Studies on Composite Solid Electrolytes with a Dual Selective Confinement Interface Structure of Anions for High-Performance Lithium Metal Batteries

Solid-state lithium batteries (SSLBs) have attracted much attention due to their good thermal stability and high energy density. However, solid-state electrolytes with low conductivity and prominent interfacial issues have hindered the further development of SSLBs. In this research, inspired from a selective confinement structure of anions, a novel HMOF-DNSE composite solid electrolyte with a dual selective confinement interface structure is proposed based on the semi-interpenetrating structure generated by poly(vinylidene fluoride)-hexafluoropropylene (PVDF-HFP), poly(di- n -butylmethylammonium) bis(trifluoromethanesulfonyl)imide (PDADMATFSI), and a metal–organic frameworks MOF derivative (HMOF) as a filler. The dual-network structure of PVDF-HFP/PDADMATFSI combined with HMOF formed a dual selective confinement interface structure to confine out the movement of large anions TFSI –, thereby enhancing the transfer ability of Li + . Subsequently, the addition of HMOF further improves the transfer of Li + by binding up TFSI – through its crystal structure. The results show that HMOF-DNSE possesses a high room-temperature ionic conductivity (0.7 mS cm –1 ), a wide electrochemical window (up to 4.5 V), and a high Li + transfer number ( t Li + ) (0.56). LiFePO 4 /HMOF-DNSE/Li cell shows an excellent capacity of 141.5 mAh g –1 at 1C rate under room temperature, with a high retention of 80.1% after 500 cycles. The material design strategy, which is based on selective confinement interface structures of anions, offers valuable insights into enhancing the electrochemical performance of solid-state lithium batteries.