The decoration of porous membranes with a dense layer of nanoparticles imparts useful functionality and can enhance membrane separation and anti-fouling properties. However, manufacturing of nanoparticle-coated membranes requires multiple steps and tedious processing. Here, we introduce a facile single-step method in which bicontinuous interfacially jammed emulsions are used to form nanoparticle-functionalized hollow fiber membranes. The resulting nanocomposite membranes prepared via solvent transfer-induced phase separation and photopolymerization have exceptionally high nanoparticle loadings (up to 50 wt% silica nanoparticles) and feature densely packed nanoparticles uniformly distributed over the entire membrane surfaces. These structurally well-defined, asymmetric membranes facilitate control over membrane flux and selectivity, enable the formation of stimuli responsive hydrogel nanocomposite membranes, and can be easily modified to introduce antifouling features. This approach forms a foundation for the formation of advanced nanocomposite membranes comprising diverse building blocks with potential applications in water treatment, industrial separations and as catalytic membrane reactors.
A facile and effective method to prepare hierarchical pine tree‐like TiO2 nanotube (PTT) arrays with an anatase phase directly grown on a transparent conducting oxide substrate via a one‐step hydrothermal reaction. The PTT arrays consist of a vertically oriented long nanotube (NT) stem and a large number of short nanorod (NR) branches. Various PTT morphologies are obtained by adjusting the water/diethylene glycol ratio. The diameter of the NTs and the size of the NR branches decreases from 300 to100 nm and from 430 to 230 nm, respectively, with increasing water content. The length of the PTT arrays could be increased up to 19 μm to significantly improve the charge transport and specific surface area. The solid‐state dye‐sensitized solar cells (ssDSSC) assembled with the 19 μm long PTT arrays exhibit an outstanding energy‐conversion efficiency of 8.0% at 100 mW/cm2, which is two‐fold higher than that of commercially available paste (4.0%) and one of the highest values obtained for N719 dye‐based ssDSSCs. The high performance is attributed to the larger surface area, improved electron transport, and reduced electrolyte/electrode interfacial resistance, resulting from the one‐dimensional, well‐aligned structure with a high porosity and large pores.
Mesoporous MgTiO3 perovskite with a high porosity and interfacial properties were synthesized via a solvothermal reaction at 150 °C for 10 h using a graft copolymer, i.e., poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) with a well-ordered micellar morphology as a structure-directing agent. A PVC-g-POEM graft copolymer with a wormlike morphology was utilized as a soft matrix to prepare a mixed matrix membrane (MMM) with mesoporous MgTiO3 perovskite through a solution-casting method. The structure and morphology of PVC-g-POEM graft copolymer was carefully tuned by controlling polymer-solvent interactions, as characterized by transmission electron microscopy (TEM). The average pore diameter of the MgTiO3 perovskite was 10.4 nm, which is effective in facilitating gas transport via Knudsen diffusion through mesopores as well as improving interfacial contact with the organic polymer matrix. Because of a high porosity (0.56), the density of mesoporous MgTiO3 (1.75 g/cm(3)) was much lower than that of dense nonporous MgTiO3 (4 g/cm(3)) and not significantly higher than that of PVC-g-POEM (1.25 g/cm(3)), leading to a uniform distribution of MgTiO3 in MMM. The permeability of MMM with MgTiO3 was greater than those of MMM with only MgO or TiO2, indicating the simultaneous improvement of solubility and diffusivity in the former, as supported by CO2 temperature-programmed desorption (TPD) measurements. The MMM with MgTiO3 25 wt % exhibited a CO2 permeability improvement of 140% up to 138.7 Barrer (1 Barrer = 1 × 10(-10) cm(3)(STP) cm cm(-2) s(-1) cmHg(-1)) without a large loss of CO2/N2 selectivity.
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