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1. Recent Progress on Dominant Sulfide‐Type Solid‐State Na Superionic Conductors for Solid‐State Sodium Batteries

   https://doi.org/10.1002/smll.202311195  

   Guo, Xiaolin; Halacoglu, Selim; Chen, Yan; Wang, Hui (August 2024, Small)

   Abstract Over the past decade, solid‐state batteries have garnered significant attentions due to their potentials to deliver high energy density and excellent safety. Considering the abundant sodium (Na) resources in contrast to lithium (Li), the development of sodium‐based batteries has become increasingly appealing. Sulfide‐based superionic conductors are widely considered as promising solid eletcrolytes (SEs) in solid‐state Na batteries due to the features of high ionic conductivity and cold‐press densification. In recent years, tremendous efforts have been made to investigate sulfide‐based Na‐ion conductors on their synthesis, compositions, conductivity, and the feasibility in batteries. However, there are still several challenges to overcome for their practical applications in high performance solid‐state Na batteries. This article provides a comprehensive update on the synthesis, structure, and properties of three dominant sulfide‐based Na‐ion conductors (Na₃PS₄, Na₃SbS₄, and Na₁₁Sn₂PS₁₂), and their families that have a variety of anion and cation doping. Additionally, the interface stability of these sulfide electrolytes toward the anode is reviewed, as well as the electrochemical performance of solid‐state Na batteries based on different types of cathode materials (metal sulfides, oxides, and organics). Finally, the perspective and outlook for the development and practical utilization of sulfide‐based SE in solid‐state batteries are discussed. 

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2. An electrochemically stable homogeneous glassy electrolyte formed at room temperature for all-solid-state sodium batteries

   https://doi.org/10.1038/s41467-022-30517-y  

   Chi, Xiaowei; Zhang, Ye; Hao, Fang; Kmiec, Steven; Dong, Hui; Xu, Rong; Zhao, Kejie; Ai, Qing; Terlier, Tanguy; Wang, Liang; et al (December 2022, Nature Communications)

   Abstract All-solid-state sodium batteries (ASSSBs) are promising candidates for grid-scale energy storage. However, there are no commercialized ASSSBs yet, in part due to the lack of a low-cost, simple-to-fabricate solid electrolyte (SE) with electrochemical stability towards Na metal. In this work, we report a family of oxysulfide glass SEs (Na 3 PS 4− x O x , where 0 <  x  ≤ 0.60) that not only exhibit the highest critical current density among all Na-ion conducting sulfide-based SEs, but also enable high-performance ambient-temperature sodium-sulfur batteries. By forming bridging oxygen units, the Na 3 PS 4− x O x SEs undergo pressure-induced sintering at room temperature, resulting in a fully homogeneous glass structure with robust mechanical properties. Furthermore, the self-passivating solid electrolyte interphase at the Na|SE interface is critical for interface stabilization and reversible Na plating and stripping. The new structural and compositional design strategies presented here provide a new paradigm in the development of safe, low-cost, energy-dense, and long-lifetime ASSSBs. 

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3. Solution Synthesis of Sb ₂ S ₃ and Na ₃ SbS ₄ Solid-State Electrolyte

   https://doi.org/10.1149/1945-7111/ac3752  

   Vaselabadi, Saeed Ahmadi; Smith, William H.; Wolden, Colin A. (November 2021, Journal of The Electrochemical Society)

   Sodium thioantimonate (Na 3 SbS 4 ) is an attractive solid-state electrolyte for sodium-ion batteries due to its high ionic conductivity and stability in protic solvents. Herein, we describe solution-based routes for its synthesis. First, we demonstrate the synthesis of the Sb 2 S 3 precursor via thermodynamically favorable metathesis between Na 2 S and SbCl 3 . This solution-based approach is further extended to couple the resulting Sb 2 S 3 with Na 2 S for the synthesis of Na 3 SbS 4 . It is shown that ethanol is a superior solvent to water for solution-based synthesis of Na 3 SbS 4 with respect to yield, morphology, and performance. Amorphous Sb 2 S 3 synthesized from low-temperature metathesis produced highly crystalline Na 3 SbS 4 with a room temperature Na + conductivity of 0.52 mS cm −1 and low activation energy, comparable to leading values reported in the literature. 

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4. Optimized Thin Film Processing of Sodium Mixed Oxy-Sulfide-Nitride Glassy Solid Electrolytes for All-Solid-State Batteries

   https://doi.org/10.1021/acsaem.3c00294  

   Olson, Madison; Wheaton, Jacob; Okkema, Mary; Oldham, Nicholas; Martin, Steve W. (June 2023, ACS Applied Energy Materials)

   Na4P2S7-6xO4.62xN0.92x (NaPSON) glassy solid electrolytes (GSEs) were prepared and tested for their electrochemical properties and processability into thin films. The x = 0.2 composition (NaPSON-2) was found to be highly conducting, non-crystallizable, largely stable against Na-metal and supports symmetric cell cycling up to >100 µA cm-2 without shorting and for these reasons was processed into thin films drawn to 50 m and tested in symmetric and asymmetric cells. Measurements of the sodium ion conductivity using symmetric cells demonstrated that the conductivity of NaPSON-2 was unchanged by film forming. Galvanostatic cycling at 5 A cm-2 of 1.3 mm NaPSON-2 showed stability over 450 hours, while cycling a 50 m thin film showed a very slow growth in the resistance. Cyclic voltammetry and x-ray photoelectron spectroscopy of the NaPSON-2 thin film GSE revealed that it did not react with Na-metal at its surface, but rather in the bulk of the film, showing S, Na2S, and Na3P reaction products. The source of the surface stability was determined to be the preferential segregation of trigonally coordinated nitrogen. These low-cost and easily processed NaPSON GSEs provide a system of materials which could provide for significantly lower cost higher energy density grid-scale batteries. 

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5. In Situ Formation of Polymer-Inorganic Solid-Electrolyte Interphase for Stable Polymeric Solid-State Lithium Metal Batteries

   https://doi.org/10.1016/j.chempr.2021.06.019  

   Deng, Tao; Cao, Longsheng; He, Xinzi; Li, Ai-Min; Li, Dan; Xu, Jijian; Liu, Sufu; Bai, Panxing; Jin, Ting; Ma, Lin; et al (January 2021, Chem)

   null (Ed.)

   Composite polymer electrolytes (CPEs) for solid-state Li metal batteries (SSLBs) still suffer from gradually increased interface resistance and unconstrained Li dendrite growth. Herein, we addressed the challenges by designing a LiF-rich inorganic solid-electrolyte interphase (SEI) through introducing a fluoride-salt concentrated interlayer on CPE film. The rigid and flexible CPE helps accommodate the volume change of electrodes, while the polymeric high-concentrated electrolyte (PHCE) surface-layer regulates Li-ion flux due to the formation of a stable LiF-rich SEI via anion reduction. The designed CPE-PHCE presents enhanced ionic conductivity and high oxidation stability of > 5.0V (vs. Li/Li+). What’s more, it dramatically reduces the interfacial resistance and achieves a high critical current density of 4.5 mA cm-2 for dendrite-free cycling. The SSLBs, fabricated with thin CPE-PHCE membrane (< 100 μm) and Co-free LiNiO2 cathode, exhibit exceptional electrochemical performance and long cycling stability. This approach of SEI design can also be applied to other types of batteries. 

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