English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 58220/91796 (63%)
造訪人次 : 13778216      線上人數 : 62
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    請使用永久網址來引用或連結此文件: http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/120221

    題名: A strategy for preparing solid polymer electrolytes via the electrospinning process
    作者: Chang, Chun-Wai;Lai, Wei-Chi
    關鍵詞: Solid polymer electrolyte;Electrospinning;Poly(ethylene oxide)
    日期: 2020-11
    上傳時間: 2021-03-17 12:11:02 (UTC+8)
    摘要: Since it is generally believed that the crystalline phase of solid polymer electrolytes (SPEs) is detrimental to ion transport, a strategy using the electrospinning technique was employed to reduce the crystallinity of SPEs. In this study, poly(ethylene oxide) (PEO)-LiClO4 SPEs fabricated by this strategy were compared with SPEs fabricated by the conventional solution casting method. Scanning electron microscopy (SEM) showed the changes in the nanofibrous structure of the electrospun SPEs when lithium salts were added. Fourier transform infrared spectroscopy (FTIR) was used to ensure that the free Li+ cations of LiClO4 are coordinated with the ether oxygen groups on the PEO chains after the electrospinning process. The results of differential scanning calorimetry (DSC) and X-ray diffraction (XRD) analyses showed that the crystalline phase is not well developed after the electrospinning process, which leads to enhanced ionic conductivities in the electrospun SPEs. Under the same chemical composition, the conductivity of the electrospun SPEs is enhanced from 1.03 × 10−7 S/cm to 3.13 × 10−5 S/cm at room temperature, compared with that of the conventional SPEs. Moreover, the ionic conductivities of the SPEs increase with temperature and obey the Arrhenius law.
    關聯: Journal of the Taiwan Institute of Chemical Engineers 116, p.279-285
    DOI: 10.1016/j.jtice.2020.11.012
    顯示於類別:[化學工程與材料工程學系暨研究所] 期刊論文


    檔案 描述 大小格式瀏覽次數



    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - 回饋