Boosting the Production of Hydrogen from an Overall Urea Splitting Reaction Using a Tri-Functional Scandium-Cobalt Electrocatalyst

Abstract

The creation of highly efficient and economical electrocatalysts is essential to the massive electrolysis of water to produce clean energy. The ability to use urea reaction of oxidation (UOR) in place of the oxygen/hydrogen evolution process (OER/HER) during water splitting is a significant step toward the production of high-purity hydrogen with less energy usage. Empirical evidence suggests that the UOR process consists of two stages. First, the metal sites undergo an electrochemical pre-oxidation reaction, and then the urea molecules on the high-valence metal sites are chemically oxidized. Here, the use of scandium-doped CoTe supported on carbon nanotubes called Sc@CoTe/CNT is reported and CoTe/CNT as a composite to efficiently promote hydrogen generation from highly durable and active electrocatalysts for the OER/UOR/HER in urea and alkali solutions. Electrochemical impedance spectroscopy indicates that the UOR facilitates charge transfer across the interface. Furthermore, the Sc@CoTe/CNT nanocatalyst has high performance in KOH and KOH-containing urea solutions as demonstrated by the HER, OER, and UOR (215 mV, 1.59, and 1.31 V, respectively, at 10 mA cm^-2 in 1 m KOH) and CoTe/CNT shows 195 mV, 1.61 and 1.3 V, respectively. Consequently, the total urea splitting system achieves 1.29 V, whereas the overall water splitting device obtaines 1.49 V of Sc@CoTe/CNT and CoTe/CNT shows 1.54, 1.48 V, respectively. This work presents a viable method of combining HER with UOR for maximally effective hydrogen production.

Keywords: hydrogen production; overall urea splitting; oxygen/hydrogen evolution reactions; pre‐oxidation of Sc@CoTe/CNT and CoTe/CNT; urea oxidation reaction.