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Three kinds of nano-concrete, i.e., 2.0% nano-SiO2 doped, 2.0% nano-CaCO3 doped and 1.0% nano-SiO2-1.0% nano-CaCO3 co-doped concretes (NS, NC, NSC) were prepared for a study on static property and dynamic property under different strain rates (50–130 s−1) using HYY series hydraulic servo test system and Φ100 mm split Hopkinson pressure bar test system, and a comparison with plain concrete (PC) as well. The results have shown that under static load, as compared with PC, NC has both strength and elastic modulus increased obviously, while NS has strength decreased and elastic modulus increased, and under dynamic load, there is an obvious strain rate effect for the dynamic compressive strength, impact toughness, energy dissipation and impact failure mode of concrete. Under the same strain rate, the dynamic compressive strength, peak strain, impact toughness and energy dissipation of NC are significantly increased, while its dynamic elastic modulus is decreased. Compared with PC, NS has dynamic compressive strength, peak strain, impact toughness and energy dissipation decreased, and dynamic elastic modulus increased, NC has static and dynamic mechanical properties improved, NS has static and dynamic mechanical properties weakened, and NSC is between PC and NC in static and dynamic mechanical properties, but generally improved. Doped with nano-CaCO3, NC has compactness improved, weak areas reduced, and pore size distribution optimized, while doped with nano-SiO2, NS has obvious internal weak areas, with pore structure degraded.

In this paper, we demonstrate an active switching of extremely high Q-factor Fano resonances using vanadium oxide (VO2)-implanted THz asymmetric double C-shaped metamaterial (MM) structures. The simulation results indicate the highly temperature-sensitive nature of the double Fano resonances that can be switched at very low external thermal pumping (68 &deg, C), which is only slightly higher than room temperature. We employ the surface current and electric field distributions of the structure to analyze the physical mechanism of the observed switching behavior in the thermally excited Fano MMs. More importantly, by optimizing the asymmetric parameter (offset length), the linewidth of the Fano resonance can reach only 0.015 THz and the Q-factor is as high as 98, which is one order of magnitude higher than that of the traditional MMs. The findings of this work would enable a thermally-induced high-Q Fano resonance MMs for ultra-sensitive sensors, modulators, low threshold switching in metadevices.

A novel adsorbent, tartaric acid modified graphene oxide (GO-TA), was successfully prepared by a simple esterification reaction and applied to remove Cu(II) and Pb(II) metal ions from aqueous solutions. The obtained composites were characterized by Fourier transform infrared (FT-IR) spectroscopy, Raman spectroscopy and transmission electron microscopy (TEM). Batch experiments were carried out to investigate the effect of pH value, contact time, concentration of metal ions and temperature on Cu(II) and Pb(II) adsorption. The maximum adsorption capacities for Cu(II) and Pb(II) are 374.53 mg g−1 and 125.63 mg g−1, respectively, which were higher than those of pristine graphene oxide (GO). The obtained experimental data showed a good correlation with the Langmuir adsorption model. The adsorption kinetics of Cu(II) and Pb(II) onto GO-TA composite was found to be well fit for the pseudo-second-order model. Moreover, thermodynamic parameters including ΔGθ 0 and ΔSθ> 0, indicating that the adsorption of Cu(II) and Pb(II) onto GO-TA composite was spontaneous and endothermic in nature. All these results indicated that GO-TA composite with such high adsorption efficiency and fast adsorption equilibrium could be used to clean up heavy metal pollution in the future.

Tunable terahertz (THz) functional devices have exhibited superior performances due to the use of active materials, such as liquid crystals, graphene, and semiconductors. However, the tunable range of constitutive parameters of materials is still limited, which leads to the low modulation depth of THz devices. Here, we demonstrate a broadband tunable THz absorber based on hybrid vanadium dioxide (VO2) metamaterials. Unlike other phase change materials, VO2 exhibits an insulator-to-metal transition characteristic and the conductivity can be increased by 4–5 orders of magnitude under external stimulus including electric fields, optical, and thermal pumps. Based on the unique transition character of VO2, the maximum tunable range of the proposed absorber can be realized from 5% to 100% by an external thermal excitation. Meanwhile, an absorption greater than 80% in a continuous range with a bandwidth about 2.0 THz can be obtained when VO2 is in its metal phase at high temperature. Furthermore, the absorber is insensitive to the incident angle up to 50° and such a broadband THz absorber can be used in applications including imaging, modulating, cloaking, and so on.

In this work, a novel activated carbon containing graphene composite was developed using a fast, simple, and green ultrasonic-assisted method. Graphene is more likely a framework which provides support for activated carbon (AC) particles to form hierarchical microstructure of carbon composite. Scanning electron microscope (SEM), transmission electron microscope (TEM), Brunauer–Emmett–Teller (BET) surface area measurement, thermogravimetric analysis (TGA), Raman spectra analysis, XRD, and XPS were used to analyze the morphology and surface structure of the composite. The electrochemical properties of the supercapacitor electrode based on the as-prepared carbon composite were investigated by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), charge/discharge, and cycling performance measurements. It exhibited better electrochemical performance including higher specific capacitance (284 F g−1 at a current density of 0.5 A g−1), better rate behavior (70.7% retention), and more stable cycling performance (no capacitance fading even after 2000 cycles). It is easier for us to find that the composite produced by our method was superior to pristine AC in terms of electrochemical performance due to the unique conductive network between graphene and AC.