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Item type:Publication, Access status: without files , Promoting Effect of the Residual Silver on the Electrocatalytic Oxidation of Methanol and Its Intermediates on Nanoporous GoldNanoporous gold (NPG) obtained by dealloying Ag75Au25 with an overall residual Ag content of less than 1% was investigated as an electrocatalyst for the oxidation of methanol, formaldehyde, and formate in aqueous 0.1 M NaOH solution. The NPG was used to fill cavity microelectrodes, which allowed the recording of well-resolved voltammetry from the porous material. NPG differs from polycrystalline Au (Au(poly)) by its microstructure and its residual Ag content and also behaves distinctly different than Au(poly). The residual Ag content is higher at the surface of the ligaments than in the bulk. By cycling the NPG electrodes in 0.1 M H2SO4, the surface concentration of Ag could be decreased. It could then be set to a defined value by underpotential deposition (UPD) of Ag. The surface structure, and specifically its evolution upon the removal of Ag from the surface, was analyzed by the characteristic voltammetric features of Pb UPD. The effect of Ag on the electrocatalytic methanol oxidation reaction (MOR) is different in different potential regions. Ag coverage shifts the onset of the methanol oxidation current to less positive potentials. In the range of the peak current density, only a defined low Ag concentration enhanced the MOR current density compared to the Ag-free NPG. The 1 0 0 and 1 1 1 facets contributed the largest current, as concluded from selective poisoning experiments. At a potential of 1.63 V vs RHE, Ag2O at the surface is oxidized to AgO. Those layers can oxidize methanol and formate to CO2. The oxidation of formaldehyde proceeds at a much higher reaction rate than the MOR and formate oxidation; the reaction leads to CO and CO2 depending on the applied potential. Given the high oxidation rate of formaldehyde, it would be immediately further oxidized should it be formed as an intermediate of MOR. This is an important difference to the methanol oxidation at Pt. The water oxidation that occurs at the same potential range in the methanol-free solution was suppressed during CO2 formation.Publicationtype: Journal Article30 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Access status: without files , Nanoporous gold dealloyed from AuAg and AuCu: Comparison of structure and chemical composition© 2018 Properties of dealloyed nanoporous gold (npAu) in catalysis, sensing or actuation applications depend on its structure and chemical composition. NpAu is obtained by corrosion of alloys of gold and a less noble metal such as silver or copper. Structural parameters can be tuned by variations in the preparation process. Due to the large number of parameters that can be varied a direct comparison of results obtained with various samples is often difficult. In this report we compare structure and chemical composition of npAu dealloyed from AuAg and AuCu alloys keeping the number of different sample preparation parameters at a minimum.Publicationtype: Journal Article189 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Access status: without files , A comparative study of alcohol oxidation over nanoporous gold in gas and liquid phase(Elsevier, 2017-08-02); ; ; ; The aerobic oxidation of methanol and ethanol in liquid phase is investigated using unsupported nanoporous gold (npAu) catalysts and compared to gas phase experiments. We pursue the question if this material is still suited as a type of model catalyst even under much more complex conditions in liquid phase. Indeed, npAu is an active catalyst for both liquid and gas phase oxidation of methanol and ethanol with O2 under mild conditions (starting at 40 °C). While in case of methanol solely the self coupling product (methyl formate) is detected, the more facile formation of the acetaldehyde in case of ethanol results in the formation of the free aldehyde (acetaldehyde) and the coupling product (ethyl acetate) in similar amounts. To further probe the surface chemistry, cross coupling reactions between both alcohols, as well as the acetaldehyde are performed. As observed also in gas phase experiments, the formation of the surface bonded aldehyde by β-H elimination of the alcoxy species is rate determining.Publicationtype: Journal Article207