Emerging Applications of Boron Nitride Nanotubes in Energy Harvesting, Electronics, and Biomedicine.

Boron nitride nanotubes (BNNTs) are structurally and mechanically similar to carbon nanotubes (CNTs). In contrast, BNNTs exhibit unique properties for being electrically insulating and optically transparent due to the polarized boron nitride bonds. All these properties have prevented the use of BNNTs for energy harvesting and electronic devices for more than 25 years. During the past few years, researchers have started to demonstrate a series of novel applications of BNNTs based on unique properties not found on CNTs. For example, these novel applications include osmotic power harvesting using the charged inner surfaces of BNNTs, room-temperature single-electron transistors using insulating BNNTs as the tunneling channels, high-brightness fluorophores that can be 1000-times brighter than regular dyes, and transistors based on Tellurium atomic chains filled inside BNNTs. We have reviewed some of these emerging applications and provided our perspective for future work.

A novel approach to low-temperature synthesis of cubic HfO2 nanostructures and their cytotoxicity.

The development of a strategy to stabilise the cubic phase of HfO2 at lower temperatures is necessary for the emergence of unique properties that are not realised in the thermodynamically stable monoclinic phase. A very high temperature (>2600 °C) is required to produce the cubic phase of HfO2, whereas the monoclinic phase is stable at low temperature. Here, a novel rapid synthesis strategy was designed to develop highly crystalline, pure cubic-phase HfO2 nanoparticles (size <10 nm) using microwave irradiation. Furthermore, the as-prepared nanoparticles were converted to different morphologies (spherical nanoparticles and nanoplates) without compromising the cubic phase by employing a post-hydrothermal treatment in the presence of surface modifiers. The cytotoxicities and proliferative profiles of the synthesised cubic HfO2 nanostructures were investigated over the MCF-7 breast cancer cell line, along with caspase-3/7 activities. The low-temperature phase stabilisation was significantly attributed to surface imperfections (defects and deformations) induced in the crystal lattice by the desirable presence of Na2S·xH2O and NaOH. Our work provides unprecedented insight into the stabilisation of nanoscale cubic-phase HfO2 in ambient environments; the method could be extended to other challenging phases of nanomaterials.

High-performance and high-sensitivity applications of graphene transistors with self-assembled monolayers.

Charge impurities and polar molecules on the surface of dielectric substrates has long been a critical obstacle to using graphene for its niche applications that involve graphene's high mobility and high sensitivity nature. Self-assembled monolayers (SAMs) have been found to effectively reduce the impact of long-range scatterings induced by the external charges. Yet, demonstrations of scalable device applications using the SAMs technique remains missing due to the difficulties in the device fabrication arising from the strong surface tension of the modified dielectric environment. Here, we use patterned SAM arrays to build graphene electronic devices with transport channels confined on the modified areas. For high-mobility applications, both rigid and flexible radio-frequency graphene field-effect transistors (G-FETs) were demonstrated, with extrinsic cutoff frequency and maximum oscillation frequency enhanced by a factor of ~2 on SiO2/Si substrates. For high sensitivity applications, G-FETs were functionalized by monoclonal antibodies specific to cancer biomarker chondroitin sulfate proteoglycan 4, enabling its detection at a concentration of 0.01 fM, five orders of magnitude lower than that detectable by a conventional colorimetric assay. These devices can be very useful in the early diagnosis and monitoring of a malignant disease.

Switching Behaviors of Graphene-Boron Nitride Nanotube Heterojunctions.

High electron mobility of graphene has enabled their application in high-frequency analogue devices but their gapless nature has hindered their use in digital switches. In contrast, the structural analogous, h-BN sheets and BN nanotubes (BNNTs) are wide band gap insulators. Here we show that the growth of electrically insulating BNNTs on graphene can enable the use of graphene as effective digital switches. These graphene-BNNT heterojunctions were characterized at room temperature by four-probe scanning tunneling microscopy (4-probe STM) under real-time monitoring of scanning electron microscopy (SEM). A switching ratio as high as 10(5) at a turn-on voltage as low as 0.5 V were recorded. Simulation by density functional theory (DFT) suggests that mismatch of the density of states (DOS) is responsible for these novel switching behaviors.

Bandgap engineering of colloidal zinc oxysulfide via lattice substitution with sulfur.

Zinc oxysulfide nanocrystals with zinc blende phase are synthesized through a wet-chemical method. An affirmation of the crystal structure, elemental homogeneity and phase transformation is obtained by X-ray diffraction and authenticated by electron micrographic studies. Theoretical observations have strongly supported the thermodynamic solubility limit for its (30%) formation. An anomalous bandgap bowing with modulation in bandgap from 3.74 eV (ZnO) to 3.93 eV (ZnS) was observed with a minimum bandgap of 2.7 eV. Tunable bandgap and a wide range of visible emission ascertain it as a potential material for optoelectronic and solar cell applications due to its large bandgap offsets.

Mechanism of uptake of ZnO nanoparticles and inflammatory responses in macrophages require PI3K mediated MAPKs signaling.

The inflammatory responses after exposure to zinc oxide nanoparticles (ZNPs) are known, however, the molecular mechanisms and direct consequences of particle uptake are still unclear. Dose and time-dependent increase in the uptake of ZNPs by macrophages has been observed by flow cytometry. Macrophages treated with ZNPs showed a significantly enhanced phagocytic activity. Inhibition of different internalization receptors caused a reduction in uptake of ZNPs in macrophages. The strongest inhibition in internalization was observed by blocking clathrin, caveolae and scavenger receptor mediated endocytic pathways. However, FcR and complement receptor-mediated phagocytic pathways also contributed significantly to control. Further, exposure of primary macrophages to ZNPs (2.5 µg/ml) caused (i) significant enhancement of Ras, PI3K, (ii) enhanced phosphorylation and subsequent activation of its downstream signaling pathways via ERK1/2, p38 and JNK MAPKs (iii) overexpression of c-Jun, c-Fos and NF-κB. Our results demonstrate that ZNPs induce the generation of reactive nitrogen species and overexpression of Cox-2, iNOS, pro-inflammatory cytokines (IL-6, IFN-γ, TNF-α, IL-17 and regulatory cytokine IL-10) and MAPKs which were found to be inhibited after blocking internalization of ZNPs through caveolae receptor pathway. These results indicate that ZNPs are internalized through caveolae pathway and the inflammatory responses involve PI3K mediated MAPKs signaling cascade.

Controlled drug release characteristics and enhanced antibacterial effect of graphene nanosheets containing gentamicin sulfate.

A novel methanol derived graphene (MDG) and gentamicin sulfate nanohybrid was prepared, and the loading and release behaviour of gentamicin on MDG is investigated. An efficient drug loading of 2.57 mg mg(-1) was obtained at pH 7. By applying release kinetic models, the mechanism of release of the drug from the MDG matrix was found to be following the Korsmeyer-Peppas model. However, the diffusional release exponent (n) value lies below 0.5 demonstrating that the mechanism controlling the drug release is the Fickian diffusion.

An ultra sensitive saccharides detection assay using carboxyl functionalized chitosan containing : nanoparticlesprobe.

A novel saccharides detection assay based on covalent immobilization of amino phenyl boronic acid (APBA) in thin films of carboxyl functionalized chitosan (HOOC-chitosan) containing <5 nm Gd2O3 : Eu3+ nanoparticles at a platinum disc electrode was developed. The resulting HOOC-chitosan/Gd2O3 : Eu3+ nanocomposite film exhibited excellent electrochemical response to changes in the pKa values of boronate esters yielded from different vicinal diols of sugars. The covalent interaction of APBA onto the HOOC-chitosan/Gd2O3 : Eu3+ Pt-disc electrode was characterized with FT-IR, SEM, contact angle and cyclic voltammetry, whereas Gd2O3 : Eu3+ nanoparticles and HOOC-chitosan/Gd2O3 : Eu3+ nanocomposite was identified using XRD, EDX and TEM. A wide linear response was measured to boronate esters ranging from 25 nM to 13.5 µM (r2 = 0.963) with good reproducibility. The excellent electrochemical activity of the assay might be attributed to the synergistic effects of the balanced de-/protonated HOOC-chitosan, APBA and Gd2O3 : Eu3+ nanoparticles. With APBA as a model, the HOOC-chitosan/Gd2O3 : Eu3+ nanocomposite-modified Pt-electrode was constructed through a simple drop coating method. The resulting assay exhibited a good potentiometric response to different saccharides including glucose, and could be a promising application for the precise electrochemical detection of vicinal diols of specific sugars for clinical diagnostics, medicine validation, bioscience research and food analysis.

Low-temperature synthesis of quantum size gadolinium monosulfide (GdS) nanoparticles and their pathogen capture efficiency.

Synthesis of paramagnetic gadolinium monosulfide nanoparticles at low temperature is achieved using dextrose ligands.