期刊文献+

PANI/MoS_2复合材料的制备及其电化学性能研究 被引量:1

Preparation and Characterization of PANI/MoS_2 Composite and Its Electrochemical Properties
下载PDF
导出
摘要 采用原位聚合法制备不同摩尔比的PANI/MoS_2纳米复合材料。通过X射线衍射、红外光谱、透射电镜等手段,对所制备的材料进行了结构和微观形貌的表征,结果表明:所制备的聚苯胺呈现棒状纳米纤维包覆在卷曲的纳米鳞片MoS_2片层上形成了PANI/MoS_2纳米复合材料。通过循环伏安法、恒流充放电等测试手段对材料的电化学性能进行了研究,结果表明:在不同电流密度下PANI∶MoS_2=1∶0.1的二元复合物比电容明显高于纯聚苯胺,在1 A/g时PANI∶MoS_2=1∶0.1的二元复合物的比电容值可达942.5 F/g,相比于同电流密度下的PANI的400.5 F/g的高出一倍。表明适量的MoS_2的掺入有助于提高PANI电极材料的电化学电容特性。 PANI/MoS2 nanocomposites with different molar ratios were prepared by in-situ polymerization. The structure and microscopy of as-prepared materials were characterized by X-ray diffraction(XRD), FTIR spectroscopy, and transmission electron microscopy(TEM). The results of analysis indicated that the prepared polyaniline exhibited rod-like nanofibers coated on the curled nanoscale MoS2 sheet. The electrochemical properties of the material were studied by cyclic voltammetry(CV) and galvanostatic charge-discharge(GCD) tests. The results showed that the specific capacitance of PANI:MoS2=1:0.1 was significantly higher than that of pure polyaniline at different current densities. The specific capacitance of the PANI:MoS2=1:0.1 composites reached 942.5 F/g, which was double that of PANI( 400.5 F/g) at the current density of 1 A/g. It showed that the proper amount of MoS2 incorporation helped to improve the electrochemical capacitance characteristics of the PANI electrode material.
作者 阿比旦.阿布都乃则尔 张艳慧 阿孜古丽.木尔赛力木 王琳 兰海蝶 Abida ABDUNAZAR;ZHANG Yan-hui;Arzugul MUSLIM;WANG Lin;LAN Hai-die(School of Chemistry and Chemical Engineering, Xinjiang Normal University, Xinjiang Urumqi 830054, China;Engineering Research Center of Electrochemical Technology and Application, Xinjiang Normal University, Xinjiang Urumqi 830054, China)
出处 《当代化工》 CAS 2018年第5期881-885,共5页 Contemporary Chemical Industry
基金 国家自然科学基金(51763023) 新疆师范大学校级科研平台招标课题项目(XJNUGCZX122017A03)
关键词 聚苯胺 二硫化钼 复合材料 电化学性能 Polyananiline Molybdenum disulfide Composite materials Electrochamical performance
  • 相关文献

参考文献4

二级参考文献58

  • 1墙蔷,倪红卫,幸伟,谢中,魏勇.银的抗菌作用机理[J].武汉科技大学学报,2007,30(2):121-124. 被引量:68
  • 2Simon, P.; Gogotsi, Y. Materials for electrochemical capacitors. Nat. Mater. 2008, 7, 845-854. 被引量:1
  • 3Xu, Y. X.; Shi, G. Q.; Duan, X. F. Self-assembled three- dimensional graphene macrostructures: Synthesis and applications in supereapacitors. Acc. Chem. Res. 2015, 48, 1666-1675. 被引量:1
  • 4Yu, D. S.; Goh, K.; Wang, H.; Wei, L.; Jiang, W. C.; Zhang, Q.; Dai, L. M.; Chert, Y. Scalable synthesis of hierarchically structured carbon nanotube-graphene fibres for capacitive energy storage. Nat. NanotechnoL 2014, 9, 555-562. 被引量:1
  • 5Augustyn, V.; Simon, P., Dunn, B. Pseudocapacitive oxide materials for high-rate electrochemical energy storage. Energy Environ. Sci. 2014, 7, 1597-1614. 被引量:1
  • 6Hercule, K. M.; Wei, Q. L.; Khan, A. M.; Zhao, Y. L.; Tian, X. C.; Mai, L. Q. Synergistic effect of hierarchical nanostructured MOOE/Co(OH)2 with largely enhanced pseudocapacitor cyclability. Nano Lett. 2013, 13, 5685-5691. 被引量:1
  • 7Yang, C.; Dong, L.; Chert, Z. X.; Lu, H. B. High-performance all-solid-state supercapacitor based on the assembly of graphene and manganese 0I) phosphate nanosheets. J. Phys. Chem. C2014, 118, 18884-18891. 被引量:1
  • 8Zhao, S. L.; Yin, H. J.; Du, L.; He, L. C.; Zlmo, K.; Chang, L.; Yin, G. P.; Zhao, H. J.; Liu, S. Q.; Tang, Z. Y. Carbonized nanoscale metal-organic frameworks as high performance electrocatalyst for oxygen reduction reaction. ACS Nano 2014, 8, 12660-12668. 被引量:1
  • 9Choi, K. M.; Jeong, H. M.; Park, J. H.; Zhang, Y. B.; Kang,J. K.; Yaghi, O. M. Supercapacitors of nanocrystalline metal-organic frameworks. ACS Nano 2014, 8, 7451-7457. 被引量:1
  • 10Yin, H. J.; Zhao, S. L.; Zhao, K.; Muqsit, A.; Tang, H. J.; Chang, L.; Zhao, H. J.; Gao, Y.; Tang, Z. Y. Ultrathin platinum nanowires grown on single-layered nickel hydroxide with high hydrogen evolution activity. Nat. Commun. 2015, 6, 6430. 被引量:1

共引文献8

同被引文献4

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部