Electrochemical capacitors featuring a modified acetonitrile (AN) electrolyte and a binder-free, activated carbon fabric electrode material were assembled and tested at <−40 °C. The melting point of the electrolyte was depressed relative to the standard pure AN solvent through the use of a methyl formate cosolvent, to enable operation at temperatures lower than the rated limit of typical commercial cells (−40 °C). Based on earlier electrolyte formulation studies, a 1:1 ratio of methyl formate to AN (by volume) was selected, to maximize freezing point depression while maintaining a sufficient salt solubility. The salt spiro-(1,1′)-bipyrrolidinium tetrafluoroborate was used, based on its improved conductivity at low temperatures, relative to linear alkyl ammonium salts. The carbon fabric electrode supported a relatively high rate capability at temperatures as low as −65 °C with a modest increase in cell resistance at this reduced temperature. The capacitance was only weakly dependent on temperature, with a specific capacitance of ∼110 F/g.

Graphene-based flexible and wearable supercapacitors have been produced by wet spinning, in which organic solvent coagulating bath was prerequisite and spacers were usually incorporated to improve the electrochemical property but sacrificing the mechanical property. In this work, a nonorganic solvent spinning technology named as interfacial polyelectrolyte complexation (IPC), which was based on the spontaneous self-assembly of two oppositely charged polyelectrolyte solutions/suspensions to form continuous fibers on drawing in their interfaces, was proposed to fabricate graphene fiber–shaped electrodes for supercapacitors. Due to the excellent mechanical performance and hydrophilicity, cellulose nanofibrils (CNFs) were added to serve as an efficient reinforcing agent and spacer of graphene fiber electrodes. Consequently, the mechanical performance and specific capacitance of the fibers were improved but electrical conductivity was declined. Taking overall consideration, CNF/rGO60 fiber electrode possessed a superior integrated performance with a capacitance of 182.6 F/g, tensile strength of 480 MPa, and electrical conductivity of 5538.7 S/m. The IPC spinning provided an environmentally friendly strategy for the fabrication of fiber-shaped functional devices.

Nanocomposites of polyvinylidene fluoride loaded with various amounts of γ-Fe2O nanoparticles, with an average size ranging between 20 and 40 nm, have been obtained by melt mixing and investigated using various experimental techniques [Superconducting Quantum Interference Device, Mössbauer, and Thermogravimetric Analysis]. Magnetic and Mössbauer measurements confirmed the presence of maghemite and a trace of a paramagnetic iron compound. Magnetic data are consistent with a blocking temperature close to room temperature (RT), showing a decrease in the coercive field as the temperature is increased. A weak exchange bias was noticed in all nanocomposites investigated at all temperatures and tentatively ascribed to surface spin disorder. The temperature dependence of the coercive field obeys the Kneller law. The nanocomposites exhibit superparamagnetic behavior near RT. Most magnetic measurements have been performed below the blocking temperature, revealing thus a complex behavior. The dependence of the mass loss derivative versus temperature, as obtained by thermogravimetric analysis, exhibits a single peak due to the thermal degradation of the polymeric matrix. A weak increase in the thermal stability of the polymeric matrix upon loading with maghemite is reported.

Structural evolution induced and driven by a dual system and simultaneous passivation of phosphorene are reported. Different nano-objects of phosphorene or black phosphorus (BP) are obtained using a new method of exfoliation, in which solvent and an ionic polymer are combined to weaken the van der Waals forces and to scissor the nanosheets. Nanoribbons, nanorods, and nanoneedles are obtained under mechanical force and ambient conditions. Ionic polymer chains assist in curling the monolayer or few-layer nanosheet. Nafion is chosen to exfoliate the bulk BP and induce a morphological transition in BP nanosheets. The exfoliation of BP nanosheets results into thin and specific structures such as nanosheets/rods/needles. The nanosheets of phosphorene are covered and passivated simultaneously by the polymeric sheath that protects the nanosheets from degradation or oxidation and can be integrated with a device directly without any further coating.

In this work, four N-TiO2/bismuth oxyiodide (BiOI)/reduced graphene oxide (RGO) composite photocatalysts with different composite ratios were prepared using a hydrothermal method. The phase, surface structure, specific surface area, and light response were characterized by X-ray diffraction, X-ray photoelectron spectrum analysis, scanning electron microscopy, specific surface area and aperture analysis, and UV-vis diffuse reflection spectrum analysis. The results indicated that the N-TiO2/BiOI/RGO (NTGB) composite prepared with a mass ratio of 1:1:2 is a promising photocatalyst for the degradation of organic pollutants by using sunlight, with a specific surface area of 139.56 (m2/g), bandgap of 1.24 eV, and strong absorption with a smaller visible region. It has the best photocatalytic properties under visible light irradiation in the degradation of methylene blue (MB): the degradation rate of MB in the presence of light for 60 min reached 99.22%, and its photocatalytic performance was significantly higher than that of TiO2, N-TiO2, BiOI, N-TiO2/BiOI, BiOI/RGO, NTGB1, NTGB2, and NTGB4.

For the first time in the literature, experimental determination of entire sets of exact interdiffusion coefficients in quaternary and quinary alloy systems is reported. Using the method of body-diagonal diffusion couple, a set of nine quaternary interdiffusion coefficients were evaluated in Fe–Ni–Co–Cr and a set of sixteen quinary interdiffusion coefficients were determined in a Fe–Ni–Co–Cr–Mn system, both at approximately equimolar compositions. Regions of uphill interdiffusion and zero flux planes were observed for nickel and cobalt in quinary couples, indicating the existence of strong diffusional interactions in Fe–Ni–Co–Cr–Mn alloys. The strong diffusional interactions were also manifested in the large magnitudes of cross coefficients in both the systems. The existence of strong diffusional interactions in high-entropy alloys (HEAs) as observed through experimentally determined interdiffusion coefficients in this study establishes beyond doubt the fact that cross interdiffusion coefficients cannot be ignored in HEAs.

In this paper, the atomic resolution high-angle annular dark-field scanning transmission electron microscope (HAADF-STEM) was used as the main research method. Using HAADF-STEM, two types of long-period stacking ordered structure (LPSO)—14H and 18R-LPSO—were observed in Mg96Gd2Y1Ni1 alloy, and the precipitates at various stages of aging were observed. Moreover, a type of rectangular β precipitates were found, and the atomic models of β precipitates along the [0001]Mg and ${\tf="TeXGyrePagella-Bold (TrueType)"\char9001} 11\bar 20\hbox{]}_{{\rm{Mg}}}$ directions were identified. At the aging peak stage, a three-dimensional network structure composed of LPSO/γ′ precipitates and β′ precipitates and β precipitates was observed. The hardness of the unaged homogenized Mg96Gd2Y1Ni1 alloy was only 87 HV and the hardness value of aging peak was 128.4 HV. Compared with the unaged alloy, the hardness of the peak-aged alloy increased by 47.59%. The composite strengthening of the three types of precipitates induced a significant strengthening to the alloy.

Regarding the effect of composition on the mechanical properties of intermetallic phases such as Laves phases, there is conflicting information in the literature. Some authors observed defect hardening when deviating from stoichiometric Laves phase composition, whereas others find defect softening. Here, we present a systematic investigation of the defect state, hardness, and elastic modulus of cubic and hexagonal NbCo2 Laves phases as a function of crystal structure and composition. For this purpose, diffusion couples were prepared which exhibit diffusion layers of the cubic C15 and hexagonal C14 and C36 NbCo2 Laves phases, with concentration gradients covering their entire homogeneity ranges from 24 to 37 at.% Nb. Direct observations of dislocations and stacking faults in the diffusion layers as a function of composition were performed by electron channeling contrast imaging, and the hardness and elastic modulus were probed in the diffusion layers along the concentration gradients by nanoindentation.

Nanoindentation and microcrystal deformation are two methods that allow probing size effects in crystal plasticity. In many cases of microcrystal deformation, scale-free and potentially universal intermittency of event sizes during plastic flow has been revealed, whereas nanoindentation has been mainly used to assess the stress statistics of the first pop-in. Here, we show that both methods of deformation exhibit fundamentally different event-size statistics obtained from plastic instabilities. Nanoindentation results in scale-dependent intermittent microplasticity best described by Weibull statistics (stress and magnitude of the first pop-in) and lognormal statistics (magnitude of higher-order pop-ins). In contrast, finite-volume microcrystal deformation of the same material exhibits microplastic event-size intermittency of truncated power-law type even when the same plastic volume as in nanoindentation is probed. Furthermore, we successfully test a previously proposed extreme-value statistics model that relates the average first critical stress to the shape and scale parameter of the underlying Weibull distribution.

The tensile yield strength of high-density polyethylene using instrumented indentation tests with a flat-ended cylindrical indenter was evaluated. The variation in the field expressed by stress and strain beneath the flat-ended cylindrical indenter is investigated using a new expanding cavity model to study the relation between tension and indentation. This model starts from the separation of forces into the compressive force on the material and the frictional one, which is generated during indentation on the sides of indenter. The authors propose a method to correct the frictional force based on the saturation of indentation hardening and obtain load–depth curve with compressive component only. For conversion of indentation force and displacement, our new representation model is applied. By modifying Johnson's model, the new assumption of conservation of indentation plastic volume is suggested. This model proves and supports conventional relations of the strain rates between indentation and tension theoretically. These are verified through the experiments: instrumented indentation and uniaxial tensile test. The authors find a good agreement between the tensile yield strengths at various strain rates.