Plasmonic-Assisted Water–Gas Shift Reaction of Gold Particles on TiO₂

The Localized Surface Plasmon (LSP) effect of 5 nm mean size Au particles deposited on TiO2 P25 was investigated during the photo-thermal water gas shift reaction (WGSR). The effects of CO concentration, excitation light flux and energy, and molecular oxygen addition during the reaction were investigated. The photocatalytic WGSR rate under light excitation with wavelengths extending from 320 to 1100 nm was found to be higher than the thermal reaction alone at the same temperature (85 °C). A H2/CO2 ratio of near unity was found at high concentrations of CO. The addition of molecular oxygen during the reaction resulted in a slight decrease in molecular hydrogen production, while the rates of CO2 formation and CO consumption changed by one order of magnitude. More importantly, it was found that the WGSR rates were still high under only visible light excitation (600–700 nm). The results prove that Au LSP alone triggers this chemical reaction without requiring the excitation of the semiconductor on which they are deposited

Plasmonic-Assisted Water–Gas Shift Reaction of Gold Particles on TiO₂

The Localized Surface Plasmon (LSP) effect of 5 nm mean size Au particles deposited on TiO2 P25 was investigated during the photo-thermal water gas shift reaction (WGSR). The effects of CO concentration, excitation light flux and energy, and molecular oxygen addition during the reaction were investigated. The photocatalytic WGSR rate under light excitation with wavelengths extending from 320 to 1100 nm was found to be higher than the thermal reaction alone at the same temperature (85 °C). A H2/CO2 ratio of near unity was found at high concentrations of CO. The addition of molecular oxygen during the reaction resulted in a slight decrease in molecular hydrogen production, while the rates of CO2 formation and CO consumption changed by one order of magnitude. More importantly, it was found that the WGSR rates were still high under only visible light excitation (600–700 nm). The results prove that Au LSP alone triggers this chemical reaction without requiring the excitation of the semiconductor on which they are deposited

NiFeOx and NiFeCoOx Catalysts for Anion Exchange Membrane Water Electrolysis

Hydrogen production using an Anion exchange membrane (AEM) electrolyzer allows the use of non-platinum group metal catalysts for oxygen evolution reaction (OER). Nickel and Cobalt-based oxides are active in an alkaline environment for OER and are relatively inexpensive compared to IrO2 catalysts used in Polymer electrolyte membrane (PEM) electrolysis. Mixed metal oxide catalysts NiFeOx and NiFeCoOx catalysts were synthesized by the coprecipitation method using NaOH. X-ray diffraction results showed mainly NiO diffraction peaks for the NiFeOx catalyst due to the low concentration of Fe, for the NiFeCoOx catalyst, NiCo2O4 diffraction peaks were observed. NiFeCoOx catalysts showed a higher Anion exchange membrane water electrolysis (AEMWE) performance compared to NiFeOx and commercial NiO, the highest current density at 2 V was 802 mA cm−2 at 70 °C using 1 M KOH as an electrolyte. The effect of electrolyte concentration was studied by using 0.01 M, 0.1 M and 1 M KOH concentrations in an electrolysis operation. Electrochemical Impedance spectroscopy was performed along with the equivalent circuit fitting to calculate ohmic and activation resistances, the results showed a decrease in ohmic and activation resistances with the increase in electrolyte concentration. Commercially available AEM (Fumasep FAA-3-50 and Sustainion dioxide membrane X-37-50 grade T) were tested at similar conditions and their performance was compared. EIS results showed that X-37-50 offered lower ohmic resistance than the FAA-3-50 membrane