Development of polyamide 6/polypyrrole conductive nanofibrous structure: the contribution of dopant type

IF 3.9 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Journal of Materials Science Pub Date : 2025-01-20 DOI:10.1007/s10853-025-10608-z
Nazanin Poursharifi, Dariush Semnani, Hossein Fashandi, Ali A. Ensafi
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Abstract

Conductive polymers, which exhibit properties of both metals and polymers, have garnered significant attention. Among the various methods considered for developing conductive polymers, chemical synthesis has gained enormous interest due to its remarkable advantages, including lightweight, cost-effectiveness, and resistance to chemical substances. Polypyrrole (PPy), a well-known conductive polymer, has found extensive use in various fields such as biosensors, supercapacitors, and solar cells. In this study, we developed a conductive nanofibrous structure through the chemical synthesis of PPy on polyamide 6 (PA6) nanofibers. We used sodium p-toluenesulfonate (NaPTS) and lithium perchlorate (LiClO4) as dopants. The structural and functional properties of the resulting conductive PA6 nanofibrous structure, including morphology, crystallinity, electrical conductivity, wettability, and electrochemical properties, were significantly influenced by the type of dopant. The average diameter of conductive PA6/PPy nanofibers increased with polymerization duration. Regardless of the dopant type, the crystallinity index (CI) of the conductive nanofibers PA6 + PPy + NaPTS (CI = 21.72%) and PA6 + PPy + LiClO4 (CI = 31.97%) was smaller compared to that of PA6 nanofibers (CI = 40.52%). This difference was attributed to the amorphous nature of PPy. When polymerization was conducted for 1 h, the electrical conductivity values were 1.76 ± 0.12 S/cm for PA6/PPy nanofibers doped with NaPTS and 4.47 ± 0.31 S/cm for those doped with LiClO4. By increasing the polymerization duration to 24 h, the electrical conductivity of PA6/PPy nanofibers improved by 99% and 92%, respectively. Coating PA6 nanofibers with PPy reduced their hydrophilicity degree, as indicated by water contact angles of 46.53 ± 2.53°. Regardless of the dopant type, water contact angles of 73.01 ± 5.92° and 72.13 ± 5.81° were obtained for NaPTS and LiClO4 dopants, respectively. Additionally, a direct linear correlation was established between the charge transfer resistance (Rct) and electrical conductivity. Overall, the developed conductive nanofibrous structure holds immense potential for high-performance sensors.

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聚酰胺6/聚吡咯导电纳米纤维结构的研制:掺杂剂类型的贡献
导电聚合物具有金属和聚合物的双重特性,引起了人们的广泛关注。在考虑开发导电聚合物的各种方法中,化学合成由于其显著的优点而获得了巨大的兴趣,包括轻质,成本效益和对化学物质的抗性。聚吡咯(PPy)是一种众所周知的导电聚合物,在生物传感器、超级电容器和太阳能电池等各个领域都有广泛的应用。在本研究中,我们通过在聚酰胺6 (PA6)纳米纤维上化学合成聚吡啶,开发了一种导电的纳米纤维结构。我们使用对甲苯磺酸钠(NaPTS)和高氯酸锂(LiClO4)作为掺杂剂。得到的导电PA6纳米纤维结构的结构和功能性能,包括形貌、结晶度、电导率、润湿性和电化学性能,受到掺杂类型的显著影响。导电PA6/PPy纳米纤维的平均直径随着聚合时间的延长而增加。无论掺杂类型如何,PA6 + PPy + NaPTS导电纳米纤维的结晶度指数(CI) (CI = 21.72%)和PA6 + PPy + LiClO4导电纳米纤维的结晶度指数(CI = 31.97%)均小于PA6纳米纤维(CI = 40.52%)。这种差异归因于PPy的无定形性质。聚合1 h后,掺NaPTS的PA6/PPy纳米纤维的电导率为1.76±0.12 S/cm,掺LiClO4的PA6/PPy纳米纤维的电导率为4.47±0.31 S/cm。将聚合时间延长至24 h, PA6/PPy纳米纤维的电导率分别提高了99%和92%。聚吡啶降低了PA6纳米纤维的亲水性,水接触角为46.53±2.53°。无论掺杂类型如何,NaPTS和LiClO4的水接触角分别为73.01±5.92°和72.13±5.81°。此外,在电荷转移电阻(Rct)和电导率之间建立了直接的线性相关关系。总的来说,所开发的导电纳米纤维结构在高性能传感器方面具有巨大的潜力。
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来源期刊
Journal of Materials Science
Journal of Materials Science 工程技术-材料科学:综合
CiteScore
7.90
自引率
4.40%
发文量
1297
审稿时长
2.4 months
期刊介绍: The Journal of Materials Science publishes reviews, full-length papers, and short Communications recording original research results on, or techniques for studying the relationship between structure, properties, and uses of materials. The subjects are seen from international and interdisciplinary perspectives covering areas including metals, ceramics, glasses, polymers, electrical materials, composite materials, fibers, nanostructured materials, nanocomposites, and biological and biomedical materials. The Journal of Materials Science is now firmly established as the leading source of primary communication for scientists investigating the structure and properties of all engineering materials.
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