The effects of structure and morphology on lithium storage in single-wall carbon nanotube (SWNT) bundles were studied by electrochemistry and nuclear magnetic resonance techniques. SWNTs were chemically etched to variable lengths and were intercalated with Li. The reversible Li storage capacity increased from LiC(6) in close-end SWNTs to LiC(3) after etching, which is twice the value observed in intercalated graphite. All the nanotubes became metallic upon intercalation of Li, with the density of states at the Fermi level increasing with increasing Li concentration. The enhanced capacity is attributed to Li diffusion into the interior of the SWNTs through the opened ends and sidewall defects.
The first systematic study on alloy formation on well‐defined nanostructured materialshas been conducted by these authors. Nanostructured silicon and germanium materials were reacted with lithium metal by solid‐state chemistry and electrochemical methods, in which nanocrystalline Si (unlike bulk material) forms Li–Si alloys already at room temperature. The Li–Si(Ge) alloys have interesting electrochemical properties, which make them attractive as anode material in lithium batteries.
X-ray radiation is widely used in medical and industrial applications. The basic design of the x-ray tube has not changed significantly in the last century. In this paper, we demonstrate that medical diagnostic x-ray radiation can be generated using a carbon nanotube (CNT) based field-emission cathode. The device can readily produce both continuous and pulsed x-ray with a programmable waveform and repetition rate. A total emission current of 28 mA was obtained from a 0.2 cm 2 area CNT cathode. The x-ray intensity is sufficient to image human extremity at 14 kVp and 180 mAs. Pulsed x-ray with a repetition rate greater than 100 kHz was readily achieved by programming the gate voltage. The CNT-based cold-cathode x-ray technology can potentially lead to portable and miniature x-ray sources for industrial and medical applications.
This feature article provides an overview of the recent research progress on the hierarchically structured carbon-based composites for electrochemical capacitors. The basic principles of electrochemical capacitors, and the design, construction and performance of hierarchically structured carbon-based composites electrode materials with good ions and electron transportation and large specific surface area are discussed. The trend of future development of high-power and large-energy electrochemical capacitors is proposed.
Many efforts are recently devoted on improving thermoelectric SnTe as an environment-friendly alternative to conventional PbTe and successful approaches include valence band convergence, nanostructuring, and substantial/interstitial defects. Among these strategies, alloying SnTe with MnTe enables the most effective reduction in the valence band offset (between L and Σ) for a convergence due to its high solubility of ≈15%, yet there is no indication that the solubility of MnTe is high enough for fully optimizing the valence band structure and thus for maximizing the electronic performance. Here, a strategy is shown to increase the MnTe solubility up to ≈25% by alloying with 5% GeTe, which successfully locates the composition (20% MnTe) to optimize the valence band structure by converging a more degenerated Λ (as compared with band L) and Σ valence bands. Through a further alloying with Cu 2 Te, the resultant Cu-interstitial defects enable a sufficient reduction in lattice thermal conductivity to its amorphous limit (0.4 W m −1 K −1 ). These electronic and thermal effects successfully realize a record-high thermoelectric figure of merit, zT of 1.8, strongly competing with that of PbTe. This work demonstrates the validity of band manipulation and interstitial defects for realizing extraordinary thermoelectric performance in SnTe.
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