Catalytic Scenarios Over Metal-Carbon Interaction Interface

Numerous efforts have been devoted to investigating the catalytic events and disclosing the catalytic nature of the metal-carbon interaction interface. Nevertheless, the local deconstruction of catalytically active metal-carbon interface was still missing. Herein, the selected four types of landmark catalytic paradigms were highlighted, which was expected to clarify their essence and thus simplify the catalytic scenarios of the metal-carbon interface—carbon-supported metal nanoparticles, carbon-confined single-atom sites, chainmail catalysis, and the Mott-Schottky effect. The potential challenges and new opportunities were also proposed in the field. This perspective is believed to give an in-depth understanding of the catalytic nature of the metal-carbon interaction interface and in turn provide rational guidance to the delicate design of novel high-performance carbon-supported metal catalysts.

Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene

Metal-supported catalyst with high activity and relatively simple preparation method is given priority to industrial production. In this work, this study reported an easily accessible synthesis strategy to prepare Mott-Schottky-type N-doped carbon encapsulated metallic Co (Co@Np+gC) catalyst by high-temperature pyrolysis method in which carbon nitride (g-C3N4) and dopamine were used as support and nitrogen source. The prepared Co@Np+gC presented a Mott-Schottky effect; that is, a strong electronic interaction of metallic Co and N-doped carbon shell was constructed to lead to the generation of Mott-Schottky contact. The metallic Co, due to high work function as compared to that of N-doped carbon, transferred electrons to the N-doped outer shell, forming a new contact interface. In this interface area, the positive and negative charges were redistributed, and the catalytic hydrogenation mainly occurred in the area of active charges. The Co@Np+gC catalyst showed excellent catalytic activity in the hydrogenation of phenylacetylene to styrene, and the selectivity of styrene reached 82.4%, much higher than those of reference catalysts. The reason for the promoted semi-hydrogenation of phenylacetylene was attributed to the electron transfer of metallic Co, as it was caused by N doping on carbon.

Влияние мультиплетных уровней Sm-=SUP=-3+-=/SUP=- и Eu-=SUP=-3+-=/SUP=- на теплоемкость мультиферроика BiFeO-=SUB=-3-=/SUB=-

The temperature dependence of the heat capacity of the multiferroics BiFeO3, Bi0.90Sm0.10FeO3, and Bi0.90Eu0.10FeO3 has been studied. It was found that the substitution of europium and samarium ions for bismuth ions in bismuth ferrite leads to the appearance of an additional heat capacity component due to transitions of 4f - electrons of rare earth ions to higher levels of the multiplet. A connection is established between the decrease in phonon thermal conductivity and the Schottky effect for the specific heat.

Visible-light-driven selective alcohol dehydrogenation and hydrogenolysis via the Mott Schottky effect

This work realized the dehydrogenation and hydrogenolysis of benzyl alcohol simultaneously.