Rare earth metal (Sm)-doped NiMnO 3 nanostructures for highly competent alkaline oxygen evolution reaction.

In the present work, samarium-doped nickel manganese oxide was produced by employing a straightforward co-precipitation method. A peak with a 2 θ of 36° corresponded to the (110) plane confirming the formation of the rhombohedral crystal structure of NiMnO 3 . The existence of Mn-O and Ni-O stretching vibration modes was confirmed by Raman spectroscopy. FTIR spectra confirmed the existence of the metal-oxygen bond of NiMnO 3 . The synthesized ternary Ni-based material was found to be spherical nanoparticles with an average diameter of 0.81 μm. The electrochemical oxygen evolution reaction (OER) performance was explored on 0.02 M samarium (Sm)-doped NiMnO 3 demonstrating outstanding OER action with low 321 mV, a low Tafel slope value (109 mV dec -1 ), and low charge-transfer resistance (0.19 Ω). Moreover, the BET results suggest that the 0.02 M Sm-doped NiMnO 3 exhibited elevated surface area (78.78 m 2 g -1 ) with a mesoporous character. Therefore, NiMnO 3 doped with high concentrations of a rare earth metal, Sm, is proposed as a suitable material for next-generation water splitting applications.