To generate green hydrogen by water electrolysis, it is vital to develop highly efficient electrocatalysts for the oxygen evolution reaction (OER). The utilization of various 3d transition metal-based layered double hydroxides (LDHs), especially NiFe− LDH, has gained vast attention for OER under alkaline conditions. However, the lack of a proper electronic structure of the NiFe− LDH and low stability under high-pH conditions limit its largescale application. To overcome these difficulties, in this study, we constructed an Sn-doped NiFe−LDH material using a simple wetchemical method. The doping of Sn will synergistically increase the active surface sites of NiFe−LDH. The highly active NiFe−LDH Sn 0 . 015(M) shows excellent OER activity by requiring an overpotential of 250 mV to drive 10 mA/cm 2 current density, whereas the bare NiFe−LDH required an overpotential of 295 mV at the same current density. Also, NiFe−LDH Sn 0 . 015(M) shows excellent long-term stability for 50 h in 1 M KOH and also exhibits a higher TOF value of 0.495 s −1 , which is almost five times higher than that of bare NiFe−LDH. This study highlights Sn doping as an effective strategy for the development of low-cost, effective, stable, self-supported electrocatalysts with a high current density for improved OER and other catalytic applications in the near future.