Enhanced Transmission at the Zeroth-Order Mode of a Terahertz Fabry-Perot Cavity.

A planar Fabry-Perot cavity with intermirror spacing of d ≪ λ is explored for its "zero-order mode" terahertz transmission. The enhanced transmission observed as d → 0 indicates that such cavities satisfy the resonance conditions across a broad terahertz bandwidth. The experimental signatures from this elusive, "technically challenging" regime are evidenced using time-domain terahertz spectroscopy and are complemented by numerical calculations. The results raise intriguing possibilities for terahertz field modulation and pave new paths for strong coupling of multiple transition frequencies simultaneously.

Enhanced molecular orientation via NIR-delay-THz scheme: Experimental results at room temperature.

Light-induced orientation of gas phase molecules is a long-pursued goal in physics and chemistry. Here, we experimentally demonstrate a six-fold increase in the terahertz-induced orientation of iodomethane (CH3I) molecules at room temperature, provided by rotational pre-excitation with a moderately intense near-IR pulse. The paper highlights the underlying interference of multiple coherent transition pathways within the rotational coherence manifold and is analyzed accordingly. Our experimental and theoretical results provide desirable and practical means for all-optical experiments on oriented molecular ensembles.

Molecular orientation echoes via concerted terahertz and near-IR excitations.

A new and efficient method for orientation echo spectroscopy is presented and realized experimentally. The excitation scheme utilizes concerted rotational excitations by both ultrashort terahertz and near-IR pulses and its all-optical detection is enabled by the molecular orientation-induced second harmonic method [J. Phys. Chem. A126, 3732 (2022)10.1021/acs.jpca.2c03237]. This method provides practical means for orientation echo spectroscopy of gas phase molecules and highlights the intriguing underlying physics of coherent rotational dynamics induced by judiciously-orchestrated interactions with both resonant (terahertz) and nonresonant (NIR) fields.

Molecular Orientation-Induced Second-Harmonic Generation: Deciphering Different Contributions Apart.

We demonstrate and explore an all-optical technique for direct monitoring of the orientation dynamics in gas-phase molecular ensembles. The technique termed "MOISH" utilizes the transiently lifted inversion symmetry of polar gas media and provides a sensitive and spatially localized probing of the second-harmonic generation signal that is directly correlated with the orientation of the gas. Our experimental results reveal selective electronic and nuclear dynamical contributions to the overall nonlinear optical signal and decipher them apart using the "reporter gas" approach. "MOISH" provides new crucial means for implementing advanced coherent rotational control via concerted excitation by both terahertz and optical fields.

Strong coupling of collective intermolecular vibrations in organic materials at terahertz frequencies.

Several years ago, strong coupling between electronic molecular transitions and photonic structures was shown to modify the electronic landscape of the molecules and affect their chemical behavior. Since then, this concept has evolved into a new field known as polaritonic chemistry. An important ingredient in the progress of this field was the demonstration of strong coupling with intra-molecular vibrations, which enabled the modification of processes occurring at the electronic ground-state. Here we demonstrate strong coupling with collective, inter-molecular vibrations occurring in organic materials in the low-terahertz region ([Formula: see text]1012 Hz). Using a cavity filled with α-lactose molecules, we measure the temporal evolution and observe coherent Rabi oscillations, corresponding to a splitting of 68 GHz. These results take strong coupling into a new class of materials and processes, including skeletal polymer motions, protein dynamics, metal organic frameworks and other materials, in which collective, spatially extended degrees of freedom participate in the dynamics.

The effects of sample conductivity on the efficacy of dynamic nuclear polarization for sensitivity enhancement in solid state NMR spectroscopy.

In recent years dynamic nuclear polarization (DNP) has greatly expanded the range of materials systems that can be studied by solid state NMR spectroscopy. To date, the majority of systems studied by DNP were insulating materials including organic and inorganic solids. However, many technologically-relevant materials used in energy conversion and storage systems are electrically conductive to some extent or are employed as composites containing conductive additives. Such materials introduce challenges in their study by DNP-NMR which include microwave absorption and sample heating that were not thoroughly investigated so far. Here we examine several commercial carbon allotropes, commonly employed as electrodes or conductive additives, and consider their effect on the extent of solvent polarization achieved in DNP from nitroxide biradicals. We then address the effect of sample conductivity systematically by studying a series of carbons with increasing electrical conductivity prepared via glucose carbonization. THz spectroscopy measurements are used to determine the extent of µw absorption. Our results show that while the DNP performance significantly drops in samples containing the highly conductive carbons, sufficient signal enhancement can still be achieved with some compromise on conductivity. Furthermore, we show that the deleterious effect of conductive additives on DNP enhancements can be partially overcome through pulse-DNP experiments.

Echo Spectroscopy in Multilevel Quantum-Mechanical Rotors.

We study the dynamics of rotational echoes in gas phase molecular ensembles and their dependence on the delay and intensity of the excitation pulses. We explore the unique dynamics of alignment echoes that arise from the multilevel nature of the molecular rotors and impose severe difficulties in utilizing echo responses for rotational spectroscopy. We show experimentally and theoretically that judicious control of both the delay and intensity of the second pulse enables multilevel "rotational echo spectroscopy." The proposed methodology paves the way to rotational spectroscopy in high-density gas samples.

Rotational Echoes: Rephasing of Centrifugal Distortion in Laser-Induced Molecular Alignment.

We study and demonstrate the rephasing property of the echo response in a multilevel rotational system of iodomethane via long time-resolved optical birefringence measurements. The strong centrifugal distortion of iodomethane is utilized as a dephasing mechanism imprinted on the echo signal and is shown to rephase throughout its evolution. The dependence of the echo signal amplitude on the driving pulses' intensities is theoretically and experimentally explored. The analogy to Hahn's spin echoes is discussed, and a quantum-mechanical version of Hahn's track runners is provided for the case of multilevel rotational system.

Coherent Radiative Decay of Molecular Rotations: A Comparative Study of Terahertz-Oriented versus Optically Aligned Molecular Ensembles.

The decay of field-free rotational dynamics is experimentally studied by two complementary methods: laser-induced molecular alignment and terahertz-field-induced molecular orientation. A comparison between the decay rates of different molecular species at various gas pressures reveals that oriented molecular ensembles decay faster than aligned ensembles. The discrepancy in decay rates is attributed to the coherent radiation emitted by the transiently oriented ensembles and is absent from aligned molecules. The experimental results reveal the dramatic contribution of coherent radiative emission to the observed decay of rotational dynamics and underline a general phenomenon expected whenever field-free coherent dipole oscillations are induced.

Rotational Control of Asymmetric Molecules: Dipole- versus Polarizability-Driven Rotational Dynamics.

We experimentally study the optical- and terahertz-induced rotational dynamics of asymmetric molecules in the gas phase. Terahertz and optical fields are identified as two distinct control handles over asymmetric molecules, as they couple to the rotational degrees of freedom via the molecular dipole and polarizability selectively. The distinction between those two rotational handles is highlighted by different types of quantum revivals observed in long-duration (>100 ps) field-free rotational evolution. The experimental results are in excellent agreement with random phase wave function (RPWF) simulations [Phys. Rev. A 91, 063420 (2015)] and provide verification of the RPWF as an efficient method for calculating asymmetric molecular dynamics at ambient temperatures, where exact calculation methods are practically not feasible. Our observations and analysis pave the way for orchestrated excitations by both optical and terahertz fields as complementary rotational handles that enable a plethora of new possibilities in three-dimensional rotational control of asymmetric molecules.