摘要
Lithium argyrodites are one of the most promising sulfide electrolytes due to their high ionic conductivity and ductile feature. Among them, Li 6 PS 5 I (LPSI) exhibits better stability against Li metal but a rather low ionic conductivity (only ≈10 −6 S cm −1 ) because of the absence of S 2− /I − disorder. Herein, argyrodite Li 6− x PS 5− x I 1+ x glass–ceramic electrolytes with high iodine content are synthesized using ultimate-energy mechanical alloying method. S 2− /I − disorder is successfully introduced into the system by doping LiI during this one-pot process. Determined by 6 Li magic angle spinning nuclear magnetic resonance and ab initio molecular dynamics simulations, the introduction of iodine promotes Li + inter-cage jumps, leading to an enhanced long-range Li + conducting. The Li 5.6 PS 4.6 I 1.4 glass–ceramic electrolyte (LPSI 1.4 -gc) possesses high ionic conductivity (2.04 mS cm −1 ) and excellent stability against Li metal. The Li symmetric cell with the LPSI 1.4 -gc electrolyte demonstrates ultralong cycling stability over 3200 h at 0.2 mA cm −2 . LiCoO 2 /Li 6 PS 5 Cl/Li all-solid-state battery applying LPSI 1.4 -gc as the anode interlayer also presents prominent cycling and rate performance. This work provides a novel type of electrolyte with high ionic conductivity and stability against Li metal.
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