Utilizing the synergistic effect between the Schottky barrier and field redistribution to achieve high-density, low-consumption, cellulose-based flexible dielectric films for next-generation green energy storage capacitors
文献情報
Hansong Wei, Shibo Zhao, Qing Guo, Yuhan Bai, Siting Wang, Peiyao Sun, Kang Du, Yating Ning, Ye Tian, Xiaohua Zhang, Hongmei Jing, Yongping Pu, Sufeng Zhang
After decades of development, the study of flexible dielectric materials has changed the focus from BOPP/PVDF/PI-based systems to those that can be biodegraded, not only because of several bottlenecks in the former systems but also because of the pollution they cause on the earth. Though various strategies were used, the improvement in the energy storage performance was slow. Recently, hydrogen bond replacement has been utilized for achieving a high energy density in sandwich-structured cellulose-based films; however, the efficiency was relatively low due to an uneven electric field distribution. In this work, a similar technology of the dissolution-regeneration route was used, and the multilayer-structured cellulose-based films were obtained by changing the sequence of fillers embedding in each sublayer. The differences in mechanical properties between films was revealed due to the different particle sizes and the presence of a slip layer effect. As a result of the synergistic effect between the field redistribution and the decreasing Fermi level, a breakdown strength as high as 6.24 MV cm−1 was achieved with a super high energy density of 31.07 J cm−3 and an efficiency of 80.03%, and the computer simulation fitted very well with the experimental data. The electric field distribution also help to reduce the energy consumption, for such a high energy density was triggered by a lower voltage. In addition, the film showed good fatigue endurance at both room temperature and 150 °C, which is caused by the intrinsic strong adiabaticity of cellulose. This work offers a unique approach to deeply understanding the electric breakdown mechanism in dielectric polymers and indicates the feasibility of cellulose in replacing petroleum-based polymers in the dielectric field.
関連文献
Efficient synthesis of discrete oligo(fluorenediacetylene)s toward chain-length-dependent optical and structural properties
Xianheng Shi, Min Liu, Lishan Li, Jiandong Zhang, Haiyan Li, Zhihao Huang, Wei Zhang, Zhengbiao Zhang, Nianchen Zhou, Xiulin Zhu
DOI: 10.1039/D1PY00165E
Oxazoline-methacrylate graft-copolymers with upper critical solution temperature behaviour in Yubase oil
Matilde Concilio, Nga Nguyen, C. Remzi Becer
DOI: 10.1039/D1PY00534K
Hierarchical ordering and multilayer structure of poly(ε-caprolactone) end-functionalized by a liquid crystalline unit: role of polymer crystallization
Wenqing Xu, Xing Li, Wenhua Yuan, Jian Zhou
DOI: 10.1039/D1PY00702E
Photo cleavable thioacetal block copolymers for controlled release
Yongjun Men, Tobias G. Brevé, Antonia G. Denkova, Rienk Eelkema
DOI: 10.1039/D1PY00514F
Helical polymer self-assembly and chiral nanostructure formation
Randall A. Scanga, James F. Reuther
DOI: 10.1039/D0PY01558J
こちらもおすすめ
噻奈普汀乙酯の物理化学的性質は何ですか?
CAS番号66981-77-9の噻奈普汀乙酯は、結晶性白色粉末であり、分子量は476.9 g/molです。この化合物は水に溶けにくく、一般的には有機溶媒で溶解し...
アミピシリン不純物Fとは何ですか?
アミピシリン不純物Fは、CAS番号124774-48-7の化合物です。これは、抗生物質アミピシリンの生産過程で生成される不純物の一つであり、(4S)-2-({[...
イリジウム(I)ヘキサフルオロフォスファートの代替品はありますか?
イリジウム(I)ヘキサフルオロフォスファートの代替品として、他の有機金属化合物や非有機金属化合物が使用されることがあります。具体的には、ダイゾニウム塩や他の金属...
含有3-(苯氧基甲基)苯硼酸频那醇酯の廃棄物はどのように処理すべきですか?
含有3-(苯氧基甲基)苯硼酸频那醇酯の廃棄物は、安全な方法で処理する必要があります。まず、廃棄物を適切な容器に収集し、避けて保管します。次に、専門の廃棄処理業者...
2-甲基辛-1-醇を取り扱う際の実験室安全事項は何ですか?
取り扱う際は、密閉のゴーグルと手袋を着用することが推奨されます。ドラフトチャンバーを使用し、漏洩時には速やかに取り扱いを中止し、適切な排気設備を使用してください...
3α-アセトキノイドコレステロールエステルはどのように保存すればよいですか?
3α-アセトキノイドコレステロールエステルは、常温から低温(0-5℃)の暗所で保存し、密閉容器に入れることで安定性を保つことが推奨されます。また、湿気や酸素から...
2-ぶンジロキシ-4-(トリフルオロメチル)フェノルビノン酸の主な用途は何ですか?
2-ぶンジロキシ-4-(トリフルオロメチル)フェノルビノン酸は、化学合成の触媒としての使用や、医薬品の合成材料としての役割があります。また、特定の合成路線で使用...
(2S,3R)-2-氨基-3-甲基丁二酸はどのように合成されますか?
(2S,3R)-2-氨基-3-甲基丁二酸は、2-ヒドロキシ-3-メチル丁酸とアミノ化反応を行うことで合成されます。触媒としてジクロロメタンが使用され、選択性と収...
1-Benzyl-2-phenyl-1H-imidazoleはどのように保存すればよいですか?
この化合物は常温で避けてください。直射日光を避け、密閉容器で保存し、湿気を防水の容器に入れて保管してください。
掲載誌
Journal of Materials Chemistry A

Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. The journals have a strong history of publishing quality reports of interest to interdisciplinary communities and providing an efficient and rigorous service through peer review and publication. The journals are led by an international team of Editors-in-Chief and Associate Editors who are all active researchers in their fields. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C. More than one Journal of Materials Chemistry journal may be suitable for certain fields and researchers are encouraged to submit their paper to the journal that they feel best fits for their particular article. Example topic areas within the scope of Journal of Materials Chemistry A are listed below. This list is neither exhaustive nor exclusive. Artificial photosynthesis Batteries Carbon dioxide conversion Catalysis Fuel cells Gas capture/separation/storage Green/sustainable materials Hydrogen generation Hydrogen storage Photocatalysis Photovoltaics Self-cleaning materials Self-healing materials Sensors Supercapacitors Thermoelectrics Water splitting Water treatment














![4-(4-{4-[4-Fluoro-3-(trifluoromethyl)phenyl]-1-methyl-1H-imidazol-2-yl}-1-piperidinyl)-1H-pyrazolo[3,4-d]pyrimidine 4-methylbenzenesulfonate (1:1) structure 4-(4-{4-[4-Fluoro-3-(trifluoromethyl)phenyl]-1-methyl-1H-imidazol-2-yl}-1-piperidinyl)-1H-pyrazolo[3,4-d]pyrimidine 4-methylbenzenesulfonate (1:1) structure](https://static.chemtradehub.com/structs/108/1082949-68-5-00b6.webp)