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Bidirectional Correlation between Mechanics and Electrochemistry of Poly(vinyl alcohol)-Based Gel Polymer Electrolytes.
Hu, Jingzhi; Li, Tong; Wei, Bingqing.
Afiliación
  • Hu J; State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University and Shaanxi Joint Laboratory of Graphene (NPU) , Xi'an 710072, China.
  • Li T; Department of Mechanical Engineering, University of Delaware , Newark, Delaware 19716, United States.
  • Wei B; State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University and Shaanxi Joint Laboratory of Graphene (NPU) , Xi'an 710072, China.
J Phys Chem Lett ; 8(24): 6106-6112, 2017 Dec 21.
Article en En | MEDLINE | ID: mdl-29211483
ABSTRACT
The electrochemical-mechanical coupling property of solid electrolyte membranes is critical to improving the performance of solid-state energy storage devices. A new phenomenon was observed in which the electrochemical charge-discharge process induced aligned wrinkles on the edge of poly(vinyl alcohol)-H2SO4 gel polymer electrolytes (GPEs), which is attributed to the deformation of polymer chains under electrochemical stimulation according to multiscale simulations. In the reverse direction, by means of modeling and testing, it was proved that the ionic conductivity of GPEs can be tuned by mediating the mechanical properties of GPEs via tailoring the polymer at the nanoscale. This bidirectional correlation reveals the coupling mechanisms between mechanical and electrochemical properties of GPEs and provides an insightful understanding of the origin and regulation of the ionic conductivity of GPEs, which is fundamental to improving the performance of GPEs.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Phys Chem Lett Año: 2017 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Phys Chem Lett Año: 2017 Tipo del documento: Article País de afiliación: China