Abstract
The pseudo-layered sulfide NiCr2 S4 exhibits outstanding electrochemical performance as anode material in sodium-ion batteries (SIBs). The Na storage mechanism is investigated by synchrotron-based X-ray scattering and absorption techniques as well as by electrochemical measurements. A very high reversible capacity in the 500th cycle of 489 mAh g-1 is observed at 2.0 A g-1 in the potential window 3.0-0.1 V. Full discharge includes irreversible generation of Ni0 and Cr0 nanoparticles embedded in nanocrystalline Na2 S yielding shortened diffusion lengths and predominantly surface-controlled charge storage. During charge, Ni0 and Cr0 are oxidized, Na2 S is consumed, and amorphous Ni and Cr sulfides are formed. Limiting the potential window to 3.0-0.3 V an unusual nickel extrusion sodium insertion mechanism occurs: Ni2+ is reduced to nanosized Ni0 domains, expelled from the host lattice, and is replaced by Na+ cations to form O3-type like NaCrS2 . Surprisingly, the discharge and charge processes comprise Na+ shuttling between highly crystalline NiCr2 S4 and NaCrS2 enabling a superior long-term stability for 3000 cycles. The results not only provide valuable insights for the electrochemistry of conversion materials but also extend the scope of layered electrode materials considering the reversible nickel extrusion sodium insertion reaction as new concept for SIBs.