Photoluminescent graphene quantum dots (GQDs) have fascinating optical and electronic properties with numerous promising applications in biomedical engineering. In this work, we first studied the in vivo biodistribution and the potential toxicity of carboxylated photoluminescent GQDs. KB, MDA-MB231, A549 cancer cells, and MDCK normal cell line were chosen as in vitro cell culture models to examine the possible adverse effects of the carboxylated photoluminescent GQDs. The carboxylated GQDs are desirable for increased aqueous solubility. All cancer cells efficiently took up the carboxylated GQDs. No acute toxicity or morphological changes were noted in either system at the tested exposure levels. A long-term in vivo study revealed that the GQDs mainly accumulated in liver, spleen, lung, kidney, and tumor sites after intravenous injection. To reveal any potential toxic effect of the GQDs on treated mice, serum biochemical analysis and histological evaluation were performed. The toxicity results from serum biochemistry and complete blood count study revealed that the GQDs do not cause appreciable toxicity to the treated animals. Finally, we observed no obvious organ damage or lesions for the GQDs treated mice after 21 days of administration at 5 mg/kg or 10 mg/kg dosages. With adequate studies of toxicity, both in vitro and in vivo, photoluminescent GQDs may be considered for biological application.

Elastomeric smart windows with switchable optical transparency and wetting properties (see Fig.) are fabricated through the combination of replica molding and surface wrinkling. The resulting smart windows, with a surface topography that is tunable via mechanical strain, exhibit not only significant changes in optical transmittance and wetting properties, but also the additional functions of self‐cleaning and antireflection.

Our results indicate that polydopamine provides a versatile platform that can reduce the in vivo toxicity of biomaterials that contact tissue or blood.

We report the fabrication of a roselike nanostructured vanadium oxide (V2O5) film with photoinduced surface wettability switching by carrying out the drop-casting of a suspension of V2O5 particles synthesized with the sol−gel method. Although a pure V2O5 film is slightly hydrophilic, the addition of alkylamine renders the nanostructured V2O5 film superhydrophobic owing to the intercalation of alkyl chains between the V2O5 layers. UV exposure switches the wettability of the V2O5 surface to superhydrophilic with a water contact angle of almost 0°, and storage in the dark reconverts the irradiated surface back to its initial superhydrophobic state. This extraordinary wetting transition is ascribed to the cooperation between the photosensitivity of V2O5 and the surface roughness of its nanostructure, which has submicron- to micron-scale apertures. Our approach provides not only the possibility of producing large homogeneous or patterned surfaces with tunable wettability, but also potential uses in catalysts, electrodes, switchable smart devices, etc., in various fields for future industrial applications.

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Rapid growth of nanotechnology is one of the most quickly emerging tendencies in cancer therapy. Gold nanoparticles roused a distinctive interest in the field, due to their incomparable light-to-thermal energy conversion efficiency, and their ability to load and deliver a variety of anticancer drugs. Therefore, simultaneous photothermal (PTT) and photodynamic (PDT) cancer therapy is available by the role of the thermal agent of the gold nanoparticle itself and the drug delivery carrier for photosensitizer (PS) transport. In this review, the physical, chemical, and biological properties of gold nanoparticle, which can promote PTT and PDT efficiency, are briefly demonstrated, and we highlight recent progression in the development of PS-containing gold nanocomposites for effective cancer therapy.

A structured polymer solar cell architecture featuring a large interface between donor and acceptor with connecting paths to the respective electrodes is explored. To this end, poly‐(3‐hexylthiophene) (P3HT) nanorods oriented perpendicularly to indium tin oxide (ITO) glass are fabricated using an anodic aluminum oxide template. It is found that the P3HT chains in bulk films or nanorods are oriented differently; perpendicular or parallel to the ITO substrate, respectively. Such chain alignment of the P3HT nanorods enhanced the electrical conductivity up to tenfold compared with planar P3HT films. Furthermore, the donor/acceptor contact area could be maximised using P3HT nanorods as donor and C60 as acceptor. In a photovoltaic device employing this structure, remarkable photoluminescence quenching (88%) and a seven‐fold efficiency increase (relative to a device with a planar bilayer) are achieved.

Rice leaves can directionally shed water droplets along the longitudinal direction of the leaf. Inspired by the hierarchical structures of rice leaf surfaces, synthetic rice leaf‐like wavy surfaces are fabricated that display a tunable anisotropic wettability by using electrostatic layer‐by‐layer assembly on anisotropic microwrinkled substrates. The nanoscale roughness of the rice leaf‐like surfaces is controlled to yield tunable anisotropic wettability and hydrophobic properties that transitioned between the anisotropic/pinned, anisotropic/rollable, and isotropic/rollable water droplet behavior states. These remarkable changes result from discontinuities in the three‐phase (solid–liquid–gas) contact line due to the presence of air trapped beneath the liquid, which is controlled by the surface roughness of the hierarchical nanostructures. The mechanism underlying the directional water‐rolling properties of the rice leaf‐like surfaces provides insight into the development of a range of innovative applications that require control over directional flow.