Abstract
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•Self-templated fabrication of hollow Mn-Co phosphide yolk-shell is reported.•Difference in inward and outer diffusion leads to hollow yolk-shell structure.•Mn-Co phosphide catalyst shows higher activity for OER than its oxide counterpart.•Mn3+ and Co3+ active sites give rise to high activity for OER.
Hierarchical nanostructures with hollow architectures can provide rich active sites, improved transport of ions, and highly robust structure for electrochemical applications. In this work, we report the self-templated fabrication of hierarchical manganese-cobalt phosphide (Mn-Co phosphide) yolk-shell spheres using highly uniform cobalt glycerate spheres as sacrificial templates. Through a simple exchange reaction with the manganese precursor solution at room temperature, these cobalt glycerate spheres are readily converted to hierarchical Mn-Co LDH yolk-shell spheres, which can be further phosphidized at 350 °C under inert atmosphere to generate hierarchical Mn-Co phosphide with distinct yolk-shell morphology. When tested as an electrocatalyst for oxygen evolution reaction (OER), the hierarchical Mn-Co phosphide yolk-shell spheres exhibit an overpotential of 330 mV at a current density of 10 mA cm−2 and a Tafel slope of 59.0 mV dec-1, which are higher than those of Mn-Co oxide yolk-shell spheres (480 mV and 113 mV dec-1) and hierarchical cobalt phosphide spheres (410 mV and 61.3 mV dec-1). Post-OER analysis by XPS reveals that the high activity of the hierarchical Mn-Co phosphide yolk-shell catalyst originates from the existence of Mn4+/Mn3+ and Co2+/Co3+ redox couples and the formation of active metal oxyhydroxide species on its surface. The proposed self-sacrificial templating strategy will provide useful guidance for future construction of hollow inorganic metal nanostructures with yolk-shell morphology for energy storage and conversion applications.