The development of cost-effective oxygen evolution catalysts is of capital importance for the deployment of large scale energy storage systems based on metal-air batteries and reversible fuel cells. In this direction, a wide range of materials have been explored, especially in more favorable alkaline conditions, and several metal chalcogenides have particularly demonstrated excellent performances. However, chalcogenides are thermodynamically less stable than the corresponding oxides and hydroxides under oxidizing potentials in alkaline media. While this instability in some cases has prevented the application of chalcogenides as oxygen evolution catalysts, and it has been disregarded in some other, we propose to use it in our favor to produce high performance oxygen evolution catalysts. We characterize here the in situ chemical, structural and morphological transformation during the oxygen evolution reaction (OER) in alkaline media of Cu2S into CuO nanowires (NWs), mediating the intermediate formation of Cu(OH)2. We also test their OER activity and stability under OER operation in alkaline media, and compare them with the OER performance of Cu(OH)2 and CuO nanostructures directly grown on the surface of a copper mesh. We demonstrate here that CuO produced during OER from Cu 2 S displays an extraordinary electrocatalytic performance toward OER, well above that of CuO and Cu(OH)2 synthesized mediating no OER in situ transformation.3