Multifunctional plasmonic Ag-hematite nano-dendrite electro-catalysts for methanol assisted water splitting: Synergism between silver nanoparticles and hematite dendrites

Hydrogen is the most environment friendly fuel and has the largest energy density but still much away from being a viable technology due to the cost associated with its production on-site on-demand. However, hydrogen production via water splitting could become potential commercial technology by designing new catalyst materials with low cost, desired surface structures and properties that govern hydrogen evolution reaction (HER) activity and stability. Here, we report the methanol assisted electrochemical water splitting using silver nanoparticles decorated hematite (Ag-hematite) dendrite nanostructures. Ag-hematite nano-dendrites prepared via two different methods viz. chemical co-precipitation and hydrothermal treatment are analysed and compared for their potential applications towards methanol assisted water splitting. It is found that Ag-hematite nano-dendrites prepared by chemical precipitation method shows much better activity as compared to both the parent materials (i.e. Ag NPs and hematite nano-dendrites) as well as Ag-hematite nano-dendrites synthesized by hydrothermal treatment. A baseline study showing the influence of methanol concentration, catalyst, catalyst support, and operating mode has been established. The analysis of the system was carried out as a function of onset potentials and kinetic parameters, including the Tafel slopes and exchange current densities. The effect of electrochemical promotion was investigated to see if it can increase the efficiency and performance of H2 production through electrochemical processes. The observed electro-catalytic enhancement could be attributed to the synergistic effect of hematite dendrites, larger surface area of dendrite structure leading to higher loading of Ag NPs on the surface of HDs. Moreover, the endurance study was performed to check the stability of the presented electrocatalyst in acidic medium under both dark and light illumination conditions which shows that the presented composite catalyst is stable for minimum 100 scans even under light illumination with no signs of photo-corrosion.