LAUSR

Abstract The huge volume change of silicon anode during cycling results in unstable solid electrolyte interface (SEI), causing rapid performance degradation. Natural SEI layer has a heterogeneous structure, results in the inhomogeneous Li+ diffusion. The repeated destruction and regeneration of SEI aggravate the inhomogeneity of Li+ diffusion at the interface, leading to non-uniform alloy reaction in the Si bulk. In this work, the silicon surface is passivated by an ultrathin uniform chitosan layer with abundant lithiophilic groups. The capacity of chitosan-coated Si (Si@CS) could reach 1500 mAh g−1 at a current density of 1 A g−1, and the capacity retention remains 91% after 400 cycles. It is demonstrated that the oxygen and nitrogen atoms in chitosan are coordinated with Li+, providing uniformly distributed Li+ transfer sites, results in a homogeneous Li+ flux in the surface layer. Interestingly, a nano-scale ordered atomic arrangement is observed in the delithiated Si@CS, which contributes to more stable and reversible lithiation/delithiation reaction of the Si@CS electrode. It is proposed that optimizing the reaction interface on the Si surface is able to alter the Li-ion diffusion kinetics and structure transition behavior of silicon, which can improve the structure reversibility and stability during cycling.