Energy density and safety are the main factors that govern the development of the rechargeable battery technology. Currently, batteries beyond typical Li-ion batteries such as those based on solid-state electrolytes (SSEs) or other active elements (e.g., Na or Mg) are being examined as alternatives. For example, SSEs that would enable stable and reliable operation of all-solid-state Li-, Na-, and Mg-based batteries, with preferably improved capacity, are considered to be one of the most desired inventions. Lightweight complex metal hydrides are a family of solid compounds that were recently discovered to have extraordinary ionic conductivities and, in some cases, electrochemical properties that enabled battery reversibility. Consequently, they have become one of the promising electrolyte materials for future development of electrochemical storage devices. In this work, we present an overview of a wide range of lightweight hydride-based materials that could be used as electrolytes and/or anodes for mono-/divalent batteries and have a pivotal role in the implementation of new technological solutions in the field of electrochemistry.

Highly radioactive waste is incorporated into a glass matrix to convert it into a safe, passive form suitable for long-term storage and disposal. It is currently known that alpha decay can generate gaseous species, which can nucleate into bubbles, either through the production of helium or from ballistic collisions with the glass network that liberate oxygen. An effective method to probe this phenomenon utilizes ion beams to either directly implant helium or investigate the damage due to ballistic collisions. This paper provides an overview of the methodology, summarizes the results of current studies, and draws comparisons between them. We find that the irradiation scheme as well as the temperature and composition of the glass are important in determining whether bubble formation will occur. We also explore how analytical techniques can promote bubble formation and suggest avenues for further work.

In this work, carbon nanotubes (CNTs)-templated binuclear metallophthalocyanines (MTAPcCF3)2C (M = Mn, Fe, Co, Ni, Cu, Zn) assemblies (MTAPcCF3)2C–COOH–CNTs are designed and obtained. Whereafter, the structure and morphology of target products are analyzed by many means such as infrared, X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy. The electrocatalytic performances of lithium-thionyl chloride battery catalyzed by (MTAPcCF3)2C–COOH–CNTs were carried out. The result shows that all catalysts can improve the battery performance including the discharge time and the initial voltage. The catalytic performance of (MTAPcCF3)2C–COOH–CNTs is ordered following the central metal: Mn > Fe > Ni > Co > Cu > Zn. The cell capacity catalyzed by optimal catalyst (MnTAPcCF3)2C–COOH–CNTs can expand to 28.08 mAˑh, with increase by 142.07%, and the (MnTAPcCF3)2C–COOH–CNTs can extend the discharge time to 551.6 s. Besides, the reaction mechanism is presented on the basis of cyclic voltammetry measurements.

To suppress the interface gap between the cell walls of wood and filled epoxy resin, a green and universal H2O2 or H2O2/HAc steam-modified delignification approach is developed to remove more lignin, thereby generating more pores to be more conveniently backfilled by epoxy resin for highly transparent wood composites. Utilizing the excellent penetration ability of steam, not only different wood species, such as basswood and pine, with different cutting directions but also the thickest (40 mm) and largest (210 × 190 mm) wood samples can be successfully delignified. Compared with the 1.9% lignin content (which is the normal content of delignified wood prepared by solution-based methods) of delignified wood, the as-prepared delignified wood has the lowest lignin content of 0.84% to date. After the infiltration of epoxy resin, not only did the mechanical strength of the 5-mm transparent wood composite increase from 12.5 to 20.6 MPa, but the transmittance (the wavelength was 550 nm) also increased from 80 to 87% due to the lower absorbance of visible light by lignin and the suppression of the interface debonding gap between the cell walls and the backfilled epoxy resin.

The excessive use of plastic, especially polystyrene (PS), has caused serious environmental pollution. The efficient utilization of plastics and the conversion of plastics into value-added carbon materials are the concerns of researchers. Herein, we propose novel “pyrolysis–deposition” method to convert one popular plastic substance, PS, into ordered mesoporous carbons (OMCs). During the synthesis process, PS is pyrolyzed into small organic gases under high temperature, which is then adsorbed through capillary adsorption into the mesoporous of SBA-15 in the presence of catalyst. The obtained OMCs have high specific surface area, uniform pore size, and ordered pore structure. The OMCs exhibit specific capacitance of 118 F/g at a current density of 0.2 A/g and electrochemical stability of 87.2% at a current density of 2 A/g after 5000 cycles. The pyrolysis–deposition strategy provides a new idea to convert waste plastics into high-performance carbon materials for electrochemical applications.

Graphene oxide (GO) is a promising material in improving the corrosion resistance properties of metals. This improvement significantly relies on the microstructure and electrical properties of GO, which nevertheless is rarely studied. Here, multiscale GOs with different flake sizes and oxidation degrees were fabricated and incorporated into waterborne alkyd resin (AR). The physical and chemical structures of GO and AR/GO composites were characterized in detail. Multiscale GOs are successfully prepared, and the corrosion resistance of AR/GO coatings is measured by electrochemical workstation. Electrochemical experiments indicate that GOs with larger flake sizes have excellent barrier properties due to the shielding effect; GOs with appropriate oxidation degrees could effectively improve the dispersion of GO and avoid the conductive path of GO in the matrix, because oxidation degree of GO could influence the dispersion and electrical properties. The corrosion protection efficiency of AR/GO(GO: 120 μm, 1.5 wt%, sp2/sp3 = 2.61) is 98.14%, which is 2.26 times higher than AR. The multiscale effects of GO on the corrosion resistance property of AR coatings are quite general, thus providing guidelines for developing highly efficient corrosion resistant coatings for practical usage.

This study investigated the compressive response of ice-templated composites and provides an understanding of their mechanical behavior based on the properties of templated ceramic and epoxy. Results suggested a dependence of properties on the microstructure of the templated porous ceramic, whereas more interestingly composites exhibited catastrophic and progressive types of failure. Compressive strength was found to be markedly greater relative to the strength of templated ceramic and polymer, and irrespective of the failure type, strength was greatly enhanced under dynamic loading relative to quasistatic loading. Compressive strength was also calculated based on the rule of mixtures and mode of failure in ice-templated ceramic. The analysis suggested that the axial mode of failure was not dominant in composites, and failures resulted from the fracture of lamella walls, possibly due to elastic instability. Fragments of the composite specimens were analyzed using scanning electron microscopy to study the fracture characteristics and rationalize the catastrophic and progressive types of failure.

This work studied the relationship between embedded particle volume fraction and magnetic particle orientation distribution in aligned 325 mesh barium hexaferrite (BHF) and polydimethylsiloxane (Sylgard 184; Dow Corning) magnetoactive elastomer (MAE) composites. BHF particles were aligned within the elastomer in the out-of-plane direction, as the material cured. Particle orientation distribution was defined herein by observations of the population of directions at which particle magnetizations resided; magnetization coincides with the physical crystallographic c-axis of BHF. The work used results of vibrating sample magnetometry experiments on MAEs with increasing volume concentrations of embedded ferromagnetic particles (10–30 v/v%) to determine changing widths of analytical particle distribution functions used to describe the range of particle orientations. With over 80% confidence, results showed that MAE composites having the intermediate 15 v/v% had the highest degree of magnetic (and thereby physical) alignment as well as magnetic remanence.

The effect of polypropylene (PP) molecular weight on the properties of styrene-butadiene-styrene block copolymer (SBS)/PP blends was studied. All SBS/PP blends (50/50 and 90/10) exhibited a sandwich structure where the co-continuous SBS/PP layer was between the top and bottom PP layers. Solvent extraction tests suggested that the continuous phase structure of PP was independent of the blending ratio and PP molecular weight, while the SBS phase changed from a dispersed phase to a continuous phase as the SBS content increased. The decrease in PP molecular weight decreased the PP layer thickness but increased the phase domain size of SBS in SBS/PP(50/50) blends. As a result, less noticeable “stress-hardening” phenomenon was observed. The mechanism for the structural change was attributed to the different melt viscosities of each component. The crystallinity of the blends did not change with the variable PP molecular weight but decreased with the increasing SBS content.

Environmental pollution and energy shortages seriously restrict the development of society. Photocatalytic oxidation technology can directly use solar energy to drive a series of chemical reactions. It has the advantages of low energy consumption, mild reaction conditions, and no secondary pollution, and is an effective method to solve organic pollutions in water. The key to achieve this process is to find and design efficient photocatalytic materials. In this paper, a novel silver-based metal–organic framework (Ag-MOF) [{Ag(H2btc)}{Ag2(Hbtc)}]n (1) (H3btc = 1,3,5-trimesic acid) is designed that exhibits a high performance in the photocatalytic degradation of methylene blue (MB). The process of photocatalytic degradation of MB conforms to pseudo first-order kinetics, and the rate is the fastest at pH 3 (K = 0.2654). Meanwhile, the photocatalytic mechanism of 1 is analyzed by in situ electron paramagnetic resonance (EPR) and ESI-MS spectra. The results are helpful for in situ research of the photocatalytic mechanism of MOFs.

Dyeing wastewater has caused serious environmental problems nowadays. In this work, nickel–phosphorus plating–titanium dioxide (Ni-P-TiO2) electroless plating polyimide (PI) fabric was fabricated as an excellent visible light response composite. First, polyaniline (PANI) was in situ polymerized on the surface of the PI fabric. Second, PANI reduced palladium ions to be active seeds for initiating electroless plating of Ni-P-TiO2 layer. Finally, the Ni-P-TiO2/PANI/PI fabric with all-in-one structure was prepared, which can effectively overcome the drawbacks of poor loading fastness and insensitivity to visible light response. It was characterized by scanning electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, thermogravimetric analysis, and ultraviolet–visible diffuse reflectance spectroscopy. The photocatalytic activity was evaluated by degrading reactive blue 19, methylene blue, and reactive red (M-3BE) under visible light irradiation. The results show that the degradation rates of the all three dyes were over 91% with robust cycle stability for repeated 5 cycles of use. The possible photocatalytic degradation mechanism of fabrics was also proposed based on free radical and hole removal experiments.

Laves phase plays a positive role in improving the strength of high-entropy alloys (HEAs); Nb and Ti elements have potential to promote Laves phase formation in some HEAs. For improving the strength of the face-centered cubic (FCC) CoCrFeMnNi HEA, a series of (CoCrFeMnNi)100−xNbx (atomic ratio: x = 0, 4, 8, 12, 16) and (CoCrFeMnNi)100−xTix (atomic ratio: x = 0, 2, 4, 6, 8, 12) HEAs were prepared by melting. The effects of Nb and Ti on the microstructure evolution and compressive properties of the CoCrFeMnNi HEAs were investigated. For (CoCrFeMnNi)100−xNbx HEAs, the second-phase (Laves and σ phase) volume fraction increased from 0 to 42%. The yield strength also increased gradually from 202 to 1010 MPa. However, the fracture strain decreased from 60% (no fracture) to 12% with increasing Nb content. For (CoCrFeMnNi)100−xTix HEAs, the yield strength increased from 202 to 1322 MPa. The Laves phase volume fraction also increased from 0 to 27%. However, the fracture strain decreased from 60% (no fracture) to 7.5% with increasing Ti content. Addition of Nb and Ti has a good effect on improving the strength of FCC CoCrFeMnNi HEA.

Atomistic simulations of 18 silicon 〈110〉 symmetric tilt grain boundaries are performed using Stillinger Weber, Tersoff, and the optimized Modified Embedded Atom Method potentials. We define a novel structural unit classification through dislocation core analysis to characterize the relaxed GB structures. GBs with the misorientation angle θ ranging from 13.44° to 70.53° are solely composed of Lomer dislocation cores. For GBs with θ less than but close to 70.53°, GB ‘step’ appears and the equilibrated states with lowest GB energies can be attained only when such GB ‘step’ is located in the middle of each single periodic GB structure. For the misorientation angles in the range of 93.37° ≤ θ ≤ 148.41°, GB structures become complicated since they contain multiple types of dislocation cores. This work not only facilitates the structural characterization of silicon 〈110〉 STGBs, but also may provide new insights into mirco-structure design in multicrystalline silicon.

In this paper, the influence of strain rate on the mechanical behavior of high-strength low-alloy (HC420LA) steel were studied. Quasi-static and dynamic tensile experiments were performed with strain rates ranging from 0.001 to 500 s−1 at room temperature. The digital image correlation technique was used to obtain the full-field strain. The experimental results showed that HC420LA steel exhibited positive strain rate sensitivity. Based on experimental results, the modified Johnson–Cook (J–C) model was used to model the constitutive behavior of HC420LA steel. Predictions of the standard and modified J–C models were compared using standard statistical parameters. The modified J–C model showed better agreement with the experimental data. Then, numerical simulation of the representative tensile test at a strain rate of 100 s−1 was performed using the finite element code LS-DYNA. Good correlation between the experimental and numerical simulation results was achieved.

M3:2 high-speed steel (HSS) billets with or without Nb addition were prepared by spray deposition. The effects of Nb and post-thermal-mechanical processing (decomposition treatment and hot forging), as well as heat treatment, on the microstructure and properties of M3:2 HSS were investigated. The microstructure of the as-deposited M3:2 HSS consisted of equiaxed grains with a mean size of approximately 25 μm and discontinuous plate-like M2C and irregular MC carbides distributed along grain boundaries. 0.5% Nb addition can refine the M2C plates and spheroidize MC carbides. With 2% Nb addition, the refined grains with a mean size of approximately 12 μm and continuous net of M6C and a uniform distribution of NbC carbides were obtained. The decomposition of metastable M2C carbides can be accelerated with 0.5% Nb addition due to the refined size and lower thermodynamic stability of M2C plates. With the increased degree of decomposition of M2C carbide, the M6C and MC carbides became refined and more uniformly distributed after optimal thermal-mechanical processing and heat treatment, which leads to a significant increase in bend strength and toughness.

To understand the effect of pH value on the corrosion and corrosion fatigue behavior of AM60 magnesium alloy, electrochemical tests, viz., electrochemical impedance spectroscopy (EIS) and fatigue tests, were carried out in PBS (phosphate buffered saline) solutions of pH 5.2, 7.4, and 9.0. The microstructure was investigated by scanning electron microscopy (SEM). Results are as follows: (i) the corrosion mechanism of AM60 under different pH values was different according to EIS; (ii) the corrosion resistance and corrosion fatigue life reduced in the following order: pH 9.0 > pH 7.4 > pH 5.2; (iii) the crack initiation was associated with hydrogen embrittlement of AM60 on the basis of fractographic analysis.

A kind of novel Ni–P gradient coating/stannate conversion film was deposited on AZ91D magnesium alloy (AZ91D alloy) by an integrative method involved stannate conversion and electroless plating. The results indicated that using sodium hypophosphite concentrations varied as 5, 10, 22, 46, and 60 g/L in the bath, the electroless Ni–P gradient coating with typical cell morphologies was successfully prepared, and the structures transited from crystalline → microcrystalline → amorphous were obtained as increasing P content from 3.31 to 12.58 wt%. Furthermore, the corrosion morphologies, polarization curves, and the electrochemical impedance spectroscopy result indicated that the corrosion resistance of AZ91D alloy substrate was significantly improved and the corrosion resistance of Ni–P gradient coating was superior than that of stannate conversion film, which might be attributed to the gradient structure and rising P content with unique function.

A new type of polyelectrolyte–Al2O3/SiO2 composite nanoparticle with excellent dispersibility and superior polishing performance was successfully fabricated using a facile method. Silica acted as a bifunctional molecule by attaching to alumina via covalent bond and adsorbing polyelectrolytes by electrostatic interaction. The material removal rate of the polyelectrolyte–Al2O3/SiO2 abrasive was 30% higher than that of the pure Al2O3 abrasive. In addition, the sapphire surface was much smoother. The material removal mechanism was investigated during CMP using the microcontact and wear model. The enhanced removal rate was mainly attributed to the well-dispersed particles, which can accelerate mechanical removal process. The remarkably smooth surface was due to the decrease in penetration depth of the abrasive into the wafer. The results of this study provided a feasible strategy to satisfy the high efficiency and damage-free polishing requirements for sapphire planarization.