Amphiphilic polymers with hydrophilic poly(N-isopropylacylamide) (PNIPAM) shell connecting hydrophobic tetraphenylthiophene (TP) core, which has the novel aggregation-induced emission (AIE) property, by ionic bonds were prepared to explore the AIE-operative emission responses toward critical micelle concentration (CMC) and lower critical solution temperature (LCST). To exercise the idea, ammonium-functionalized TP2NH(3)(+) and sulfonate-terminated PNIPAM were separately prepared and mixed in different molar ratios to yield three amphiphilic TP-PNIPAMn complexes for the evaluations of CMC and LCST by fluorescence responses. The nonemissive dilute aqueous solutions of TP-PNIPAMn became fluorescent when increasing concentrations above CMC. Heating micelles solution to temperatures above LCSTs causes further enhancement on the emission intensity. The fluorescence responses are explained by the extent of aggregation in the micelles and in the globules formed at room temperature and at high temperatures, respectively.
This paper describes a simple, reproducible, and scalable procedure for the preparation of a SiO 2 -containing supercapacitor with high cycle stability. A carbon mesoporous material (CMM) with a high specific surface area, CMK-3, was adopted as an electric double-layer capacitor (EDLC) active material for the preparation of electrodes for the supercapacitor. The optimized SiO 2 content decreased as the microsphere diameter decreased, and the optimal specific capacitance was obtained with 6 wt % SiO 2 microspheres (100 nm size). The capacitance improved from 133 to 298 F/g. The corresponding capacitance retention rate after 1000 cycles increased from 68.04 to 91.53%. In addition, the energy density increased from 21.05 to 26.25 Wh/kg with a current density of 1 A/g. Finally, similar results based on active carbon, CeO 2 /CMK-3, and graphene/CNT/ MnO v composite electrodes demonstrated that the proposed method exhibits wide compatibility with diverse electrode materials.
In an attempt to improve the photocatalytic activity of anatase TiO2, we developed a composite photocatalyst composed of hollow TiO2 microspheres (hTS) and graphene. The hTS were prepared through a two-step hydrothermal process, where SiO2 microspheres with desirable diameters of 100–400 nm were used as sacrificial templates. Accordingly, the effect of the hTS cavity size on the activity of the catalyst in wet CO2 photoreduction (CO2PR) was studied. Furthermore, it was established that the hydrothermal pH value crucially influences the photocatalytic activity of the hTS photocatalyst, as well as its composition and microstructure. The hTS photocatalyst was also combined with graphene (0–90 wt%) to improve its photocatalytic activity. This study provides insight into the optimal microsphere diameter, hydrothermal pH value, and graphene/hTSx ratio required for designing hollow microsphere-based photocatalysts with enhanced CO2PR performances.
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