Mechanistic insight into oxygen evolution electrocatalysis of surface phosphate modified cobalt phosphide nanorod bundles and their superior performance for overall water splitting

- Co-Pi/CoP/Ti requires only 310 mV to deliver a current density of 10 mA cm−2 for OER.
- Co-Pi/CoP/Ti affords 10 mA cm−2 by a cell voltage of only 1.60 V for overall water splitting.
- The overall water-splitting device based on Co-Pi/CoP/Ti can be powered by a 1.5 V AAA battery.
- OER mechanism of Co-Pi/CoP/Ti was systematically investigated.

We here design and fabricate a catalytic electrode by direct growth of cobalt phosphide nanorod bundles with simultaneous surface phosphate (denoted Pi) modification on Ti plate through a simple one-step low-temperature phosphorization process. When the resultant electrodes act as an electrocatalyst for alkaline water splitting, the Co-Pi/CoP/Ti exhibits the superior activity for electrocatalytic oxygen evolution reaction (OER). The Co-Pi/CoP/Ti requires only 310 mV to deliver a current density of 10 mA cm−2 for OER catalysis, which is competitive with state-of-the-art RuO2 and superior to most of cobalt-based phosphides. Mechanistic study suggests that the Co-Pi/CoP undergoes composition and structure conversion during OER catalysis, which endows this electrode with the synergetically improved electrocatalytic OER activity. Serving as a robust bifunctional electrode in a two-electrode configuration for alkaline water electrolyzer, the Co-Pi/CoP/Ti affords current density of 10 mA cm−2 by a cell voltage of only about 1.60 V and maintains its stable performance for at least 24 h. Even the overall water-splitting device based on Co-Pi/CoP/Ti electrodes can be powered by a 1.5 V AAA battery. The present finding offers an attractive electrode for cost-effective and energy-efficient water electrolysis.

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