Aluminum Acetylacetonate-Confined In-Situ Polymer as Dynamic Active Medium for Sustainable Solid-State Lithium–Sulfur Batteries
Solid polymer electrolyte (SPE)-based lithium-sulfur (Li-S) batteries attract significant interest due to their high theoretical energy densities and enhanced safety profiles. However, the clogging of the cathode-SPE interface with ″dead″ lithium polysulfide (LiPS) is the core failure mechanism of the SPE-based Li-S battery. This induces a sluggish, irreversible electrochemical environment, hindering redox processes and limiting the practical implementation of high-energy-density solid-state Li-S batteries (SSLSBs). To address this problem, this study proposes the generation of a dynamic active medium (DAM) electrolyte system at the cathode interface. Based on the coordination effect between aluminum acetylacetonate and 1,3-dioxolane (DOL), this system is introduced between the cathode and in situ-polymerized polyDOL-based SPE, synergistically realizing three functions: (1) optimizing the electrode-electrolyte interfacial compatibility, (2) adsorbing and reactivating the LiPS accumulated at the interface, and (3) reducing the energy barriers of the S redox reactions and accelerating the sulfide conversion kinetics. This approach enables the SSLSB to reach a high energy density of 347 Wh kg<sup>-1</sup> at a high S loading of 4.5 mg cm<sup>-2</sup>. The pouch cell configuration maintains a capacity retention rate as high as 85.3% after 80 cycles. Moreover, this interfacial DAM strategy provides an innovative engineering concept to suppress the accumulation of LiPS in SSLSBs.
Authors
- Youqi Zhang (ORCID: https://orcid.org/0000-0003-4555-5061)
- Myoung-Chan Kim
- Hun Uk Kim
- Xiaosheng Song
- Wenyi He
- Yang-Kook Sun
- Yong Zhao
Institutions
- Henan University (CN)
- Ministry of Education (IR)
- Hanyang University (KR)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-02-23
- DOI
- https://doi.org/10.1021/jacs.5c14765
- Primary Topic
- Advanced Battery Materials and Technologies
- Type
- article
- Field-Weighted Citation Impact
- 0.00