Developing a highly efficient, cost-effective, and stable bifunctional electrode for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is still a major challenge. This work reports on a novel method for fabricating TiN ceramic membrane supported nitrogen-incorporating NiCo 2 nanowires (NiCo 2 -N/TiN) as a bifunctional electrode. Owing to its unique structure, the ample reaction sites available, and the enhanced mass/charge transport ability, the NiCo 2 -N/TiN electrode exhibits efficient catalytic performance both in HER and OER, with overpotentials of 131 mV at 20 mA·cm −2 for HER and 330 mV at 20 mA·cm −2 for OER, together with excellent stability in alkaline solution. The NiCo 2 -N/TiN electrode only requires a cell voltage of 1.71 V to drive the current density of 20 mA·cm −2 for overall water splitting, which exhibits excellent stability for more than 100000 s. Accordingly, the produced ceramic membrane electrode has a great potential for application in industrial hydrogen production.
The development of high-performance electrocatalytic electrodes for overall water splitting is a crucial issue to realize renewable hydrogen production . This paper presents the in situ growth of N -modified Co-based nanorods on porous TiN ceramic membranes using the hydrothermal method and thermal NH 3 treatment, resulting in a novel self-supported electrocatalytic electrode with abundant heterointerfaces, denoted as NCTN-x-y (x: nitridation temperature; y: nitridation time). In the alkaline medium (1 M KOH), the NCTN-350-2 electrode displays the best hydrogen evolution reaction (HER) activity (ƞ 10 = 66 mV), and the NCTN-250-3 electrode manifests the best oxygen evolution reaction (OER) performance (ƞ 10 = 270 mV). Accordingly, these two electrodes comprise an electrolyzer, which features a current density of 10 mA cm −2 at a low cell voltage of 1.63 V. The good electrocatalytic performance can be attributed to the abundant heterointerfaces formed between the porous TiN ceramic membrane and the N -modified Co-based nanorods , in conjunction with the hierarchical pore structure of the TiN ceramic membrane. Theoretical calculations identify that the construction of heterointerfaces modulates the electronic structure of active sites, thereby promoting the dissociation of H 2 O, optimizing the H* adsorption energy (ΔG H* ), and accelerating the reaction kinetics, which ultimately improve the electrocatalytic activity of electrode.
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