TY - JOUR
T1 - Surface-functionalized Li1.3Al0.3Ti1.7(PO4)3 with synergetic silane coupling agent and ionic liquid modification for PEO-based all-solid-state lithium metal batteries
AU - Wu, Yuchen
AU - Chao, Ming
AU - Lu, Chengyi
AU - Xu, Hanyu
AU - Zeng, Kai
AU - Li, Decheng
AU - Yang, Ruizhi
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/4/15
Y1 - 2024/4/15
N2 - Surface functionalization is one effective strategy for optimizing the stability of Li1.3Al0.3Ti1.7(PO4)3 (LATP) with Li metal anodes and the compatibility between the components of an electrolyte for lithium battery. Herein, a bifunctional modification layer induced by the silane coupling agent (SCA) and ionic liquid (IL) are successfully introduced onto the surface of LATP particles (defined as LATP@SCA-0.25IL) through chemical grafting and ion exchange strategies. Benefitting from the synergistic effect between the protection of modification layer and the effectively reduced interaction of PEO chain segments with Li+, the compatibility of LATP with the Li metal anode is improved, and the dispersion of LATP in PEO matrix is enhanced, a faster Li+ transfer is thereby enabled. As a result, thus-prepared LATP@SCA-0.25IL composite polymer electrolyte (CPE) shows an excellent electrochemical property with high ionic conductivity (1.455 × 10−3 S cm−1 at 60 °C), enhanced Li-ion transference number (0.40), wide electrochemical stability window (4.76 V vs. Li+/Li) and favorable Li metal compatibility (over 1200 h). Furthermore, separately assembled Li/LATP@SCA-0.25IL CPE/LFP coin full cells and pouch cells verify the operational feasibility under extreme conditions. This work paves a new way to protect LATP and promote its practical application in all-solid-state lithium batteries.
AB - Surface functionalization is one effective strategy for optimizing the stability of Li1.3Al0.3Ti1.7(PO4)3 (LATP) with Li metal anodes and the compatibility between the components of an electrolyte for lithium battery. Herein, a bifunctional modification layer induced by the silane coupling agent (SCA) and ionic liquid (IL) are successfully introduced onto the surface of LATP particles (defined as LATP@SCA-0.25IL) through chemical grafting and ion exchange strategies. Benefitting from the synergistic effect between the protection of modification layer and the effectively reduced interaction of PEO chain segments with Li+, the compatibility of LATP with the Li metal anode is improved, and the dispersion of LATP in PEO matrix is enhanced, a faster Li+ transfer is thereby enabled. As a result, thus-prepared LATP@SCA-0.25IL composite polymer electrolyte (CPE) shows an excellent electrochemical property with high ionic conductivity (1.455 × 10−3 S cm−1 at 60 °C), enhanced Li-ion transference number (0.40), wide electrochemical stability window (4.76 V vs. Li+/Li) and favorable Li metal compatibility (over 1200 h). Furthermore, separately assembled Li/LATP@SCA-0.25IL CPE/LFP coin full cells and pouch cells verify the operational feasibility under extreme conditions. This work paves a new way to protect LATP and promote its practical application in all-solid-state lithium batteries.
KW - Ionic liquids
KW - LATP
KW - Silane coupling agent
KW - Solid-state batteries
KW - Surface functionalization
UR - http://www.scopus.com/inward/record.url?scp=85185533325&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2024.234206
DO - 10.1016/j.jpowsour.2024.234206
M3 - 文章
AN - SCOPUS:85185533325
SN - 0378-7753
VL - 599
JO - Journal of Power Sources
JF - Journal of Power Sources
M1 - 234206
ER -