Unbounding the Future: Designing NiAl-Based Catalysts for Dry Reforming of Methane.

Dry reforming of methane (DRM), the catalytic conversion of CH and CO into syngas (H+CO), is an important process closely correlated to the environment and chemical industry. NiAl-based catalysts have been reported to exhibit excellent activity, low cost, and environmental friendliness. At the same time, the rapid deactivation caused by carbon deposition, Ni sintering, and phase transformation exerts great challenges for its large-scale applications.

Nitrogen-incorporation activates NiFeO catalysts for efficiently boosting oxygen evolution activity and stability of BiVO photoanodes.

Developing low-cost and highly efficient catalysts toward the efficient oxygen evolution reaction (OER) is highly desirable for photoelectrochemical (PEC) water splitting. Herein, we demonstrated that N-incorporation could efficiently activate NiFeO catalysts for significantly enhancing the oxygen evolution activity and stability of BiVO photoanodes, and the photocurrent density has been achieved up to 6.4 mA cm at 1.

Unveiling the Activity and Stability Origin of BiVO Photoanodes with FeNi Oxyhydroxides for Oxygen Evolution.

Understanding the origin of formation and active sites of oxygen evolution reaction (OER) cocatalysts is highly required for solar photoelectrochemical (PEC) devices that generate hydrogen efficiently from water. Herein, we employed a simple pH-modulated method for in situ growth of FeNi oxyhydroxide ultrathin layers on BiVO photoanodes, resulting in one of the highest currently known PEC activities of 5.8 mA cm (1.

Facile synthesis of ordered mesoporous zinc alumina catalysts and their dehydrogenation behavior.

Ordered mesoporous Zn/AlO materials with varying Zn content were simply prepared an evaporation-induced self-assembly (EISA) method. Dehydrogenation of isobutane to isobutene was carried out on these materials; an isobutane conversion of 45.0% and isobutene yield of 39.

An efficient ordered mesoporous molybdate-zirconium oxophosphate solid acid catalyst with homogeneously dispersed active sites: Synthesis, characterization and application.

Ordered mesoporous molybdate-zirconium oxophosphate (M-ZrPMo) solid acid catalysts with controllable molybdenum contents (0-20%) are designed and synthesized through a one-pot evaporation-induced self-assembly strategy. Afterwards, ordered mesostructure and molybdenum species in the materials are systematically researched by a variety of means. The results show that M-ZrPMo has highly ordered mesoporous structure with large specific surface area (∼200 m·g), big pore volume (∼0.

Mesoporous Mn-Zr composite oxides with a crystalline wall: synthesis, characterization and application.

Mesoporous Mn-Zr composite oxides (M-MnZr) with a crystalline wall were designed and achieved by a facile one-pot evaporation-induced self-assembly (EISA) strategy. As proved by XRD, HRTEM and SAED characterization, the wall of the obtained mesoporous materials exhibited a typical tetragonal phase of ZrO2. In addition, the introduced manganese species were homogeneously dispersed in the mesoporous skeleton.

Remarkable charge transfer between CdSe seeded CdS nanorods and its metallic and semiconducting tips and its effect on Rhodamine B photodegradation.

Hybrid colloids (HCs) have shown distinct optical, electric, and optoelectronic properties from the components, mainly because of electronic interplay between the components. Here we investigate different charge transfer behaviors of dumbbell-structured CdSe-seeded CdS nanorods with metallic and semiconducting tip materials respectively studied by UV-vis and photoluminescence (PL) spectra, i.e.

Hydrolysis of cellulose in SO₃H-functionalized ionic liquids.

Influence of acidity and structure of ionic liquids on microcrystalline cellulose (MCC) hydrolysis was investigated. MnCl₂-containing ionic liquids (ILs) were efficient catalysts and achieved MCC conversion rates of 91.2% and selectivities for 5-hydroxymethyl furfural (HMF), furfural and levulinic acid (LA) of 45.

Catalytic conversion of cellulose to chemicals in ionic liquid.

A simple and effective route for the production of 5-hydroxymethyl furfural (HMF) and furfural from microcrystalline cellulose (MCC) has been developed. CoSO(4) in an ionic liquid, 1-(4-sulfonic acid) butyl-3-methylimidazolium hydrogen sulfate (IL-1), was found to be an efficient catalyst for the hydrolysis of cellulose at 150°C, which led to 84% conversion of MCC after 300min reaction time. In the presence of a catalytic amount of CoSO(4), the yields of HMF and furfural were up to 24% and 17%, respectively; a small amount of levulinic acid (LA) and reducing sugars (8% and 4%, respectively) were also generated.

Hydrolysis of cellulose by using catalytic amounts of FeCl₂ in ionic liquids.

Microcrystalline cellulose (MCC) is hydrolyzed to an appreciable extent (70 %) by using 1-(4-sulfonic acid) butyl-3-methylimidazolium hydrogen sulfate (IL-1) as effective catalyst. Valuable chemicals, such as 5-hydroxymethyl furfural (HMF) and furfural, are obtained in relatively high yields (15 % and 7 %, respectively). Interestingly, the introduction of FeCl₂ as catalyst into IL-1 further enhances the catalytic activity, as proved by the higher conversion of MCC (84 %) and higher yields of HMF and furfural (34 % and 19 %, respectively) under the same experimental conditions, although small amounts of levulinic acid (LA) and total reducing sugars (TRS) were also found.

CeO2-promoted W-Mn/SiO2 catalysts for conversion of methane to C3-C4 hydrocarbons at elevated pressure.

A CeO2-doped Na-Mn-W/SiO2 catalyst for oxidative conversion of methane has been studied in a micro-stainless-steel reactor under elevated pressure; a CH4 conversion of 47.2% with a C3-C4 selectivity of 47.3% (C2:C3:C4 = 1:1:3.