Photomixing of two near-infrared lasers is well established for continuous-wave terahertz spectroscopy. Photomixing of three lasers allows us to measure at three terahertz frequencies simultaneously. Similar to Fourier spectroscopy, the spectral info
rmation is contained in an nterferogram, which is equivalent to the waveform in time-domain spectroscopy. We use one fixed terahertz frequency u_ref to monitor temporal drifts of the setup, i.e., of the optical path-length difference. The other two frequencies are scanned for broadband high-resolution spectroscopy. The frequency dependence of the phase is obtained with high accuracy by normalizing it to the data obtained at u_ref, which eliminates drifts of the optical path-length difference. We achieve an accuracy of about 1-2 microns or 10^{-8} of the optical path length. This method is particularly suitable for applications in nonideal environmental conditions outside of an air-conditioned laboratory.
In a continuous-wave terahertz system based on photomixing, the measured amplitude of the terahertz signal shows an uncertainty due to drifts of the responsivities of the photomixers and of the optical power illuminating the photomixers. We report on
a simple method to substantially reduce this uncertainty. By normalizing the amplitude to the DC photocurrents in both the transmitter and receiver photomixers, we achieve a significant increase of the stability. If, e.g., the optical power of one laser is reduced by 10%, the normalized signal is expected to change by only 0.3%, i.e., less than the typical uncertainty due to short-term fluctuations. This stabilization can be particularly valuable for terahertz applications in non-ideal environmental conditions outside of a temperature-stabilized laboratory.
The electronic properties of as-prepared and purified unoriented single-walled carbon nanotube films were studied by transmission measurements over a broad frequency range (far-infrared up to visible) as a function of temperature (15 K - 295 K) and e
xternal pressure (up to 8 GPa). Both the as-prepared and the purified SWCNT films exhibit nearly temperature-independent properties. With increasing pressure the low-energy absorbance decreases suggesting an increasing carrier localization due to pressure-induced deformations. The energy of the optical transitions in the SWCNTs decreases with increasing pressure, which can be attributed to pressure-induced hybridization and symmetry-breaking effects. We find an anomaly in the pressure-induced shift of the optical transitions at $sim$2 GPa due to a structural phase transition.
We present measurements of the infrared response of the quasi-one-dimensional organic conductor (TMTSF)2$SO3 along (E||a) and perpendicular (E||b) to the stacking axis as a function of temperature. Above the metal-insulator transition related to the
anion ordering the optical conductivity spectra show a Drude-like response. Below the transition an energy gap of about 1500 cm-1 (185 meV) opens, leading to the corresponding charge transfer band in the optical conductivity spectra. The analysis of the infrared-active vibrations gives evidence for the long-range crystal structure modulation below the transition temperature and for the short-range order fluctuations of the lattice modulation above the transition temperature. Also we report about a new infrared mode at around 710 cm-1 with a peculiar temperature behavior, which has so far not been observed in any other (TMTSF)2X salt showing a metal-insulator transition. A qualitative model based on the coupling between the TMTSF molecule vibration and the reorientation of electrical dipole moment of the FSO3 anion is proposed, in order to explain the anomalous behavior of the new mode.
