Issue 35, 2022

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

Abstract

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 Cu3P@Co-Cu3P (CH@PBA-P/CF) sub-microwire arrays as an active electrocatalyst for alkaline water splitting. The Co-Cu3P shell derived from the Cu3[Co(CN)6]2 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−2 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.

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

Supplementary files

Article information

Article type
Paper
Submitted
24 Jun 2022
Accepted
11 Aug 2022
First published
17 Aug 2022

Dalton Trans., 2022,51, 13451-13461

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

J. Chen, Y. Li, H. Ye, P. Zhu, X. Fu and R. Sun, Dalton Trans., 2022, 51, 13451 DOI: 10.1039/D2DT02013K

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