A processable Prussian blue analogue-mediated route to promote alkaline electrocatalytic water splitting over bifunctional copper phosphide.

Prussian blue analogues (PBAs) as a class of metal-organic frameworks demonstrate a promising platform to develop cost-effective high-performance electrocatalysts. However, the construction of delicate micro/nanostructures and controllable doping are still a challenging task for the fabrication of highly efficient copper-based electrocatalysts. Herein, we report a facile synthesis of copper foam supported CuP@Co-CuP (CH@PBA-P/CF) sub-microwire arrays as an active electrocatalyst for alkaline water splitting. The Co-CuP shell derived from the Cu[Co(CN)] PBA serves as the source of active sites. Co doping and construction of core-shell structures endow the CH@PBA-P/CF electrocatalyst with abundant catalytic sites, enhanced intrinsic activity, and low charge transport resistance. The catalytic electrode integrated with 3D copper foam and 1D sub-microwire arrays is highly conductive and stable, which promotes the charge transport and improves the structural stability. As a consequence, CH@PBA-P/CF shows impressive catalytic performances toward the HER and OER in terms of low overpotentials of 231 and 312 mV at a current density of 50 mA cm in 1 M KOH, respectively. Notably, the water electrolyzer using the CH@PBA-P/CF electrode exhibits better water splitting performance than the one using noble metal-based couples.