Evaluating DNA Derived and Hydrothermally Aided Cobalt Selenide Catalysts for Electrocatalytic Water Oxidation.

Electrocatalysts with engaging oxygen evolution reaction (OER) activity with lesser overpotentials are highly desired to have increased cell efficiency. In this work, cobalt selenide catalysts were prepared utilizing both wet-chemical route (CoSe and CoSe-DNA) and hydrothermal route (CoSe-hyd). In wet-chemical route, cobalt selenide is prepared with DNA (CoSe-DNA) and without DNA (CoSe). The morphological results in the wet-chemical route had given a clear picture that, with the assistance of DNA, cobalt selenide had formed as nanochains with particle size below 5 nm, while it agglomerated in the absence of DNA. The morphology was nano networks in the hydrothermally assisted synthesis. These catalysts were analyzed for OER activity in 1 M KOH. The overpotentials required at a current density of 10 mA cm were 352, 382, and 383 mV for CoSe-hyd, CoSe, and CoSe-DNA catalysts, respectively. The Tafel slope value was lowest for CoSe-hyd (65 mV/dec) compared to CoSe-DNA (71 mV/dec) and CoSe (80 mV/dec). The chronoamperometry test was studied for 24 h at a potential of 394 mV for CoSe-hyd and was found to be stable with a smaller decrease in activity. From the OER study, it is clear that CoSe was found to be superior to others. This kind of related study can be useful to design the catalyst with increased efficiency by varying the method of preparation.