RESUMEN
Thermoresponsive smart windows (TRSWs) take great advantages in energy-efficient buildings and on-demand devices owing to their self-adaptiveness and external energy consumption-free nature. Currently used TRSWs largely rely on thermal-induced phase transitions in single-material systems, however, the intrinsic characteristics of which may not be suited for practical window utilization, such as poor luminous transparency and fixed critical temperature (Tc ). Herein, an adaptive TRSW based on dynamic refractive index (RI) matching between two phases is demonstrated, which is facilely fabricated by embedding ethylene glycol solution microdroplets into polydimethylsiloxane (PDMS) via a one-step emulsification approach, realizing a smart temperature response in PDMS. The TRSW presents high transparency (≈92%) and bidirectional transparency-temperature response (≈20% at 73 °C, ≈40% at 8 °C). Moreover, the RI dispersion generates a unique effect of wavelength selectivity with temperature. Notably, the effective optical-temperature response with variable Tc could be tuned over a wide range of 13-68 °C by adjusting the EGS concentration. The proposed strategy with dynamic RI matching allows TRSW construction to extend beyond phase transitional materials and greatly broadens the applicable scope of TRSWs, which is promising in the fields of smart optical devices such as smart windows, anti-counterfeiting, optical switches, and optical selection.
RESUMEN
In nature, many organisms (e.g., chameleons) protect themselves by changing their colors in response to environmental changes. Inspired by these organisms, we present a multi-responsive, flexible, and structurally colored hydrogel film with a one-dimensional (1D) ordered periodic groove structure. The groove structure endows the film with bright, highly angle-dependent structural colors, which can be reversibly tuned by stretching and releasing. In addition, because of the thermosensitive properties of the hydrogel, the film can be switched between colored state and opaque white state with temperature. In addition, the optical state of the film is sensitive to solvent and can be reversibly changed between colored state and transparent state with soaking and evaporation of the solvent. This reversible, multi-responsive, flexible, and structurally colored hydrogel film has great potential to be used in the fields of color display, sensors, anti-counterfeiting, and so on because of its flexible and diverse tuning methods, excellent optical performance, and convenient preparation process.
RESUMEN
Smart optical materials are drawing more and more attention because of their wide application in energy conservation, wearable sensors, optical tuning, and medical devices. However, current smart optical materials, including electroresponsive, thermoresponsive, and mechanoresponsive materials, are greatly restricted in practical applications because of their long response time, complicated preparation, and high cost. This study develops a novel, magnetically tunable, smart optical material with swift and high-contrast optical switching based on one-dimensional (1D) Fe3O4@SiO2 nanochains (NCs), which have the large shape anisotropy of the 1D structure and the superparamagnetic properties of Fe3O4 particles. The material exhibited a clear transparent state when NCs were arranged parallel to the viewing direction under an applied magnetic field, whereas it showed good shielding effect when the NCs were randomly oriented upon removal of the field. The light transmittance could be dynamically adjusted over the wide range of 20-80% through a small applied magnetic field of 50-100 Oe, which is superior to most of the currently reported systems. This swift, sensitive, and reversible response is attributed to the good responsivity of magnetic NCs. Also, an effective model was proposed to explain the transmittance modulation scheme and forecast its optical potential. The large tunable range and the low triggered field make Fe3O4@SiO2 NCs an advantageous candidate for application in smart windows, optical switchers, and other fields.
RESUMEN
Fe3O4-Ag Janus composites were synthesized using a two-step solvothermal method. The optimal growth process was determined by investigating the relationship between the particle morphologies and reaction time. Magnetic and Raman spectroscopic measurements showed that the as-synthesized Janus composites have both good magnetic response and significant surface-enhanced Raman scattering (SERS) effects, as well as reproducibility. The calculated Raman enhancement factor reached an unprecedented magnitude of 109 compared with the values of other Fe3O4-Ag compounds. Furthermore, the SERS effect was exhibited even at a concentration of probe molecules as low as 10-13 M. This demonstrates that the as-synthesized Fe3O4-Ag Janus composite particles have promise for application as separable, highly sensitive SERS substrates.
RESUMEN
This paper describes a new synthesis and lithium ion charge-discharge property of tin dioxide (SnO(2)) hollow nanocubes. SnO(2) is one of the best-known anode materials for lithium-ion battery application because of its high lithiation-delithiation capacity. Hollow nanostructures with high surface area are preferred, because they accommodate large volume changes and maintain the structural stability of electrode materials during charge-discharge cycles. The SnO(2) hollow cubes made in this study had a discharge capacity of up to 1783 mA h g(-1) for the initial cycle and 546 mA h g(-1) after 30 cycles at a current density of 0.2 C between 0.02 and 2.0 V (vs Li/Li(+)).