Carbon Quantum Dots with High Photothermal Conversion Efficiency and Their Application in Photothermal Modulated Reversible Deformation of Poly(N-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 59.4% under 650 nm laser irradiation were synthesized by a simple one-pot microwave-assisted solvothermal method using citric acid (CA) and urea (UR) as the precursors and N,N-dimethylformamide as the solvent under an optimized condition (CA/UR = 1/7, 150 °C, and 1 h). The as-prepared CQDs were demonstrated to have unique surface chemical states; i.e., abundant pyrrole, amide, carboxyl, and hydroxyl groups were found on the surfaces of CQDs, which ensure a high PCE. These CQDs were introduced into a thermoresponsive poly(N-isopropylacrylamide) (PNIPAM) to form a CQDs@PNIPAM nanocomposite, and then, a bilayer hydrogel composed of CQDs@PNIPAM and polyacrylamide (PAM) was fabricated. The bilayer hydrogel can be reversibly deformed just by a light switching on/off operation. Based on the excellent photothermal performance, the developed CQDs are expected to be used in photothermal therapy, photoacoustic imaging, and other biomedical fields, and the CQDs@PNIPAM hydrogel nanocomposite is promising to be applied in intelligent device systems as a light-driven smart flexible material.

Atomically Dispersed Mn for Electrochemical CO2 Reduction with Tunable Performance.

Electrochemical CO2 reduction (ECR) is recognized as a sustainable and promising approach for the production of high-value chemicals. To facilitate widespread application of this technology, the design and construction of efficient cathodic electrocatalysts is critically important. Here we report the synthesis of atomically dispersed manganese on nitrogen-doped porous carbon (Mn SAs/NC) using a facile and scalable annealing method for catalyzing the ECR reaction. The as-obtained Mn SAs/NC delivers high activity and selectivity toward CO formation with a faradaic efficiency of 80.5±0.6%, over 5 times that of bare NC. The high activity is preserved even after 10 h of continuous polarization. The catalytic properties of our cost-effective Mn SAs/NC catalyst are readily tuned by regulating the nitrogen configurations and the percentage of Mn SAs via modulation of the nitrogen precursor and the thermal treatment conditions.

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. In this regard, we develop an algorithm to extract CI based on per-pixel physiognomy. To be specific, the algorithm is based on the Google Earth Engine (GEE) platform and constructs a high temporal (10 days) spatial (30 m) resolution dataset with the fusion of Landsat 7/8 and Sentinel-2 A/B image data and extracts CI information using a time series of peak discovery method, threshold method and phenological period feature extraction to obtain the 2018 Chinese Huai River Basin (HRB) CI map. Our results suggest that the overall accuracy (OA) of CI extraction in the HRB is 92.72%, with a kappa coefficient of 0.864. The single-season crop, double-season crop and three-season crop account for 41.6%, 57.7% and 0.7% of the total farmland area, respectively. Compared to existing CI identification and extraction methods, this approach achieves higher accuracy in the identification and extraction of CI information over a larger area.

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. The gases produced in the formation process of the particles played key role in the formation of the porous structure. The obtained porous magnetite was used as support to immobilize Au nanoparticles with size less than 2 nm with the assistance of L-cysteine. The as-prepared Fe(3)O(4) particles can effectively catalyze epoxidation of styrene, and the immobilization of Au nanoparticles on the Fe(3)O(4) support significantly improved the activity of the catalyst.

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. It was found that the as-obtained ZnO nanorods were single crystals with uniform diameter around 150 nm and length of 4 microm. The nanorod crystals were prismatic with hexagonal cross sections, consistent with the wurtzite lattice structure. Moreover, the sensing properties of the as-prepared ZnO nanorods were also investigated. It was demonstrated that they exhibited good performance for detecting ethanol vapor even at 380 and 250 degrees C.

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. As a result, the catalyst showed high thermal stability against metal particle agglomeration or sintering even after being subjected to harsh treatments up to 500 °C. In addition, degradation in catalytic activity was minimized for the hydrogenation of nitrobenzene over the catalyst treated at 300 °C for 2 h. The scheme was also extended to coat porous silica onto the surfaces of CuRu(@)CNT and the resultant catalyst thereby can be reusable at least four times without loss of activity for the hydrogenolysis of glycerol. These results suggest that the as-prepared nanostructured CNT-supported catalysts may find promising applications, especially in those processes requiring rigorous 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 2.6 nm, as confirmed by TEM examination. The activities of the resultant catalysts for Heck reactions of iodobenzene and its derivatives with olefins and selective hydrogenation of citral were investigated. It was demonstrated that the as-prepared catalysts exhibited very high efficiency for these reactions.

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. On the basis of the surface redox reaction between the Ce(III) oxide support and noble metal ions, an effective and novel approach was presented to prepare noble metal/CeO(2) nanocatalysts, and a series of AuPd/CeO(2) nanocomposites with different Au:Pd molar ratios and metal loadings were obtained in the absence of any extra reducing and protective agents. The resultant composites were characterized by different techniques including X-ray diffraction, transmission electron microspectroscopy, X-ray photoelectron microspectroscopy, and ICP-AES analysis. It was demonstrated that in the AuPd/CeO(2) composites the content of Ce(III) reached about 30%, and the AuPd bimetallic particles with average size of 2.6 or 3.3 nm and narrow size distribution were uniformly distributed on the CeO(2) nanorods. The AuPd/CeO(2) composites were found to be excellent heterogeneous nanocatalysts for the selective oxidation of benzyl alcohol under solvent-free conditions. It was shown that all the AuPd/CeO(2) catalysts exhibited good selectivity toward benzaldehyde; especially, the catalyst with Au:Pd = 1:5 and metal loading of 1.2 wt % displayed extremely high activity with a TOF = 30.1 s(-1) at 160 °C.

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 HT-Arg-Pd composites were used to catalyze transfer hydrogenation of aromatic ketones, which exhibited high efficiency for this kind of reaction. It was demonstrated that arginine played an important role in the high activity and stability of the catalyst, which not only mediated Pd nanoparticles to be immobilized on the HT support firmly but also promoted the transfer hydrogenation reactions.

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. The activities of these resultant polymer- and silica-based catalysts were investigated for CO(2) cycloaddition reactions with epoxides. It was demonstrated that these catalysts could effectively catalyze CO(2) cycloaddition. In particular, the polymer supports generated synergistic effects with the IL in the coupling reaction of CO(2) with propylene oxide, and the turnover frequency could reach about 1700 h(-1) when the IL attached to the NH(2)-functionalized polymer was used as the catalyst.

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. It was demonstrated that the diameters of the resultant TiO2 spheres could be tuned in the range of 380-800 nm by changing the APA:TTIP molar ratio (1:3 to 3:1) and water content (1-3 v/v%) in the reaction medium, and that increasing the APA:TTIP molar ratio led to larger TiO2 hybrid spheres while increasing the water content decreased their size. The loading content of APA in the hybrid spheres could reach 20 wt.% as they were prepared with the APA:TTIP ratio of 3:1. The possible formation mechanism of the hybrid spheres was also investigated. It was found that APA slowed down the hydrolysis rate of the titanium precursor so that resulted in the formation of the TiO2 spheres. In addition, the APA present in TiO2 spheres acted as a reducing agent to in situ convert HAuCl4 into metallic Au on the surface of the TiO2 spheres. The catalytic activity of the resultant Au/APA-TiO2 composite was examined using transfer hydrogenation of phenylacetone with 2-propanol, and it was indicated that the catalyst displayed high efficiency for this reaction.

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.