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A laser-based angle resolved photoemission (ARPES) system utilizing 6 eV photons from the fourth harmonic of a mode-locked Ti:sapphire oscillator is described. This light source greatly increases the momentum resolution and photoelectron count rate, while reducing extrinsic background and surface sensitivity relative to higher energy light sources. In this review, the optical system is described, and special experimental considerations for low-energy ARPES are discussed. The calibration of the hemispherical electron analyzer for good low-energy angle-mode performance is also described. Finally, data from the heavily studied high T(c) superconductor Bi(2)Sr(2)CaCu(2)O(8+delta) (Bi2212) is compared to the results from higher photon energies.

The JILA multidimensional optical nonlinear spectrometer (JILA-MONSTR) is a robust, ultrastable platform consisting of nested and folded Michelson interferometers that can be actively phase stabilized. This platform generates a square of identical laser pulses that can be adjusted to have arbitrary time delay between them while maintaining phase stability. The JILA-MONSTR provides output pulses for nonlinear excitation of materials and phase-stabilized reference pulses for heterodyne detection of the induced signal. This arrangement is ideal for performing coherent optical experiments, such as multidimensional Fourier-transform spectroscopy, which records the phase of the nonlinear signal as a function of the time delay between several of the excitation pulses. The resulting multidimensional spectrum is obtained from a Fourier transform. This spectrum can resolve, separate, and isolate coherent contributions to the light-matter interactions associated with electronic excitation at optical frequencies. To show the versatility of the JILA-MONSTR, several demonstrations of two-dimensional Fourier-transform spectroscopy are presented, including an example of a phase-cycling scheme that reduces noise. Also shown is a spectrum that accesses two-quantum coherences, where all excitation pulses require phase locking for detection of the signal. [ABSTRACT FROM AUTHOR]

The article presents a research report on multidimensional coherent spectroscopy reveals triplet state coherences in cesium lead-halide perovskite nanocrystals. Topics include advances in optoelectronics require materials with novel and engineered characteristics; and picosecond time scale dephasing times are measured for both triplet and inter-triplet coherences, from which we infer a unique exciton fine structure level ordering composed of a dark state.

Using optical two-dimensional Fourier transform spectroscopy, we report temperature- and excitation-density-dependent measurements of the homogeneous linewidth of the exciton ground-state transition in a single layer of interfacial GaAs quantum dots (QDs). We show that the homogeneous linewidth increases nonlinearly with temperature from 6 to 50 K and that the thermal broadening is well described by an activation term and offset. The absence of a phonon-activation peak in the two-dimensional spectra reveals that elastic scattering of excitons with acoustic phonons via virtual transitions between the ground and excited states significantly contributes to the thermal broadening. We find that the combination of increasing virtual activation energy and exciton-phonon coupling strength with decreasing QD size results in greater thermal broadening for excitons localized in smaller QDs. The homogeneous linewidth also exhibits a strong excitation-density dependence and is shown to increase linearly as the photon density increases from 2×1011 to 1×1012 photons pulse-1 cm-2 at 6 K. This trend is attributed to strong coupling of excitons within the same QD and is independent of the quantum-well exciton population density. [ABSTRACT FROM AUTHOR]