“…To solve the above problem of slow Li + transfer kinetics of the SSEs, a great deal of work is mainly focused on the exploration of enhancing the ionic conductivity by introducing aliovalent atoms into the crystal structure of inorganic SSEs. − Li 7 La 3 Zr 2 O 12 (LLZO), as a typical SSE, exhibits higher ionic conductivity (2.4 × 10 –4 S cm –1 ) in cubic phase than that of its counterpart in tetragonal phase (2.3 × 10 –5 S cm –1 ), while the cubic phase is unstable at room temperature. − Recently, many types of aliovalent ions (Ta 5+ , W 6+ , Te 6+ , and Nb 5+ ) are introduced into the crystal structure of LLZO, creating additional vacancies at Li + sites and further reducing the free energy of Li + transfer. , Through aliovalent atoms doping and vacancy regulation, Li 7– x La 3 Zr 2– x M x O 12 (M = Nb and Ta) delivers a higher ionic conductivity of 4 × 10 –4 S cm –1 than LLZO at room temperature, benefited from the stabilized phase with high conductivity and fast transport of lithium ions . However, current inorganic SSEs including LLZO and Li 1.3 Al 0.3 Ti 1.7 P 3 O 12 (LATP) are inevitably limited by their poor mechanical properties and complicated processing conditions, greatly hampering the practical applications. − On this occasion, polymers or their monomers are introduced into inorganic SSEs to fabricate composite electrolytes by physical-mechanical mixing, guaranteeing the ion transport properties and enhancing the mechanical strength to a certain extent. ,, For instance, poly(propylene oxide) (PEO) elastomer is introduced into the LLZO, greatly improving its mechanical strength (∼1.0 MPa) and meanwhile improving the movement of PEO segments and the transport of Li + .…”