In situ formed oxy/hydroxide antennas accelerating the water dissociation kinetics on a Co@N-doped carbon core-shell assembly for hydrogen production in alkaline solution

Dalton Trans. 2019 Aug 21;48(31):11927-11933. doi: 10.1039/c9dt02301a. Epub 2019 Jul 18.

Abstract

The hydrogen evolution reaction (HER) in alkaline electrolytes is restricted severely by sluggish water dissociation in the Volmer step. Here, we embedded Co crystals into a N-doped carbon (Co@NC) on nickel foam (NF) framework and electrochemically oxidized them in situ to construct a CoOxHy [a mixture of Co(OH)2 and CoOOH] antenna-modified Co@NC core-shell assembly (NF/Co@NC/CoOxHy). The CoOxHy antennas significantly decreased the activation energy of water dissociation to protons (the Volmer step), and hydrogen production over the Co core activated NC shell may follow a multi-carbon catalytic mechanism activated by Co and N atoms. As a result, the NF/Co@NC/CoOxHy configuration exhibits a 40 mV onset potential, a low HER overpotential of 51 mV at 10 mA cm-2, and a current density still reaching around 20 mA cm-2 after 55 h of stability testing in alkaline electrolyte. Our material functionalization strategy may open up a new approach for developing water-alkali electrolysers for use in efficient renewable energy conversion.