TY - JOUR
T1 - Bio-based interfacial engineering enables extreme-temperature dielectric energy storage in polymer nanocomposites
AU - Zhang, Qian
AU - Zuo, Miaomiao
AU - Ma, Xiaoqin
AU - Wang, Jian
AU - Zhang, Yifei
AU - Peng, Biyun
AU - Gong, Honghong
AU - Gong, Xusheng
AU - Xie, Yunchuan
AU - Ma, Wei
AU - Zhou, Di
N1 - Publisher Copyright:
© 2026 Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
PY - 2026/11/15
Y1 - 2026/11/15
N2 - Dielectrics capable of simultaneous high energy density (Ud), high efficiency (η), and reliable operation at elevated temperatures are urgently needed for advanced electronics and power systems, yet remain a formidable challenge. Here, we report a bio-based interfacial engineering strategy that employs wide-bandgap, polar cellulose to conformally coat high-k TiO2 nanosheets, creating a core-shell structured filler. When incorporated into a polyetherimide (PEIs) matrix, the cellulose shell simultaneously enhances filler dispersion and introduces deep charge traps at the interface. This synergistic effect yields a remarkable combination of high dielectric polarization and strongly suppressed conduction loss at high temperatures. The resulting nanocomposite with only 2 wt% filler achieves an electrical breakdown strength of 600 MV m−1 and a Ud of 4.05 J cm−3 at 150 °C, retaining a high Ud of 2.89 J cm−3 with 90% η even at 200 °C. Combining thermally stimulated depolarization current analysis and finite-element modelling, we reveal the mechanism by which the cellulose interlayer homogenizes the electric field distribution and immobilizes space charges. This work demonstrates a nature-derived interfacial strategy for high-performance dielectrics under extreme conditions, offering a sustainable pathway to high-energy-density capacitive energy storage.
AB - Dielectrics capable of simultaneous high energy density (Ud), high efficiency (η), and reliable operation at elevated temperatures are urgently needed for advanced electronics and power systems, yet remain a formidable challenge. Here, we report a bio-based interfacial engineering strategy that employs wide-bandgap, polar cellulose to conformally coat high-k TiO2 nanosheets, creating a core-shell structured filler. When incorporated into a polyetherimide (PEIs) matrix, the cellulose shell simultaneously enhances filler dispersion and introduces deep charge traps at the interface. This synergistic effect yields a remarkable combination of high dielectric polarization and strongly suppressed conduction loss at high temperatures. The resulting nanocomposite with only 2 wt% filler achieves an electrical breakdown strength of 600 MV m−1 and a Ud of 4.05 J cm−3 at 150 °C, retaining a high Ud of 2.89 J cm−3 with 90% η even at 200 °C. Combining thermally stimulated depolarization current analysis and finite-element modelling, we reveal the mechanism by which the cellulose interlayer homogenizes the electric field distribution and immobilizes space charges. This work demonstrates a nature-derived interfacial strategy for high-performance dielectrics under extreme conditions, offering a sustainable pathway to high-energy-density capacitive energy storage.
KW - Cellulose
KW - Electrical properties
KW - High-temperature performance
KW - Interfacial engineering
KW - Nanocomposites
UR - https://www.scopus.com/pages/publications/105045125716
U2 - 10.1016/j.est.2026.123654
DO - 10.1016/j.est.2026.123654
M3 - 文章
AN - SCOPUS:105045125716
SN - 2352-152X
VL - 178
JO - Journal of Energy Storage
JF - Journal of Energy Storage
M1 - 123654
ER -