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Multifunctional Epoxy-Based Solid Polymer Electrolytes for Solid-State Supercapacitors
- Kwon, Suk Jin;
- Kim, Taehoon;
- Jung, Byung Mun;
- Lee, Sang Bok;
- Choi, U. Hyeok
WEB OF SCIENCE
111초록
Solid polymer electrolytes (SPEs) have drawn attention for promising multifunctional electrolytes requiring very good mechanical properties and ionic conductivity. To develop a safe SPE for energy storage applications, mechanically robust cross-linked epoxy matrix is combined with fast ion-diffusing ionic liquid/lithium salt electrolyte (ILE) via a simple one-pot curing process. The epoxy-rich SPEs show higher Young's modulus (E), with higher glass transition temperature (T-g) but lower ionic conductivity (sigma(dc)) with a higher activation energy, compared to the ILE-rich SPEs. The incorporation of inorganic robust Al2O3 nanowire simultaneously provides excellent mechanical robustness (E approximate to 1 GPa at 25 degrees C) and good conductivity (sigma(dc) approximate to 2.9 x 10(-4) S/cm at 25 degrees C) to the SPE. This suggests that the SPE has a bicontinuous microphase separation into ILE-rich and epoxy-rich microdomain, where ILE continuous conducting phases are intertwined with a sturdy cross-linked amorphous epoxy framework, supported by the observation of the two T(g)s and low tortuosity as well as the microstructural investigation. After assembling the SPE with activated carbon electrodes, we successfully demonstrate the supercapacitor performance, exhibiting high energy and power density (75 W h/kg at 382 W/kg and 9.3 kW/kg at 44 W h/kg). This facile strategy holds tremendous potential to advance multifunctional energy storage technology for next-generation electric vehicles.
키워드
- 제목
- Multifunctional Epoxy-Based Solid Polymer Electrolytes for Solid-State Supercapacitors
- 저자
- Kwon, Suk Jin; Kim, Taehoon; Jung, Byung Mun; Lee, Sang Bok; Choi, U. Hyeok
- 발행일
- 2018-10-17
- 유형
- Article
- 권
- 10
- 호
- 41
- 페이지
- 35108 ~ 35117
- 언어
- ENG
- 출판사
- AMER CHEMICAL SOC
- 발행국가
- 미국
- 분량
- 10 페이지
- ISSN
- E 1944-8252
P 1944-8244