摘要
Owing to the sluggish kinetics of oxygen evolution reaction (OER) in electrochemical water electrolysis process, efficient and durable OER electrocatalysts are crucially needed. However, it is a great challenge to improve the comprehensive performance of OER electrocatalysts by utilizing various synergistic methodologies. To solve these issues, herein, Ir-doped Co-based compounds with regulated anions were synthesized using a coprecipitation method as the electrodes for boosting the OERs. Doping with Ir atoms modified the coordination environments and electronic structures of the CoOx-CO32- lattice, and the generated Co3+ species promoted the generation of active species for the OER. It is worthwhile noting that a hybrid crystalline/amorphous IrCoOx-CO32- compound was obtained with an Ir content of 10.09 wt.% and a large amount of Co3+, and demonstrated excellent electrocatalytic OER performance. The overpotential required for the developed IrCoOx-CO32- to achieve 10 mA cm-2 was as low as 207 mV with a very low Tafel slope of 61.7 mV dec-1, which is better than the commercial IrO2. Furthermore, anions created in the IrCoOx significantly promoted the OER, and their effects were decreased in the order of CO32- > PO43- > OH-. This work clarifies the synergistic mechanism of cations and anions on the electrocatalytic OER performance of Co-based compounds, providing new insights for designs of high-performance OER electrocatalysts for water electrolysis.
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