RESUMEN
Hydrophilic coating can prevent surface from fogging but its application is limited by low mechanical performance. In this study, a hydrophilic coating was prepared by crosslinking the Si-doped carbonized polymer dot (Si-CPD) with 3-glycidyloxypropyltrimethoxysilane (GPTMS) and ethylene oxide (EO). The hydrophilic coating can be used as robust hydrophilic anti-fogging coating. The Si-CPD derived from ethylene diamine tetraacetic acid (EDTA) and aminopropyl oligosiloxanes (APOS) was successfully prepared via one-step hydrothermal method. Then, a resin solution was prepared by mixing Si-CPD, GPTMS and EO. Epoxy group of GPTMS and EO can react with amino group of Si-CPD. Finally, a composite coating with antifogging function can be obtained by simple heating curing. Due to the introduction of hydroxyl which derived from EO, the coating shows excellent antifogging performance. Meanwhile, the presence of inorganic component endows the coating with outstanding mechanical performance. The coating has great potential in related applications, such as optical lenses, mirrors and other transparency substrates.
RESUMEN
Perovskite nanocrystals (PNCs)/polymer nanocomposites can combine the advantages of each other, but extremely few works can achieve the fabrication of PNCs/polymer nanocomposites by bulk polymerization. We originally adopt a two-type ligand strategy to fabricate bulk PNCs/polystyrene (PS) nanocomposites, including a new type of synthetic polymerizable ligand. The CsPbCl3 PNCs/PS nanocomposites show extremely high transparency even the doping content up to 5 wt%. The high transparency can be ascribed to the Rayleigh scattering as the PNCs distribute uniformly without obvious aggregation. Based on this behavior, we first exploit the potential of PNCs to serve as scatters inside light guided plate (LGP), whose surface illuminance and uniformity can be improved, and this new kind of LGP is compatible with the advanced liquid crystal display technology. Thanks to the facile composition adjustment of CsPbClxBr3-x (1 ≤ x ≤ 3) PNCs, the Rayleigh scattering behavior can also be adjusted so as to the performance of LGP. The best-performing 5.0-inch LGP based on CsPbCl2.5Br0.5 PNCs/PS nanocomposites shows 20.5 times higher illuminance and 1.8 times higher uniformity in display than the control. The LGP based on PNCs/PS nanocomposite exhibits an enormous potential in commercialization no matter based on itself or combined with the LGP-related technology.
RESUMEN
Flexible transparent hydrophobic coating films with excellent scratch resistance have important applications in many fields, especially for optical materials. Herein, a hydrophobic composite coating film was prepared and used as a polymer film protective material by combining 3-glycidyloxypropyltrimethoxysilane (GPTMS)-modified Si-doped carbonized polymer dots (Si-CPDs) with mono-trimethoxysilyl-terminated poly(dimethyl siloxane) (PDMS). The Si-CPDs derived from tetramethyl disiloxane propylamine tetraacetic acid and multi-amino oligosiloxanes were successfully prepared via one-step hydrothermal method and then grafted by GPTMS to obtain modified Si-CPDs (mSi-CPDs). Among them, mSi-CPDs act as a matrix layer, and PDMS acts as a low-surface energy layer. Cross-linking the Si-O-Si network of the coating film was formed through sol-gel chemistry. Driven by the hydrophilic-hydrophobic effect, PDMS trends to aggregate at the film surface, thus avoiding the phase separation which can affect transparency. The highly cross-linked network and the presence of hard silica core provide a high hardness to stand the steel-wool scratch. Flexible polymer chains impart the coating film an outstanding bendability. Introduction of PDMS makes the coating film possess hydrophobicity and anti-graffiti function.
RESUMEN
Seeking clean energy as an alternative to traditional fossil fuels is the inevitable choice to realize the sustainable development of the society. Photocatalytic technique is considered a promising energy conversion approach to store the abundant solar energy into other wieldy energy carriers like chemical energy. Carbon dots, as a class of fascinating carbon nanomaterials, have already become the hotspots in numerous photoelectric researching fields and particularly drawn keen interests as metal-free photocatalysts owing to strong UV-vis optical absorption, tunable energy-level configuration, superior charge transfer ability, excellent physicochemical stability, facile fabrication, low toxicity, and high solubility. In this review, the classification, microstructures, general synthetic methods, optical and photoelectrical properties of carbon dots are systematically summarized. In addition, recent advances of carbon dots based photoinduced reactions including photodegradation, photocatalytic hydrogen generation, CO2 conversion, N2 fixation, and photochemical synthesis are highlighted in detail, deep insights into the roles of carbon dots in various systems combining with the photocatalytic mechanisms are provided. Finally, several critical issues remaining in photocatalysis field are also proposed.
RESUMEN
The rapid development of optical and electronic devices has driven up the demand of high performance optical protective films to avoid exterior influence and extend the service life. But it is not easy to obtain an ideal coating film with high transmittance, high hardness, and good flexibility. Herein, by taking advantage of the special core-shell structure of carbonized polymer dots (CPDs), we propose a strategy to build up a nanoscale soft-hard segment microstructure for optical protective coating materials. The CPDs with hard core and soft polymer chain shell are prepared from citric acid and (3-aminopropyl)triethoxysilane. The as-prepared CPDs can be converted directly to the coating film by the dehydration and cross-linking. In addition to the good optical transmittance, the final film exhibits simultaneously ultrahigh 9H pencil hardness to stand 4000 cycles of a steel-wool wear test, and excellent flexibility to stand bending and rolling-up.
RESUMEN
Crystallographic orientation control is an effective method to improve the photoelectrochemical water splitting efficiency of BiVO4 photoanodes. Herein, textured and transparent Mo-BiVO4 photoanodes are fabricated by spin-coating Mo-doped BiVO4 nanoparticles on FTO. The photoelectrodes exhibit a current density of 4.15 mA cm-2 and 2.50 mA cm-2 for sulfite and water oxidation, respectively. By connecting the photoelectrode with a CsPbBrI2 perovskite solar cell, a stand-alone tandem water splitting device with a current density of 2.13 mA cm-2 and an STH of 2.43% can be achieved.
RESUMEN
The anilide anion (m/z 92) generated directly from aniline, or indirectly as a fragmentation product of deprotonated acetanilide, captures CO2 readily to form the carbamate anion (m/z 136) in the collision cell, when CO2 is used as the collision gas in a tandem-quadrupole mass spectrometer. The gas-phase affinity of the anilide ion to CO2 is significantly higher than that of the phenoxide anion (m/z 93), which adds to CO2 only very sluggishly. Our results suggest that the efficacy of CO2 capture depends on the natural charge density on the nitrogen atom, and relative nucleophilicity of the anilide anion. Generally, conjugate bases generated from aniline derivatives with proton affinities (PA) less than 350 kcal/mol do not tend to add CO2 to form gaseous carbamate ions. For example, the anion generated from p-methoxyaniline (PA = 367 kcal/mol) reacts significantly faster than that obtained from p-nitroaniline (PA = 343 kcal/mol). Although deprotonated p-aminobenzoic acid adds very poorly because the negative charge is now located primarily on the carboxylate group, it reacts more efficiently with CO2 if the carboxyl group is esterified. Moreover, mixture of CO2 and He as the collision gas was found to afford more efficient adduct formation than CO2 alone, or as mixtures made with nitrogen or argon, because helium acts as an effective "cooling" gas and reduces the internal energy of reactant ions.
RESUMEN
On contrary to the widely accepted conviction that the m/z 93 ion derived from phenol does not react with CO2, we demonstrate that it makes an adduct with CO2 to a small but demonstrable extent. For example, the product-ion mass spectrum recorded for the m/z 98 ion derived from [(2)H6]phenol showed a small peak at m/z 142 when CO2 was used as the collision gas. The formation of an m/z 137 adduct ion from the m/z 93 ion (generated either directly from phenol, or indirectly from salicylic acid by in-source decarboxylation) was demonstrated also by multiple-reaction-monitoring tandem mass spectrometric experiments. According to literature, the m/z 93 ion derived from salicylic acid does not undergo CO2 addition because it is deemed to exist only in the phenoxide form. This reaction has been previously proposed as a method for differentiating phenoxide ion from its isomeric hydroxyphenide ions. We propose that the m/z 93 ion, albeit small, exists also as the phenide form together with the predominant phenoxide ion.
RESUMEN
We investigated the role of the pygidial gland on foraging behavior in two ecologically dominant column foraging Nearctic harvesting ants (Messor pergandei and Messor andrei). Using chemical analyses and behavioral tests, we show that n-tridecane is the major biologically active compound of pygidial gland secretions in both species, and that this chemical functions as a powerful alarm-recruitment pheromone. Another major compound of pygidial gland contents is benzaldehyde; this substance does not release behavioral reactions in M. pergandei workers but might function as a defensive secretion. Six solitary foraging Nearctic Messor and two column foraging Palearctic Messor species, did not have large pygidial gland reservoirs.
