Vibrational Strong Coupling Research Articles

Manipulating the Self-Assembly of Phenyleneethynylenes under Vibrational Strong Coupling.

The chemical and physical properties of molecules and materials are known to be modified significantly under vibrational strong coupling (VSC). To gain insight into the effects of VSC on π-π interactions involved in molecular self-assembly, themselves sensitive to vacuum electromagnetic field fluctuations, the aggregation of two structural isomers (linear and V-shaped) of phenyleneethynylene under cooperative coupling was investigated. By coupling the aromatic C═C stretching band, the assembly of one of the molecules results in the formation of spheres as opposed to flakes under normal conditions. As a consequence, the electronic absorption and emission spectra of the self-assembled structures are also modified significantly. The VSC-induced changes depend not only on the type of vibration that is coupled but also on the symmetry of the phenyleneethynylene isomer. These results confirm that VSC can be used to drive molecular assemblies to new structural minima and thereby provide a new tool for supramolecular chemistry.

Effective mass of cavity-vibration polaritons formed in etalons with liquid carbon tetrachloride.

Etalons are pairs of parallel plate mirrors with wavelength-scale spacing that exhibit cavity modes, giving transmission maxima (fringes) due to constructive interference. Infrared transmission measurements as a function of angle were used to determine the effective mass of etalon cavity modes using a gap filled with air and then liquid carbon tetrachloride. The air-filled etalon gives results in agreement with pure photon expectations established herein. Liquids with vibrations having strong infrared transition intensity (vibrational strong coupling mode) can strongly perturb the pattern of transmission resonances, creating mixed states of infrared cavity modes and molecular vibrations, i.e., cavity-vibration polaritons. The effective mass of one cavity-vibration polariton close to the strong vibration of carbon tetrachloride is 4.36 times heavier than the pure photon cavity mode expectation, i.e., the mass factor vs pure light. The mass factors are largest when closest to the strong vibrational frequency, and they converge to the one far away from the strong vibration. This work gives quantitative values of the effective mass of cavity-vibration polariton states and is a diagnostic for the mixing of vibrations with etalon transmission.

Vibration-Cavity Polariton Chemistry and Dynamics.

Molecular polaritons result from light-matter coupling between optical resonances and molecular electronic or vibrational transitions. When the coupling is strong enough, new hybridized states with mixed photon-material character are observed spectroscopically, with resonances shifted above and below the uncoupled frequency. These new modes have unique optical properties and can be exploited to promote or inhibit physical and chemical processes. One remarkable result is that vibrational strong coupling to cavities can alter reaction rates and product branching ratios with no optical excitation whatsoever. In this work we review the ability of vibration-cavity polaritons to modify chemical and physical processes including chemical reactivity, as well as steady-state and transient spectroscopy. We discuss the larger context of these works and highlight their most important contributions and implications. Our goal is to provide insight for systematically manipulating molecular polaritons in photonic and chemical applications.

Vibrational Strong Coupling between Surface Phonon Polaritons and Organic Molecules via Single Quartz Micropillars.

Vibrational strong coupling (VSC), the strong coupling between optical resonances and the dipolar absorption of molecular vibrations at mid-infrared frequencies, holds the great potential for the development of ultrasensitive infrared spectroscopy, the modification of chemical properties of molecules, and the control of chemical reactions. In the realm of ultracompact VSC, there is a need to scale down the size of mid-infrared optical resonators and to elevate their optical field strength. Herein, by using single quartz micropillars as mid-infrared optical resonators, the strong coupling is demonstrated between surface phonon polariton (SPhP) resonances and molecular vibrations from far-field observation. The single quartz micropillars support sharp SPhP resonances with an ultrasmall mode volume, which strongly couples with the molecular vibrations of 4-nitrobenzyl alcohol (C7 H7 NO3 ) molecules featuring pronounced mode splitting and anticrossing dispersion. The coupling strength depends on the molecular concentration and reaches the strong coupling regime with only 7300 molecules. The findings pave the way for promoting the VSC sensitivity, miniaturing the VSC devices, and will boost the development of ultracompact mid-infrared spectroscopy and chemical reaction control devices.

Cavity catalysis: modifying linear free-energy relationship under cooperative vibrational strong coupling.

Here, we used an unconventional idea of cooperative vibrational strong coupling of solute and solvent molecules to enhance the rate of an esterification reaction. Different derivatives of p-nitrophenyl benzoate (solute) and isopropyl acetate (solvent) are cooperatively coupled to an infrared Fabry–Perot cavity mode. The apparent rates are increased by more than six times at the ON resonance condition, and the rate enhancement follows the lineshape of the vibrational envelope. Very interestingly, a strongly coupled system doesn't obey the Hammett relations. Thermodynamics suggests that the reaction mechanism remains intact for cavity and non-cavity conditions. Temperature-dependent experiments show an entropy-driven process for the coupled molecules. Vacuum field coupling decreases the free energy of activation by 2–5 kJ mol−1, supporting a catalysis process. The non-linear rate enhancement can be due to the reshuffling of the energy distribution between the substituents and the reaction center across the aromatic ring. These findings underline the non-equilibrium behavior of cavity catalysis.

Negligible rate enhancement from reported cooperative vibrational strong coupling catalysis.

We report the results of an attempt to reproduce a reported cavity catalysis of the ester hydrolysis of para-nitrophenyl acetate due to vibrational strong coupling. While we achieved the same light-matter coupling strength and detuning, we did not observe the reported ten-fold increase in the reaction rate constant. Furthermore, no obvious detuning dependence was observed. The inconsistency with the reported literature suggests that cavity catalysis is sensitive to experimental details beyond the onset of vibrational strong coupling. This indicates that other important factors are involved and have been overlooked so far. We find that more investigation into the limits, key factors, and mechanisms to reliably actualize cavity modified reactions is needed.

Probing Vibrational Strong Coupling of Molecules with Wavelength‐Modulated Raman Spectroscopy

AbstractRaman spectroscopy is a powerful technique that enables fingerprinting of materials, molecules, and chemical environments by probing vibrational resonances. In many applications, the desired Raman signals are masked by fluorescence, either from the molecular system being studied, or from adjacent metallic nanostructures. Here, it is shown that wavelength‐modulated Raman spectroscopy provides a powerful way to significantly reduce the strength of the fluorescence background, thereby allowing the desired Raman signals to be clearly recorded. This approach is made use of to explore Raman scattering in the context of vibrational strong coupling, an area that has thus far been problematic to visualise. Specifically, strong coupling between the vibrational modes in a polymer and two types of confined light field, the fundamental mode of a metal‐clad microcavity, and the surface‐plasmon modes of an adjacent thin metal film are looked at. While clear advantages in using the wavelength‐modulated Raman approach are found, these results on strong coupling are inconclusive, and highlight the need for more work in this exciting topic area.

Vibrational Coupling of Water from Weak to Ultrastrong Coupling Regime via Cavity Mode Tuning

Vibrational strong coupling is an emerging method for modulation of ground-state molecular properties. Spectroscopic information about the vibrational coupling state is essential for determination ...

Chemistry under Vibrational Strong Coupling.

Over the past decade, the possibility of manipulating chemistry and material properties using hybrid light-matter states has stimulated considerable interest. Hybrid light-matter states can be generated by placing molecules in an optical cavity that is resonant with a molecular transition. Importantly, the hybridization occurs even in the dark because the coupling process involves the zero-point fluctuations of the optical mode (a.k.a. vacuum field) and the molecular transition. In other words, unlike photochemistry, no real photon is required to induce this strong coupling phenomenon. Strong coupling in general, but vibrational strong coupling (VSC) in particular, offers exciting possibilities for molecular and, more generally, material science. Not only is it a new tool to control chemical reactivity, but it also gives insight into which vibrations are involved in a reaction. This Perspective gives the underlying fundamentals of light-matter strong coupling, including a mini-tutorial on the practical issues to achieve VSC. Recent advancements in "vibro-polaritonic chemistry" and related topics are presented along with the challenges for this exciting new field.

Quantum Effects in Chemical Reactions under Polaritonic Vibrational Strong Coupling.

The electromagnetic field in an optical cavity can dramatically modify and even control chemical reactivity via vibrational strong coupling (VSC). Since the typical vibration and cavity frequencies are considerably larger than thermal energy, it is essential to adopt a quantum description of cavity-catalyzed adiabatic chemical reactions. Using quantum transition state theory (TST), we examine the coherent nature of adiabatic reactions in cavities and derive the cavity-induced changes in eigenfrequencies, zero-point energy, and quantum tunneling. The resulting quantum TST calculation allows us to explain and predict the resonance effect (i.e., maximal kinetic modification via tuning the cavity frequency), collective effect (i.e., linear scaling with the molecular density), and selectivity (i.e., cavity-induced control of the branching ratio). The TST calculation is further supported by perturbative analysis of polariton normal modes, which not only provides physical insights to cavity-catalyzed chemical reactions but also presents a general approach to treat other VSC phenomena.

Mode-Specific Chemistry through Vibrational Strong Coupling (or A Wish Come True)

Mode-Specific Chemistry through Vibrational Strong Coupling (or <i>A Wish Come True</i>)

Supramolecular Assembly of Conjugated Polymers under Vibrational Strong Coupling

AbstractStrong coupling plays a significant role in influencing chemical reactions and tuning material properties by modifying the energy landscapes of the systems. Here we study the effect of vibrational strong coupling (VSC) on supramolecular organization. For this purpose, a rigid‐rod conjugated polymer known to form gels was strongly coupled together with its solvent in a microfluidic IR Fabry–Perot cavity. Absorption and fluorescence studies indicate a large modification of the self‐assembly under such cooperative VSC. Electron microscopy confirms that in this case, the supramolecular morphology is totally different from that observed in the absence of strong coupling. In addition, the self‐assembly kinetics are altered and depend on the solvent vibration under VSC. The results are compared to kinetic isotope effects on the self‐assembly to help clarify the role of different parameters under strong coupling. These findings indicate that VSC is a valuable new tool for controlling supramolecular assemblies with broad implications for the molecular and material sciences.

Supramolecular Assembly of Conjugated Polymers under Vibrational Strong Coupling.

Strong coupling plays a significant role in influencing chemical reactions and tuning material properties by modifying the energy landscapes of the systems. Here we study the effect of vibrational strong coupling (VSC) on supramolecular organization. For this purpose, a rigid-rod conjugated polymer known to form gels was strongly coupled together with its solvent in a microfluidic IR Fabry-Perot cavity. Absorption and fluorescence studies indicate a large modification of the self-assembly under such cooperative VSC. Electron microscopy confirms that in this case, the supramolecular morphology is totally different from that observed in the absence of strong coupling. In addition, the self-assembly kinetics are altered and depend on the solvent vibration under VSC. The results are compared to kinetic isotope effects on the self-assembly to help clarify the role of different parameters under strong coupling. These findings indicate that VSC is a valuable new tool for controlling supramolecular assemblies with broad implications for the molecular and material sciences.

Theory of Mode-Selective Chemistry through Polaritonic Vibrational Strong Coupling.

Recent experiments have demonstrated remarkable mode-selective reactivities by coupling molecular vibrations with a quantized radiation field inside an optical cavity. The fundamental mechanism behind such effects, on the other hand, remains elusive. In this work, we provide a theoretical explanation of the basic principle of how cavity frequency can be tuned to achieve mode-selective reactivities. We find that the dynamics of the radiation mode leads to a cavity frequency-dependent dynamical caging effect of a reaction coordinate, resulting in suppression of the rate constant. In the presence of competitive reactions, it is possible to preferentially cage a reaction coordinate when the barrier frequencies of competing reactions are different, resulting in a selective slow down of a given reaction. Our theoretical results illustrate the cavity-induced mode-selective chemistry through polaritonic vibrational strong couplings, revealing the fundamental mechanism for changing chemical selectivities through cavity quantum electrodynamics.

Strong Coupling in a Self-Coupled Terahertz Photonic Crystal

Vibrational strong coupling is a phenomenon in which a vibrational transition in a material placed inside a photonic structure is hybridized with its optical modes to form composite light–matter excitations known as vibro-polaritons. Here we demonstrate a new concept of vibrational strong coupling: we show that a monolithic photonic crystal, made of a resonant material, can exhibit strong coupling between the optical modes confined in the structure and the terahertz vibrational excitations of the same material. We study this system both experimentally and numerically to characterize the dispersion of the photonic modes for various sample thicknesses and reveal their coupling with the vibrational resonances. Finally, our time-domain THz measurements allow us to isolate the free induction decay signal from the grating modes as well as from the vibro-polaritons.

Collective Vibrational Strong Coupling Effects on Molecular Vibrational Relaxation and Energy Transfer: Numerical Insights via Cavity Molecular Dynamics Simulations**

AbstractFor a small fraction of hot CO2 molecules immersed in a liquid‐phase CO2 thermal bath, classical cavity molecular dynamics simulations show that forming collective vibrational strong coupling (VSC) between the C=O asymmetric stretch of CO2 molecules and a cavity mode accelerates hot‐molecule relaxation. This acceleration stems from the fact that polaritons can be transiently excited during the nonequilibrium process, which facilitates intermolecular vibrational energy transfer. The VSC effects on these rates 1) resonantly depend on the cavity mode detuning, 2) cooperatively depend on Rabi splitting, and 3) collectively scale with the number of hot molecules. For larger cavity volumes, the average VSC effect per molecule can remain meaningful for up to N≈104 molecules forming VSC. Moreover, the transiently excited lower polariton prefers to relax by transferring its energy to the tail of the molecular energy distribution rather than distributing it equally to all thermal molecules. As far as the parameter dependence is concerned, the vibrational relaxation data presented here appear analogous to VSC catalysis in Fabry–Pérot microcavities.

Collective Vibrational Strong Coupling Effects on Molecular Vibrational Relaxation and Energy Transfer: Numerical Insights via Cavity Molecular Dynamics Simulations*.

For a small fraction of hot CO2 molecules immersed in a liquid-phase CO2 thermal bath, classical cavity molecular dynamics simulations show that forming collective vibrational strong coupling (VSC) between the C=O asymmetric stretch of CO2 molecules and a cavity mode accelerates hot-molecule relaxation. This acceleration stems from the fact that polaritons can be transiently excited during the nonequilibrium process, which facilitates intermolecular vibrational energy transfer. The VSC effects on these rates 1) resonantly depend on the cavity mode detuning, 2) cooperatively depend on Rabi splitting, and 3) collectively scale with the number of hot molecules. For larger cavity volumes, the average VSC effect per molecule can remain meaningful for up to N≈104 molecules forming VSC. Moreover, the transiently excited lower polariton prefers to relax by transferring its energy to the tail of the molecular energy distribution rather than distributing it equally to all thermal molecules. As far as the parameter dependence is concerned, the vibrational relaxation data presented here appear analogous to VSC catalysis in Fabry-Pérot microcavities.

Reproducibility of cavity-enhanced chemical reaction rates in the vibrational strong coupling regime.

One of the most exciting and debated aspects of polariton chemistry is the possibility that chemical reactions can be catalyzed by vibrational strong coupling (VSC) with confined optical modes in the absence of external illumination. Here, we report an attempt to reproduce the enhanced rate of cyanate ion hydrolysis reported by Hiura et al. [chemRxiv:7234721 (2019)] when the collective OH stretching vibrations of water (which is both the solvent and a reactant) are strongly coupled to a Fabry-Pérot cavity mode. Using a piezo-tunable microcavity, we reproduce the reported vacuum Rabi splitting but fail to observe any change in the reaction rate as the cavity thickness is tuned in and out of the strong coupling regime during a given experiment. These findings suggest that there are subtleties involved in successfully realizing VSC-catalyzed reaction kinetics and therefore motivate a broader effort within the community to validate the claims of polariton chemistry in the dark.

Vibrational strong coupling between Tamm phonon polaritons and organic molecules

Phonon polaritons (PhPs) have a long lifetime and high confinement of light fields compared with their plasmonic counterparts in the mid-infrared range. Thus, PhPs are promising candidates for realizing vibrational strong coupling (VSC) with molecules. However, VSCs of PhPs in nanoresonators and thin films require the near-field technique and are limited to the transverse magnetic mode. Here we propose a new configuration based on the Tamm structure, which supports PhPs excited by the free-space incident light in both transverse-electric and transverse-magnetic modes. The VSC of a 300 nm thick molecular layer can be achieved with 21 c m − 1 Rabi splitting, according to the numerically obtained angle resolved reflectivity spectra with the transfer matrix method. Our findings provide a promising platform for applications in free-space sensing of vibrational modes and control of chemical reactions in compact devices.

Vibrational Strong Coupling in Subwavelength Nanogap Patch Antenna at the Single Resonator Level.

Vibrational strong coupling (VSC) between a vacuum field and molecules in a cavity offers promising applications in cavity-modified chemical reactions and ultrasensitive vibrational spectroscopy. At present, in order to realize VSC, bulky microcavities with large mode volume are utilized, which limits their potential applications at the nanoscale. Here, we report on the experimental realization of strong coupling between molecular vibrations and infrared photons confined within a deeply subwavelength nanogap patch antenna cavity. Our system exhibits a characteristic anticrossing dispersion, indicating a Rabi splitting of 108 cm-1 at the single resonator level with excellent angular insensitivity. The numerical simulations and theoretical analyses quantitatively reveal that the strength of coupling depends on the cavity field-molecule overlap integral and the image charge effect. VSC at the single nanogap patch antenna level paves the way for molecular-scale chemistry, ultrasensitive biosensors, and the development of ultralow-power all-optical devices in the mid-infrared spectral range.