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排序方式: 共有716条查询结果,搜索用时 46 毫秒
1.
Harry G. Sherman Jacqueline M. Hicks Akhil Jain Jeremy J. Titman Prof. Cameron Alexander Snow Stolnik Frankie J. Rawson 《Chembiochem : a European journal of chemical biology》2019,20(8):1008-1013
A model cancer cell line was used to initiate polymerisation of pyrrole to form the conducting material polypyrrole. The polymerisation was shown to occur through the action of cytosolic exudates rather than that of the membrane redox sites that normally control the oxidation state of iron as ferricyanide or ferrocyanide. The data demonstrate for the first time that mammalian cells can be used to initiate synthesis of conducting polymers and suggest a possible route to detection of cell damage and/or transcellular processes through in situ and amplifiable signal generation. 相似文献
2.
为赋予棉针织物导电和储电的新功能并将其用于可穿戴器件中,将吡咯单体原位聚合到棉针织物上。借助扫描电子显微镜和红外光谱仪对棉针织物和聚吡咯的微观形貌以及化学结构进行表征,并测试了聚吡咯/棉针织物在不同拉伸应变时的表面电阻及电化学性能。结果表明:聚吡咯充分附着在针织棉纤维上;当拉伸应变从0%增至40%时,织物电阻值从429.2 Ω降至231.4 Ω;织物在5 mV/s条件下的储电面积容量为680.6 mF/cm 2,在2 mA/cm2 条件下为1 014.2 mF/cm2;由聚吡咯/棉针织物组装成的对称型超级电容器在1、5 mA/cm2时的面积容量分别为229.8、161.5 mF/cm2,经过10 000次恒流充放电循环后容量保留率为76.3%。 相似文献
3.
纳米纤状聚吡咯导电涂料的制备与性能研究 总被引:1,自引:0,他引:1
以十六烷基三甲基溴化铵(CTAB)胶束作为软模版,过硫酸铵(APS)为氧化剂制备纳米纤状聚吡咯(C-PPy)导电聚合物;利用电子转移再生催化剂原子转移自由基聚合(ARGET-ATRP)法合成羟基丙烯酸酯氟树脂,对其结构、形貌进行表征。将C-PPy与氟化丙烯酸酯树脂、固化剂复合,制成复合导电涂料,测试涂层力学性能与导电性能。实验结果表明:当C-PPy用量占涂料体系的质量分数为15%时,复合涂层的耐冲击性提高约133%,导电性能达到0.006 S/cm,涂层综合性能优异。 相似文献
4.
In the present investigation, Greigite-conducting polypyrrole nanocomposite (GPPy nanocomposite) was prepared, characterized and used to remove arsenite and arsenate from aqueous solution. Fe3S4 was synthesized using solvothermal synthetic method and it was grafted to conducting polypyrrole matrix. The nanocomposite was characterized using FE-SEM, EDX, XRD, FTIR, TGA/DSC and BET surface area. Kinetic studies revealed that the removal process followed first order kinetics. Batch isotherm studies were performed to determine the binding capacity. Thermodynamic parameters were also computed and it indicated the spontaneous nature of the process. Electrophoretic studies were carried out to determine the point of zero charge. 相似文献
5.
Electrochemical properties of free‐standing polypyrrole/graphene oxide/zinc oxide flexible supercapacitor 下载免费PDF全文
We report the preparation of a polypyrrole/graphene oxide/zinc oxide nanocomposite on a nickel foam using a simple and rapid single‐step electrochemical deposition process under ambient conditions. A free‐standing flexible supercapacitor was fabricated by sandwiching a polyvinyl alcohol hydrogel polymer electrolyte between two layers of the as‐prepared ternary nanocomposite electrodes. The electrochemical properties of the free‐standing supercapacitor were analyzed using a two‐electrode system. The supercapacitor achieved a specific capacitance of 123.8 F/g at 1 A/g, which was greater than its single (39.1 F/g) and binary (81.3 F/g) counterparts. This suggests that ZnO acts as a spacer and support that hinders the ternary structure from collapsing and subsequently enhances the diffusion of ions within the matrix. The flexible supercapacitor exhibited remarkable electrochemical stability when subjected to bending at various angles. The cycling stability of the ternary nanocomposite showed a favorable specific capacitance retention of more than 90% after 1000 cycles for mild alkaline electrolytes compared with strong alkali electrolytes. The presence of glycerin in the polymer electrolyte enabled the supercapacitor to perform better under the vigorous cycling condition. The potential of the as‐fabricated supercapacitor for real applications was manifested by its ability to light up a light‐emitting diode after being charged. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
6.
为研究制备纳米银-聚吡咯(Ag-PPy)导电复合薄膜的最佳聚合工艺,分别采用静置、超声和磁力搅拌三种聚合工艺制备了纳米银-聚吡咯导电复合薄膜。用四探针法测量了复合薄膜的表面电阻值,用三维视频显微镜(3-DVM)观测其表面形貌并测定了膜层的厚度,用X射线衍射仪(XRD)分析了膜层物质的晶型。结果表明:采用频率为25kHz、功率为70 W的超声工艺制备的Ag-PPy导电复合薄膜的综合性能最好,在该条件下得到的复合薄膜表面平整,纳米银粒子在聚吡咯中分布连续且均匀,表面电阻值可达到0.68kΩ,复合物粒子在基体上沉积的厚度为56.28μm,沉积速率为8.67mg·cm-2·h-1。 相似文献
7.
N‐Oligo(3‐hydroxybutyrate)‐functionalized polypyrroles: towards bio‐erodible conducting copolymers 下载免费PDF全文
Anna Domagala Wojciech Domagala Przemyslaw Ledwon Marta Musiol Henryk Janeczek Agnieszka Stolarczyk Piotr Kurcok Grazyna Adamus Mieczyslaw Lapkowski 《Polymer International》2016,65(12):1395-1404
New copolymer materials have been prepared by chemical grafting of oligomeric 3‐hydroxybutyric acid (OHB) onto polypyrrole (PPy) derivatives. The influence of grafting density and molecular weight of OHB brushes on the physicochemical properties of prepared copolymers was investigated. PPy substrates were prepared by FeCl3‐driven oxidative homopolymerization of N‐(2‐carboxyethyl)pyrrole or its copolymerization with pyrrole. The grafting method employed involved controlled anionic polymerization of β‐butyrolactone on pyrrole‐tethered potassium carboxylate active sites. Obtained PPy‐g‐OHB copolymers of varying grafting density and pendant polyester chain length were characterized and the observed structure–property relationships discussed. The impact of real time exposure to phosphate‐buffered saline environment was investigated and the residue products were characterized. Cross‐correlation of spectroscopic, thermal, electrical and elemental analysis data afforded comprehensive evaluation of the structure of prepared materials and their behaviour in hydrolytic medium. Erosion and degradation pathways have been identified, indicating ways to consciously tailor the physicochemical properties of these new biomimetic materials. © 2016 Society of Chemical Industry 相似文献
8.
CuBr2‐induced charge screening on photoactive nanocolloidal polypyrrole:poly(styrene sulfonate) composite multilayer thin‐film counter electrodes for high‐efficiency dye‐sensitized solar cells 下载免费PDF全文
S Maruthamuthu J Chandrasekaran D Manoharan SN Karthick Hee‐Je Kim B Saravanakumar 《Polymer International》2016,65(5):584-595
Nanocolloidal polypyrrole (PPy):poly(styrene sulfonate) (PSS) particles were synthesized by chemical oxidative polymerization using 15 wt% of PSS. The highly processable polymer composite (PPy:PSS) was spin‐coated at 4000 rpm on fluorine‐doped tin oxide glass and subsequently employed as a counter electrode (CE) for dye‐sensitized solar cells (DSCs). PPy:PSS multilayer (one, three, five) CEs were treated with CuBr2 salt, which enhances the efficiency of the DSCs. Optical studies reveal that a bulkier counterion hinders interchain interactions of PPy which on salt treatment shows a moderate redshift in absorption maxima. Salt‐treated PPy:PSS films exhibit lower charge transfer resistance, higher surface roughness and better catalytic performance for the reduction of I3?, when compared with untreated films. The improved catalytic performance of salt‐treated PPy:PSS multilayer films is attributed to charge screening and conformational change of PPy, along with the removal of excess PSS. Under standard AM 1.5 sunlight illumination, salt treatment is shown to boost the efficiency of multilayer PPy:PSS composite film‐based DSCs, leading to enhanced power conversion efficiency of 6.18, 6.33 and 6.37% for one, three and five layers, respectively. These values are significantly higher (ca 50%) than those for corresponding devices without CuBr2 salt treatment (3.48, 2.90 and 2.01%, respectively). © 2016 Society of Chemical Industry 相似文献
9.
Miguelina Vasquez‐Ortega Mauricio Ortega Juan Morales M Guadalupe Olayo Guillermo J Cruz Roberto Olayo 《Polymer International》2014,63(12):2023-2029
Polypyrrole hollow nanoparticles were prepared by atmospheric pressure plasma polymerization. The structure of the nanoparticles was studied using Fourier transform infrared and X‐ray photoelectron spectroscopies, thermogravimetric analysis, scanning and transmission electron microscopies and atomic force microscopy. In contrast to low‐pressure plasma polymerization of pyrrole, which can produce films and solid nanoparticles, we obtained two types of hollow nanoparticles: a fraction with single spherical core and another with a core composed of small bubbles. Thermal characterization allowed us to determine that the nanoparticles are composed of highly crosslinked polymer. A mechanism that explains the formation of both types of hollow nanoparticles as well as solid nanoparticles is proposed. Chemical characterization shows that, in addition to the expected chemical structures due to pyrrole polymerization, the high energy of the plasma at atmospheric pressure produces intense dehydrogenation and oxidation processes. The fluorescence spectrum of the nanoparticles, however, shows a peak at 482 nm indicating that some degree of π‐conjugation is present in the material. © 2014 Society of Chemical Industry 相似文献
10.
Afarin Bahrami Zainal Abidin Talib Wan Mahmood Mat Yunus Kasra Behzad Mahnaz M. Abdi Fasih Ud Din 《International journal of molecular sciences》2012,13(11):14917-14928
Polypyrrole (PPy) and polypyrrole-carboxylic functionalized multi wall carbon nanotube composites (PPy/f-MWCNT) were synthesized by in situ chemical oxidative polymerization of pyrrole on the carbon nanotubes (CNTs). The structure of the resulting complex nanotubes was characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). The effects of f-MWCNT concentration on the electrical properties of the resulting composites were studied at temperatures between 100 K and 300 K. The Hall mobility and Hall coefficient of PPy and PPy/f-MWCNT composite samples with different concentrations of f-MWCNT were measured using the van der Pauw technique. The mobility decreased slightly with increasing temperature, while the conductivity was dominated by the gradually increasing carrier density. 相似文献