Enlightening the ultrahigh electrical conductivities of doped double-wall carbon nanotube fibers by Raman spectroscopy and first-principles calculations.

Highly aligned, packed, and doped carbon nanotube (CNT) fibers with electrical conductivities approaching that of copper have recently become available. These fibers are promising for high-power electrical applications that require light-weight, high current-carrying capacity cables. However, a microscopic understanding of how doping affects the electrical conductance of such CNT fibers in a quantitative manner has been lacking. Here, we performed Raman spectroscopy measurements combined with first-principles calculations to determine the position of the average Fermi energy and to obtain the temperature of chlorosulfonic-acid-doped double-wall CNT fibers under high current. Due to the unique way in which double-wall CNT Raman spectra depend on doping, it is possible to use Raman data to determine the doping level quantitatively. The correspondence between the Fermi level shift and the carbon charge transfer is derived from a tight-binding model and validated by several calculations. For the doped fiber, we were able to associate an average Fermi energy shift of ∼-0.7 eV with a conductance increase by a factor of ∼5. Furthermore, since current induces heating, local temperature determination is possible. Through the Stokes-to-anti-Stokes intensity ratio of the G-band peaks, we estimated a temperature rise at the fiber surface of ∼135 K at a current density of 2.27 × 108 A m-2 identical to that from the G-band shift, suggesting that thermalization between CNTs is well achieved.

Plasmonic pumping of excitonic photoluminescence in hybrid MoS2-Au nanostructures.

We report on the fabrication of monolayer MoS2-coated gold nanoantennas combining chemical vapor deposition, e-beam lithography surface patterning, and a soft lift-off/transfer technique. The optical properties of these hybrid plasmonic-excitonic nanostructures are investigated using spatially resolved photoluminescence spectroscopy. Off- and in-resonance plasmonic pumping of the MoS2 excitonic luminescence showed distinct behaviors. For plasmonically mediated pumping, we found a significant enhancement (∼65%) of the photoluminescence intensity, clear evidence that the optical properties of the MoS2 monolayer are strongly influenced by the nanoantenna surface plasmons. In addition, a systematic photoluminescence broadening and red-shift in nanoantenna locations is observed which is interpreted in terms of plasmonic enhanced optical absorption and subsequent heating of the MoS2 monolayers. Using a temperature calibration procedure based on photoluminescence spectral characteristics, we were able to estimate the local temperature changes. We found that the plasmonically induced MoS2 temperature increase is nearly four times larger than in the MoS2 reference temperatures. This study shines light on the plasmonic-excitonic interaction in these hybrid metal/semiconductor nanostructures and provides a unique approach for the engineering of optoelectronic devices based on the light-to-current conversion.

A table-top, repetitive pulsed magnet for nonlinear and ultrafast spectroscopy in high magnetic fields up to 30 T.

We have developed a mini-coil pulsed magnet system with direct optical access, ideally suited for nonlinear and ultrafast spectroscopy studies of materials in high magnetic fields up to 30 T. The apparatus consists of a small coil in a liquid nitrogen cryostat coupled with a helium flow cryostat to provide sample temperatures down to below 10 K. Direct optical access to the sample is achieved with the use of easily interchangeable windows separated by a short distance of ~135 mm on either side of the coupled cryostats with numerical apertures of 0.20 and 0.03 for measurements employing the Faraday geometry. As a demonstration, we performed time-resolved and time-integrated photoluminescence measurements as well as transmission measurements on InGaAs quantum wells.