Boosting overall electrochemical water splitting via rare earth doped cupric oxide nanoparticles obtained by co-precipitation technique

초록

The development of electrocatalyst based on nonprecious metals has been a persistent issue as electro-chemical water splitting requires electrocatalyst with advanced activity and stability. Further, the electrocatalyst must require low overpotential above the standard potential (> 1.23 V) of water splitting to produce hydrogen. This study presents the facile co-precipitation derived rare earth dysprosium (Dy) doped cupric oxide nanoparticles (Cu1-xDyxO) as a non-noble transition metal oxide nanoparticle. The 3 % Dy doped CuO (3 % Dy/CuO) and 1 % Dy doped CuO (1 % Dy/CuO) electrocatalysts showed excellent Oxygen Evolution Reaction (OER) at 1.55 V vs RHE and Hydrogen Evolution Reaction (HER) at -0.036 V vs RHE in aqueous 1 M KOH aqueous electrolyte to attain the benchmark current density (10 mA cm(-2)). The stability of the driven electrocatalyst in a bi-functional electrocatalytic setup was monitored for 24 h and was found to be exhibiting a cell voltage of about 2.1 V at 30 mA cm(-2) constant current density. Further, the retention capability of the electrode was observed to be 99 % with a very minimal loss. This study hugely suggests the promising consequence of doping rare earth onto a non-precious metal oxide-based electrocatalyst, making it a highly effective bifunctional material for water splitting. (C) 2022 Elsevier B.V. All rights reserved.

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