TY - JOUR
T1 - Double-network composite solid electrolyte with stable interface for dendrite-free Li metal anode
AU - Wu, Feng
AU - Wen, Ziyue
AU - Zhao, Zhikun
AU - Bi, Jiaying
AU - Shang, Yanxin
AU - Liang, Yaohui
AU - Li, Li
AU - Chen, Nan
AU - Li, Yuejiao
AU - Chen, Renjie
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/6
Y1 - 2021/6
N2 - The application of solid polymer electrolytes for Li metal batteries (LMBs) is hindered by the Li/electrolyte interface instability and poor mechanical strength. Herein, a flexible composite solid electrolyte with a cross-linked double-network structure of inorganic particles and polymer was constructed by an in situ gel-sol method. The as-prepared electrolyte promoted the formation of a stable solid electrolyte interface on the Li metal surface and suppressed the formation of Li dendrites more than pure polymer electrolytes. Particularly, X-ray photoelectron spectroscopy results demonstrated the beneficial effect of inorganic particles for suppressing the side reactions between the Li metal and polymer. Additionally, the as-prepared electrolyte exhibited a reduction of polymer crystallinity, which can facilitate Li+ transport by weaking the interactions between Li+ and the polymer chains. The Li|Li symmetric batteries were stabilized to maintain successive electrodeposition over 1400 h of the plating/stripping process. Furthermore, the Li|LiFePO4 batteries displayed excellent cycling performance at a rate of 0.3 C, revealing tremendous potential in promoting the large-scale application of future LMBs.
AB - The application of solid polymer electrolytes for Li metal batteries (LMBs) is hindered by the Li/electrolyte interface instability and poor mechanical strength. Herein, a flexible composite solid electrolyte with a cross-linked double-network structure of inorganic particles and polymer was constructed by an in situ gel-sol method. The as-prepared electrolyte promoted the formation of a stable solid electrolyte interface on the Li metal surface and suppressed the formation of Li dendrites more than pure polymer electrolytes. Particularly, X-ray photoelectron spectroscopy results demonstrated the beneficial effect of inorganic particles for suppressing the side reactions between the Li metal and polymer. Additionally, the as-prepared electrolyte exhibited a reduction of polymer crystallinity, which can facilitate Li+ transport by weaking the interactions between Li+ and the polymer chains. The Li|Li symmetric batteries were stabilized to maintain successive electrodeposition over 1400 h of the plating/stripping process. Furthermore, the Li|LiFePO4 batteries displayed excellent cycling performance at a rate of 0.3 C, revealing tremendous potential in promoting the large-scale application of future LMBs.
KW - Composite solid electrolyte
KW - Li metal batteries
KW - Li/electrolyte interface
KW - Polymer crystallinity
UR - http://www.scopus.com/inward/record.url?scp=85103689684&partnerID=8YFLogxK
U2 - 10.1016/j.ensm.2021.03.020
DO - 10.1016/j.ensm.2021.03.020
M3 - Article
AN - SCOPUS:85103689684
SN - 2405-8297
VL - 38
SP - 447
EP - 453
JO - Energy Storage Materials
JF - Energy Storage Materials
ER -