4.8 Article

Synergistic effects of chlorine substitution in sulfide electrolyte solid state batteries

Journal

ENERGY STORAGE MATERIALS
Volume 45, Issue -, Pages 484-493

Publisher

ELSEVIER
DOI: 10.1016/j.ensm.2021.12.008

Keywords

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Funding

  1. Dean's Competitive Fund for Promising Scholarship at Harvard University, Data Science Initiative Competitive Research Award at Harvard University
  2. Global Innovation Contest (GIC) of LG Energy Solution, Ltd.
  3. Harvard Climate Change Solutions Fund
  4. Harvard Physical Sciences and Engineering Accelerator Award
  5. Real Colegio Complutense (RCC) at Harvard
  6. Chinese Scholarship Council (CSC)
  7. home institution of Shanghai Jiaotong University
  8. Vehicle Technology Office of the U.S. DOE through the Advanced Battery Materials Research (BMR) Program [DE-SC0012704]
  9. Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory [DE-AC02-06CH11357]
  10. National Science Foundation

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The chlorine substitution effect in sulfide electrolytes improves the ionic conductivity and stability of all-solid-state batteries. Chlorine-substituted sulfide solid electrolytes can better inhibit instabilities caused by bulk decompositions and interfacial reactions through increased voltage stability. This understanding provides an important design principle for all-solid-state batteries.
All-solid-state battery is considered as one of the most promising competitors to Li ion batteries. Two widely known performance metrics for solid electrolytes, among others, are ionic conductivity and stability. Here it is found that both can be improved by the synergistic effects of chlorine substitution in sulfide-based solid electrolytes. Particularly, instabilities arising from both bulk decompositions and interfacial reactions to electrodes can be better inhibited in the chlorine substituted sulfide solid electrolytes through the increased susceptibility to the mechanical constriction induced enhancement of voltage stability. As a result, the stability window of some chlorine-rich Li-argyrodites can be systematically higher than some other chlorine-deficient or chlorine-free electrolytes, especially under the implementation of the mechanical constriction battery assembly and test conditions. Thus, a solid-state battery system of 4 V to 5 V-class cathodes paired with lithium metal anode is demonstrated using these chlorine-rich Li-argyrodites without additional coatings. Furthermore, since Cl composition modulates the stability and instability of Li-argyrodite at low voltages, it allows us to design a multilayer configuration with a hierarchy of Li metal stabilities to demonstrate the stable cycling at relatively high current densities for solid-state batteries. It is found that a moderate Cl composition in the electrolyte is the best to inhibit Li dendrite penetration as the central electrolyte layer, emphasizing a slightly increased instability as the hidden performance metric of relevance here, in addition to the two well-known metrics of stability and ionic conductivity. The understanding of the chlorine substitution effect in sulfide electrolytes provides an important design principle for all-solid-state batteries.

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