Most active electrocatalysts include platinum-group metals (PGMs) and their alloys for electrochemical water splitting, but they are strongly limited by material cost and scarcity. [1] On the other hand, transition metal nitrides overcome this bottleneck and show high electrical conductivity, making them catalytically active for water electrolysis. The high conductivity is based on the incorporation of nitrogen atoms into the unit cell of metal, leading to their d-band contraction with electron density enhancement below Fermi level. [2] For instance, metallic nickel nitride (Ni3N) has been widely reported as a promising electrocatalyst material to accelerate the oxygen evolution reaction (OER) by in-situ forming a nickel (oxy)hydroxide [Ni(OH)2 and NiOOH] layer. [3] The Ni3N materials can be prepared by single step soft-urea route to obtain pure crystal phase [4] or a composite with carbon [5], which rises the following two research questions: 1. What are the optimal synthesis parameters of the soft-urea route to control the structure of Ni3N? 2. What is the relationship between structure and OER activity for Ni3N materials?In this work, we used the soft-urea route to prepare Ni3N materials by varying the ratios of NiCl2, urea and ethanol as precursor chemicals. The precursors were made into a gel by magnetic stirring having metal:urea ratio of 1:5, and then heated up to 400 ºC in a tubular furnace with constant flow of argon. The as-prepared Ni3N were then characterized by X-ray diffraction (XRD), elemental analysis (CHN), transmission electron microscopy (TEM) equipped with an energy-dispersive X-ray spectroscopy (EDX) and X-ray absorption spectroscopy (XAS).Based on the quantitative Rietveld refinement, the formation of pristine Ni3N materials is strongly controlled by the annealing temperature. In addition to the Ni3N phase, we observed the formation of the fcc Ni phase (0 – 10 wt.%) as a minor phase. The TEM images show individual particles of below 100 nm in size. Rotating disc electrode (RDE) technique was employed to establish the electrochemical OER activity of Ni3N materials by sweeping the potential from 1.3 to 1.8 VRHE at 10 mV s-1 in Ar-saturated 0.1 M KOH. Polycrystalline Ni and Ni particles are taken as reference materials. We observed an improvement of the OER activity as the overpotential at 10 mA cm-2 (normalized by the geometric surface area) reduced from 379 mV (poly-Ni) to 358 mV (Ni3N). Furthermore, in-situ XAS studies were performed to better understand the nature of the redox reactions between Ni species and the in-situ formation of nickel (oxy)hydroxide [Ni(OH)2 and NiOOH] layers before and during the OER as a function of the applied potential. Based on the in-situ XANES data, we correlated the structure of Ni3N/fcc-Ni/carbon composite with observed OER activity under alkaline conditions.To summarize, we were able to prepare a composite of Ni3N/fcc-Ni/carbon material with improved OER activity via soft-urea route. The in-situ formation of the layered nickel (oxy)hydroxide [Ni(OH)2 and NiOOH] layers as the catalytically active OER species were probed by in-situ XANES data.