RESUMEN
Hollow silica particles are desirable for numerous applications, however, designing hollow silica materials with varying hollow structures and shapes remains a significant challenge. Herein, a strategy for the precisely controlled synthesis of hexagonal-shaped hollow silica plate (HHSP) particles was successfully prepared via a sol-gel method at room temperature, using tetraethyl orthosilicate (TEOS) as a silica precursor and zinc oxide (ZnO) particles as a colloidal template. The effect of reaction time was carried out to control the structure and morphology of HHSP particles, and the thickness of silica shell can be tuned in the range from 12.2 to 43.2 nm by adjusting the TEOS/ZnO molar ratios. In addition, the polymer/HHSP composite thin films were prepared using poly(methyl methacrylate) (PMMA) matrix and surface modified HHSP particles by grafting silane coupling agents. High transmittance values were observed (>95%) for the composite thin films (5 µm in thickness, 0.1-1.0 wt% HHSP) in the ultraviolet and visible regions. Furthermore, the refractive index of HHSP particles was observed to be 1.28, which is significantly lower than dense silica (n = 1.46). These results suggest that the approach adopted herein will open up opportunities for the development of a new generation of film materials with a low refractive index.
RESUMEN
Creating hollow structures is one strategy for tuning the optical properties of materials. The current study aimed to increase the optical transmittance of silica (SiO2) particles. To this end, hexagonal-shaped hollow silica plate (HHSP) particles were synthesized from tetraethyl orthosilicate (TEOS) and zinc oxide (ZnO) template particles, using a microwave-assisted hydrothermal method. The size and shell thickness of the HHSP particles could be adjusted by using different TEOS/ZnO molar ratios and different ZnO template sizes, respectively. The optical transmittance of the HHSP particles depended on the shell thickness and particle size. The highest transmittance was 99% in the ultraviolet and visible region (300-800 nm) and was exhibited by HHSP particles with the thinnest shell thickness of 6.3 nm. This transmittance was higher than that exhibited by spherical hollow silica particles with a similar shell thickness. This suggested morphology-dependent transmittance for the semiconducting material. These preliminary results illustrate the promising features of the HHSP particles and suggest their potential application in future transparent devices.
RESUMEN
Monodisperse, nitrogen-doped hollow carbon spheres of submicron size were synthesized using hexamethoxymethylmelamine as both a carbon and nitrogen source in a short (1 h) microwave-assisted synthesis. After carbonization at 550 °C, porous carbon spheres with a remarkably high nitrogen content of 37.1% were obtained, which consisting mainly of highly basic pyridinic moieties. The synthesized hollow spheres exhibited high selectivity for carbon dioxide (CO2) over nitrogen and oxygen gases, with a capture capacity up to 1.56 mmol CO2 g-1. The low adsorption enthalpy of the synthesized hollow carbon spheres permits good adsorbent regeneration. Evaluation of the feasibility of scaling up shows their potential for large-scale applications.
RESUMEN
A C/SiO2 composite was produced from 3-aminophenol and tetraethyl orthosilicate (TEOS) by a synthesis protocol that involved microwave irradiation. This protocol featured simultaneous 3-aminophenol polymerization and TEOS hydrolysis and condensation, which were achieved rapidly in a microwave reactor. The SiO2 component was formed from low-concentration TEOS confined in cetyltrimethylammonium bromide micelles. We demonstrated a control of the SiO2 particle size, ranging from 20 to 90 nm, by varying the 3-aminophenol concentration. The carbon component provided a microporous structure that greatly contributed to the high specific surface area, 375 m2/g, and served as a host for the nitrogen functional groups with a content of 5.34%, 74% of which were pyridinic type. The composite formation mechanism was clarified from time-series scanning electron microscopy images and dynamic light scattering analysis. An understanding of the composite formation mechanism in this protocol will enable the design of composite morphologies for specific applications.