Heterostructured FeNi hydroxide for effective electrocatalytic oxygen evolution.

Hydrogen production technology by water splitting has been heralded as an effective means to alleviate the envisioned energy crisis. However, the overall efficiency of water splitting is limited by the effectiveness of the anodic oxygen evolution reaction (OER) due to the high energy barrier of the 4e - process. The key to addressing this challenge is the development of high-performing catalysts. Transition-metal hydroxides with high intrinsic activity and stability have been widely studied for this purpose. Herein, we report a gelatin-induced structure-directing strategy for the preparation of a butterfly-like FeNi/Ni heterostructure (FeNi/Ni HS) with excellent catalytic performance. The electronic interactions between Ni 2+ and Fe 3+ are evident both in the mixed-metal "torso" region and at the "torso/wing" interface with increasing Ni 3+ as a result of electron transfer from Ni 2+ to Fe 3+ mediated by the oxo bridge. The amount of Ni 3+ also increases in the "wings", which is believed to be a consequence of charge balancing between Ni and O ions due to the presence of Ni vacancies upon formation of the heterostructure. The high-valence Ni 3+ with enhanced Lewis acidity helps strengthen the binding with OH - to afford oxygen-containing intermediates, thus accelerating the OER process. Direct evidence of FeNi/Ni HS facilitating the formation of the Ni-OOH intermediate was provided by in situ Raman studies; the intermediate was produced at lower oxidation potentials than when Ni 2 (CO 3 )(OH) 2 was used as the reference. The Co congener (FeCo/Co HS), prepared in a similar fashion, also showed excellent catalytic performance.