Abstract

<h2>Summary</h2> Lithium-sulfur (Li-S) batteries promise high energy density for next-generation energy storage systems, yet many challenges remain. Li-S batteries follow a conversion chemistry, which radically differs from intercalation-based lithium-ion batteries. Recently, it has become clear that the chemistry of electrolyte solutions and their ability to stabilize polysulfide Li<sub>2</sub>S<sub>x</sub> species formed by sulfur reduction have a critical effect on energy density and cycling performance. This review evaluates the key role of solution properties and polysulfide solvation. Factors that determine the solvation are discussed, including the solvent, salt, concentration, and interaction with Li-polysulfide species. Three fundamental types of electrolyte solution—moderately (conventional), sparingly, and highly solvating—are presented along with a multi-dimensional analysis of solution chemistry, polysulfide solubility, sulfur reaction pathway, Li<sub>2</sub>S deposition, and solution quantity. The stability of lithium metal anodes with these solutions is discussed with respect to side reactions, protective surface film formation, and dendritic Li deposition. Emphasis is placed on options to reduce the electrolyte solution/sulfur ratio and prolong battery cycle life. The advantages and disadvantages of the three systems are compared in accordance with the multifaceted requirements. In conclusion, we offer our perspective for future development of Li-S batteries.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.