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A Functional Air-Stable Li 9.8 GeP 1.7 Sb 0.3 S 11.8 I 0.2 Superionic Conductor for High-Performance All-Solid-State Lithium Batteries.

Cailing FanMuhammad Khurram TufailChaoyuan ZengSajid MahmoodXiaoxiao LiangXianzhe YuXinting CaoQinxi DongNiaz Ahmad
Published in: ACS applied materials & interfaces (2024)
Solid-state electrolytes (SSEs) based on sulfides have become a subject of great interest due to their superior Li-ion conductivity, low grain boundary resistance, and adequate mechanical strength. However, they grapple with chemical instability toward moisture hypersensitivity, which decreases their ionic conductivity, leading to more processing requirements. Herein, a Li 9.8 GeP 1.7 Sb 0.3 S 11.8 I 0.2 (LGPSSI) superionic conductor is designed with a Li + conductivity of 6.6 mS cm -1 and superior air stability based on hard and soft acids and bases (HSAB) theory. The introduction of optimal antimony (Sb) and iodine (I) into the Li 10 GeP 2 S 12 (LGPS) structure facilitates fast Li-ion migration with low activation energy ( E a ) of 20.33 kJ mol -1 . The higher air stability of LGPSSI is credited to the strategic substitution of soft acid Sb into (Ge/P)S 4 tetrahedral sites, examined by Raman and X-ray photoelectron spectroscopy techniques. Relatively lower acidity of Sb compared to phosphorus (P) realizes a stronger Sb-S bond, minimizing the evolution of toxic H 2 S (0.1728 cm 3 g -1 ), which is ∼3 times lower than pristine LGPS when LGPSSI is exposed to moist air for 120 min. The NCA//Li-In full cell with a LGPSSI superionic conductor delivered the first discharge capacity of 209.1 mAh g -1 with 86.94% Coulombic efficiency at 0.1 mA cm -2 . Furthermore, operating at a current density of 0.3 mA cm -2 , LiNbO 3 @NCA/LGPSSI/Li-In cell demonstrated an exceptional reversible capacity of 117.70 mAh g -1 , retaining 92.64% of its original capacity over 100 cycles.
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