Abstract
The development of non-noble metal electrocatalyst with high-efficiency and clear underlying of the related reaction mechanism towards the sluggish oxygen evolution reaction (OER) is critical for large-scale hydrogen production. In this study, tri-metallic Prussian blue analogue (PBA) of FeCoNi-PBA was synthesized using a facile and low-energy consumption co-precipitation method. The FeCoNi-PBA was found to be etched by the high-pH 1 M KOH electrolyte such that under anodic applied potential during electrolysis the formation of metal (oxy)hydroxide is accelerated. Operando Raman and post-mortem characterizations reveal that the applied anodic potential promotes the phase transformation so that the PBA undergoes self-reconstruction to form metal (oxy)hydroxide embedded in a carbon matrix with fully exposed active sites. The metal (oxy)hydroxide serves as the real active sites while the carbon matrix is believed to enhance the conductivity and hydrophilicity, which facilitates the electron transfer and electrolyte diffusion to improve the OER performance. In alkaline media, FeCoNi-PBA demonstrates excellent OER performance with a low overpotential of 236 mV at 10 mA cm−2, small Tafel slope of 43.8 mV dec-1, and long-term durability.
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