Search

Rational design and precise engineering are needed to optimize the structural and chemical parameters of functional materials. In this work, we demonstrate how pre-formed binary metal selenides can be an excellent synthetic choice for the synthesis of ternary coinage metal selenide nanoparticles (NPs) with controlled composition. The mild conditions required to obtain these ternary coinage metal selenide NPs offered an easy synthesis of n% CuAgSe–TiO2 (n = 0.01, 0.1, 0.3 and 1.0 mol%) nanocomposites for photocatalytic applications without compromising the structural and morphological characteristics of TiO2 and without having any organic ligands around the NPs. The use of ternary metal selenide nanocomposites CuAgSe–TiO2 results in a clear improvement in their photocatalytic activity for the photodegradation of formic acid as compared to the well-known benchmark for photocatalysis, TiO2 (P25), and its binary metal selenide nanocomposites Cu2−xSe–TiO2. DFT calculations establish semi-metallic behavior of CuAgSe NPs and show that CuAgSe–TiO2 forms a semimetallic-semiconductor heterojunction allowing a better charge separation to enhance its photocatalytic activity. [ABSTRACT FROM AUTHOR]

Site poisoning is a powerful method to unravel the nature of active sites or reaction intermediates. The nature of the intermediates involved in the hydrogenation of CO was unraveled by poisoning alumina-supported cobalt catalysts with various concentrations of tin. The rate of formation of the main reaction products (methane and propylene) was found to be proportional to the concentration of multi-bonded CO, likely located in hollow sites. The specific rate of decomposition of these species was sufficient to account for the formation of the main products. These hollow-CO are proposed to be main reaction intermediates in the hydrogenation of CO under the reaction conditions used here, while linear CO are mostly spectators. [ABSTRACT FROM AUTHOR]

Ge-containing ITQ-22 zeolites have been almost completely degermanated under strong acidic conditions without modifications of the framework topology. Simultaneous to Ge extraction, the framework was partially dissolved; mesopores were formed but the structure was maintained through the re-incorporation of some of silicon species at vacant sites. The presence of many defects in the degermanated framework enabled the incorporation of tetrahedral aluminum, opening the way to the preparation of new and stable acid catalysts with original topologies. [ABSTRACT FROM AUTHOR]

Rational design and precise engineering are needed to optimize the structural and chemical parameters of functional materials. In this work, we demonstrate how pre-formed binary metal selenides can be an excellent synthetic choice for the synthesis of ternary coinage metal selenide nanoparticles (NPs) with controlled composition. The mild conditions required to obtain these ternary coinage metal selenide NPs offered an easy synthesis of n% CuAgSe–TiO2 (n = 0.01, 0.1, 0.3 and 1.0 mol%) nanocomposites for photocatalytic applications without compromising the structural and morphological characteristics of TiO2 and without having any organic ligands around the NPs. The use of ternary metal selenide nanocomposites CuAgSe–TiO2 results in a clear improvement in their photocatalytic activity for the photodegradation of formic acid as compared to the well-known benchmark for photocatalysis, TiO2 (P25), and its binary metal selenide nanocomposites Cu2−xSe–TiO2. DFT calculations establish semi-metallic behavior of CuAgSe NPs and show that CuAgSe–TiO2 forms a semimetallic-semiconductor heterojunction allowing a better charge separation to enhance its photocatalytic activity. [ABSTRACT FROM AUTHOR]

Rational design and precise engineering are needed to optimize the structural and chemical parameters of functional materials. In this work, we demonstrate how pre-formed binary metal selenides can be an excellent synthetic choice for the synthesis of ternary coinage metal selenide nanoparticles (NPs) with controlled composition. The mild conditions required to obtain these ternary coinage metal selenide NPs offered an easy synthesis of n% CuAgSe-TiO2 (n = 0.01, 0.1, 0.3 and 1.0 mol%) nanocomposites for photocatalytic applications without compromising the structural and morphological characteristics of TiO2 and without having any organic ligands around the NPs. The use of ternary metal selenide nanocomposites CuAgSe-TiO2 results in a clear improvement in their photocatalytic activity for the photodegradation of formic acid as compared to the well-known benchmark for photocatalysis, TiO2 (P25), and its binary metal selenide nanocomposites Cu2-xSe-TiO2. DFT calculations establish semi-metallic behavior of CuAgSe NPs and show that CuAgSe-TiO2 forms a semimetallic-semiconductor heterojunction allowing a better charge separation to enhance its photocatalytic activity.

Site poisoning is a powerful method to unravel the nature of active sites or reaction intermediates. The nature of the intermediates involved in the hydrogenation of CO was unraveled by poisoning alumina-supported cobalt catalysts with various concentrations of tin. The rate of formation of the main reaction products (methane and propylene) was found to be proportional to the concentration of multi-bonded CO, likely located in hollow sites. The specific rate of decomposition of these species was sufficient to account for the formation of the main products. These hollow-CO are proposed to be main reaction intermediates in the hydrogenation of CO under the reaction conditions used here, while linear CO are mostly spectators., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)