Academic Journal List

Hydrogen production via photocatalytic water splitting using sunlight has enormous potential in solving the worldwide energy and environmental crisis. The key challenge in this process is to develop efficient photocatalysts which must satisfy several criteria such as high chemical and photochemical stability, effective charge separation and strong sunlight absorption. The combination of different semiconductors to create composite materials offers a promising way to achieve efficient photocatalysts because doing so can improve the charge separation, light absorption and stability of the photocatalysts. In this review article, we summarized the most recent studies on semiconductor composites for hydrogen production under visible light irradiation. After a general introduction about the photocatalysis phenomenon, typical heterojunctions of widely studied heterogeneous semiconductors, including titanium dioxide, cadmium sulfide and graphitic carbon nitride are discussed in detail.

A novel dual-emission ratiometric fluorescence probe is designed and developed by linking two parts, positively charged aggregation-induced emission (AIE) organic fluorescence nanoparticles (OFNs) as the reference and negatively charged Au nanoclusters (Au NCs) as the response, by electrostatic attraction for the first time. This probe can be used for not only visual but quantitative determination of Hg2+ as well as melamine, because red fluorescence of Au NCs can be quenched by mercury ions and recovered by melamine, due to the strong affinity metallophilic Hg2+–Au interaction and stronger affinity Hg2+–N. During this process, the green fluorescence of AIE-OFNs remains constant owing to the protection of ε-polylysine (ε-Ply). In addition, the prepared dual-emission ratiometric fluorescence probe has good biocompatibility, indicating the potential of the probe in applications of biological imaging and detection. The results revealed that this dual-emission ratiometric fluorescence probe broadens the application of AIE-based organic fluorescent nanoparticles, and presents a new method to prepare more sensitive, biocompatible, and visual ratiometric fluorescent probes.

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The formation of fullerene crystals represents a major degradation pathway of polymer/fullerene bulk-heterojunction thin films that inexorably deteriorates their photovoltaic performance. Currently no tools exist that reveal the origin of fullerene crystal formation vertically through the film. Here, we show that electron tomography can be used to study nucleation and growth of fullerene crystals. A model bulk-heterojunction blend based on a thiophene-quinoxaline copolymer and a fullerene derivative is examined after controlled annealing above the glass transition temperature. We image a number of fullerene nanocrystals, ranging in size from 70 to 400 nanometers, and observe that their center is located close to the free-surface of spin-coated films. The results show that the nucleation of fullerene crystals predominately occurs in the upper part of the films. Moreover, electron tomography reveals that the nucleation is preceded by more pronounced phase separation of the blend components.

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Nanoscale topographies and chemical patterns can be used as synthetic cell interfaces with a range of applications including the study and control of cellular processes. Herein, we describe the fabrication of high aspect ratio nanostructures using electron beam lithography in the epoxy-based polymer SU-8. We show how nanostructure geometry, position and fluorescence properties can be tuned, allowing flexible device design. Further, thiol–epoxide reactions were developed to give effective and specific modification of SU-8 surface chemistry. SU-8 nanostructures were made directly on glass cover slips, enabling the use of high resolution optical techniques such as live-cell confocal, total internal reflection and 3D structured illumination microscopy to investigate cell interactions with the nanostructures. Details of cell adherence and spreading, plasma membrane conformation and actin organization in response to high aspect ratio nanopillars and nanolines were investigated. The versatile structural and chemical properties combined with the high resolution cell imaging capabilities of this system are an important step towards the better understanding and control of cell interactions with nanomaterials.

Gold glyconanoparticles (GlycoNPs) are full of promise in areas like biomedicine, biotechnology and materials science due to their amazing physical, chemical and biological properties. Here, siRNA GlycoNPs (AuNP@PEG@Glucose@siRNA) in comparison with PEGylated GlycoNPs (AuNP@PEG@Glucose) were applied in vitro to a luciferase-CMT/167 adenocarcinoma cancer cell line and in vivo via intratracheal instillation directly into the lungs of B6 albino mice grafted with luciferase-CMT/167 adenocarcinoma cells. siRNA GlycoNPs but not PEGylated GlycoNPs induced the expression of pro-apoptotic proteins such as Fas/CD95 and caspases 3 and 9 in CMT/167 adenocarcinoma cells in a dose dependent manner, independent of the inflammatory response, evaluated by bronchoalveolar lavage cell counting. Moreover, in vivo pulmonary delivered siRNA GlycoNPs were capable of targeting c-Myc gene expression (a crucial regulator of cell proliferation and apoptosis) via in vivo RNAi in tumour tissue, leading to an ∼80% reduction in tumour size without associated inflammation.

In this work, anodically grown ZrO2 nanotubes (NTs) are examined for the first time for use in micro solid oxide fuel cell (μ-SOFC) applications. This is due to their high surface area to volume ratio and useful nanoscale morphological features (e.g., 5–100 nm thick NT bases that could serve as the electrolyte layer). To understand their full potential for these applications, the determination of their electrical properties is necessary. Therefore, ZrO2 NTs, in the form of a uniform and crack-free film, were obtained by the two-step anodization of Zr foil in aqueous solutions. The films exhibited excellent adhesion to the Zr substrate, which facilitated impedance spectroscopy analyses, used for the first time to obtain the resistivity of the nanotubular array separately from the contact resistances. This gave a conductivity of the ZrO2 NTs of 1.6 × 10−6 S cm−1 at 600 °C in N2, approximately twice that reported for dense ZrO2 films measured at the same temperature in air, and also a very reasonable activation energy of 0.90 eV in the 400–600 °C temperature range.