Because of the interesting and multifunctional properties, recently, ZnO nanostructures are considered as excellent material for fabrication of highly sensitive and selective gas sensors. Thus, ZnO nanomaterials are widely used to fabricate efficient gas sensors for the detection of various hazardous and toxic gases. The presented review article is focusing on the recent developments of NO2 gas sensors based on ZnO nanomaterials. The review presents the general introduction of some metal oxide nanomaterials for gas sensing application and finally focusing on the structure of ZnO and its gas sensing mechanisms. Basic gas sensing characteristics such as gas response, response time, recovery time, selectivity, detection limit, stability and recyclability, etc are also discussed in this article. Further, the utilization of various ZnO nanomaterials such as nanorods, nanowires, nano-micro flowers, quantum dots, thin films and nanosheets, etc for the fabrication of NO2 gas sensors are also presented. Moreover, various factors such as NO2 concentrations, annealing temperature, ZnO morphologies and particle sizes, relative humidity, operating temperatures which are affecting the NO2 gas sensing properties are discussed in this review. Finally, the review article is concluded and future directions are presented.

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Zinc Oxide Nanostructures for NO2 Gas–Sensor Applications: A Review

Conducting PANI stimulated ZnO system for visible light photocatalytic degradation of coloured dyes

Polymeric nanoparticles: A study on the preparation variables and characterization methods

A two-bit magnetic memory is demonstrated, based on the magnetic states of individual holmium atoms, which are read and written in a scanning tunnelling microscope set-up and are stable over many hours. The ultimate limit of miniaturized classical data storage would be to use single-atom magnetic bits. Holmium atoms are seen as promising candidates because they have long magnetic relaxation times, so they do not easily lose their information. Fabian Natterer et al. now achieve the reading and writing of the magnetism of single holmium atoms, using a scanning tunnelling microscope, and show that individual atoms keep their state for many hours. They use these atoms to make a two-bit memory, to which they write the four possible states. They then use nearby magnetic iron atoms as sensors to confirm the magnetic states. This work suggests that single-atom magnetic memory should be possible. The single-atom bit represents the ultimate limit of the classical approach to high-density magnetic storage media. So far, the smallest individually addressable bistable magnetic bits have consisted of 3–12 atoms1,2,3. Long magnetic relaxation times have been demonstrated for single lanthanide atoms in molecular magnets4,5,6,7,8,9,10,11,12, for lanthanides diluted in bulk crystals13, and recently for ensembles of holmium (Ho) atoms supported on magnesium oxide (MgO)14. These experiments suggest a path towards data storage at the atomic limit, but the way in which individual magnetic centres are accessed remains unclear. Here we demonstrate the reading and writing of the magnetism of individual Ho atoms on MgO, and show that they independently retain their magnetic information over many hours. We read the Ho states using tunnel magnetoresistance15,16 and write the states with current pulses using a scanning tunnelling microscope. The magnetic origin of the long-lived states is confirmed by single-atom electron spin resonance17 on a nearby iron sensor atom, which also shows that Ho has a large out-of-plane moment of 10.1 ± 0.1 Bohr magnetons on this surface. To demonstrate independent reading and writing, we built an atomic-scale structure with two Ho bits, to which we write the four possible states and which we read out both magnetoresistively and remotely by electron spin resonance. The high magnetic stability combined with electrical reading and writing shows that single-atom magnetic memory is indeed possible.

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Reading and writing single-atom magnets

We have produced ultrathin epitaxial graphite films which show remarkable 2D electron gas (2DEG) behavior. The films, composed of typically 3 graphene sheets, were grown by thermal decomposition on the (0001) surface of 6H-SiC, and characterized by surface-science techniques. The low-temperature conductance spans a range of localization regimes according to the structural state (square resistance 1.5 kOhm to 225 kOhm at 4 K, with positive magnetoconductance). Low resistance samples show characteristics of weak-localization in two dimensions, from which we estimate elastic and inelastic mean free paths. At low field, the Hall resistance is linear up to 4.5 T, which is well-explained by n-type carriers of density 10^{12} cm^{-2} per graphene sheet. The most highly-ordered sample exhibits Shubnikov - de Haas oscillations which correspond to nonlinearities observed in the Hall resistance, indicating a potential new quantum Hall system. We show that the high-mobility films can be patterned via conventional lithographic techniques, and we demonstrate modulation of the film conductance using a top-gate electrode. These key elements suggest electronic device applications based on nano-patterned epitaxial graphene (NPEG), with the potential for large-scale integration.

Ultrathin epitaxial graphite: 2D electron gas properties and a route toward graphene-based nanoelectronics

The ability to engineer nearly perfect ultrathin oxide layers, up to the limit of monolayer thickness, is a key issue for nanotechnological applications. Here we face the difficult and important case of ultrathin MgO films on Ag(100), for which no extended and well-ordered layers could thus far be produced in the monolayer limit. We demonstrate that their final morphology depends not only on the usual growth parameters (crystal temperature, metal flux, and oxygen partial pressure), but also on aftergrowth treatments controlling so far neglected thermodynamics constraints. We thus succeed in tuning the shape of the oxide films from irregular, nanometer-sized, monolayer-thick islands to slightly larger, perfectly squared, bilayer islands, to extended monolayers limited apparently only by substrate steps.

Morphology of monolayer MgO films on Ag(100): switching from corrugated islands to extended flat terraces.

The interest in thin and ultrathin oxide films is increasing rapidly due to the new properties and the many possible technological applications of such materials. In this frame the interaction with...

Enhanced Reactivity at Metal-Oxide Interface: Water Interaction with MgO Ultrathin Films

In spite of the relevance of ultrathin MgO films for the study of model systems as well as for technological applications, great difficulties have been found so far in the growth of extended, well-ordered, ultrathin films. Combining scanning tunneling microscopy, X-ray photoemission spectroscopy, and high-resolution electron energy loss spectroscopy experiments with ab initio calculations, we demonstrate here that the structure of sub-monolayer MgO films grown on Ag(100) by reactive deposition is strongly affected not only by the growth conditions but also by after-growth treatments. The latter ones allow one to quench the thermodynamically most stable configuration at the deposition temperature or let the system evolve toward the low-temperature equilibrium state. Moreover, we give experimental and theoretical evidence of the accumulation of oxygen atoms at the MgO/Ag interface at the highest deposition temperature, which reduces the stress of the oxide film favoring the formation of extended terraces. T...

How Growing Conditions and Interfacial Oxygen Affect the Final Morphology of MgO/Ag(100) Films

Flash nanoprecipitation (FNP) is a widely used technique to prepare particulate carriers based on various polymers, and it was proven to be a promising technology for the industrial production of drug loaded nanoparticles. However, up to now, only its application to hydrophobic compounds has been deeply studied and the encapsulation of some strongly hydrophilic compounds, such as caffeine, remains a challenge. Caffeine loaded poly-e-caprolactone (PCL) nanoparticles were produced in a confined impinging jet mixer using acetone as the solvent and water as the antisolvent. Caffeine was dissolved either in acetone or in water to assess the effects of two different process conditions. Nanoparticles properties were assessed in terms of loading capacity (LC%), encapsulation efficiency (EE%), and in vitro release kinetics. Samples were further characterized by dynamic light scattering, scanning electron microscopy, X-ray photo electron spectroscopy, and infrared spectroscopy to determine the size, morphology, and structure of nanoparticles. FNP was proved an effective technique for entrapping caffeine in PCL and to control its release behavior. The solvent used to solubilize caffeine influences the final structure of the obtained particles. It was observed that the active principle was preferentially adsorbed at the surface when using acetone, while with water, it was embedded in the matrix structure. The present research highlights the possibility of extending the range of applications of FNP to hydrophilic molecules.

Overcoming the limits of flash nanoprecipitation: effective loading of hydrophilic drug into polymeric nanoparticles with controlled structure

The vibrational modes of clean MgO films are investigated vs film thickness by means of high-resolution electron energy-loss spectroscopy. For thin films (20\char21{}30 monolayers) we observe, in accord with the literature, the Fuchs-Kliewer phonon at $677{\mathrm{cm}}^{\ensuremath{-}1}$ and the Wallis mode at $524{\mathrm{cm}}^{\ensuremath{-}1}.$ For ultrathin films standing wave optical phonons confined in the overlayer are present, whose frequencies depend strongly on film thickness. Comparison with theoretical calculations for MgO slabs on a perfect conductor shows that the experimental frequencies are lower than expected, indicating the presence of compressive stress. At and below one-monolayer thickness an intense loss peak at $427{\mathrm{cm}}^{\ensuremath{-}1}$ is observed.

Edvige Celasco

Papers

Morphology of monolayer MgO films on Ag(100): switching from corrugated islands to extended flat terraces.

Enhanced Reactivity at Metal-Oxide Interface: Water Interaction with MgO Ultrathin Films

How Growing Conditions and Interfacial Oxygen Affect the Final Morphology of MgO/Ag(100) Films

Overcoming the limits of flash nanoprecipitation: effective loading of hydrophilic drug into polymeric nanoparticles with controlled structure

MgO/Ag(100): Confined vibrational modes in the limit of ultrathin films