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The activity of Au nanoparticle-loaded P25 TiO2 (Au/P25) plasmonic photocatalysts, evaluated by the oxidative decomposition of formic acid in water under visible light irradiation, was enhanced up to 3 times by simply mixing Au/P25 with photocatalytically inactive h-BN nanosheets as a result of electron transfer from photoexcited Au/TiO2 to the h-BN nanosheets and retardation of the charge recombination.
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OBJECTIVE: This article illustrates the development of psychiatric register research and discusses the strengths, limitations, and possible directions for future activities. METHOD: Examples illustrating the development from the post-World War II introduction of psychiatric register research until today are selected. RESULTS: The strengths of register research are seen especially within health service. Until recently, when starting linking registers to biobanks, register research had limited value in cause-seeking. Register research benefits from the possibilities for following identifiable persons over long time (lifelong) and the possibilities for linking to other registers and databases. Important limitations of register research are the heterogeneity and questionable validity of the clinical data collected. CONCLUSION: Future register research can go in the direction of big is beautiful collecting data from all possible sources creating giga-registers. In that case, low data quality will still be an unsolved problem. Or it can take the direction of smaller local clinical databases which has many advantages, for example, integrating clinical knowledge and experience into register research. However, in that case, registers will not be able to deal with rare conditions and diseases.
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Coleta de Dados , Pesquisa sobre Serviços de Saúde , Psiquiatria , Sistema de Registros , Coleta de Dados/história , Coleta de Dados/normas , Coleta de Dados/tendências , Pesquisa sobre Serviços de Saúde/história , Pesquisa sobre Serviços de Saúde/normas , Pesquisa sobre Serviços de Saúde/tendências , História do Século XX , História do Século XXI , Humanos , Psiquiatria/história , Psiquiatria/normas , Psiquiatria/tendênciasRESUMO
Centimeter-long Ta3N5 nanobelts were synthesized by a reaction of centimeter-long TaS3 nanobelt templates with flowing NH3 at 800 °C for 2 h. The nanobelts have cross-sections of about 50 × 100 nm(2), and lengths up to 0.5 cm. A field effect transistor (FET) made of a single Ta3N5 nanobelt was fabricated on silica/silicon substrate. The electric transport of the individual nanobelt revealed that the nanobelt is a semiconductor with a room-temperature resistivity of 11.88 Ω m, and can be fitted well with an empirical formula ρ = 10831 exp(-T/43.8) - 22.6, where ρ is resistivity (Ω m) and T is absolute temperature (K). The FET showed decent photoconductive performance under light irradiation in the range 250-630 nm. The photocurrent increased by nearly 10 times the dark current under 450 nm light irradiation at an applied voltage of 5.0 V.
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Excellent photoconductive properties have been found in Sb(2)O(3) nanobelts synthesized by a surfactant-assisted solvothermal method. Visible-light photodetectors have been designed from Sb(2)O(3) nanobelt networks using micrometer-wide gold wires as masks. Photodetectors show high sensitivity to visible light, high stability, and reproducibility. Fast response and decay times (<0.3 s) are comparable or even better than these parameters in many other metal oxide nanoscale photodetectors. The dominant mechanism of excellent photoconductivity is attributed to the barrier height modulations in the nanobelt-to-nanobelt contact regions. These results demonstrate that Sb(2)O(3) nanobelt networks can indeed serve as high-performance photodetectors in the visible light range.
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Nanoestruturas/química , Nanoestruturas/ultraestrutura , Fotometria/instrumentação , Compostos de Estanho/química , Desenho de Equipamento , Análise de Falha de Equipamento , Luz , Nanoestruturas/efeitos da radiação , Compostos de Estanho/efeitos da radiaçãoRESUMO
A submicrometer-sized pH sensor based on biotin-fluorescein-functionalized multiwalled BN nanotubes with anchored Ag nanoparticles is designed. Intrinsic pH-dependent photoluminescence and Raman signals in attached fluorescein molecules enhanced by Ag nanoparticles allow this novel nanohybrid to perform as a practical pH sensor. It is able to work in a submicrometer-sized space. For example, the sensor may determine the environmental pH of sub-units in living cells where a traditional optical fiber sensor fails because of spatial limitations.
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Técnicas Biossensoriais/métodos , Compostos de Boro/química , Nanotecnologia/métodos , Nanotubos/química , Concentração de Íons de Hidrogênio , Medições Luminescentes/métodos , Microscopia Eletrônica de Varredura , Nanopartículas/química , Nanopartículas/ultraestrutura , Nanotubos/ultraestrutura , Espectrometria de FluorescênciaRESUMO
We report on experimental synthesis and theoretical studies of ultrasharp BN-nanocones. Using scanning and transmission electron microscopy, the cone-like morphology of synthesized products was confirmed. Theoretical analysis of the dipole moment nature in h-BN nanocones reveals that the moment has contributions from the polarity of B-N bonds and electronic flexoelectric effect associated with a curved h-BN lattice. The latter phenomenon is predicted on the basis of the extension of the theory of flexoelectric effects in the h-BN lattice through establishing universality of the linear dependence of flexoelectric dipole moments on local curvature in various nano- h-BN networks (nanotubes and fullerenes). Our study of the atomic structure response and its polarization under deformation of nanocones with different apex angles shows the advantageous properties of cones with the smallest angles.
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We have used Raman spectroscopy to study the behavior of multi-walled boron nitride nanotubes and hexagonal boron nitride crystals under high pressure. While boron nitride nanotubes show an irreversible transformation at about 12 GPa, hexagonal boron nitride exhibits a reversible phase transition at 13 GPa. We also present molecular dynamics simulations which suggest that the irreversibility of the pressure-induced transformation in boron nitride nanotubes is due to the polar nature of the bonds between boron and nitrogen.
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Compostos de Boro/química , Cristalização/métodos , Modelos Químicos , Modelos Moleculares , Nanotecnologia/métodos , Nanotubos/química , Nanotubos/ultraestrutura , Simulação por Computador , Substâncias Macromoleculares/química , Teste de Materiais , Conformação Molecular , Tamanho da Partícula , Pressão , Propriedades de SuperfícieRESUMO
For the first time the surface of decellularized extracellular matrix (DECM) was modified via deposition of a multicomponent bioactive nanostructured film for improvement of the DECM's mechanical properties. TiCaPCON films were deposited onto the surface of intact and decellularized ulna, radius, and humerus bones by magnetron sputtering of TiC0.5 + 10%Ca3(PO4)2 and Ti targets in a gaseous mixture of Ar + N2. The film structure was studied using x-ray diffraction, scanning and transmission electron microscopy, and Raman spectroscopy. The films were characterized in terms of their wettability, as well as adhesion strength to the intact bone and DECM substrates. The mechanical properties of TiCaPCON-coated samples were investigated by compression testing. In addition, humerus bones were evaluated during three-point bending tests. The results indicate that the tightly adhered films, uniformly covering the DECM surfaces, possessed hydrophilic characteristics. A maximum improvement in mechanical properties (250%) was observed for coated humerus samples. In case of decellularized radius bones, the compressive strength also increased by 150% after coating. The positive role of TiCaPCON films was less noticeable for ulna bones because of large data scattering. These results clearly indicate that the films acted as a rigid frame that increased the material compressive strength. Compared with intact bones, fracture in the TiCaPCON-coated DECM samples was characterized by rarer and larger cracks generated under higher critical loads. As a result, the samples were crushed into several large pieces and numerous tiny fragments. Although the film deposition increased the bone stiffness, the bending tests revealed that the flexural strength of the coated samples became 20%-25% lower than the strength of the film-free samples.
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Substitutos Ósseos/química , Osso e Ossos/química , Fosfatos de Cálcio/química , Materiais Revestidos Biocompatíveis/química , Matriz Extracelular/química , Titânio/química , Adesividade , Animais , Argônio/química , Sistema Livre de Células/química , Força Compressiva , Cães , Módulo de Elasticidade , Teste de Materiais , Nanoestruturas/química , Nanoestruturas/ultraestrutura , Nitrogênio/química , Estresse Mecânico , Propriedades de Superfície , Resistência à TraçãoRESUMO
Record high values of Young's modulus and tensile strength of graphene and BN nanoribbons as well as their chemically active edges make them promising candidates for serving as fillers in metal-based composite materials. Herein, using ab initio and analytical potential calculations we carry out a systematic study of the mechanical properties of nanocomposites constructed by reinforcing an Al matrix with BN and graphene nanoribbons. We consider a simple case of uniform distribution of nanoribbons in an Al matrix under the assumption that such configuration will lead to the maximum enhancement of mechanical characteristics. We estimate the bonding energy and the interfacial critical shear stress at the ribbon/metal interface as functions of ribbon width and show that the introduction of nanoribbons into the metal leads to a substantial increase in the mechanical characteristics of the composite material, as strong covalent bonding between the ribbon edges and Al matrix provides efficient load transfer from the metal to the ribbons. Using the obtained data, we apply the rule of mixtures in order to analytically assess the relationship between the composite strength and concentration of nanoribbons. Finally, we study carbon chains, which can be referred to as the ultimately narrow ribbons, and find that they are not the best fillers due to their weak interaction with the Al matrix. Simulations of the electronic transport properties of the composites with graphene nanoribbons and carbyne chains embedded into Al show that the inclusion of the C phase gives rise to deterioration in the current carrying capacity of the material, but the drop is relatively small, so that the composite material can still transmit current well, if required.
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GaN nanowires with P doping were synthesized via a simple thermal evaporation process. The P-doped GaN nanowires have average diameters of approximately 100 nm and lengths up to tens of micrometers. Scanning electron microscope and high-resolution field-emission transmission electron microscope analyses revealed that P doping results in a rough surface morphology of GaN nanowires. Field-emission measurements showed that P doping effectively decreases the turn-on field of GaN nanowire to 5.1 V/mum, holding promise of application as an electron emitter. The rough surface is responsible for enhancement of the field-emission properties of GaN nanowires.
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Carbon nanotubes are known to be metallic or semiconducting, depending on their helicity and diameter. However, boron nitride (BN) nanotubes are the only nanotubular product known to date that are predicted to have stable insulating properties that are independent of their atomic structure and morphology. Thus, the BN tube has attracted prime attention as an advanced nanoinsulating shield for all types of encapsulated conducting material, i.e., metal wires, clusters, etc. However, so far there have been no successes in controlled one-dimensional filling of BN nanotubes with conductive material. We report the first experimental results on the synthesis, high-resolution transmission electron microscopy, energy dispersion X-ray analysis, and electron energy loss spectroscopy of BN nanotubes that are filled with Mo clusters over their entire length. This was accomplished by means of two-step thermochemical treatment of chemically vapor-deposited C nanotubes with B2O3, CuO, and MoO3 oxides in a flowing N2 atmosphere. The first examples of BN nanotubes filled with molybdenum clusters are reported and the formation of the first nanocable (approximately 10 nm in length), consisting of a conductive metal core and an insulating BN nanotubular shield is demonstrated.
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Compostos de Boro/química , Cristalização/métodos , Molibdênio/química , Nanotecnologia/métodos , Nanotubos de Carbono/química , Compostos de Boro/isolamento & purificação , Condutividade Elétrica , Instalação Elétrica/instrumentação , Instalação Elétrica/métodos , Substâncias Macromoleculares , Teste de Materiais , Microscopia Eletrônica , Microesferas , Conformação Molecular , Molibdênio/isolamento & purificação , Movimento (Física) , Tamanho da PartículaRESUMO
Theoretical analysis of experimental data on unzipping multilayered WS2 nanotubes by consequent intercalation of lithium atoms and 1-octanethiol molecules [C. Nethravathi, et al., ACS Nano, 2013, 7, 7311] is presented. The radial expansion of the tube was described using continuum thin-walled cylinder approximation with parameters evaluated from ab initio calculations. Assuming that the attractive driving force of the 1-octanethiol molecule is its reaction with the intercalated Li ions ab initio calculations of a 1-octanethiol molecule bonding with Li(+) were carried out. In addition, the non-chemical interactions of the 1-octanethiol dipole with an array of positive point charges representing Li(+) were taken into account. Comparing between the energy gain from these interactions and the elastic strain energy of the nanotube allows us to evaluate a value for the tube wall deformation after the implantation of 1-octanethiol molecules. The ab initio molecular dynamics simulation confirmed our estimates and demonstrated that a strained WS2 nanotube, with a decent concentration of 1-octanethiol molecules, should indeed be unzipped into the WS2 nanoribbon.
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We first describe the synthesis of novel and highly porous boron nitride (BN) nanospheres (100-400 nm o.d.) that exhibit a rough surface consisting of open BN nanocones and corrugated BN ribbons. The material was produced by reacting B2O3 with nanoporous carbon spheres under nitrogen at ca. 1750 degrees C. The BN nanospheres were characterized using scanning electron microscopy, high-resolution electron microscopy, and electron energy loss spectroscopy. The porous BN spheres show relatively large surface areas of ca. 290 m2/g and exhibit surprisingly stable field emission properties at low turn-on voltages (e.g., 1-1.3 V/microm). We attribute these outstanding electron emission properties to the presence of finite BN ribbons located at the surface of the nanospheres (exhibiting zigzag edges), which behave like metals as confirmed by first-principles calculations. In addition, our ab initio theoretical results indicate that the work function associated to these zigzag BN ribbons is 1.3 eV lower when compared with BN-bulk material.
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Novel coaxial structures consisting of nitrogen-doped carbon nanotube (MWNTs-CNx) cores with external concentric shells of pure carbon were produced by the pyrolysis of toluene over Fe-coated MWNTs-CNx. These materials were thoroughly characterized by SEM, HRTEM, X-ray diffraction, and TGA; a possible growth scenario for their formation is also proposed. In addition, these coaxial structures were able to form 2D and 3D covalent networks that mainly exhibited T-, Y-, and on-type morphologies. The two-step technique presented here could be further developed to fully control the growth of these new coaxial structures, study of individual junctions, and it could be used to create periodic nanotube networks, in which the heterocable structure could find applications in nanoelectronics.
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Cristalização/métodos , Nanotecnologia/métodos , Nanotubos de Carbono/química , Nanotubos de Carbono/ultraestrutura , Nitrogênio/química , Condutividade Elétrica , Substâncias Macromoleculares/química , Teste de Materiais , Conformação Molecular , Tamanho da Partícula , Propriedades de SuperfícieRESUMO
Direct synthesis of large-scale ternary boron carbonitride single-walled nanotubes (BCN-SWNTs) via a bias-assisted HFCVD process was presented. The BCN-SWNTs were grown over the powdery Fe-Mo/MgO catalyst by using CH4, B2H6, and ethylenediamine vapor as the reactant gases. As high as 16 atom % nitrogen can be incorporated within the nanotube shells, with the boron content in the range of 2-4 atom %. The ternary covalent bonding nature of the BCN-SWNTs was well characterized, and the B, C, and N elemental maps were clearly imaged by energy-filtered transmission electron microscopy.
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Single-crystalline Al4 O4 C nanowires can be synthesized at a high yield via a simple high-temperature solid reaction. A two-step method has been developed to convert the prepared nanowires into single-crystalline α-Al2 O3 nanotubes. These nanotubes may find high-temperature applications due to their unmatched refractory properties.
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We describe the synthesis of novel monocrystalline FeCo nanowires encapsulated inside multiwalled carbon nanotubes (MWNTs). These FeCo nanowires exhibit homogeneous Fe and Co concentrations and do not contain an external oxide layer due to the presence of insulating nanotube layers. The method involves the aerosol thermolysis of toluene-ferrocene-cobaltocene solutions in inert atmospheres. The materials have been carefully characterized using state-of-the-art high-resolution transmission electron microscopy (HRTEM), electron-energy-loss spectroscopy (EELS), scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDX), electron diffraction, HREELS-STM elemental mapping, X-ray powder diffraction, and SQUID magnetometry. We noted that the formation of FeCo alloys occurs at relatively low pyrolytic temperatures (e.g., 650-750 degrees C). These single-crystal nanowires, which have not been reported hitherto, always exhibit the FeCo (110) plane parallel to the carbon nanotube axis. The FeCo nanomaterials have shown large coercive fields at room temperature (e.g., 900 Oe). We envisage that these aligned ferromagnetic nanowires could be used in the fabrication of high-density magnetic storage devices and magnetic composites.