Sub‐Nanowires Boost Superior Capacitive Energy Storage Performance of Polymer Composites at High Temperatures

Author:

Yang Minzheng1,Yuan Feng234,Shi Wenxiong5,Ren Weibin1,Guo Mengfan16,Ouyang Chen2,Zhou Le1,Sun Nannan1,Xiao Yao1,Xu Erxiang1,Zhang Xuanhe7,Wei Yan34,Deng Xuliang34,Nan Cewen1,Wang Xun2,Shen Yang16ORCID

Affiliation:

1. State Key Lab of New Ceramics and Fine Processing, School of Materials Science and Engineering Tsinghua University Beijing 100084 China

2. Engineering Research Center of Advanced Rare Earth Materials Department of Chemistry Tsinghua University Beijing 100084 China

3. Institute of Medical Technology Peking University Health Science Center Beijing 100191 China

4. Beijing Laboratory of Biomedical Materials Department of Geriatric Dentistry Peking University School and Hospital of Stomatology Beijing 100081 China

5. Institute for New Energy Materials and Low Carbon Technologies School of Materials Science and Engineering Tianjin University of Technology Tianjin 300384 China

6. Center for Flexible Electronics Technology Tsinghua University Beijing 100084 China

7. Department of Mechanical Engineering Tsinghua University Beijing 100084 China

Abstract

AbstractPolymer dielectrics with high breakdown strength (Eb) and high efficiency are urgently demanded in advanced electrical and electronic systems, yet their energy density (Ue) is limited due to low dielectric constant (εr) and high loss at elevated temperatures. Conventional inorganic fillers with diameters from nano to micrometers can only increase εr at the cost of compromised Eb and Ue due to their poor compatibility with polymer matrix. Herein, hydroxyapatite (HAP) sub‐nanowires with a diameter of ≈0.9 nm are incorporated in polyetherimide (PEI) matrix to form HAP/PEI sub‐nanocomposites. εr and Eb of the composites are concomitantly enhanced with only 0.5 wt.% of HAP sub‐nanowires, leading to high Ue of 5.14 (@150 °C) and 3.1 J cm−3 (@200 °C) with efficiency of 90% and high‐temperature stability up to 3 × 105 charge‐discharge cycles at 200 °C. Microstructural analysis and molecular dynamics simulations indicate that the sub‐nanowires with comparable diameter as polymer chains induce enormous interfacial area, substantially increase mobility of polymer chains and form dense traps for charge carriers. This work extends the current research scope of polymer‐inorganics composite dielectrics to the sub‐nano‐level incorporation and provides a novel strategy for fabricating high performance polymer dielectrics at elevated temperatures.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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