2 research outputs found

    Efficient Visible-Light-Driven Photocatalytic Degradation with Bi<sub>2</sub>O<sub>3</sub> Coupling Silica Doped TiO<sub>2</sub>

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    A new TiO<sub>2</sub>-based visible light photocatalyst (Bi<sub>2</sub>O<sub>3</sub>/Si–TiO<sub>2</sub>) was synthesized by both Bi<sub>2</sub>O<sub>3</sub> coupling and Si doping via a two-step method. The structural, morphological, light absorption, and photocatalytic properties of as-prepared samples were studied using various spectroscopic and analytical techniques. The results showed that Bi<sub>2</sub>O<sub>3</sub>/Si–TiO<sub>2</sub> catalysts held an anatase phase and possessed high thermal stability. The doped Si was woven into the lattice of TiO<sub>2</sub>, and its content had a significant effect on the surface area and the crystal size of Bi<sub>2</sub>O<sub>3</sub>/Si–TiO<sub>2</sub>. The introduced Bi species mainly existed as oxides on the surface of TiO<sub>2</sub> particles, and the Bi<sub>2</sub>O<sub>3</sub> photosensitization extended the light absorption into the visible region. Bi<sub>2</sub>O<sub>3</sub> coupling also favored the separation and transfer of photoinduced charge carriers to inhibit their recombination and Si doping enlarged the surface area of photocatalysts. Compared to bare TiO<sub>2</sub>, Bi<sub>2</sub>O<sub>3</sub>/TiO<sub>2</sub>, and Si–TiO<sub>2</sub>, Bi<sub>2</sub>O<sub>3</sub>/Si–TiO<sub>2</sub> samples showed better activities for the degradation of methyl orange (MO) and bisphenol A (BPA) under visible light irradiation (λ > 420 nm). The highest activity was observed for 1.0% Bi<sub>2</sub>O<sub>3</sub>/15% Si–TiO<sub>2</sub> calcined at 500 °C. The superior performance was ascribed to the high surface area, the ability to absorb visible light, and the efficient charge separation associated with the synergetic effects of appropriate amounts of Si and Bi in the prepared samples. The adsorbed hydroxyl radicals (<sup>•</sup>OH) were also found to be the most reactive species in the photocatalytic degradation

    Scalable Fabrication and Integration of Graphene Microsupercapacitors through Full Inkjet Printing

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    A simple full-inkjet-printing technique is developed for the scalable fabrication of graphene-based microsupercapacitors (MSCs) on various substrates. High-performance graphene inks are formulated by integrating the electrochemically exfoliated graphene with a solvent exchange technique to reliably print graphene interdigitated electrodes with tunable geometry and thickness. Along with the printed polyelectrolyte, poly­(4-styrenesulfonic acid), the fully printed graphene-based MSCs attain the highest areal capacitance of ∼0.7 mF/cm<sup>2</sup>, substantially advancing the state-of-art of all-solid-state MSCs with printed graphene electrodes. The full printing solution enables scalable fabrication of MSCs and effective connection of them in parallel and/or in series at various scales. Remarkably, more than 100 devices have been connected to form large-scale MSC arrays as power banks on both silicon wafers and Kapton. Without any extra protection or encapsulation, the MSC arrays can be reliably charged up to 12 V and retain the performance even 8 months after fabrication
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