Bionic Structural Coloration of Textiles Using the Synthetically Prepared Liquid Photonic Crystals.

The structural coloration of textiles with bionic photonic crystals (PCs) is expected to become a critical approach to the ecological coloration of textiles. Rapid and large-area preparation of PC structurally colored textiles can be achieved via self-assembly of high mass fractions of liquid photonic crystals (LPCs). However, the rapid and large-scale manufacturing of LPCs remains a challenge. In this work, the pH regulator is added in the process of emulsion polymerization to solve the problem of phase transformation caused by the thermal decomposition of the initiator to produce H+ , directly achieving 40 wt.% PS nanospheres in the dispersion. Then oligomers and small-molecule salts are removed from the system via dialysis, and the pre-crystallized LPC system is efficiently prepared. Adjusting the particle size and the mass fraction of nanospheres is shown to be an efficient way to control the optical properties of LPCs. The rapid and large-area preparation of PC structural color fabric and the patterned PC structural color fabric with an iridescent effect is implemented by using LPCs as the assembly intermediate. By constructing the encapsulation layer on the surface of the PC structural color fabric, the consistency of high structural stability and high color saturation of the PC is realized.

Patterned SiO2/Polyurethane Acrylate Inverse Opal Photonic Crystals with High Color Saturation and Tough Mechanical Strength.

Patterned structural color photonic crystals (PCs) based on periodic photonic nanostructures have attracted great interest in developing high-performance sensors and other smart optical materials as well as tunable structurally colored fashion textiles. However, previously reported patterned PCs with both high color saturation and tough mechanical strength were difficult to achieve, which restricts their practical applications. Herein, arbitrarily patterned silica/polyurethane acrylate (SiO2/PUA) inverse opal photonic crystals (IOPCs) with high color saturation and tough mechanical strength were innovatively designed and fabricated by writing with photopolymerizable PUA "ink" on a self-assembled hollow SiO2 PC template. The high color saturation of the prepared SiO2/PUA IOPCs originated from the high refractive index contrast between the encapsulated air-filled core and the SiO2/PUA composite skeleton. The cross-linked flexible PUA matrix tightly warped the self-assembled hollow SiO2 nanospheres together, endowing the obtained SiO2/PUA IOPCs a structural color pattern with tough mechanical strength. The structural colors of SiO2/PUA IOPCs could be finely tuned by regulating their basic parameters, and a redshift in the resultant structural color was observed due to an increase in the lattice constant when increasing the core size and/or shell thickness of the hollow SiO2 nanospheres.

La2O2CO3 Encapsulated La2O3 Nanoparticles Supported on Carbon as Superior Electrocatalysts for Oxygen Reduction Reaction.

Constructing nanoscale hybrid materials with unique interfacial structures by using various metal oxides and carbon supports as building blocks are of great importance to develop highly active, economical hybrid catalysts for oxygen reduction reaction (ORR). In this work, La2O2CO3 encapsulated La2O3 nanoparticles on a carbon black (La2O2CO3@La2O3/C) were fabricated via chemical precipitation in an aqueous solution containing different concentrations of cetyltrimethyl ammonium bromide (CTAB), followed by calcination at 750 °C. At a given CTAB concentration 24.8 mmol/L, the obtained lanthanum compound nanoparticles reach the smallest particle size (7.1 nm) and are well-dispersed on the carbon surface. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) results demonstrate the formation of La2O2CO3 located on the surface of La2O3 nanoparticles in the hybrid. The synthesized La2O2CO3@La2O3/C hybrid exhibits a significantly enhanced electrocatalytic activity in electrocatalysis experiments relative to pure La2O3, La2O2CO3, and carbon in an alkaline environment, by using the R(R)DE technique. Moreover, its long-term stability also outperforms that obtained by commercial Pt/C catalysts (E-TEK). The exact origin of the fast ORR kinetics is mainly ascribed to the La2O2CO3 layer sandwiched at the interface of carbon and La2O3, which contributes favorable surface-adsorbed hydroxide (-OH(-)(ad)) substitution and promotes active oxygen adsorption at the interfaces. The unique covalent -C-O-C(═O)-O-La-O- bonds, formed at the interfaces between La2O2CO3 and carbon, can act as active sites for the improved ORR kinetics over this hybrid catalyst. Therefore, the fabrication of lanthanum compound-based hybrid material with an unique interfacial structure maybe open a new way to develop carbon-supported metal oxides as next-generation of ORR catalysts.

[Reversible temperature dependence of surface-enhanced Raman scattering of adenine, purine and pyrene].

The surface-enhanced Raman scattering (SERS) spectra of adenine, purine and pyrene adsorbed on a SERS-active silver surface roughened by nitric acid have been measured over the -190 degrees C-30 degrees C surface temperature range. The results show that the Raman shifts and SERS intensity of the vibrations, which are enhanced by electromagnetic mechanism, are affected by temperature, those by chemical mechanism are not. However, it has been found that the observed temperature dependence can be explained by postulating the reorientation of the absorbates. Adenine molecules and purine molecules prefer to adopt a more perpendicular stance on the surface at high temperature, but for a planar symmetric molecule, such as pyrene, the preferred orientation is parallel and temperature has no effect on its orientation.