Cobalt disulfide (CoS₂) features highly active catalytic sites and is regarded as a promising candidate for electrocatalytic hydrogen evolution. In this study, molybdenum-doped cobalt disulfide (CoS₂:Mo) was synthesized via a facile hydrothermal approach. XRD analysis confirms that the obtained samples crystallize in a cubic pyrite structure, with diffraction peaks consistently shifting towards lower angles. SEM characterization reveals that the samples exhibit microrod-like morphologies with an average size of approximately 1 μm. Integrated analyses from XRD, XPS, and EDS mapping demonstrate that Mo is uniformly distributed across the surface and successfully doped into the CoS₂ lattice. Electrochemical measurements indicate that the CoS₂:Mo sample delivers a low overpotential of 122 mV and a Tafel slope of 128 mV dec⁻¹ at a current density of 10 mA cm⁻² in alkaline media, significantly surpassing the performance of pure CoS₂ and MoS₂. Moreover, the CoS₂:Mo exhibits an enhanced double-layer capacitance, with a C_dl value of 2.72 mF cm⁻², superior to that of pure CoS₂ (1.63 mF cm⁻²) and MoS₂ (0.31 mF cm⁻²). Mo doping enhances conductivity and active sites, thereby boosting electrocatalysis. This work presents an effective strategy for the development of cost-efficient and high-performance non-precious metal electrocatalysts.