低温球磨制备高热稳定性纳米晶Al-Zn-Mg-Cu合金块体材料

利用液氮球磨和真空热压技术制备纳米晶Al-10Zn-3Mg-1.8Cu(质量分数,%)合金块体材料。采用X射线衍射(XRD)和透射电镜(TEM)对材料在制备过程中的固态相变、晶粒尺寸和热稳定性进行分析。结果表明,材料经过液氮球磨15 h后晶粒尺寸为37 nm,真空热压后材料晶粒保持在100 nm,热挤压后晶粒尺寸约为300 nm,热处理后晶粒尺寸保持不变。材料的高热稳定性原因在于大量合金元素和杂质元素超饱和固溶于Al基体中阻止了晶粒的长大,以及细小析出MgZn2相和Al2O3颗粒对于晶界的钉扎作用。     

Light-Responsive Programmable Shape-Memory Soft Actuator Based on Liquid Crystalline Polymer/Polyurethane Network

Liquid crystalline polymers (LCPs), especially liquid crystalline elastomers (LCEs) can generate ultrahigh shape change amplitude but has lower mechanical strength. Although some attempts have been tried to improve the mechanical performance of LCE, there are still limitations including complicated fabrication and high actuation temperature. Here, a versatile method is reported to fabricate light-driven actuator by covalently cross-linking polyurethane (PU) into LCP networks (PULCN). This new scheme is distinct from the previous interpenetrating network strategy, the hydrogen bonds and covalent bonds are used in this study to improve the miscibility of non-liquid-crystalline PU and LCP materials and enhance the stability of the composite system. This material not only possesses the shape memory properties of PU but shows shape-changing behavior of LCPs. With a shrinkage ratio of 20% at the phase transition temperature, the prepared materials reached a maximum mechanical strength of 20 MPa, higher than conventional LCP. Meanwhile, the resulting film shows diverse and programmable initial shapes by constructing crosslinking density gradient across the thickness of the film. By integration of PULCN with near-infrared light-responsive polydopamine, local and sequential light control is achieved. This study may provide a new route for the fabrication of programmable and mechanically robust light-driven soft actuator.     

Hot corrosion behavior of porous nickel-based alloys containing molybdenum in the presence of NaCl at 750 °C

The hot corrosion of porous Ni-23Cr-xMo (0%, 4.5%, 9.0%, 13.5%, mass fraction) alloys tested at 750 °C under cyclic procedure was investigated in order to elucidate the effect of Mo addition on hot corrosion in the presence of NaCl. The hot corrosion experiments were performed at 750 °C in air with 4 mg cm^− 2 NaCl deposit. The performance of the alloys was evaluated by the results of weight change kinetics. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS) were used to characterize the corrosion products. The results indicate that NaCl accelerated the oxidation of the alloys by chloridized elements Mo and Cr. Among the porous Ni-23Cr-xMo alloys, Ni-23Cr-9Mo alloy exhibited the best hot corrosion resistance due to the formation of NiO-NiCr₂O₄-Cr₂O₃ oxide scales. Furthermore, these oxide scales were confirmed more effective to protect the alloys after adding of Mo.     

A modified θ projection model for constant load creep curves-II. Application of creep life prediction

To minimize the deviation of the predicted creep curves obtained under constant load conditions by the original θ projection model, a new modified version that can be expressed by $\epsilon ={\theta }_1\left(1-e^{-{\theta }_{2}t}\right)+{\theta }_3\left(e^{{\theta }_4{e}^{{\theta }_5\epsilon }t}-1\right)$, was derived and experimentally validated in our last study. In the present study, the predictive capability of the modified θ projection model was investigated by comparing the simulated and experimentally determined creep curves of K465 and DZ125 superalloys over a range of temperatures and stresses. Furthermore, the linear relationship between creep temperature and initial stress was extended to the 5-parameter model. The results indicated that the modified model could be used as a creep life prediction method, as it described the creep curve shape and resulted in predictions that fall within a specified error interval. Meanwhile, this modified model provides a more accurate way of describing creep curves under constant load conditions. The limitations and future direction of the modified model were also discussed. In addition, this modified θ projection model shows great potential for the evaluation and assessment of the service safety of structural materials used in components governed by creep deformation.     

Low-valence ion addition induced more compact passive films on nickel-copper nano-coatings

Ni-Cu nano-coatings were prepared by pulsed electroplating technique in the baths containing various amount of boric acid. Their microstructure, morphologies and corrosion resistance were characterized in detail. The addition of boric acid strongly influences on the microstructure of the Ni-Cu coatings. The coating with a grain size of 130 nm, obtained from the bath containing 35 g L⁻¹ boric acid, shows the highest corrosion resistance. This is attributed to the low-valence Cu ion (Cu⁺) additions in nickel oxide, which could significantly decrease the oxygen ion vacancy density in the passive film to form a more compact passive film. The higher Cu⁺ additions and the lower diffusivity of point defects (D₀) are responsible for the formation of more compact passive film on the coating obtained from the bath with 35 g L⁻¹ boric acid.     

Prediction of stable high-pressure structures of tantalum nitride TaN2

Structure searches based on a combination of first-principles calculations and a particle swarm optimization technique unravel two new stable high-pressure structures (C2/m and Cmce) for TaN₂. The structural features, mechanical properties, formation enthalpies, electronic structure, and phase diagram of TaN₂ are fully investigated. Being mechanically and dynamically stable, the two phases could be made metastable experimentally at ambient conditions.     

Oligothiophene-based small molecules with 3,3′-difluoro-2,2′-bithiophene central unit for solution-processed organic solar cells

Two new oligothiophene-based small molecules, namely DRCN6T-F and DRCN8T-F, with 3,3′-difluoro-2,2′-bithiophene as the central building block and 2-(1,1-dicyanomethylene)-rhodanine as end groups, were designed and synthesized. Compared to their non-fluorinated counterparts DRCN6T and DRCN8T, DRCN6T-F and DRCN8T-F exhibit enhanced intermolecular interactions and lower HOMO energy levels. However, PCEs of 2.26% and 5.07% were obtained for DRCN6T-F and DRCN8T-F based optimized devices, respectively, lower than those of non-fluorinated molecules DRCN6T and DRCN8T. The relatively poor performance for the DRCN6T-F and DRCN8T-F were mainly caused by their low short-circuit current densities, due to their unfavorable morphologies and low charge carrier mobilities.     

Effect of pore structure on the compressive property of porous Ti produced by powder metallurgy technique

Porous Ti with an average macro-pore size of 200–400 μm and porosity in the range of 10–65% has been manufactured using polymethyl methacrylate (PMMA) powders as spacer particles. The compressive strength and elastic modulus of resultant porous Ti are observed in the range of 32–530 MPa and 0.7–23.3 GPa, respectively. With the increasing of the porosity and macro-pore size, the compressive strength and modulus decrease as described by Gibson–Ashby model. The failure due to cracking (complete fracture) of the struts on porous Ti is controlled primarily by macro-pores. Fractography shows evidence of the brittle cleavage fracture mainly, but containing a few fine shallow dimples and a small amount of transcrystalline fracture of similarly oriented laths. The failure mechanism has been discussed by taking the intrinsic microstructural features into consideration.     

A preliminary study on optimizing the heat treatment of high strength Al–Cu–Mg–Zn alloys

The design of critical aerospace alloys is primarily built on optimizing strength and ductility, both of which can be enhanced by controlling the alloying element additions as well as heat treatment conditions. The 7075 alloy is one such aerospace alloy. The main objective of this study was to optimize the 7075 strength. Several experimental alloys were prepared and tensile test bars were cast using an ASTM B-108 type permanent metallic mold. The as-cast samples were then solution heat-treated at 470 °C for times up to 48 h. The solution heat-treated bars were also aged in order to improve the alloy strength through precipitation hardening. Line scans for Mg, Cu and Zn were obtained from the various heat-treated alloy samples using an electron probe microanalyzer equipped with Energy Dispersive X-ray (EDX) and Wavelength Dispersive Spectroscopic (WDS) facilities. Peaks corresponding to the Mg, Cu and Zn concentrations in the as-cast samples disappeared after solution treatment, reflecting optimized homogeneity structures. The newly developed versions of the 7075 alloy displayed an ultimate tensile strength (UTS) of ∼1 GPa.     

Atomistic tight-binding computations of the electronic properties of ZnSe/ZnS core/shell nanocrystals under applied electric field

The effect of applied electric field on the electronic properties of spherical ZnSe/ZnS core/shell nanocrystals of experimentally relevant size is investigated by the atomistic tight-binding theory. Using this model, the calculations show that a range of electronic properties, including the single-particle spectra, atomistic characters, charge densities, excitonic energies, ground-state coulomb energies, overlaps of the electron and hole wave functions and oscillation strengths, all depend on the strengths of the applied electric field. The spatial distributions of the electron and hole wave functions are induced by the applied electric field. The analysis demonstrates a clear manipulation of the electronic properties of ZnSe/ZnS core/shell nanocrystals by introducing and varying the applied electric field strengths. According to the comprehensive investigations, I suppose that these atomistic computations will be of prospective help for experimental works concentrated on the new optoelectronic devices based on the applied electric field.