Surface Engineering of Cr-Doped Cobalt Molybdate toward High-Performance Hydrogen Evolution

Replacing commercial noble metal catalysts with earth-abundant metal catalysts for hydrogen production is an important research direction for electrolytic water. Improving the catalytic performance of non-noble metals while maintaining stability is a key challenge for alkaline hydrogen evolution. Herein, we combined alkali etching and surface phosphating to regulate the properties of Cr-doped CoMoO4 material, forming a surface structure in which amorphous cobalt phosphate and Crdoped Co(Mo)Ox coexist. As expected, the as-prepared catalytic material exhibits remarkable hydrogen evolution activity in 1.0 M KOH, only requiring a low overpotential of 52.7 mV to achieve a current density of 10 mA cm-2, and can maintain this current density for 24 h. The characterization and analysis of the catalyst before and after the stability test reveal that the Cr doping and surface engineering (i.e., alkali etching and phosphating) synergistically increase the adsorption and dissociation of water, optimize the desorption of H, and ultimately accelerate hydrogen evolution. This work provides a new strategy for tailoring nonprecious metal materials to improve the hydrogen production from water electrolysis.

Automated summary

Replacing commercial noble metal catalysts with earth-abundant metal catalysts for hydrogen production is an important research direction. This study demonstrates a new strategy for tailoring non-precious metal materials to improve hydrogen production from water electrolysis. By combining alkali etching and surface phosphating processes, the researchers were able to enhance the catalytic performance of a Cr-doped CoMoO4 material, resulting in efficient and stable hydrogen evolution.