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2.
《Carbon》2015
We report a simple route to synthesize iron carbide/carbon yolk–shell composite via a facile two-step process including polymerization of pyrrole using Fe3O4 as a sacrificial template to form a Fe3O4/polypyrrole composite, followed by annealing at high temperature in N2 atmosphere. The yolk–shell composite, with iron carbide (Fe2.5C) embedded in nitrogen-doped carbon layers, shows impressively high catalytic activity and stability for oxygen reduction reaction in alkaline solution. Both the pyridinic-N and graphic-N in the shell of Fe3O4–PPy-700, together with the Fe2.5C confined in carbon layers are believed to be the active sites for the ORR. 相似文献
3.
The visible light driven Bi2MoO6 photocatalyst doped with different contents of Ag nanoparticles was successfully synthesized by a combination of hydrothermal and sonochemical methods. The as-synthesized samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning and transmission electron microscopy (SEM and TEM) and UV–visible spectroscopy to investigate crystalline structure, morphology, composition and photocatalytic properties. XRD patterns and TEM images of the samples revealed pure phase orthorhombic Bi2MoO6 nanoplates without any detection of Ag dopant due to its low concentration and very tiny particle size. TEM images showed that Ag nanoparticles with the size of 10–15 nm were dispersed randomly on the surface of Bi2MoO6. The XPS analysis of Ag/Bi2MoO6 nanocomposites revealed the presence of additional metallic Ag. Photocatalytic activities of the Ag/Bi2MoO6 nanocomposites were evaluated by determining the degradation of rhodamine B (RhB) under visible light radiation. In this research, the 10 wt% Ag/Bi2MoO6 nanocomposites showed the best photocatalytic activity. The results suggest that the dispersion of Ag nanoparticles on the surface of Bi2MoO6 significantly enhances its photocatalytic activity. 相似文献
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《International Journal of Hydrogen Energy》2020,45(53):28860-28869
Developing highly active, stable and sustainable electrocatalysts for overall water splitting is of great importance to generate renewable H2 for fuel cells. Herein, we report the synthesis of electrocatalytically active, nickel foam-supported, spherical core-shell Fe-poly(tetraphenylporphyrin)/Ni-poly(tetraphenylporphyrin) microparticles (FeTPP@NiTPP/NF). We also show that FeTPP@NiTPP/NF exhibits efficient bifunctional electrocatalytic properties toward both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER). Electrochemical tests in KOH solution (1 M) reveal that FeTPP@NiTPP/NF electrocatalyzes the OER with 100 mA cm−2 at an overpotential of 302 mV and the HER with 10 mA cm−2 at an overpotential of 170 mV. Notably also, its catalytic performance for OER is better than that of RuO2, the benchmark OER catalyst. Although its catalytic activity for HER is slightly lower than that of Pt/C (the benchmark HER electrocatalyst), it shows greater stability than the latter during the reaction. The material also exhibits electrocatalytic activity for overall water splitting reaction at a current density of 10 mA cm−2 with a cell voltage of 1.58 V, along with a good recovery property. Additionally, the work demonstrates a new synthetic strategy to an efficient, noble metal-free-coordinated covalent organic framework (COF)-based, bifunctional electrocatalyst for water splitting. 相似文献
6.
《Hydrometallurgy》2006,81(3-4):234-240
The oxidation of glucose during the reductive leaching of pure MnO2 and manganese ore in sulphuric acid at 90 °C MnO2 was investigated. The aim was to identify the derivatives and the chemical pathway of glucose oxidation. Organic derivatives were monitored by HPLC using an Aminex HPX-78H column and UV detection. Chromatographic patterns of leaching solutions showed that major compound formed was formic acid. Minor quantities of glycolic, glyceric and traces of gluconic acids were identified. Results suggest that during the leaching reaction, the carbon chain of glucose is shortened by detachment of one carbon atom as formic acid. 相似文献
7.
《Materials Letters》2007,61(11-12):2247-2250
We report on the fouling of Focused Ion Beam (FIB)-fabricated silicon oxide nanopores after exposure to tap water for two weeks. Pore clogging was monitored by Scanning Electron Microscopy (SEM) on both bare silicon oxide and chemically functionalized nanopores. While fouling occurred on hydrophilic silicon oxide pore walls, the hydrophobic nature of alkane chains prevented clogging on the chemically functionalized pore walls. These results have implications for nanopore sensing platform design. 相似文献
8.
Ren Qinggang Chen Yaju Qiu Yongjian Tao Leiming Ji Hongbing 《Catalysis Letters》2021,151(10):2919-2927
Catalysis Letters - Porous materials with heterogeneous nature occupy a pivotal position in the chemical industry. This work described a facile pre- and post-synthetic approach to modify porous... 相似文献
9.
1 Introduction Lithium manganese oxides are the most attractive cathode materials for rechargeable lithium-ion batteries because of their low-cost and less toxicity when compared with either cobaltates or nickelates[1?3]. Among these oxides, the spinel-fr… 相似文献
10.
《Fuel》2006,85(12-13):1772-1780
With a view to developing onboard generation of selective reductants for NOx removal from diesel engine exhaust we compared the performance of a primary, secondary and tertiary amine to NH3 using a typical mini core NH3-SCR catalyst. Primary amines with short hydrocarbon chains, e.g. CH3NH2 (maximum NOx conversion, 50%) approached the NOx conversion obtained using NH3 (maximum NOx conversion, 70%). Increasing the amine to NOx ratio greater than 1 results in NOx conversions closer to those of NH3 (maximum NOx conversion increased to 60%). Secondary and tertiary amines had smaller NOx conversions as a function of temperature and the drop in NO and NOx conversion decreased with increasing amine hydrogen substitution. Also, the maximum NOx conversion for each reductant tends to move to a lower temperature as the degree of substitution increases.Unlike NH3, the amines can react in the gas phase at temperatures within the range of diesel engine exhaust. Due to this gas phase reactivity the NOx conversions measured using the mini core SCR catalyst also contain a gas phase conversion component. Gas phase conversions were investigated by replacing the mini core SCR catalyst with an equivalent length of quartz beads. Subtraction of the two results highlighted the differences between the mini core catalytic and gas phase conversions measured in this manner over the temperature range investigated. These differential NOx conversions for the three amines had maxima at about 375 °C. 相似文献