Titanium Oxycarbide as Platinum-Free Electrocatalyst for Ethanol Oxidation.

The compound material titanium oxycarbide (TiOC) is found to be an effective electrocatalyst for the electrochemical oxidation of ethanol to CO. The complete course of this reaction is one of the main challenges in direct ethanol fuel cells (DEFCs). While TiOC has previously been investigated as catalyst support material only, in this study we show that TiOC alone is able to oxidize ethanol to acetaldehyde without the need of expensive noble metal catalysts like Pt.

Electroreduction of CO in a Non-aqueous Electrolyte-The Generic Role of Acetonitrile.

Transition metal carbides, especially MoC, are praised to be efficient electrocatalysts to reduce CO to valuable hydrocarbons. However, on MoC in an aqueous electrolyte, exclusively the competing hydrogen evolution reaction takes place, and this discrepancy to theory was traced back to the formation of a thin oxide layer at the electrode surface. Here, we study the CO reduction activity at MoC in a non-aqueous electrolyte to avoid such passivation and to determine products and the CO reduction reaction pathway.

Fundamental Study of the Optical and Vibrational Properties of Fx-AZB@MOF systems as Functions of Dye Substitution and the Loading Amount.

Controlling the switching efficiency of photoactive hybrid systems is an obligatory key prerequisite for systematically improving the design of functional materials. By modulating the degree of fluorination and the amount being embedded into porous hosts, the / ratios of fluorinated azobenzenes were adjusted as both functions of substitution and the degree of loading. Octafluoroazobenzene (F8-AZB) and perfluoroazobenzene (F10-AZB) were inserted into porous DMOF-1.

True Nature of the Transition-Metal Carbide/Liquid Interface Determines Its Reactivity.

Compound materials, such as transition-metal (TM) carbides, are anticipated to be effective electrocatalysts for the carbon dioxide reduction reaction (CORR) to useful chemicals. This expectation is nurtured by density functional theory (DFT) predictions of a break of key adsorption energy scaling relations that limit CORR at parent TMs. Here, we evaluate these prospects for hexagonal MoC in aqueous electrolytes in a multimethod experiment and theory approach.