电极具有较好的循环稳定性, 单电极比电容达到522 F·g-1. 相似文献
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制备了金纳米粒子修饰玻碳电极(Au/GCE),用循环伏安法研究L-色氨酸(L-Trp)在修饰电极上的电化学行为,以及支持电解质、溶液p H、扫描速率等对L-Trp伏安响应的影响。实验表明:在p H=3.5的HAcNa Ac支持电解质中,L-Trp在Au/GCE上有一灵敏的氧化峰(Epa=0.93)。氧化峰电流与L-Trp浓度在5.0×10-7~1.0×10-4mol·L-1范围内呈良好的线性关系,相关系数为0.9990,检出限1.6×10-7mol·L-1。测得L-Trp样品平均回收率为98%。 相似文献
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阿霉素在纳米钴/碳纳米管/ITO修饰电极上的电化学行为 总被引:2,自引:1,他引:1
以固定在氧化铟锡(ITO)电极上的多壁碳纳米管为基底吸附纳米钴,制备了复合纳米材料修饰的电极(Co/CNT/ITO)。采用扫描电子显微镜(SEM)和电子能谱(EDS)等对其进行了表征。用纳米钴/碳纳米管/ITO电极,研究了阿霉素(ADM)的电化学行为。实验表明,该体系具有吸附性的不可逆过程,峰电位为-0.65V(vs.Ag/AgCl),峰电流与ADM浓度在1.0×10-9~5.0×10-7mol/L范围内呈线性关系;检出限为1.0×10-9mol/L。本法灵敏、简便。 相似文献
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Ali Grinou Hyeonseong Bak Young Soo Yun 《Journal of Dispersion Science and Technology》2013,34(5):750-755
A simple method was used to synthesize the hybrid nanocomposites consisting of the functionalized multiwalled carbon nanotube composites (MWCNTs) with the polyaniline incorporated silver nanoparticles (a-MWCNT/PANI-Ag) through an emulsion polymerization at room temperature in order to enhance the electrical conductivity of polyaniline. The electrical conductivity of the composite with the incorporated Ag nanoparticles was 5% higher than the same weight percent for the composite without Ag nanoparticles, and the thermal stability was dramatically increased from 54% for the composite (a-MWCNT/PANI) to 69% through the incorporation of the Ag nanoparticles at 830°C. Additionally, the advantages of the Ag nanoparticles, including the improved electrical and thermal properties without damage to the polyaniline structure, were confirmed using FTIR and Raman spectroscopy. 相似文献
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聚苯胺/碳纳米纤维复合材料的制备及电容性能 总被引:1,自引:0,他引:1
采用原位聚合法制备了聚苯胺/碳纳米纤维(PANI/CNF)复合材料,用傅里叶变换红外(FT-IR)光谱、热重分析(TGA)、扫描电镜(SEM)和孔分布及比表面积测定仪研究了复合材料的表面官能团、组成、表面形貌及比表面积,并运用循环伏安(CV)法和计时电位法测试了PANI/CNF布作为电极材料的电化学性能.研究结果表明:PANI/CNF复合材料具有粗糙的毛刺结构,PANI沿碳纳米纤维均匀分布;PANI/CNF电极氧化还原反应的可逆性良好;在100mA·g-1电流密度下,当PANI含量为44.4%(w)时,复合材料比电容量高达587.1F·g-1,比能量为66.1Wh·kg-1,电流密度为800mA·g-1时比功率可达1014.2W·kg-1;在5A·g-1的电流密度下,1000次循环充放电后,复合材料的比电容量衰减28%.PANI/CNF复合材料具有良好的导电性和快速充放电能力,是一种优良的超级电容器电极材料. 相似文献
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分别采用粉末碳纳米管(CNT)和带连接点的碳纳米管网(CNTN)为模板,通过与聚苯胺(PANI)有限域聚合得到了CNT/PANI和CNTN/PANI 2种复合材料.采用透射电子显微镜和扫描电子显微镜对材料的形貌进行了表征,采用氮气吸附-脱附分析研究了材料的孔结构参数,运用双电四探针测试仪对材料的导电性能进行了测试,利用恒流充放电、循环伏安、循环寿命及交流阻抗等电化学测试手段表征了材料的电化学储能性能.结果表明,CNTN/PANI复合材料比CNT/PANI复合材料表现出更好的导电性能和电化学储能性能,其放电比容量可达到143.2 F/g(有机电解液). 相似文献
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KONG Ling-bin ZHANG Jing CAI Jian-jun YANG Zhen-sheng LUO Yong-chun KANG Long . State Key Laboratory of Gansu Advanced Non-ferrous Metal Materials . School of Materials Science Engineering Lanzhou University of Technology Lanzhou P. R. China 《高等学校化学研究》2011,(2):295-299
Chemically modified ordered mesoporous carbon CMK-3 materials were prepared by means of an easy wet-oxidative method in 2 mol/L nitric acid aqueous solution. A large amount of oxygen-containing functional groups were introduced onto the CMK-3 surface. Modified CMK-3(m-CMK-3) and aniline monomer were polymerized via an in situ chemical oxidative polymerization method. Morphological characterizations of m-CMK-3/PANI (polyaniline) composites were carried out via field emission scanning electron microscopy(SEM)... 相似文献
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A sensitive electrochemical method for the detection of DNA hybridization based on the probe labeled with multiwall carbon‐nanotubes (MWNTs) loaded with silver nanoparticles (Ag‐MWNTs) has been developed. MWNTs were electroless‐plated with a large number of silver nanoparticles to form Ag‐MWNTs. Probe single strand DNA (ss‐DNA) with a thiol group at the 3′‐terminal labeled with Ag‐MWNTs by self‐assembled monolayer (SAM) technique was employed as an electrochemical probe. Target ss‐DNA with a thiol group was immobilized on a gold electrode by SAM technique and then hybridized with the electrochemical probe. Binding events were monitored by differential pulse voltammetric (DPV) signal of silver nanoparticles. The signal difference permitted to distinguish the match of two perfectly complementary DNA strands from the near perfect match where just three base pairs were mismatched. There was a linear relation between the peak current at +120 mV (vs. SCE) and complementary target ss‐DNA concentration over the range from 3.1×10?14 to 1.0×10?11 mol/L with a detection limit of 10 fmol/L of complementary target ss‐DNA. The proposed method has been successfully applied to detection of the DNA sequence related to cystic fibrosis. This work demonstrated that the MWNTs loaded with silver nanoparticles offers a great promising approach for sensitive detection of DNA hybridization. 相似文献
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碳纳米管微结构的改变对其容量性能的影响 总被引:9,自引:0,他引:9
以KOH为活性剂,通过在高温下将碳纳米管进行活化处理来实现对碳纳米管管壁结构的改变,得到了比表面积和孔容分别是活化处理前约3倍和1.5倍的活性碳纳米管.将活化处理前后两种碳纳米管分别制作成电化学超级电容器电极,在充满氩气的无水手套箱组装成模拟电化学超级电容器,在恒流充放电模式下进行电化学可逆容量的测试,发现活性碳纳米管的电化学容量远高于活化前碳纳米管,是它的2倍.从而发现碳纳米管被打断,管壁变粗糙的活性碳纳米管比一般碳纳米管更适合用于电化学超级电容器电极材料. 相似文献