Cr颗粒尺寸对Ni-Cr复合镀层氧化行为的影响

利用Ni与不同粒度的Cr颗粒通过复合电镀的方法分别制备了Nip7．5Cr（平均粒度为21nm）、Ni-10．9Cr（平均粒度为39nm）和Ni-12．4Cr（平均粒度为2．4μm）的Ni-Cr复合镀层．Ni-Cr纳米复合镀层与Ni—Cr复合微米颗粒镀层相比，其颗粒分布更为均匀，颗粒间距减少2～3个数量级．900℃恒温氧化实验结果表明：复合微米颗粒的Ni—Cr镀层只形成NiO膜，不能形成连续的Cr2O3膜，氧化速率很快；而Ni—Cr纳米复合镀层。由于能形成连续的Cr2O3膜，氧化速率显著降低，并且这种颗粒尺寸效应随粒度越细越明显．文中对颗粒尺寸效应进行了探讨．

铁磁纳米颗粒系统磁性质对尺寸和各向异性效应的依赖

研究了随机分布颗粒系统的尺寸、各向异性、矫顽力和温度之间的关系.从FexCu1-x,Fe/SiO2,Fe/Al2O3颗粒膜实验结果入手,以Néel-Bron理论和Storner-Wohlfartly模型为依据,建立了描述细磁性颗粒矫顽力Hc与颗粒大小d、热力学温度T的函数关系,并得出在粒径小于dm（=18～20 nm）范围内,矫顽力随着颗粒的尺寸的增加而迅速地增大,而在颗粒尺寸大于这个范围,则按照Hc∝1/d规律变化.

Ag-Ni alloy nanoparticles for electrocatalytic reduction of benzyl chloride

Ag-based nanocatalysts exhibit good catalytic activity for the electrochemical reduction of organic halides. Ag-Ni alloy nanoparticles（NPs） were facilely prepared by chemical reduction, and the as-prepared nanocatalysts were characterized by X-ray diffraction, ultraviolet-visible spectroscopy, transmission electron microscopy and energy-dispersive X-ray spectroscopy. The electrocatalytic activity of Ag-Ni NPs for benzyl chloride reduction was studied in organic medium using cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy. The results show that the addition of Ni element can obviously decrease the size of Ag-Ni NPs, shift the reduction peak potential（φp） of benzyl chloride positively, and increase the catalytic activity of Ag-Ni NPs. However, when the Ni content reaches a certain value, the catalytic activity of Ag-Ni NPs decreases. Meanwhile, the synergistic catalytic effect of Ag-Ni NPs was also discussed.

Metal–organic-framework-based catalysts for hydrogenation reactions

Metal-organic-framework （MOF）-based materials with novel physicochemical properties have emerged as promising catalysts for various hydrogenation reactions. In addition to metal clusters and multifunctional organic ligands, MOF-based catalysts can incorporate other functional species, and thus provide various active sites for hydrogenation processes. The structural properties of the catalysts play significant roles in enhancing the interactions among the reactants, products, and catalytic sites, which can be rationally designed. Because of the synergistic effects between the ac-tive sites and the structural properties, MOF-based catalysts can achieve higher activities and selec- tivities in hydrogenation reactions than can be obtained using traditional heterogeneous catalysts. This review provides an overview of recent developments in MOF-based catalysts in the hydro-genation of alkenes, alkynes, nitroarenes, cinnamaldehyde, furfural, benzene, and other compounds. Strategies for improving the catalytic performances of MOF-based catalysts are discussed as well as the different active sites and structural properties of the catalysts.

Effects of Au-Ce strong interactions on catalytic activity of Au/CeO_2/3DOM Al_2O_3 catalyst for soot combustion under loose contact conditions

Au/3DOM（three-dimensionally ordered macroporous） Al2O3 and Au/CeO2/3DOM Al2O3 were prepared using a reduction-deposition method and characterized using scanning electron microscopy,N2 adsorption-desorption,X-ray diffraction,transmission electron microscopy,ultraviolet-visible spectroscopy,temperature-programmed hydrogen reduction,and X-ray photoelectron spectroscopy.Au nanoparticles of similar sizes were well dispersed and supported on the inner walls of uniform macropores.The norminal Au loading is 2%.Al-Ce-O solid solution in CeO2/3DOM Al2O3 catalysts can be formed due to the incorporation of Al^3＋ ions into the ceria lattice,which causes the creation of extrinsic oxygen vacancies.The extrinsic oxygen vacancies improved the oxygen-transport properties.The strong metal-support interactions between Au and CeO2 increased the amount of active oxygen on the Au nanoparticle surfaces,and this promoted soot oxidation.The activities of the Au-based catalysts were higher than those of the supports（Al2O3 or CeO2/3DOM Al2O3） at low temperature.Au/CeO2/3DOM Al2O3 had the highest catalytic activity for soot combustion,with T（10）,T（50）,and T（90） values of 273,364,and 412℃,respectively.

Ultrasonic-Assisted Synthesis of Monodisperse Ag Nanoparticles and Their Applications in Surface Enhanced Raman Scattering and Fluorescence Enhancement

Monodisperse Ag nanoparticles with diameters of about 3.4 nm were synthesized by a facile ultrasonic synthetic route at room temperature with the reduction of borane-tert-butylamine in the presence of oleylamine （OAm） and oleic acid （OA）. The reaction parameters of time, the molar ratios of OAm to OA were studied, and it was found that these parameters played important roles in the morphology and size of the products. Meanwhile, surface enhanced Raman spectrum （SERS） property suggested the Ag nanoparticles exhibited high SERS effect on the model molecule Rhodamine 6G. And also, two-photon fluorescence images showed that the silver nanoparticles had high performances in fluorescence enhancement.

Promoting reaction kinetics of lithium polysulfides by cobalt polyphthalocyanine derived ultrafine Co nanoparticles mono-dispersed on graphene flakes for Li-S batteries

Lithium-sulfur(Li-S)batteries have been considered as the next generation high energy storage devices.However,its commercialization has been hindered by several issues,especially the dissolution and shuttle of the soluble lithium polysulfides(LiPSs)as well as the slow reaction kinetics of LiPSs which may make shuttling effect even worse.Herein,we report a strategy to address this issue by in-situ transformation of Co−N_(x) coordinations in cobalt polyphthalocyanine(CoPPc)into Co nanoparticles(Co NPs)embedded in carbon matrix and mono-dispersed on graphene flakes.The Co NPs can provide rich binding and catalytic sites,while graphene flakes act as ideally LiPSs transportation and electron conducting platform.With a remarkable enhanced reaction kinetics of LiPSs via these merits,the sulfur host with a sulfur content up to 70 wt%shows a high initial capacity of 1048 mA∙h/g at 0.2C,good rate capability up to 399 mA·h/g at 2C.

Dependence of Optical Absorption in Silicon Nanostructures on Size of Silicon Nanoparticles

The amorphous silicon nanoparticles （Si NPs） embedded in silicon nitride （SiNx） films prepared by helicon wave plasma-enhanced chemical vapor deposition （HWP-CVD） technique are studied. From Raman scattering investigation, we determine that the deposited film has the structure of silicon nanocrystals embedded in silicon nitride （nc-Si/SiNx） thin film at a certain hydrogen dilution amount. The analysis of optical absorption spectra implies that the Si NPs is affected by quantum size effects and has the nature of an indirect-band-gap semiconductor. Further, considering the effects of the mean Si NP size and their dispersion on oscillator strength, and quantum-confinement, we obtain an analytical expression for the spectral absorbance of ensemble samples. Gaussian as well as lognormal size-distributions of the Si NPs are considered for optical absorption coefficient calculations. The influence of the particle size-distribution on the optical absorption spectra was systematically studied. We present the fitting of the optical absorption experimental data with our model and discuss the results.

Sponge-templating synthesis of sandwich-like reduced graphene oxide nanoplates with confined gold nanoparticles and their enhanced stability for solar evaporation

Solar evaporation based on plasmonic metal nanoparticles(MNPs)is emerging as a promising technology.However,the fine structure of MNPs is unstable,and both the high temperature generated by intensive light and corrosive ions in water could damage them.The performance will decline after recycling and long-time usage.To address these issues,we adopted a sponge-templating method for preparing sandwich-like nanoplates with the gold nanoparticles(Au NPs)confined in reduced graphene oxide(rGO)nanosheets.Due to the confinement effect,both the surface melting and ion diffusion were suppressed.The solar evaporator based on the sandwich-like nanoplates showed a high solar-vapor conversion efficiency of 85.2%under a high light intensity of 10 kW.After 30 times recycle of seawater desalination,the conversion efficiency scarcely decreased.These sandwich-like nanoplates with enhanced thermal and chemical stability of Au NPs are promising in the practical application of seawater desalination.

NiRh nanoparticles supported on nitrogen-doped porous carbon as highly efficient catalysts for dehydrogenation of hydrazine in alkaline solution

Well-dispersed bimetallic NiRh nanoparticles （NPs） with different compositions supported on nitrogen-doped porous carbon （NPC） derived from metal-organic frameworks （ZIF-8） were synthesized through a co-reduction method. The NPC-900 supported NiRh catalyst exhibits the highest catalytic activity and 100% hydrogen selectivity toward hydrogen generation from hydrazine. These properties might be attributed to the high surface area and high graphitization of the NPC. This strategy may open up a new avenue for designing high-performance catalysts by utilizing NPC as a support to anchor active metal NPs for additional applications.

Synthesis and luminescence properties of the europium quaternary complexes nanoparticles

In this paper,the nanometer-sized(200 nm)quaternary rare-earth complex Eu(BA)(TTA)2phen was successfully prepared by using the method of optimizing chemical precipitation.The characterizations of these nanoparticles were performed by using elemental analysis,thermogravimetric analysis,infrared spectroscopy,fluorescence spectroscopy,transmission electron microscopy and luminescence quantum-yield.The results indicate that they are better than common ternary complexes at light-emitting performance,luminescence properties,thermal stability,uniformity and particle size;they can also be further mixed with a suitable polymer to form functional rare earth polymers.Compared to the common solid materials,the quaternary complex has better and unique characteristics such as nanoparticle size effect and surface effect.A foundation had been laid for the further expansion of its application in the field of light-emitting and magnetic materials.

Oxidation behavior of cobalt nanoparticles studied by in situ environmental transmission electron microscopy

The dynamics of oxidation of cobalt nanoparticles were directly revealed by in situ environmental transmission electron microscopy.Firstly,cobalt nanoparticles were oxidized to polycrystalline cobalt monoxide,then to polycrystalline tricobalt tetroxide,in the presence of oxygen with a low partial pressure.Numerous cavities(or voids) were formed during the oxidation,owing to the Kirkendall effect.Analysis of the oxides growth suggested that the oxidation of cobalt nanoparticles followed a parabolic rate law,which was consistent with diffusion-limited kinetics.In situ transmission electron microscopy allowed potential atomic oxidation pathways to be considered.The outward diffusion of cobalt atoms inside the oxide layer controlled the oxidation,and formed the hollow structure.Irradiation by the electron beam,which destroyed the sealing effect of graphite layer coated on the cobalt surface and resulted in fast oxidation rate,played an important role in activating and promoting the oxidations.These findings further our understanding on the microscopic kinetics of metal nanocrystal oxidation and knowledge of energetic electrons promoting oxidation reaction.

Spectrofluorimetric analysis of captopril based on its obstruction effect of the nanomaterial surface energy transfer between acridine orange and gold nanoparticles

A simple and sensitive method for detection of captopril was established based on its obstructive effect on nanomaterial sur- face energy transfer （NSET）. It was found that the acridine orange （AO） could be adsorbed onto the surface of citrated-gold nanoparticles （AuNPs） through electrostatic interaction. Incidentally, the fluorescence of AO was quenched owing to the dipole-dipole interaction of NSET between AO fluorophore and the AuNPs. However, captopril could obstruct the occurrence of NSET between AO and AuNPs effectively with the formation of Au-S covalent bonds between it and the AuNPs. Consequently, AO molecules were moved away from the surface of AuNPs leading to a decline of the energy transfer efficiency. Moreover, the fluorescence of AO could be gradually restored with the addition of captopril. Under the optimal conditions, the recovered fluorescence intensity correlated linearly with the concentration of captopril in the range of 400 nmol/L-2.0μmol/L with a detection limit of 71 μmol/L. Besides, the proposed method was successfully applied for the detection of captopril in troches with the recovery of 93%-102% and the RSD lower than 2.24%. The results were in good agreement with those obtained from the HPLC method,

Flower-like Bi^0/CeO2-δ plasmonic photocatalysts with enhanced visible-light-induced photocatalytic activity for NO removal

Plasmonic bismuth(Bi^0)nanoparticle-decorated flower-like CeO2-δ(Bi^0/CeO2-δ)photocatalysts with abundant oxygen vacancies(OVs)were synthesized via a solvothermal method.The OVs can not only improve the separation of electron-hole pairs,but also facilitate the adsorption and activation of gas molecules(NO/O2).In addition,the Bi^0 nanoparticles can enhance the visible light response and prevent the recombination of charge carriers by virtue of the surface plasmon resonance(SPR)effect,achieving an excellent ability for NO elimination and NO2 inhibition under visible light irradiation.Density functional theory(DFT)calculations confirm that the Schottky barrier between Bi^0 and CeO2-δaccompanied with the OVs are pivotal for the migration of photogenerated charge carriers to involve in the photocatalytic NO removal.Trapping experiments and in situ FTIR spectroscopy were conducted to explore the mechanism of the photocatalytic NO removal,suggesting that the photocatalytic NO removal can be significantly enhanced by introducing abundant OVs and the involvement of Bi^0 metal nanoparticles.