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The batch removal of Cr(VI) from simulated wastewater with Fe@Fe2O3 core-shell nanowires (FCSNs) was investigated in this study. Itwas found that each gram of the FCSNs could remove 7.78 mg of Cr(VI) from simulated wastewater containing 8.0 mg L(-1) of Cr(VI) with an initial pH of 6.5 at room temperature. The Freundlich adsorption isotherm was applicable to describe the removal processes. Kinetics of the Cr(VI) removal was found to follow pseudo-second-order rate equation. Furthermore, the as-prepared and Cr(VI)-adsorbed FCSNs were carefully examined by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopic analysis (XPS). The characterization results suggested that the adsorbed Cr(VI) was partially reduced to Cr(lll) in Cr2O3/Cr(OH)3 on the FCSNs. The possible mechanism of removal of Cr(VI) on FCSNs was proposed, which involved the dominant Cr(VI) adsorption, followed by the partial reduction of Cr(VI) to Cr(III) (chromium(III) oxyhydroides) on the surface of FCSNs. These Fe@Fe2O3 core-shell nanowires with high specific surface area and strong magnetic property are very attractive for the removal of Cr(VI) from wastewater.

Material composition engineering and device fabrication of perovskite nanocrystals (PNCs) in solution can introduce organic contamination and entail several synthetic, processing, and stabilization steps. We report three-dimensional (3D) direct lithography of PNCs with tunable composition and bandgap in glass. The halide ion distribution was controlled at the nanoscale with ultrafast laser–induced liquid nanophase separation. The PNCs exhibit notable stability against ultraviolet irradiation, organic solution, and high temperatures (up to 250°C). Printed 3D structures in glass were used for optical storage, micro–light emitting diodes, and holographic displays. The proposed mechanisms of both PNC formation and composition tunability were verified.

Nanoparticles have a wide range of electrical and optical properties owing to the quantum-size effect, surface effect, and conjoint effect of nanostructures. [1] Materials doped with noble-metal nanoparticles exhibit large third-order nonlinear

Monodispersed porous crystalline TiO(2), SrTiO(3), and BaTiO(3) spheres were produced through a one-step hydrothermal process from amorphous TiO(2) spheres. The resulting samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and nitrogen sorption measurements. On the basis of the characterization results, we proposed a formation process of these porous spheres according to a mechanism analogous to the Kirkendall effect. This study provides a general way to synthesize porous titania-based spheres.

Monochalcogenides of germanium (or tin) are considered as isoelectronic and isostructural analogues of black phosphorus. Here, we demonstrate the synthesis of atomically thin GeSe by direct sonication-assisted liquid phase exfoliation (LPE) of bulk microcrystalline powders in organic solvents. The thickness of the GeSe sheets is dependent on the exfoliation conditions, and highly crystalline few-layer GeSe sheets of 4−10 layer stacks with lateral sizes over 200 nm were obtained. In ambient atmosphere, the LPE sheets deposited on the substrate demonstrate strong resistance against degradation, while decomposition into elemental Ge and Se nanostructures occurs at a moderate rate for ethanol dispersions. Density functional theory calculation together with optical characterizations confirm the blue-shifted bandgap for the GeSe sheets as a result of strong quantum confinement effect. In addition, we show that the few-layer GeSe sheets with favorable optical bandgap allow for efficient solar light harvesting for photocurrent generation based on a photoelectrochemical cell. Our joint theoretical and experimental results suggest that GeSe sheets of atomic thickness could be a new two-dimensional semiconductor that can be exploited for potential applications in optoelectronics and photonics.

Pulsed lasers operating in the mid-infrared (3-25 µm) are increasingly becoming the light source of choice for a wide range of industrial and scientific applications such as spectroscopy, biomedical research, sensing, imaging, and communication. Up to now, one of the factors limiting the mid-infrared pulsed lasers is the lack of optical switch with a capability of pulse generation, especially for those with wideband response. Here, a semiconductor material of bismuth oxyselenide (Bi O Se) with a facile processibility, constituting an ultrabroadband saturable absorber for the mid-infrared (actually from the near-infrared to mid-infrared: 0.8-5.0 µm) is exhibited. Significantly, it is found that the optical response is associated with a strong nonlinear character, showing picosecond response time and response amplitude up to ≈330.1% at 5.0 µm. Combined with facile processibility and low cost, these solution-processed Bi O Se materials may offer a scalable and printable mid-infrared optical switch to open up the long-sought parameter space which is crucial for the exploitation of compact and high-performance mid-infrared pulsed laser sources.

Field effect relies on the nonlinear current-voltage relation in semiconductors; analogously, materials that respond nonlinearly to an optical field can be utilized for optical modulation. For instance, nonlinear optical (NLO) materials bearing a saturable absorption (SA) feature an on-off switching behavior at the critical pumping power, thus enabling ultrafast laser pulse generation with high peak power. SA has been observed in diverse materials preferably in its nanoscale form, including both gaped semiconductor nanostructures and gapless materials like graphene; while the presence of optical bandgap and small carrier density have limited the active spectral range and intensity. We show here that solution-processed plasmonic semiconductor nanocrystals exhibit superbroadband (over 400 THz) SA, meanwhile with large modulation depth (∼7 dB) and ultrafast recovery (∼315 fs). Optical modulators fabricated using these plasmonic nanocrystals enable mode-locking and Q-switching operation across the near-infrared and mid-infrared spectral region, as exemplified here by the pulsed lasers realized at 1.0, 1.5, and 2.8 μm bands with minimal pulse duration down to a few hundreds of femtoseconds. The facile accessibility and superbroadband optical nonlinearity offered by these nonconventional plasmonic nanocrystals may stimulate a growing interest in the exploiting of relevant NLO and photonic applications.