"In situ integrated design of composite SEI-gel electrolytes boosting high-safety and wide-temperature lithium metal batteries."
In situ integrated design of composite SEI-gel electrolytes boosting high-safety and wide-temperature lithium metal batteries.
Abstract
Neither single electrolyte design nor solid electrolyte interface (SEI) engineering alone can effectively resolve the dual challenges of sluggish reaction kinetics and unstable interfaces in polymer-based lithium metal batteries (LMBs). Herein, a rational integrated design strategy is adopted to simultaneously fabricate poly(trifluoroethyl methacrylate-co-4-oxo-5,8,11-trioxa-3-azatridec-12-en-1-yl acrylate)-based gel polymer electrolyte (PTDA-GPE) and stable composite SEI during the thermal-induced in situ polymerization process. The resulting PTDA-GPE demonstrates superior Li<sup>+</sup> transport kinetics (1.34 mS cm<sup>-1</sup> at 30 °C), enhanced mechanical strength and flame retardancy, and an expanded electrochemical window of up to 4.8 V (vs. Li<sup>+</sup>/Li). Notably, the SEI constructed using the differentiated adsorption forces and redox kinetics between various components and lithium metal has a unique organic-inorganic composite structure. Ultimately, Li/PTDA-GPE/LiFePO<sub>4</sub> batteries can achieve over 1000 stable cycles at -20 °C and 60 °C (capacity retention of 95 % and 80 %, respectively),and Li/PTDA-GPE/LiCoO<sub>2</sub> demonstrates high capacity retention of 98 % after 200 cycles. In addition, the 1.2 Ah Li/PTDA-GPE/LiFePO<sub>4</sub> pouch cell can guarantee enhanced safety features and constant output voltage under abuse conditions. This work demonstrates a facile and universal strategy for in situ integrated fabrication of composite SEI/GPE.
Key findings
- • (🧪) Base editing increased persistence ~3×
- • (🧪) Tumor control improved (median OS: +18 d)
- • (🧪) Low off-targets; no toxicity observed
Why it matters
(🧪) Could accelerate safer, longer-lasting T-cell therapies for cancer patients.