Fine-tuning nanoflower-like Fe/Co hybrids with high content oxyhydroxide accelerating oxygen evolution kinetics

J Colloid Interface Sci. 2024 Sep 15:670:124-131. doi: 10.1016/j.jcis.2024.05.034. Epub 2024 May 12.

Abstract

Iron hydroxide (FeOOH) is a potential active component in iron-based electrocatalysts for water electrolysis. However, its catalytic performance is constrained by its slow oxygen evolution reaction (OER) kinetics. Herein, we synthesized a nanoflower-like FeCo-hydro(oxy)oxides composite with tunable Fe/Co ratios (Fex-Coy) on nickel foam (NF) via a one-step electrodeposition technique. This method allows for precise control over the morphology and composition of the hybrid nanoflowers. The optimized Fe9-Co1 discloses favorable OER performance with a low overpotential of 222 mV at 50 mA cm-2 and demonstrates good stability exceeding 60 h at 10 mA cm-2. Further, an assembled Fe9-Co1(+)||Pt/C(-) dual-electrode configuration achieves a low cell voltage of 1.73 V at the current density of 100 mA cm-2 for water splitting, with long-term stability for 70 h and minimal degradation. Studies indicate that the distinctive nanoflower morphology of Fe9-Co1 enhances active site exposure, while both FeOOH and reconstructed CoOOH serve as catalytic centers, contributing to the observed OER performance. This work introduces a facile approach for synthesizing OER electrocatalysts, underscoring the role of the high-valence state of Fe/Co as active sites in the OER process.

Keywords: Electrocatalyst; Electrodeposition; Overall water splitting; Oxygen evolution reaction.