Microscopic growth mechanism and edge states of monolayer 1T'-MoTe_(2)

Transition metal ditellurides(TMTDs)have versatile physical properties,including non-trivial topology,Weyl semimetal states and unique spin texture.Controlled growth of high-quality and large-scale monolayer TMTDs with preferred crystal phases is crucial for their applications.Here,we demonstrate the epitaxial growth of 1T'-MoTe_(2) on Au(111)and graphitized silicon carbide(Gr/SiC)by molecular beam epitaxy(MBE).We investigate the morphology of the grown1T'-MoTe_(2) at the atomic level by scanning tunnelling microscopy(STM)and reveal the corresponding microscopic growth mechanism.It is found that the unique ordered Te structures preferentially deposited on Au(111)regulate the growth of monolayer single crystal 1T'-MoTe_(2),while the Mo clusters were preferentially deposited on the Gr/SiC substrate,which impedes the ordered growth of monolayer MoTe_(2).We confirm that the size of single crystal 1T'-MoTe_(2) grown on Au(111)is nearly two orders of magnitude larger than that on Gr/SiC.By scanning tunnelling spectroscopy(STS),we observe that the STS spectrum of the monolayer 1T'-MoTe_(2) nano-island at the edge is different from that at the interior,which exhibits enhanced conductivity.

Growth Mechanism of Microcrystalline Silicon Films by Scaling Theory and Monte Carlo Simulation

Hydrogenated microcrystalline silicon （~c-Si：H） films with a high deposition rate of 1.2nm/s were prepared by hot-wire chemical vapor deposition （HWCVD）. The growth-front roughening processes of the μc-Si..H films were investi- gated by atomic force microscopy. According to the scaling theory, the growth exponent β≈0.67, the roughness exponent α≈0.80,and the dynamic exponent 1/z = 0.40 are obtained. These scaling exponents cannot be explained well by the known growth models. An attempt at Monte Carlo simulation has been made to describe the growth process of μc-Si： H film using a particle reemission model where the incident flux distribution,the type and concentration of growth radical, and sticking,reemission,shadowing mechanisms all contributed to the growing morphology.

Corrosion fatigue crack growth mechanisms in welded joints of marine steel structures

This paper presents a model of fatigue crack growth in a welded joint and a two-dimensional model of anodic dissolution based on Donahue model and anodic dissolution mechanism,respectively.In addition,a model for predicting the corrosion fatigue crack growth rate in welded joints of steel marine structures is established and crack growth mechanisms are analyzed.The results show that during early stages of crack growth,corrosion fatigue crack growth rate in welded joints is mainly controlled by corrosion action,whereas cyclic loading becomes more influential during the later stage of crack propagation.Loading frequency and effective stress ratio can affect rupture period of protective film at the corrosion fatigue crack tip and the length of corrosion crack increment,respectively,which changes the influence of corrosion action on crack growth rate.However,the impact of stress amplitude on crack growth rate is only significant when crack propagation is caused by cyclic loading.Welding residual stress not only improves the effective stress ratio of cyclic loading,but also promotes crack closure and increases corrosion fatigue crack growth rate in welded joints.Compared to corrosion action,welding residual stress has a more significant influence on crack growth caused by cyclic loading.

Research of growth mechanism of ceramic coatings fabricated by micro-arc oxidation on magnesium alloys at high current mode

Micro-arc oxidation(MAO)coatings of ZK60 magnesium alloys were formed in a self-developed dual electrolyte composed of sodium silicate and phosphate at the high constant current of 1.8 A(15 A/dm^(2)).The MAO process and growth mechanism were investigated by scanning electron microscopy(SEM)coupled with an energy dispersive spectrometer(EDS),confocal laser scanning microscopy and X-ray diffraction(XRD).The results indicate that the growth process of MAO coating mainly goes through“forming→puncturing→rapid growth of micro-arc oxidation→large arc discharge→self-repairing”.The coating grows inward and outward at the same time in the initial stage,but outward growth of the coating is dominant later.Mg,Mg_(2)SiO_(4) and MgO are the main phases of ceramic coating.

Recent progresses in the suppression method based on the growth mechanism of lithium dendrite

Lithium secondary batteries（LSBs） with high energy densities need to be further developed for future applications in portable electronic devices, electric vehicles, hybrid electric vehicles and smart grids. Lithium metal is the most promising electrode for next-generation rechargeable batteries. However, the formation of lithium dendrite on the anode surface leads to serious safety concerns and low coulombic efficiency.Recently, researchers have made great efforts and significant progresses to solve these problems. Here we review the growth mechanism and suppression method of lithium dendrite for LSBs’ anode protection. We also establish the relationship between the growth mechanism and suppression method. The research direction for building better LSBs is given by comparing the advantages and disadvantages of these methods based on the growth mechanism.

GROWTH MECHANISM OF TiC WHISKERS PREMRED BY A MODIFIED CHEMICAL VAPOR DEPOSITION METHOD

High quality TiC whiskers have been prepared by a modified chemical vapor deposition (CVD) method using TiCl4 and CH4 as reactant gases and Ni as substrate. The deposition temperature and gas flow mies have ampreciable effect on the whisker growth.The whisker orientations and morphology are determined by X-my diffraction (XRD),scanning electron micmpmph (SEM) and transmission electron microgmph (TEM).In addition to the spherical tips, spiral growth microsteps and obvious terraces are observed at the tips and side faces of whiskers in the present eoperiment. The whiskers grow mostly along (100) direction. The whisker growth mechanism is discussed in detail.

Origin and growth mechanisms of strike-slip faults in the central Tarim cratonic basin, NW China

Through fault structure analysis and chronology study, we discuss the origin and growth mechanisms of strike-slip faults in the Tarim Basin.(1) Multiple stages strike-slip faults with inherited growth were developed in the central Tarim cratonic basin. The faults initiation time is constrained at the end of Middle Ordovician of about 460 Ma according to U-Pb dating of the fault cements and seismic interpretation.(2) The formation of the strike-slip faults was controlled by the near N-S direction stress field caused by far-field compression of the closing of the Proto-Tethys Ocean.(3) The faults localization and characteristics were influenced by the pre-existing structures of the NE trending weakening zones in the basement and lithofacies change from south to north.(4) Following the fault initiation under the Andersonian mechanism, the strike-slip fault growth was dominantly fault linkage, associated with fault tip propagation and interaction of non-Andersonian mechanisms.(5) Sequential slip accommodated deformation in the conjugate strike-slip fault interaction zones, strong localization of the main displacement and deformation occurred in the overlap zones in the northern Tarim, while the fault tips, particularly of narrow-deep grabens, and strike-slip segments in thrust zones accumulated more deformation and strain in the Central uplift. In conclusion, non-Andersonian mechanisms, dominantly fault linkage and interaction, resulted in the small displacement but long intraplate strike-slip fault development in the central Tarim Basin. The regional and localized field stress, and pre-existing structures and lithofacies difference had strong impacts on the diversity of the strike-slip faults in the Tarim cratonic basin.

Growth mechanisms for spherical Ni_(0.815)Co_(0.15)Al_(0.035)(OH)_(2) precursors prepared via the ammonia complexation precipitation method

The microstructures of precursors strongly affect the electrochemical performance of Ni-rich layerstructured cathode materials.In this study,the growth behaviour of Ni_(0.815)Co_(0.15)Al_(0.035)(OH)_2(NCA) prepared via the ammonia complexation precipitation method in a 50-L-volume continuously stirred tank reactor(CSTR) is studied in detail.The growth of Ni(OH)2-based hydroxide can be divided into a nucleation process,an agglomeration growth process,a process in which multiple growth mechanisms coexist,and an interface growth process over time,while the inner structure of the CSTR can be divided into a nucleation zone,a complex dissolution zone,a growth zone,and a maturation zone.The concentration of ammonium ions affects the growth habit of the primary crystal significantly due to its specific adsorption on the electronegative crystal plane.When the ammonia concentration is <1.5 mol L^(-1) at 60℃ at pH=11.5,the precursors grow preferentially along the(1 0 1) crystal plane,whereas they grow preferentially along the(0 0 1) crystal plane when the concentration is >2.0 mol L^(-1).The LiNi_(0.815)Co_(0.15)Al_(0.035)O_2 materials inherit the grain structure of the precursor.Materials prepared from precursors with(1 0 1)preferential primary particles show a higher specific capacity and better rate performance than those that were prepared from(0 0 1) preferential primary particles,but the latter realize a better cycling performance than the former.

Growth mechanism and photocatalytic evaluation of flower-like ZnO microstructures prepared with SDBS assistance

Flower-like ZnO microstructures were successfully produced using a hydrothermal method employing ZnSO_(4)/(NH_(4))_(2)SO_(4) as a raw material.The effect of the operating parameters of the hydrothermal temperature, OH^(-)/Zn^(2+) molar ratio, time, and amount of dispersant on the phase structure and micromorphology of the ZnO particles were investigated.The synthesis conditions of the flower-like ZnO microstructures were: hydrothermal temperature of 160℃, OH^(-)/Zn^(2+) molar ratio of 5:1, reaction time of 4 h, and 4 mL of dispersant.The flower-like ZnO microstructures were comprised of hexagon-shaped ZnO rods arranged in a radiatively.Degradation experiments of Rhodamine B with the flower-like ZnO microstructures demonstrated a degradation efficiency of 97.6% after 4 h of exposure to sunshine, indicating excellent photocatalytic capacity.The growth mechanism of the flower-like ZnO microstructures was presented.

Preparation and growth mechanism of nickel nanowires under applied magnetic field

Nickel nanowires with large aspect ratio of up to 300 have been prepared by a hydrazine hydrate reduction method under applied magnetic field. The diameter of nickel nanowires is about 200 nm and length up to 60 μm. The role of magnetic field on the growth of magnetic nanowires is discussed and a magnetic nanowire growth mechanism has been proposed. Nickel ions are firstly reduced to nickel atoms by hydrazine hydrates in a strong alkaline solution and grow into tiny spherical nanoparticles. Then, these magnetic particles will align under a magnetic force and form linear chains. Furthermore, the as-formed chains can enhance the local magnetic field and attract other magnetic particles nearby, resulting finally as linear nanowires. The formation and the size of nanowires depend strongly on the magnitude of applied magnetic field.

Template growth mechanism of spherical Ni(OH)_2

The microstructures and growth process characteristics precipitation-crystallization method were investigated by SEM, TEM of spherical Ni（OH）2 particles synthesized by the aqueous and XRD, and their growth mechanism was discussed. With the reaction beginning and continuing, amorphous Ni（OH）2 nano-crystallites grow up to spherical micron-particles with radially arranged crystallites. The nucleation, crystallization and re-crystallization led by Ostwald ripening simultaneously take place through the whole growth processes. With the course from reversible aggregation to irreversible agglomeration, the Ni（OH）2 particles tend to grow according to the template growth model： the growth on the crystallite templates stretching in the radius directions is free and quick, while the growth rate for crystallites in other directions is confined due to lower monomers concentration and tends to dissolve So it is only the radially arranged crystallites that predominate in the particle and lead to characteristic microstructures.

Morphology control of ultrafine cuprous oxide powder and its growth mechanism

Four shapes of Cu2O particles as sphere,cube,truncated octahedron and octahedron were prepared via glucose reduction of Cu(Ⅱ)under alkaline condition.The products were characterized by XRD and SEM.The effects of the precursor(CuO,Cu(OH)2), reaction temperature and glucose concentration on morphology of Cu2O particles were investigated,and the mechanism of morphology control was discussed on the basic theory of crystal nucleation and growth.It is found that the Cu+supersaturation is remarkably influenced by the precursor kind,reaction temperature and glucose concentration,and the morphology of Cu2O particles can be controlled by the Cu+supersaturation.

Growth mechanism and modification of electronic and magnetic properties of silicene

Silicene, a monolayer of silicon atoms arranged in a honeycomb lattice, has been undergoing rapid development in recent years due to its superior electronic properties and its compatibility with mature silicon-based semiconductor technology. The successful synthesis of silicene on several substrates provides a solid foundation for the use of silicene in future microelectronic devices. In this review, we discuss the growth mechanism of silicene on an Ag(111) surface, which is crucial for achieving high quality silicene. Several critical issues related to the electronic properties of silicene are also summarized, including the point defect effect, substrate effect, intercalation of alkali metal, and alloying with transition metals.

Synthesis and growth mechanism of SiC/SiO2 nanochains by catalyst-free thermal evaporation method in Ar/CO atmosphere

SiC/SiO2 nanochains were synthesized on a carbon fiber substrate by a catalyst-free thermal evaporation method in the Ar/CO atmosphere.X-ray diffraction(XRD),Fourier-transform infrared spectroscopy(FT-IR),scanning electron microscopy(SEM)and transmission electron microscopy(TEM)revealed that the as-synthesized SiC/SiO2 nanochains are composed of single-crystalline SiC nanowires and amorphous SiO2 beads.The introduction of CO can promote the formation of SiO2,so that the SiC/SiO2 nanochains are subsequently formed during cooling.In addition,the photoluminescence spectrum of SiC/SiO2 nanochains showed a broad emission peak at around 350 nm,which is ascribed to the oxygen discrepancy in the SiO2 beads as well as the SiC/SiO2 interfacial effect.These findings can provide guidance for further study of the vapor growth of 1D SiC-based materials.

Electrodeposited PtNi nanoparticles towards oxygen reduction reaction:A study on nucleation and growth mechanism

In this work,highly monodispersed Pt-Ni alloy nanoparticles were directly deposited on carbon substrate through a facile electrodeposition strategy in the solvent system of N,N-dimethylformamide(DMF).A series of carbon supported Pt-Ni alloy electrocatalysts were synthesized under different applied electrode potentials.Among all as-obtained samples,the Pt-Ni/C electrocatalyst deposited at-1.73 V exhibits the optimal specific activity up to 1.850 mA cm^(-2)at 0.9 V vs.RHE,which is 6.85 times higher than that of the commercial Pt/C.Comprehensive physiochemical characterizations and computational evaluations via density functional theory were conducted to unveil the nucleation and growth mechanism of PtNi alloy formation.Compared to the aqueous solution,DMF solvent molecule must not be neglected in avoiding particle agglomeration and synthesis of monodispersed nanoparticles.During the alloy co-deposition process,Ni sites produced through the reduction of Ni(Ⅱ)precursor not only facilitates Pt-Ni alloy crystal nucleation but also in favor of further Pt reduction on the Ni-inserted Pt surface.As for the deposition potential,it adjusts the final particle size.This work provides a hopeful extended Pt-based catalyst layer production strategy for proton exchange membrane fuel cells and a new idea for the nucleation and growth mechanism exploration for electrodeposited Pt alloy.

Mg_2(OH)_2CO_3·3H_2O Whiskers Growth Mechanism

From the perspective of growth units, the growth mechanism of Mg2（OH）2CO3.3H2O whisker is investigated in this paper. Results show that the growth morphology of Mg2（OH）2CO33H2O whisker is consistent with the model of anion coordination polyhedron growth units. The growth solution Raman shift of Mg2（OH）2CO;3H2O was monitored using Raman spectroscopy. The growth units are [Mg-（OH）4]2- and H2COv The growth process of Mg2（OH）2COf3H2O whisker is as follows： growth unit [Mg-（OH）4]2- first incorporates into the larger dimension [Mg-（OH）4]2-, then the [Mg-（OH）4]2-n combines with H2CO3 into a linear skeleton Mg2（OH）2CO3 in the same line. Mg2（OH）2CO3 combines with H2O by hydrogen bonds and ultimately transforms into Mg2（OH）2COf3H2O whisker. Magnesium carbonate whiskers have a layered structure, each of which is made of magnesium, carbon, oxygen, with H2O in between each layer. When skeletons are superimposed within the same plane as a parallelepiped one, they grow into solid cuboid-shaped whiskers. When the parallelepiped skeletons planes combine with each other through the cascading links, they grow into hollow cylindrical whiskers.

Shape controlled synthesis and growth mechanism of one-dimensional zinc oxide nanomaterials

Some types of ZnO nanostructures with various shape and size, including tetrapod-like ZnO (T-ZnO) nanorods, nanowires and nanonbbons, have been obtained by controlled growth process. The nanostructures of ZnO have been investigated by means of field-emission scanning electron microscope, transmission electron microscopy and high-resolution transmission electron microscopy. The growth mechanisms of various ZnO nanostructures were proposed and discussed.

Controllable synthesis,characterization,and growth mechanism of hollow Zn_x Cd_(1-x) S spheres generated by a one-step thermal evaporation method

Novel hollow ZnxCdl xS spheres that are uniform in size are synthesized through the one-step thermal evaporation of a mixture of Zn and CdS powder. From an X-ray diffraction （XRD） study, the hexagonal wurtzite phase of ZnxCdl_xS is verified, and the Zn mole fraction （x） is determined to be 0.09. According to the experimental results, we propose a mechanism for the growth of Zn0.09Cd0.91S hollow spheres. The results of the cathodoluminescence investigation indicate uniform Zn, Cd, and S distribution of alloyed Zn0.09Cd0.91S, instead of separate CdS, ZnS, or nanocrystals of a core- shell structure. To the best of our knowledge, the fabrication of ZnxCd1-xS hollow spheres of this kind by one-step thermal evaporation has never been reported. This work would present a new method of growing and applying hollow spheres on Si substrates, and the discovery of the Zn0.09Cd0.91S hollow spheres would make the investigation of ZnxCd1-xS micro/nanostructures more interesting and intriguing.

Growth Mechanism and Characterization of ZnO 3D Nanocrystals by Laser Irradiation & Coaxially Transporting O_2

Different three-dimension （3D） nanotetrapods, containing club-like nanocrystals, nanotetrapods and four-foot-like nanocrystals were synthesized from Zinc sheet via CO2 laser irradiation and coaxially transporting O2. Different nanoproducts were fabricated by changing the content of oxygen in the experiment. The morphologies, components, phase structures and optical properties of the products were investigated by a field-emission scanning electron microscopy, an X-ray diffraction, an energy dispersed X-ray spectrometer and a photoluminescence spectroscope. The X-ray diffraction spectra were obtained on a Rigaku D/max 2500PC diffractometer. The experimental results reveal that high quality ZnO nanotetrapods can be fabricated on the special parameters, and growth of ZnO nanotetrapods depends on Vapour-Liquid-Solid（VLS） model, and the content of oxygen in the gas, namely, oxygen partial pressure is one of main factors to control morphologies and optical properties ofZnO nanotetrapods; these advantages above are important for realization of optoelectronic devices.

Massive Si Phase and Its Growth Mechanism in Al-Si Casting Alloy

Optical microscope and scanning electron microscope were used to observe the microstructure of the AI-11.6%Si and AI-11.6%Si-0.4%Mg alloys and the morphology of the massive silicon particles. It is found that the massive silicon phase, observed in the unfully modified alloys with 0.010%Sr, disappears completely in the alloys fully modified with 0.020%Sr. The serrations and reentrant edges shown in the massive silicon particles with the conventional casting indicate that the TPRE mechanism plays an important role in the growth of the massive silicon phase. The ripples and steps suggest that the "lateral microscopic growth" may be another operating mechanism.