Abstract Carbon coating on SiO X surface is crucial for enhancing initial Coulombic efficiency (ICE) and cycling performance in batteries, while also buffering volume expansion. Despite its market prevalence, the effects of the carbon layer's quality and structure on the electrochemical properties of SiO X remain underexplored. This study compares carbon layers produced via gas‐phase and solid‐phase coating methods, introducing an innovative technique that sequentially uses two gases to develop a low‐impedance hybrid carbon structure. In this approach, C 3 H 8 is first deposited to create a short‐range, vertically ordered carbon architecture, followed by C 2 H 2 to establish a long‐range, layered structure, effectively filling the gaps. This results in a dense hybrid carbon layer characterized by minimal defects, high crystallinity, and excellent electronic conductivity. The dominant vertical configuration enhances Li‐ion migration. The SiO@C 3 H 8 @C 2 H 2 prepared through this method yields a specific surface area of 1.14 m 2 g⁻¹ and a high reversible capacity of 1574.9 mAh g⁻¹, alongside an ICE of 83.7%. It showcases remarkable cycling stability, retaining 86.6% capacity after 1000 cycles at room temperature, and performs effectively under varied temperatures and discharging conditions. This low‐impedance carbon structure provides a significant reference for other anodes that also require a carbon layer.