Composite polymer electrolytes (CPEs)
that integrate
the advantages
of both inorganic and polymer electrolytes show considerable scope
for all-solid-state lithium metal batteries (ASSLMBs) by virtue of
their enhanced ionic conductivity, excellent mechanical strength,
and low interfacial resistance. Here, NASICON-type Li<sub>1.5</sub>Al<sub>0.43</sub>Y<sub>0.07</sub>Ti<sub>1.5</sub>(PO<sub>4</sub>)<sub>3</sub> (YLATP) is used as an inorganic filler for incorporation
into a poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) organic
matrix. The 7 wt % YLATP CPE exhibits a wide electrochemically stable
potential window of over 5 V and the highest ionic conductivity of
6.28 × 10<sup>–4</sup> S cm<sup>–1</sup> at room
temperature, with a lithium-ion transference number of 0.78. It also
exhibits a self-extinguishing phenomenon, which suggests fireproof
properties in comparison to the prevalent lithium-ion battery separator.
Consequently, the ASSLMB using LiFePO<sub>4</sub> as the cathode demonstrates
a high initial discharge capacity of 168 mAh g<sup>–1</sup> at a 0.1 C-rate, with a capacity retention of 94% after 50 cycles
and improved rate capability in comparison to the pristine (Li<sub>1.5</sub>Al<sub>0.5</sub>Ti<sub>1.5</sub>(PO<sub>4</sub>)<sub>3</sub>) inorganic filler. Post-cycling analysis confirms the formation
of a favorable solid electrolyte interphase (SEI) in the 7 wt % YLATP-based
CPE, which exhibits a significantly lower concentration of CO<sub>3</sub><sup>2–</sup>. This indicates that the low lithium-ion-conducting
inorganic byproduct, Li<sub>2</sub>CO<sub>3</sub>, does not substantially
contribute to the interfacial processes. The synergistic effects of
the YLATP filler, namely its ability to reduce the crystallinity of
the PVDF-HFP matrix and to enhance Li<sup>+</sup> transport via immobilization
of TFSI<sup>–</sup> anions, collectively contribute to the
development of a high-performance CPE suitable for advanced all-solid-state
lithium metal batteries (ASSLMBs).