TY - JOUR
T1 - Solid electrolyte membranes prepared from poly(arylene ether sulfone)-g-poly(ethylene glycol) with various functional end groups for lithium-ion battery
AU - Tian, Zhenchuan
AU - Kim, Dukjoon
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/3/1
Y1 - 2021/3/1
N2 - A series of poly(arylene ether sulfone)-g-poly(ethylene glycol)s (PAES-g-PEG)s with different functional groups of –CH3, –OH, -2OH, and –CN were synthesized for the application of solid polymer electrolyte membranes in the lithium-ion battery. Several essential material and membrane properties, including thermal, mechanical, dimensional stability, lithium-ion conductivity, interfacial compatibility, Li-ion transference number, and cell performance, were investigated. The phase separation behavior in the presence of ionic liquid was also examined using small-angle X-ray scattering. As this provision of functional groups led to the suppression of crystallinity but the increment of dielectric permittivity of the electrolytes, both the lithium-ion conductivity and Li-ion transference number were significantly affected. Among them, the PAES-g-PEG membrane containing –CN end group showed the highest lithium-ion conductivity of 8.97 × 10−4 S cm−1 and the Li-ion transference number of tLi+ = 0.4, maintaining the rigid solid-state with the tensile strength beyond 1.5 MPa at room temperature. These excellent physical and electrochemical properties of solid-state electrolyte membranes led to quite a high cell capacity of over 138 mAh g−1 during the 50 charge-discharge cycling tests and stable lithium stripping/plating cyclic performance during 500 cycles.
AB - A series of poly(arylene ether sulfone)-g-poly(ethylene glycol)s (PAES-g-PEG)s with different functional groups of –CH3, –OH, -2OH, and –CN were synthesized for the application of solid polymer electrolyte membranes in the lithium-ion battery. Several essential material and membrane properties, including thermal, mechanical, dimensional stability, lithium-ion conductivity, interfacial compatibility, Li-ion transference number, and cell performance, were investigated. The phase separation behavior in the presence of ionic liquid was also examined using small-angle X-ray scattering. As this provision of functional groups led to the suppression of crystallinity but the increment of dielectric permittivity of the electrolytes, both the lithium-ion conductivity and Li-ion transference number were significantly affected. Among them, the PAES-g-PEG membrane containing –CN end group showed the highest lithium-ion conductivity of 8.97 × 10−4 S cm−1 and the Li-ion transference number of tLi+ = 0.4, maintaining the rigid solid-state with the tensile strength beyond 1.5 MPa at room temperature. These excellent physical and electrochemical properties of solid-state electrolyte membranes led to quite a high cell capacity of over 138 mAh g−1 during the 50 charge-discharge cycling tests and stable lithium stripping/plating cyclic performance during 500 cycles.
KW - Functional end group effect
KW - Grafting polymer
KW - Lithium-ion battery
KW - Lithium-ion conductivity
KW - Phase separation
KW - Solid polymer electrolyte
UR - https://www.scopus.com/pages/publications/85098739262
U2 - 10.1016/j.memsci.2020.119023
DO - 10.1016/j.memsci.2020.119023
M3 - Article
AN - SCOPUS:85098739262
SN - 0376-7388
VL - 621
JO - Journal of Membrane Science
JF - Journal of Membrane Science
M1 - 119023
ER -