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Daniel D. Kohler

Publications and source records attributed to Daniel D. Kohler.

4 recordsLinked to original sources

Quantum interference between the optical Stark effect and resonant harmonic generation in WS2

An applied field can modulate optical signals by resonance shifting via the Stark effect. The optical Stark effect (OSE) uses ultrafast light in the transparency region of a material to shift resonances with speeds limited by the pulse duration or system coherence. In this Letter we investigate the OSE in resonant optical harmonic generation (OHG) using the ground state exciton transition of WS2 with a variety of morphologies. Multidimensional pump-harmonic-probe measurements, in which the probe is second- or third-harmonic emission, reveal not only large Stark shifts that are commensurate with the large optical susceptibilities common to WS2 excitons, but also behaviors more complex than simple OSE treatments predict. We show how a new manifestation of the Stark Effect, brought forth by coherent photon exchange between the pump and OHG fundamental fields, can strongly enhance or suppress OHG.

physics.optics

Pump-triple sum-frequency-probe spectroscopy of transition metal dichalcogenides

Triple sum-frequency (TSF) spectroscopy measures multidimensional spectra by resonantly exciting multiple quantum coherences of vibrational and electronic states. In this work we demonstrate pump-TSF-probe spectroscopy in which a pump excites a sample and some time later three additional electric fields generate a probe field which is measured. We demonstrate pump-TSF-probe spectroscopy on polycrystalline, smooth, thin films and spiral nanostructures of both MoS2 and WS2. The pump-TSF-probe spectra are qualitatively similar to the more conventional transient-reflectance spectra. While transient-reflectance sensitivity suffers under low surface coverage, pump-TSF-probe sensitivity is independent of the sample coverage and nanostructure morphologies. Our results demonstrate that pump-TSF-probe is a valuable methodology for studying microscopic material systems.

physics.optics

Multidimensional Triple Sum-Frequency Spectroscopy of MoS2 and Comparisons with Absorption and Second Harmonic Generation Spectroscopies

Triple sum-frequency (TSF) spectroscopy is a recently-developed methodology that enables collection of multidimensional spectra by resonantly exciting multiple quantum coherences of vibrational and electronic states. This work reports the first application of TSF to the electronic states of semiconductors. Two independently tunable ultrafast pulses excite the A, B, and C features of a MoS2 thin film. The measured TSF spectrum differs markedly from absorption and second harmonic generation spectra. The differences arise because of the relative importance of transition moments and the joint density of states. We develop a simple model and globally fit the absorption and harmonic generation spectra to extract the joint density of states and the transition moments from these spectra. Our results validate previous assignments of the C feature to a large joint density of states created by band nesting.

physics.optics

Group and phase velocity mismatch fringes in triple sum-frequency spectroscopy

The effects of group and phase velocity mismatch are well-known in optical harmonic generation, but the non-degenerate cases remain unexplored. In this work we develop an analytic model which predicts velocity mismatch effects in non-degenerate triple sum-frequency mixing, TSF. We verify this model experimentally using two tunable, ultrafast, short-wave-IR lasers to demonstrate spectral fringes in the TSF output from a 500 $μ$m thick sapphire plate. We find the spectral dependence of the TSF depends strongly on both the phase velocity and the group velocity differences between the input and output fields. We define practical strategies for mitigating the impact of velocity mismatches.

physics.optics