基因编辑递送系统:将“手术刀”送进突变细胞

随着第三代基因编辑技术——CRISPR/Cas9技术斩获2020年诺贝尔化学奖,“基因编辑”一词便频繁地出现在大众视野中。然而,这把基因的“手术刀”只有被送到靶细胞才能发挥其特定作用,因此,在体内精准递送基因编辑系统仍然是该技术应用于医药学领域的重大挑战之一。

A review of applications of poly(diallyldimethyl ammonium chloride) in polymer membrane fuel cells: From nanoparticles to support materials

Polymer membrane fuel cells represent important sustainable energy devices because their operation involves zero emissions and low temperatures and their components exhibit low toxicity. Among the various components of such cells, the electrocatalyst plays the vital role of enhancing the output power density and/or working lifetime. Over the past several decades, numerous strategies have been proposed to address the challenges of electrocatalyst activity and/or durability. Herein, we review the applications of polyelectrolytes in electrocatalysts, including the enhancement of both catalytic nanoparticles and support materials. The effects of polyelectrolytes with regard to controlling the size, composition and morphology of catalytic nanoparticles, as well as the modification of support materials were summarized. In addition, the future possibilities for the research and development of polyelectrolytes in the field of catalyst design and synthesis are discussed.

A review of significant factors in the synthesis of hetero-structured dumbbell-like nanoparticles

This paper reviews several important factors that influence the synthesis of dumbbell‐like nanoparticles,which can significantly enhance the catalyst activity in catalytic combustion. The dumbbell‐like nanoparticles discussed in this article refer to a hetero‐structure with two nanoparticles of different materials in contact with each other. This nanostructure can be considered as a special intermediate between individual spherical nanoparticles and a core–shell nanostructure. Therefore,the synthesis of dumbbell‐like nanoparticles is more difficult than other structures. The controllability of the synthesis process, the nanoparticle size and size distribution, and the morphology of the final products depend on many factors： the seed size and size ratio could be used to influence the controllability of epitaxial growth. The component sizes and size distribution could be varied by carefully controlling the reaction temperature and reaction time. The morphology of the dumbbell‐like nanoparticles is closely related to the solvent polarity, the precursor ratio, the lattice mismatch between the two components, and the surfactant concentration. Some related synthesis methods are also briefly introduced in each section to facilitate understanding. This summary will benefit the development of new dumbbell‐like nanoparticles with various components, which have great potential in catalytic combustion of more dysoxidizable gases.

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.

Reverse Microemulsion Synthesis and Characterization of Pd-Ag Bimetallic Alloy Catalysts Supported on Al_2O_3 for Acetylene Hydrogenation

Pd-Ag bimetallic alloy nanoparticles were synthesized by the reverse microemulsion method, and then deposited on A1203 to form the supported catalyst. The nanoparticles of Pd-Ag and Pd-Ag/AI203 samples were characterized by UV/ Vis, HRTEM, EDX, XRD, and XPS. The test results indicated that Pd-Ag bimetallic alloy nanoparticles with a size of about 2 nm and a face-centered cubic （fcc） structure were formed in the measured area of microemulsion. The growth of nanopar- ticles was effectively limited within the droplet of micoremulsion. TEM image exhibited that the Pd-Ag alloy nanoparticles were well-dispersed on the A1203 support. The catalytic performance of various catalysts for selective hydrogenation of acetylene showed that a higher acetylene conversion and selectivity to ethylene upon acetylene hydrogenation was achieved on a nano-sized Pd-Ag bimetallic catalyst with a Pd/Ag alloy supported molar ratio of 1：1.5.

Facile synthesis of porous LiNiVO_4 powder as high-voltage cathode material for lithium-ion batteries

Porous LiNiVO4 powder was synthesized via solution combustion synthesis method using lithium nitrate, nickel nitrate,ammonium metavanadate and citric acid as raw materials. Thermogravimetry (TG) and differential scanning calorimetry (DSC),X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy and transmission electron microscopy (TEM) were used toevaluate the structures and morphologies of samples. The results show that the calcination temperature has significant effect on thecrystallinity and morphologies. Pure LiNiVO4 flaky nanoparticles with a mean particle size around 20 nm can be readily prepared bycalcining the precursor in air at 500 °C for 2 h. As a cathode material for lithium-ion batteries, the porous LiNiVO4 powder exhibits agood structural reversibility.

Effect of Zr additions and annealing temperature on electrical conductivity and hardness of hot rolled Al sheets

The influence of annealing cycles up to 650 °C on the specific conductivity and hardness（HV） of hot-rolled sheets of Al alloys containing up to 0.5% Zr（mass fraction） was studied.Using analytical calculations of phase composition and experimental methods（scanning electron microscopy,transmission electron microscopy,electron microprobe analysis,etc）,it is demonstrated that the conductivity depends on the content of Zr in the Al solid solution which is the minimum after holding at 450 °C for 3 h.On the other hand,the hardness of the alloy is mainly caused by the amount of nanoparticles of the L12（Al3Zr） phase that defines the retention of strain hardening.It is shown that the best combination of electrical conductivity and hardness values can be reached within an acceptable holding time at the temperature about 450 °C.

Straightforward synthesis of beta zeolite encapsulated Pt nanoparticles for the transformation of 5-hydroxymethyl furfural into 2,5-furandicarboxylic acid

Encapsulating noble metal nanoparticles(NPs)within the zeolite framework enhances the stability and accessibility of active sites;however,direct synthesis remains a challenge because of the easy precipitation of noble metal species under strong alkali crystallization conditions.Herein,beta zeolite-encapsulated Pt NPs(Pt@Beta)were synthesized via a hydrothermal approach involving an unusual acid hydrolysis preaging step.The ligand—(3-mercaptopropyl)trimethoxysilane—and Pt precursor were cohydrolyzed and cocondensed with a silica source in an initially weak acidic environment to prevent colloidal precipitation by enhancing the interaction between the Pt and silica species.Thus,the resultant 0.2%Pt@Beta was highly active in the transformation of 5-hydroxymethylfurfural into 2,5-furandicarboxylic acid(FDCA)under atmospheric O2 conditions by using water as the solvent while stably evincing a high yield(90%)associated with a large turnover number of 176.The excellent catalysis behavior is attributable to the enhanced stability that inhibits Pt leaching and strengthens the intermediates that accelerate the rate-determining step for the oxidation of 5-formyl-2-furan carboxylic acid into FDCA.

Sustainable solid-state synthesis of uniformly distributed PdAg alloy nanoparticles for electrocatalytic hydrogen oxidation and evolution

New sustainable syntheses based on solid-state strategies have sparked enormous attention and provided novel routes for the synthesis of supported metallic alloy nanocatalysts(SMACs).Despite considerable recent progress in this field,most of the developed methods suffer from either complex operations or poorly controlled morphology,which seriously limits their practical applications.Here,we have developed a sustainable strategy for the synthesis of PdAg alloy nanoparticles(NPs)with an ultrafine size and good dispersion on various carbon matrices by directly grinding the precursors in an agate mortar at room temperature.Interestingly,no solvents or organic reagents are used in the synthesis procedure.This simple and green synthesis procedure provides alloy NPs with clean surfaces and thus an abundance of accessible active sites.Based on the combination of this property and the synergistic and alloy effects between Pd and Ag atoms,which endow the NPs with high intrinsic activity,the PdAg/C samples exhibit excellent activities as electrocatalysts for both the hydrogen oxidation and evolution reactions(HOR and HER)in a basic medium.Pd9Ag1/C showed the highest activity in the HOR with the largest j0,m value of 26.5 A g Pd^–1 and j0,s value of 0.033 mA cmPd^–2,as well as in the HER,with the lowest overpotential of 68 mV at 10 mA cm^–2.As this synthetic method can be easily adapted to other systems,the present scalable solid-state strategy may open opportunity for the general synthesis of a wide range of well-defined SMACs for diverse applications.

Synthesis of γ-Al_2O_3 nanoparticles by chemical precipitation method

Highly pure active γ-Al2O3 nanoparticles were synthesized from aluminum nitrate and ammonium carbonate with a little surfactant by chemical precipitation method. The factors affecting the synthesis process were studied. The properties of γ-Al2O3 nanoparticles were characterized by DTA, XRD, BET, TEM, laser granularity analysis and impurity content analysis. The results show that the amorphous precursor AI（OH）3 sols are produced by using 0.1 mol/L Al（NO3）3·9H2O and 0.16 mol/L （NH4）2CO3·H2O reaction solutions, according to the volume ratio 1.33, adding 0.024%（volume fraction） surfactant PEG600, and reacting at 40℃, 1000 r/min stirring rate for 15min. Then, after stabilizing for 24 h, the precursors were extracted and filtrated by vacuum, washed thoroughly with deionized water and dehydrated ethanol, dried in vacuum at 80℃ for 8h, final calcined at 800℃ for 1h in the air, and high purity active γ-Al2O3 nanoparticles can be prepared with cubic in crystal system, OH^7-FD3M in space group, about 9 nm in crystal grain size, about 20 nm in particle size and uniform size distribution, 131.35 m^2/g in BET specific surface area, 7 - 11 nm in pore diameter, and not lower than 99.93% in purity.

Size-dependent melting properties of Sn nanoparticles by chemical reduction synthesis

Tin nanoparticles with different size distribution were synthesized using chemical reduction method by applying NaBH4 as reduction agent.The Sn nanoparticles smaller than 100 nm were less agglomerated and no obviously oxidized.The melting properties of these synthesized nanoparticles were studied by differential scanning calorimetry.The melting temperatures of Sn nanoparticles in diameter of 81,40,36 and 34 nm were 226.1,221.8,221.1 and 219.5？欲espectively.The size-dependent melting temperature and size-dependent latent heat of fusion have been observed.The size-dependent melting properties of tin nanoparticles in this study were also comparatively analyzed by employing different size-dependent theoretical melting models and the differences between these models were discussed.The results show that the experimental data are in accordance with the LSM model and SPI model,and the LSM model gives the better understanding for the melting property of the Sn nanoparticles.

Study on the Electrical Conductivity of Au Nanoparticle/Chloroform and Toluene Suspensions

Au nanoparticles capped by hexadecanethiol and dodecanethiol were chemically synthesized. The characteristics of electrical conductivity for the capped nanoparticles dissolved in chloroform and toluene solvents were investigated. The electrical conductivity of the samples is conspicuously Au nanoparticle concentration dependent. The results show that a rapid conductivity increases when the nanoparticle concentration increases from low value to a moderate value of 5.47 g/L and 11.22 g/L, which is capped by hexadecanethiol and dodecanethiol in chloroform solvent, and 2.77 g/L and 7.88 g/L in toluene solvent. The room-temperature dc conductivity σ dc of Au nanoparticle capped by hexadecanethiol is smaller than that capped by dodecanethiol in the whole range of Au nanoparticle concentrations. The conductivity of Au nanoparticle suspensions increases almost linearly in the temperature range in above two solvents.

Solid state synthesis of nano-mineral particles

Many researchers in academia and industries are interested in reducing particle sizes from few submicrometers to nano-meter levels.These nano-particles find application in several areas including ceramics,paints,cosmetics,microelectronics,sensors,textiles and biomedical,etc.This article reviews the present state of the art for solid state synthesis of mineral nano-particles by wet milling,including their operating variables such as ball size,solid mass fraction and suspension stability.This article concludes and recommends with a critical discussion of nano-particles synthesis and a few common strategies to overcome stability issues.

Extracellular green synthesis of silver nanoparticles using Amazonian fruit Araza(Eugenia stipitata McVaugh)

An eco-friendly method for the extracellular synthesis of silver nanoparticles（AgNPs） using aqueous Araza fruit extract and their antioxidant activity was investigated. It was observed that UV–Vis absorption peak is dependent on various parameters such as pH, temperature, and change of time. The initial appearance of the yellow color with intense surface plasmon bands at 430-450 nm, then transmission electron microscopy, scanning electron microscopy and X-ray diffraction analysis revealed the formation of 15-45 nm sized, spherical and crystalline Ag NPs. Fourier transform infrared spectroscopy depicted that malic acid, citric acid, and carotenoids of Araza fruit involved in the synthesis of Ag NPs. In addition, the surface modified AgNPs（77.42%, 1mL） showed nearly double antioxidant efficiency than Araza fruit extract（35.30%, 1 mL） against 1, 1-diphenyl-2-picrylhydrazyl. The present study highlights the possibility of using the Araza fruit to synthesize AgNPs, which could be used effectively in the present and future antioxidant agent.

Green synthesis of silver nanoneedles using shallot and apricot tree gum

A green synthesis method to produce silver nanoneedles was described using shallot and apricot tree gum（ATG）.A fast,simple,and low cost method was used to synthesize silver with nanoparticle and nanoneedle shape from the silver nitrate solution.Shallot as a reducing agent and apricot tree gum（ATG） as a stabilizer and a capping agent were utilized to reduce and form silver ions into silver atoms with needle and particle shape.Moreover,high crystalline structures of silver nanoparticles（AgNPs） with diameters of 8-20 nm and silver nanoneedles with average diameters of 50-60 nm and lengths of 5-10 μm were consequently synthesized by shallot and the mixture of shallot and ATG.A self-assembly mechanism was proposed to indicate the formation of needle-like structures of spherical Ag NPs via carbon chains of ATG.The results indicate that the presence of ATG with shallot can transfer the reduced Ag NPs into the silver nanoneedle.The findings were characterized using X-ray diffraction（XRD）,ultra violet visible（UV-Vis） spectrometry,field emission scanning electron microscopy（FESEM）,and transmission electron microscopy（TEM） techniques.

Solution-based Synthesis of Ni Sb Nanoparticles for Electrochemical Activity in Hydrogen Evolution Reaction

A cost-effective,facile solution-based hot-injection synthetic route has been developed to synthesize NiSb nanoparticles in oleylamine(OAm)using commercially available inexpensive precursor with reducing toxicity at a relatively low temperature of 160℃.Especially,an organic reductant of borane-tert-butylamine complex is intentionally involved in the reaction system to promote a fast reduction of metallic Ni and Sb for the formation of the NiSb nanoparticles.Structural characterizations reveal that the NiSb nanoparticles are hexagonal phase with space group P63/mmc and they are composed of small granules with size about 10 nm that tend to form agglomerates with porous-like geometries.This is the first report on the generation of transition metal antimonide via solution-based strategy,and the asfabricated nanoparticles possess actively electrocatalytic hydrogen evolution reaction(HER)property in acidic electrolytes when the long-chain ligand of OAm adhered on the surface of the nanoparticles is exchanged by ligand-removal and exchange procedure.It is found that the NiSb nanoparticles as a new kind of non-noble-metal HER electrocatalysts only require overpotentials of 437 and 531 mV to achieve high current densities of 10 and 50 mA/cm^2 respectively,as well as exhibit low charge transfer resistance and excellent HER stability.

Effect of 0.3% Sc on microstructure, phase composition and hardening of Al-Ca-Si eutectic alloys

The phase composition,microstructure and hardening of aluminum-based experimental alloys containing0.3%Sc,0?14%Si and0?10%Ca(mass fraction)were studied.The experimental study(electron microscopy,thermal analysis and hardnessmeasurements)was combined with Thermo-Calc software simulation for the optimization of the alloy composition.It wasdetermined that the maximum hardening corresponded to the annealing at300?350°С,which was due to the precipitation of Al3Scnanoparticles with their further coarsening.The alloys falling into the phase region(Al)+Al4Ca+Al2Si2Ca have demonstrated asignificant hardening effect.The ternary eutectic(Al)+Al4Ca+Al2Si2Ca had a much finer microstructure as compared to the Al?Sieutectic,which suggests a possibility of reaching higher mechanical properties as compared to commercial alloys of the A356type.Unlike commercial alloys of the A356type,the model alloy does not require quenching,as hardening particles are formed in thecourse of annealing of castings.

Synthesis and Characterization of MgSb2O6 Trirutile-Type in Low Presence Concentrations of Ethylenediamine

The nanoparticles MgSb206 with trirutile-type structure were prepared by colloidal method using ethylanediamine （0.5 and 0.75 mL）, following a calcination at 800 ℃. After, those powders were analyzed by x-ray obtaining a tetragonal structure with cell parameters, a = 4.64 A and c = 9.25 A and special group P42/mnm. Using a scanning electron microscopy were analyzed the powders calcined at 800 ℃, showing the formation of micro-plates, micro-rods, nanoparticles and morphology as rice grains. Employing a transmission electron microscopy, were found nanostructures hexagonal shaped with sizes of- 33.6 nm （0.5 mL） and 28.6 nm （0.75 mL）.

Synthesis of Ni-Zn ferrite and its microstructure and magnetic properties

Nanometer Ni0.5Zn0.5Fe2O4 powders with spinel phase were prepared by the hydrothermal method using purified FeSO4 solution from sodium jarosite＇s slag as materials. The results show that the spinel phase of Ni0.5Zn0.5Fe2O4 powders begins to form at a relatively low temperature （130 ℃） and a shorter holding time （1 h） when pH=8. The crystallization kinetics equation at 200℃ is ln[-ln（1-x）] =-0.78＋0.951n t. The growth activation energy of Ni0.5Zn0.5Fe2O4 grains is 41.6 kJ/moL in hydrothermal synthesis process. With the increase of sintering temperature, the density and diameter shrinkage of ferrite circulus increase, whereas its pores decrease. The results of magnetic measurements show that saturation magnetic flux density Bs increases and the coercivity Hc decreases with the increase of their sintering temperature. Magnetic parameters of all the investigated samples satisfy the character demand of high Bs, low Br and low Hc of soft magnetic ferrite materials.

Synthesis and characterization of FeAl nanoparticles by flow-levitation method

The synthesis of high purity intermetallic FeAI nanoparticles using the flow-levitation （FL） method was reported. Iron and aluminium droplets were levitated stably at about 2 230℃. The morphology, clystal structure and chemical composition of FeAI nanoparticles were investigated by transmission electron microscopy （TEM）, high-resolution TEM, X-ray diffraction and energy dispersive spectrometry. The results show that the average particle size of these nanoparticles is about 34.5 nm. Measurements of the d-spacing from X-ray diffraction and electron diffraction studies confirm that the intermetallic nanoparticles have the same crystal structure （B2） as the bulk FeA1. A thin oxidation coating is formed around the particles when being exposed to air. Based on the XPS measurements, the surface coating of the FeAI nanoparticles is composed of Fe2O3 and FeAl2O4. Besides, hysteresis curve reveals that saturation magnetization （Ms） of FeA1 is 1.66 A/m2, and the coercivity is about 1.214×10^3 A/re.