Co─Mn Bimetallic Nanowires by Interfacial Modulation with/without Vacancy Filling as Active and Durable Electrocatalysts for Water Splitting

Abstract Active and stable nonnoble electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are required for water splitting by sustainable electricity. Here, Mn bonded with O and P is incorporated to modulate Co 3 S 4 and Co 2 P respectively to enhance the catalytic activity and extend the catalyst lifetime. Mn 3 O 4 adjusts the electronic structure of Co 3 S 4 and Co atom fills the oxygen vacancy in Mn 3 O 4 . The interfacial interaction endows Co 3 S 4 /Mn 3 O 4 to a lower reaction barrier due to ideal binding energies for OER intermediates. Structure stability of active sites and enhanced Co─S bonds by Operando Raman spectroscopy and theoretical calculations reduce the dissolution of Co 3 S 4 /Mn 3 O 4 , resulting in a lifetime of 500 h at 50 mA cm −2 for OER. The modulation of Co 2 P by MnP weakens the interaction between Co sites and adsorbed H * , achieving a high activity under a large current for HER. The assembled electrolyzer affords 50 mA cm −2 at 1.58 V and exhibits a lifetime of 350 h at 50 mA cm −2 . The calculations disclose the electron interaction for the activity and stability, as well as the enhanced conductivity. The findings develop new avenues toward promoting catalytic activity and stability, making Co─Mn bimetallic nanowires efficient electrocatalysts for nonnoble water electrolyzers.