纤维素
电介质
材料科学
无定形固体
复合材料
复合数
化学工程
氢键
溶解
高分子化学
分子
有机化学
光电子学
化学
工程类
作者
De-Long Li,Shao-Cong Shi,Ke-Yu Lan,Chunyan Liu,Yue Li,Ling Xu,Jun Lei,Gan‐Ji Zhong,Hua‐Dong Huang,Zhong‐Ming Li
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2023-06-21
卷期号:12 (7): 880-887
被引量:14
标识
DOI:10.1021/acsmacrolett.3c00224
摘要
Cellulose-based dielectrics with attractive dielectric performance are promising candidates to develop eco-friendly electrostatic energy storage devices. Herein, all-cellulose composite films with superior dielectric constant were fabricated by manipulating the dissolution temperature of native cellulose, where we revealed the relationship among the hierarchical microstructure of the crystalline structure, the hydrogen bonding network, the relaxation behavior at a molecular level, and the dielectric performance of the cellulose film. The coexistence of cellulose I and cellulose II led to a weakened hydrogen bonding network and unstable C6 conformations. The increased mobility of cellulose chains in the cellulose I-amorphous interphase enhanced the dielectric relaxation strength of side groups and localized main chains. As a result, the as-prepared all-cellulose composite films exhibited a fascinating dielectric constant of as high as 13.9 at 1000 Hz. This work proposed here provides a significant step toward fundamentally understanding the dielectric relaxation of cellulose, thus developing high-performance and eco-friendly cellulose-based film capacitors.
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