纖維素當作基底並使用聚苯胺(Polyaniline, PANi)和聚吡咯(Polypyrrole, PPy)以及加入奈米碳點獨立形成複合材料，並使用原位聚合法(in-situ polymerization method)合成不同重量(胺的單體為: 60, 90, 120, 150 and 180μl 吡咯單體為: 60, 120, 180, 240μl 吡咯奈米碳點系列: 吡咯單體為180μl 奈米碳點: 50, 100, 300, 500μl)的聚合材料。
　　本實驗發現在聚苯胺系列的電極系列中，當在胺單體120μl時其比電容值達到最高(174 F/g在掃描速率為5mV /s時)。同時，在聚吡咯系列電極中，比電容值隨吡咯含量降低而逐漸變小。儘管180μl吡咯量的比電容值低於240μl吡咯量，但由於180μl吡咯量做出的膜電極柔韌性較240μl吡咯量做出的膜電極好出許多，根據實驗目的是為了做出柔性電極，因此取180μl吡咯量做出的膜為我們最好的重量比，這些電化學結果表明聚吡咯複合材料比聚苯胺系列有著更好的特性，這兩種聚合材料都修正了纖維素沒有導電度的問題，因此複合材料膜電極不僅有更好的機械性能，而且擁有更快的電荷轉移促進了聚合物和纖維素之間的加強協同作用。
　　此外，複合膜電極的穩定度有些微不同，在經過三千次循環後聚苯胺膜電極穩定性為81%，但聚吡咯為97，聚吡咯被塗覆在纖維素上可以製造良好的柔性電極。
　　但以上兩種聚合物指出它們不能使薄膜具有優異的充電和放電，因此將碳點加入到用吡咯原位聚合以提高充放電的比電容，與沒有碳點的電極相比，有碳點的膜電極表現出優異的電化學改變。順帶一提，100μl碳點與吡咯的複合膜的比電容為1073 F/g，這個值比沒有碳點薄膜高1.9倍。另外，這些複合材料薄膜的充放電比沒有碳點的情況下顯示出更好的充電和放電的比電容值，表明這種材料可以高效率地製造用於能量存儲設備的柔性電極。

Composite materials were synthesized by polyaniline, polypyrrole and carbon dots on cellulose-based substrates, independently. The materials at different weights were prepared by the in-situ polymerization method.
　　In the case of Polyaniline-series electrodes, the specific capacitance was maximum (174 F/g at a scan rate of 5mV/s) in 120μl of aniline monomer. Meanwhile, in the Polypyrrole-series film electrodes, the specific capacitance significantly decreased from 571 F/g at 5 mV/s of 240μl (pyrrole amounts) with decreasing content of pyrrole amounts. Although the specific capacitance of 180μl pyrrole amount electrode was lower than that of 240μl pyrrole amount electrode, the flexibility of 180μl pyrrole amount electrode was better than that of 240μl amount. These electrochemical results indicate that Polypyrrole-composites have better properties than PANi-series. Furthermore, the stability of polyaniline was 81% after 3000 cycles, but polypyrrole and Cdot-ppy were almost 100%.
　　Since two polymers above indicated the inferior charge/discharge profile, carbon dots as added into in-situ polymerization with pyrrole to enhance their specific capacitance. The addition of carbon dots on composite films consisting of polypyrrole showed superior electrochemical performance in comparison with the electrode without carbon dots. Incidentally, the specific capacitance was 1073 F/g for the composite film added 100μl carbon dots. This value is 1.9 times higher than that electrode without carbon dots. Moreover, these composites film also showed better charge/discharge shape than that without carbon dots. These results indicate that this composite can produce a flexible electrode for energy storage devices with high efficiency.

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