Rechargeable sodium-ion batteries are facing the challenge of highly electrochemical active anode for their realization. In this study, we report a dual coating strategy of CoS 2 with metallic Co particles and carbon to boost the charge transfer and stability. The phase of CoS 2 and the existence of Co metallic particles were confirmed using x-ray diffraction (XRD). x-ray photoelectron spectroscopy (XPS) results corroborate the presence of carbon and Co S bonding. The prepared CoS 2 @Co@C anode reveals high performance where it shows a capacity of 712 mA h g −1 at 0.05 C rate. The CoS 2 @Co@C electrode exhibits exceptional high rate capability where it exhibits a capacity of 260 mA h g −1 at elevated rate of 10.0 C. The cyclability of CoS 2 @Co@C anode is tested at 0.05 C and 0.5 C rates where the electrode shows 78% and 45% capacity retention of stabilized capacity. The reaction mechanism of the CoS 2 @Co@C electrode is determined using x-ray absorption spectroscopy (XAS) and the results show reversibility of the material. K E Y W O R D S anode, CoS 2 @co@C, dual coating, sodium-ion batteries, x-ray absorption spectroscopy 1 | INTRODUCTION Recently, rechargeable sodium-ion batteries (SIBs) have emerged as the strongest candidates as an alternative to the existing lithium-ion batteries (LIBs). This is due to the extensive usage of energy storage gadgets from small (electronics) to medium (electric vehicles) to large (energy storage system) scale applications. Currently, it seems difficult to replace LIBs from electronic devices and electric vehicles, however, their use in the energy storage system is obstructed due to the high cost and inadequate sources. 1,2 In comparison, SIBs have the