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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Kočí, Jan | Prague |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Dorozhkin, P. S.
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article
Structure, transport and field-emission properties of compound nanotubes
Abstract
<p>Transport and field-emission properties of assynthesized CN<sub>x</sub> and BNC<sub>x</sub> (x < 0.1) multi-walled nanotubes were compared in detail. Individual ropes made of these nanotubes and macrofilms of those were tested. Before measurements, the nanotubes were thoroughly characterized using high-resolution and energy-filtered electron microscopy, electron diffraction and electron-energy-loss spectroscopy. Individual ropes composed of dozens of CN<sub>x</sub> nanotubes displayed well-defined metallic behavior and low resistivities of ∼ 10-100 kΩ or less at room temperature, whereas those made of BNC<sub>x</sub> nanotubes exhibited semiconducting properties and high resistivities of ∼ 50-300 MΩ. Both types of ropes revealed good field-emission properties with emitting currents per rope reaching ∼ 4 μA (CN<sub>x</sub>) and ∼ 2 μA (BNC<sub>x</sub>), albeit the latter ropes severely deteriorated during the field emission. Macrofilms made of randomly oriented CN<sub>x</sub> or BNC<sub>x</sub> nanotubes displayed low and similar turn-on fields of ∼ 2-3 V/μm. 3 mA/cm<sup>2</sup> (BNC<sub>x</sub>) and 5.5 mA/cm<sup>2</sup> (CN<sub>x</sub>) current densities were reached at 5.5 V/μm macroscopic fields. At a current density of 0.2-0.4 mA/cm<sup>2</sup> both types of compound nanotubes exhibited equally good emission stability over tens of minutes; by contrast, on increasing the current density to 0.2-0.4 A/cm<sup>2</sup>, only CN<sub>x</sub> films continued to emit steadily, while the field emission from BNC<sub>x</sub> nanotube films was prone to fast degradation within several tens of seconds, likely due to arcing and/or resistive heating.</p>