Patterned growth of carbon nanotubes on Si substrates without predeposition of metal catalysts

Aligned carbon nanotubes (CNTs) can be readily synthesized on quartz or silicon-oxide-coated Si substrates using a chemical vapor deposition method, but it is difficult to grow them on pure Si substrates without predeposition of metal catalysts. We report that aligned CNTs were grown by pyrolysis of iron phthalocyanine at 1000 °C on the templates created on Si substrates with simple mechanical scratching. Scanning electron microscopy and x-ray energy spectroscopy analysis revealed that the trenches and patterns created on the surface of Si substrates were preferred nucleation sites for nanotube growth due to a high surface energy, metastable surface structure, and possible capillarity effect. A two-step pyrolysis process maintained Fe as an active catalyst.

New effective catalysts based on mesoporous nanofibrous carbon for selective oxidation of hydrogen sulfide

The systems based on granular mesoporous nanofibrous carbonaceous (NFC) materials synthesized by decomposition of hydrocarbons over nickel- containing catalysts are promising catalysts for selective oxidation of hydrogen sulfide. Sample series of nanofibrous carbon with three main types of their fiber structures and different contents of metal catalysts inherited from the catalysts for their synthesis were studied in this reaction. The correlation between NFC structure and its activity and selectivity in hydrogen sulfide oxidation was determined. The metal inherited from the initial catalysts for the synthesis of NFC influences the activity and selectivity of the resulting carbon catalysts. A particular influence is observed in the case of the catalyst withdrawn from the synthesis reactor at the stage of stationary operation of the metal catalyst (low specific carbon yields per unit weight of the catalyst). The presence of the metal phase results in an increase in the carbon catalyst activity and in a decrease in the selectivity to sulfur. NFC samples with the highest activity and selectivity are nanotubes and those with graphite planes perpendicular to the axis of the fibers. Carbon nanotubes have high selectivity, while samples obtained on copper–nickel catalysts also possess high activity. The promising NFC catalysts provide high conversion and selectivity (almost independent of the molar oxygen/hydrogen sulfide ratio) when a large excess of oxygen is contained in the reaction mixture.

Bronsted acidic ionic liquids derived from alkylamines as catalysts and mediums for Fischer esterification : study of structure–activity relationship

Esterification of acetic acid with 1-octanol was studied using a series of alkylammonium salts as Brønsted acidic ionic liquids. The following
ionic liquids were prepared and used as catalysts and mediums in the esterification reaction; [Et₃NH][HSO₄], [Et₃NH][H₂PO₄], [Et₃NH][BF₄],
[Et₃NH][p-CH₃C₆H₄SO₃], [Et₂(PhCH₂)NH][HSO₄], [n-Bu₃NH][HSO₄], [n-Oct₃NH][HSO₄], [Et₂NH₂][HSO₄], [Et₂NH₂][H₂PO₄], [Et₂NH₂]
[BF₄], [i-Pr₂NH₂][HSO₄], [EtNH₃][HSO₄], [EtNH₃][H₂PO₄], and [EtNH₃][BF₄]. Higher acidity of the anion in the ionic liquid resulted in high yield of the ester. Yield of the ester decreased with increase in the size of the cation. There was no phase separation in the reactions where size of anion and/or cation was bigger

Highly efficient LaCoO3 nanofibers catalysts for photocatalytic degradation of rhodamine B

Perovskite-type oxide LaCoO₃ nanofibers have been fabricated by electrospinning and subsequent calcination technology. Scanning electron microscopy, transmission electron microscopy, and X-ray diffraction were used to characterize the morphology and structure. Rhodamine B (RhB) was used to evaluate the ultraviolet photocatalytic activity of the as-prepared nanofibers. The effect of calcination temperature and pH of the reaction solution on the decolorization of RhB were investigated. Results showed that the samples calcined at 600°C exhibited the best photocatalytic activity at pH 4. Additionally, the recycling experiments confirmed the attractive stability of the catalysts.

Toward design of synergistically active carbon-based catalysts for electrocatalytic hydrogen evolution

Replacement of precious Pt catalyst with cost-effective alternatives would be significantly beneficial for hydrogen production via electrocatalytic hydrogen evolution reaction (HER). All candidates thus far are exclusively metallic catalysts, which suffer inherent corrosion and oxidation susceptibility during acidic proton-exchange membrane electrolysis. Herein, based on theoretical predictions, we designed and synthesized nitrogen (N) and phosphorus (P) dual-doped graphene as a nonmetallic electrocatalyst for sustainable and efficient hydrogen production. The N and P heteroatoms could coactivate the adjacent C atom in the graphene matrix by affecting its valence orbital energy levels to induce a synergistically enhanced reactivity toward HER. As a result, the dual-doped graphene showed higher electrocatalytic HER activity than single-doped ones and comparable performance to some of the traditional metallic catalysts.