Dual-Network Quasi-Solid Polymer Electrolyte Enabling Polysulfide Immobilization and Dendrite Suppression for Stable Lithium–Sulfur Batteries
Source abstract
Abstract
A dual-network quasi-solid polymer electrolyte (QSPE-DN) is prepared via sequential temperature-programmed cationic ring-opening polymerization and Ritter reaction, integrating crystalline poly(oxymethylene) (POM) lamellae with a chemically cross-linked PMHA ( c -PMHA) network. This hierarchical architecture synergistically combines nanoscale confinement and chemisorption to suppress polysulfide shuttling, enabling the Li–S battery with negligible self-discharge capacity loss. QSPE-DN demonstrates a high Li + transference number (0.78). It can protect the Li anode and promote dendrite-free Li deposition. The Li|QSPE-DN|S battery has an initial capacity of 1003 mAh g –1 at 0.2C and shows a low decay rate of 0.094% per cycle over 300 cycles. Further analysis confirms the structural integrity of sulfur cathodes and negligible Li 2 S/Li 2 S 2 deposition on the anodes, validating effective polysulfide confinement.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry
Beijing Normal University
College of Textiles & Clothing
Qingdao University
Funding
National Natural Science Foundation of China
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