Chemical Competing Diffusion for Practical All-Solid-State Batteries

The thermal safety issues of currently available Ni-rich cathode-based power supplies brought in the development of all-solid-state batteries, yet the cascade reactions in Ni-rich materials and the chemo-mechanical degradation between the cathode and solid electrolyte diminished the cycle life. Here, by introducing a new heteroatom chemical competing diffusion strategy, we successfully stabilize the Ni-rich cathode and the contact face with an solid electrolyte. Combining extensive explorations in theoretical calculation and multiscale in/ex situ characterization, we elucidate the atomic-level chemical competing diffusion upon the topological lithiation of layered materials. The heteroatoms with higher binding energy to the coordinated oxygen served as the "oxygen anchor" in the bulk and alleviated the excessive oxygen oxidation through charge compensation, thus easing the chemical aggression of the solid electrolyte by evolved oxygen. Comparably, others were enriched in the surface and formed an ionic "diffusion regulator" with residual lithium, and the special ionic transfer regulation mechanism of the piezoelectric layer validly improved the interface compatibility with the solid electrolyte and weakened the space-charge layer in solid-state batteries. This helped the designed Ni-rich cathode-based sulfide solid-state battery exhibit excellent cyclability under 4.5 V (97.3% after 120 cycles). Our findings unlocked the structure-function relationship between the polarization field generated by the piezoelectric material and the electrode.