The one-pot synthesis of methyl isobutyl ketone（MIBK） from acetone using multifunctional catalysts is an important sustainable organic synthesis method with high atom and energy efficiency.Herein. we report a series...The one-pot synthesis of methyl isobutyl ketone（MIBK） from acetone using multifunctional catalysts is an important sustainable organic synthesis method with high atom and energy efficiency.Herein. we report a series of Pd supported on mixed metal oxide（MMO） catalysts with controllable acidic/basic/metallic sites on the surface. We study the relationship between the nature, synergy,and proximity of active sites and the catalytic performance of the multifunctional catalyst in the tandem reaction, in detail. In the existence of Lewis acid and base sites, the catalysts with medium-strength acidic/basic sites show preferred activity and/or MIBK selectivity. For multifunctional catalysts, the catalytic properties are more than just a collection of active sites, and the Pd/Mg_3Al-MMO catalyst possessing 0.1% Pd loading and ~0.4 acid/base molar ratio exhibits the optimal 42.1% acetone conversion and 37.2% MIBK yield, which is among the best reported so far for this tandem reaction under similar conditions. Moreover, the proximity test indicates that the intimate distance between acidic/basic/metallic sites can greatly shorten the diffusion time of the intermediate species from each active site, leading to an enhancement in the catalytic performance.展开更多
Electrocatalytic CO_(2) reduction plays an important role in the reduction of the CO_(2) concentration in atmosphere and consequently the mitigation of greenhouse effects.Pd has been extensively inves‐tigated as an e...Electrocatalytic CO_(2) reduction plays an important role in the reduction of the CO_(2) concentration in atmosphere and consequently the mitigation of greenhouse effects.Pd has been extensively inves‐tigated as an electrocatalyst for the CO_(2) reduction to formate,which is an important raw material in the production of organic chemicals.However,the low selectivity and competitive reaction(hydro‐gen evolution reaction(HER))have hindered the performance of monometallic Pd catalysts.In this paper,intermetallic PdBi nanosheets(NSs)are prepared for efficient CO_(2) reduction to formate.The highest Faradaic efficiency(FE)of formate on fully ordered PdBi NSs reaches 91.9%at−1.0 V vs.RHE,which outperforms that of the disordered PdBi and pure Pd catalysts.Density functional theo‐ry calculations suggest that compared to disordered PdBi NSs,the ordered structure can decrease the free energy barrier of*OCHO(a key intermediate of formate formation)and inhibit H_(2) evolution as well,thereby enhancing the activity and selectivity for formate production.展开更多
The Solvated Metal Atom Impregnation (SMAI) technique was employed to prepare macroporous resin immobilized Pd--Cu bimetallic cluster catalysts. The X--ray diffraction (XRD) and transmission electron micrograph (TEM) ...The Solvated Metal Atom Impregnation (SMAI) technique was employed to prepare macroporous resin immobilized Pd--Cu bimetallic cluster catalysts. The X--ray diffraction (XRD) and transmission electron micrograph (TEM) showed that Pd--Cu alloy was formed and the particle sizes of Pd--Cu clusters were very small, with average diameters <3nm. X--ray photoelectron spectroscopy indicated that both Pd and Cu were in zero--valent state. The catalytic activities of the macroporous resin immobilized Pd--Cu catalysts in hydrogenation of 4--methyl--3--penten--2--one were much greater than that of the carbon supported Pd--Cu catalysts.展开更多
文摘The one-pot synthesis of methyl isobutyl ketone（MIBK） from acetone using multifunctional catalysts is an important sustainable organic synthesis method with high atom and energy efficiency.Herein. we report a series of Pd supported on mixed metal oxide（MMO） catalysts with controllable acidic/basic/metallic sites on the surface. We study the relationship between the nature, synergy,and proximity of active sites and the catalytic performance of the multifunctional catalyst in the tandem reaction, in detail. In the existence of Lewis acid and base sites, the catalysts with medium-strength acidic/basic sites show preferred activity and/or MIBK selectivity. For multifunctional catalysts, the catalytic properties are more than just a collection of active sites, and the Pd/Mg_3Al-MMO catalyst possessing 0.1% Pd loading and ~0.4 acid/base molar ratio exhibits the optimal 42.1% acetone conversion and 37.2% MIBK yield, which is among the best reported so far for this tandem reaction under similar conditions. Moreover, the proximity test indicates that the intimate distance between acidic/basic/metallic sites can greatly shorten the diffusion time of the intermediate species from each active site, leading to an enhancement in the catalytic performance.
文摘Electrocatalytic CO_(2) reduction plays an important role in the reduction of the CO_(2) concentration in atmosphere and consequently the mitigation of greenhouse effects.Pd has been extensively inves‐tigated as an electrocatalyst for the CO_(2) reduction to formate,which is an important raw material in the production of organic chemicals.However,the low selectivity and competitive reaction(hydro‐gen evolution reaction(HER))have hindered the performance of monometallic Pd catalysts.In this paper,intermetallic PdBi nanosheets(NSs)are prepared for efficient CO_(2) reduction to formate.The highest Faradaic efficiency(FE)of formate on fully ordered PdBi NSs reaches 91.9%at−1.0 V vs.RHE,which outperforms that of the disordered PdBi and pure Pd catalysts.Density functional theo‐ry calculations suggest that compared to disordered PdBi NSs,the ordered structure can decrease the free energy barrier of*OCHO(a key intermediate of formate formation)and inhibit H_(2) evolution as well,thereby enhancing the activity and selectivity for formate production.
文摘The Solvated Metal Atom Impregnation (SMAI) technique was employed to prepare macroporous resin immobilized Pd--Cu bimetallic cluster catalysts. The X--ray diffraction (XRD) and transmission electron micrograph (TEM) showed that Pd--Cu alloy was formed and the particle sizes of Pd--Cu clusters were very small, with average diameters <3nm. X--ray photoelectron spectroscopy indicated that both Pd and Cu were in zero--valent state. The catalytic activities of the macroporous resin immobilized Pd--Cu catalysts in hydrogenation of 4--methyl--3--penten--2--one were much greater than that of the carbon supported Pd--Cu catalysts.
