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Solid-state batteries (SSBs) are developed with the use of inflammable solid-state electrolytes to realize higher energy density and improved safety. However, the densification temperature of solid electrolytes via conventional sintering methods is usually high, especially for oxide-type electrolytes. Advanced sintering techniques such as spark plasma sintering have been developed to decrease the heat-treatment temperature and time. Recently, a novel cold sintering process (CSP) has been developed, which offers an alternative route to the densification of many solid-state electrolyte materials below 300 °C. Generally, the CSP involves multi-stage non-equilibrium processes such as dissolution-precipitation under external stress, viscous flow of saturated solutions and diffusion of species. Herein, the CSP application in different solid electrolytes and electrodes are summarized. It is expected that the CSP has great potential in preparing solid-state batteries and solid electrolytes in the future. [ABSTRACT FROM AUTHOR]

In this paper, the microstructure and ionic conductivity of Li 1.5 Al 0.5 Ge 1.5 (PO 4) 3 (LAGP) solid electrolytes prepared by spark plasma sintering (SPS) were investigated by XRD, SEM, TEM and EIS, respectively. The results showed that as the sintering temperature was increased, both the relative density and the ionic conductivity of the sintered LAGP samples first increased and then decreased, achieving a maximum value of 97% and 2.12 × 10−4 S cm−1 simultaneously at 700 °C. At the same time, the crystallinity of the sintered samples was improved, while a few impurity phases, such as AlPO 4 and GeO 2 , appeared in the samples. It was also found that carbon contamination and oxycarbide gas was be brought in during SPS. Carbon contamination could produce an extra grain boundary impedance to the samples and could be removed by annealing at 500 °C in an air atmosphere. Oxycarbide gas could affect the relative density of the sintered LAGP samples and could be mitigated by choosing a suitable SPS process. Moreover, the shear modulus of the sintered LAGP was measured to be 49.6 GPa, which exceeded the minimum value of 8.5 GPa that was necessary to suppress Li dendrite growth. [ABSTRACT FROM AUTHOR]

The low coulombic efficiency and poor cycle performance deriving from uncontrolled growth of dendrites have caused a serious obstacle to the practical application of lithium metal. Herein we propose a bifunctional regular-random dual cross-linking network solid polymer electrolyte (RRa-SPE) for dendrite-free all-solid-state lithium metal batteries. Under the synergistic effect of regular polymerization skeleton and random cross-linking network, the RRa-SPE effectively regulates the lithium deposition and facilitates the generation of a highly homogeneous and robust solid-electrolyte interphase (SEI) layer on lithium metal. Besides, this RRa-SPE shows benign ionic conductivity of 4.36 × 10−4 S cm−1 (at 30 °C), high lithium ion transference number of 0.76 and enhanced mechanical strength. The Li/RRa-SPE/Li symmetric cell maintains low and stable voltage polarization (0.15 V) after circulating for 1200 h at 0.5 mA cm−2. Improved LiFePO 4 /RRa-SPE/Li cell exhibits excellent rate capability and prominent cycle performance with a capacity retention of 99.6% after 240 cycles at 0.5 C at 30 °C. Image 1 The SPE is prepared via a facile UV-derived dual-reaction. With bifunctional network, the SPE effectively regulates the lithium deposition. The SPE shows enhanced ionic conductivity of 4.36 × 10−4 S cm−1 at 30 °C. The SPE exhibits high lithium ion transference number of 0.76. [ABSTRACT FROM AUTHOR]

Sulfide-based composite solid-state electrolyte has been deemed as "Holy Grail" for unlocking solid-state lithium metal batteries (SSLMBs) with high-energy density, combining the extremely high ionic conductivity of sulfide and machinability of organic polymer. However, this appealing system is hitherto stymied by two hindrances, difficult to synthesize due to the chemical incompatibility of sulfide with moisture and polar solvents, moreover, interfacial instability with lithium (Li) anode inducing severe Li dendrite grown. Herein, by utilizing perfluoropolyethers as bifunctional adjuvant, we initiatively fabricate sulfide-based composite electrolyte, Poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)/Li 10 GeP 2 S 12 and assemble SSLMBs. Perfluoropolyethers with low molecular weight facilitate the stable dispersion of Li 10 GeP 2 S 12 in casting solution, ascribed to their strong electronegativity of C–F bonds. In addition, high molecular weight perfluoropolyethers function as interfacial stabilizer, dramatically improving the interfacial compatibility with Li anode by in-situ forming a LiF-rich solid electrolyte interphase layer. This composite electrolyte exhibits high room temperature ionic conductivity (0.18 mS cm−1), outstanding lithium ion transfer number (0.68), good mechanical strength and nonflammability. The solid-state LiFePO 4 ǁLi battery presents superior long-term cycling stability and rate capability. Our study paves a new way for fabricating the sulfide-based composite electrolyte, provides an effective strategy for constructing compatible solid-state electrolyteǁLi interface. Image 1 • PVDF-HFP/Li 10 GeP 2 S 12 electrolyte is prepared by binary solution casting method. • PFPE 500 as dispersing solvents exhibit good chemical compatibility with Li 10 GeP 2 S 12. • A high ion conductivity (σ RT = 10−4 S cm−1) and Li+ transfer number (0.68) are obtained. • PFPEs as interfacial stabilizers enhance the compatibility of Li 10 GeP 2 S 12 with Li. • LiFePO 4 ‖Li battery shows good cycling stability and rate capability. [ABSTRACT FROM AUTHOR]