Carbon Quantum Dots with High Photothermal Conversion Efficiency and Their Application in Photothermal Modulated Reversible Deformation of Poly(-isopropylacrylamide) Hydrogel.

The fluorescence of carbon quantum dots (CQDs) has been paid a lot of attention, but its photothermal performance attracts less attention since preparing CQDs with high photothermal conversion efficiency (PCE) is a big challenge. In this work, CQDs with an average size of 2.3 nm and a PCE of up to 59.

Research on cropping intensity mapping of the Huai River Basin (China) based on multi-source remote sensing data fusion.

As a key input variable to many global climates, land surfaces and crop models, cropping intensity (CI) accurately assesses and predicts crops' output, in view of the global decline in food production in recent years due to declining natural resources, urban expansion and declining quality of arable land. Hence, research on CI mapping can have a contribution to solve this problem. Unfortunately, existing remote sensing data for CI mapping research, including Moderate Resolution Imaging Spectroradiometer (MODIS) and Landsat images, are not adequate for obtaining CI information at higher spatial and temporal resolution.

Porous Fe3O4 nanoparticles: synthesis and application in catalyzing epoxidation of styrene.

A facile route was employed to synthesize porous magnetite via reaction of FeCl(3)·6H(2)O with N(2)H(4)·H(2)O in ethylene glycol without any structure-directing agent. The resultant Fe(3)O(4) particles were characterized by transmission electron microscopy, N(2) adsorption, X-ray photoelectron spectroscopy, and thermal gravimetric analysis. It was demonstrated that the particle size varied in the range of 40-220 nm, and the pore size of particles was centered around 2 nm.

Thermal-stable carbon nanotube-supported metal nanocatalysts by mesoporous silica coating.

A universal strategy was developed for the preparation of high-temperature-stable carbon nanotube (CNT) -supported metal nanocatalysts by encapsulation with a mesoporous silica coating. Specifically, we first showed the design of one novel catalyst, Pt(@)CNT/SiO(2), with a controllable mesoporous silica coating in the range 11-39 nm containing pores ≈3 nm in diameter. The hollow porous silica shell offers a physical barrier to separate Pt nanoparticles from contact with each other, and at the same time the access of reactant species to Pt was not much affected.

CO2-mediated synthesis of ZnO nanorods and their application in sensing ethanol vapor.

High-purity ZnO nanorods have been synthesized via a two-step route using zinc acetate as a precursor without any surfactant and additive. In this method, ZnCO3 fibers were first formed in the CO2-ethanol solution, which directed the formation of ZnO nanorods by subsequent treatment in KOH aqueous solution. The as-prepared nanorods were fully characterized by transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy and Fourier transform Infrared spectroscopy.

In-situ loading ultrafine AuPd particles on ceria: highly active catalyst for solvent-free selective oxidation of benzyl alcohol.

Ce(III) oxide was synthesized under the protection of nitrogen gas, which had strong ability to reduce noble metal ions (e.g., Au, Pd ions) into metallic forms under oxygen-free conditions.

In situ loading of palladium nanoparticles on mica and their catalytic applications.

Mica supported Pd nanocatalysts were prepared by a two-step approach, in which SnCl(2) was first grafted onto mica via its reaction with hydroxyl groups on mica, followed by the in situ reduction of Pd(2+) by Sn(2+) on the surface of mica. The as-prepared Pd-Sn/mica catalysts were characterized by different techniques including transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and ICP analysis. The loaded Pd particles existed in the form of Pd(0) confirmed by XPS analysis, and distributed uniformly on mica with average size about 2.

Arginine-mediated synthesis of highly efficient catalysts for transfer hydrogenations of ketones.

Palladium-hydrotalcite catalysts were prepared by immobilizing Pd(2+) on hydrotalcite (HT) via an amino acid, arginine (Arg), followed by reduction with NaBH(4) at room temperature. The resulting composite was characterized by different techniques. X-ray photoelectron spectroscopy analysis showed that the loaded Pd on hydrotalcite mainly existed in the form of Pd(0), and distributed uniformly on the support with particle size around 4 nm, as confirmed by transmission electron microscopy examination.

The immobilization of glycidyl-group-containing ionic liquids and its application in CO2 cycloaddition reactions.

Covalent immobilization of glycidyl-group-containing ionic liquids (ILs) on organic and inorganic supports with functional surfaces was achieved, based on the fact that the glycidyl group can actively react with almost all nucleophilic, electrophilic, neutral, and free-radical species. By using polymer spheres with amino- and carboxyl-group-functionalized surfaces as organic supports and silicas (including SBA15 and silica gel) with amino groups attached as inorganic supports, the ionic liquid 1-glycidyl-butylimidazolium chloride was successfully grafted onto these polymer and silica supports, respectively, through reactions between the glycidyl group in the IL and the polar groups on the support surfaces. The resultant samples were examined by transmission electron microscopy, solid-state (13)C NMR spectroscopy, IR spectroscopy, and ion chromatography.

p-Aminophenylacetic acid-mediated synthesis of monodispersed titanium oxide hybrid microspheres in ethanol solution.

Monodispersed TiO2 hybrid microspheres were prepared via the hydrolysis of titanium isopropoxide (TTIP) in ethanol solution containing p-aminophenylacetic acid (APA). The effects of the APA:TTIP molar ratio, water content, reaction time and reaction temperature on the morphology of the resultant spheres were investigated. The products were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, and X-ray diffraction.

In situ controllable loading of ultrafine noble metal particles on titania.

Herein we present a novel and facile approach to controllably load ultrafine noble metal nanoparticles on titania through in situ redox reaction between the reductive titanium(III) oxide support and metal salt precursors in aqueous solution. A series of noble metal/TiO(2) nanocomposites with uniform metal dispersion, tunable metal particle size, and narrow metal particle size distribution were obtained.