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arXiv:2310.09108 · Physical Review A

Nonlinear optovibronics in molecular systems

Quansheng Zhang, Muhammad Asjad, Michael Reitz, Christian Sommer, Burak Gurlek, Claudiu Genes

Published Feb 20, 2024• 1 citation
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Abstract

We analytically tackle optovibronic interactions in molecular systems driven by either classical or quantum light fields. In particular, we examine a simple model of molecules with two relevant electronic levels, characterized by potential landscapes with different positions of minima along the internuclear coordinates and of varying curvatures. Such systems exhibit an electron-vibron interaction, which can be composed of linear and quadratic terms in the vibrational displacement. By employing a combination of conditional displacement and squeezing operators, we present analytical expressions based on a quantum Langevin equations approach, to describe the emission and absorption spectra of such nonlinear molecular systems. Furthermore, we examine the imprint of the quadratic interactions onto the transmission properties of a cavity-molecule system within the collective strong-coupling regime of cavity quantum electrodynamics. Published by the American Physical Society 2024

DOI
10.1103/physreva.109.023714

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We analytically tackle optovibronic interactions in molecular systems driven by either classical or quantum light fields. In particular, we examine a simple model of molecules with two relevant electronic levels, characterized by potential landscapes with different positions of minima along the internuclear coordinates and of varying curvatures. Such systems exhibit an electron-vibron interaction, which can be composed of linear and quadratic terms in the vibrational displacement. By employing a combination of conditional displacement and squeezing operators, we present analytical expressions based on a quantum Langevin equations approach, to describe the emission and absorption spectra of such nonlinear molecular systems. Furthermore, we examine the imprint of the quadratic interactions onto the transmission properties of a cavity-molecule system within the collective strong-coupling regime of cavity quantum electrodynamics. Published by the American Physical Society 2024
We investigate the interaction between light and molecular systems modeled as quantum emitters coupled to a multitude of vibrational modes via a Holstein-type interaction. We follow a quantum Langevin equations approach that allows for analytical derivations of absorption and fluorescence profiles of molecules driven by classical fields or coupled to quantized optical modes. We retrieve analytical expressions for the modification of the radiative emission branching ratio in the Purcell regime and for the asymmetric cavity transmission associated with dissipative cross-talk between upper and lower polaritons in the strong coupling regime. We also characterize the Forster resonance energy transfer process between donor-acceptor molecules mediated by the vacuum or by a cavity mode.
We investigate the interaction between light and molecular systems modeled as quantum emitters coupled to a multitude of vibrational modes via a Holstein-type interaction. We follow a quantum Langevin equations approach that allows for analytical derivations of absorption and fluorescence profiles of molecules driven by classical fields or coupled to quantized optical modes. We retrieve analytical expressions for the modification of the radiative emission branching ratio in the Purcell regime and for the asymmetric cavity transmission associated with dissipative cross talk between upper and lower polaritons in the strong coupling regime. We also characterize the Förster resonance energy transfer process between donor-acceptor molecules mediated by the vacuum or by a cavity mode.
Strong coupling between molecular excitations and quantized electromagnetic fields in optical cavities provides a powerful means to control the physical and chemical properties of molecular systems. Here, we study electron transfer (ET) dynamics in cavity-coupled molecules using the numerically exact hierarchical equations of motion (HEOM) method, which captures nonperturbative and non-Markovian effects beyond standard perturbative theories. We identify distinct resonance and collective effects associated with polariton formation and show that the ET rate saturates in the strong-coupling regime, a feature not captured by perturbative approaches. We further extend the cavity-modified ET model by incorporating the nuclear-coordinate dependence of molecular electric dipole moments, which gives rise to a three-body interaction involving molecular electronic and vibrational degrees of freedom and cavity photons. This vibronic polariton formation leads to non-monotonic, oscillatory dependencies of the ET rate on the light-matter coupling strength and cavity frequency, which we attribute to quantum interference among multiple transfer pathways. These findings establish cavity-modified electron transfer as a multichannel quantum process governed by the interplay of electronic, vibrational, and photonic degrees of freedom.
For decades, ultrafast light-matter interactions have provided a powerful means to observe electrons in motion across a wide range of physical systems. This dissertation builds new theoretical frameworks to make sense of the emergent phenomena that arise when light drives matter into the strong-field regime, spanning atomic, molecular, and condensed-matter systems. The resulting dynamics leave their fingerprints on a variety of observables, such as photoionization spectra, high-harmonic generation, and nonlinear spectroscopic signals, each of which provides a different window onto the underlying electronic motion. The work is organized into two parts.The first part focuses on the electric-field observables of nonlinear optical signals. Because both the amplitude and phase of the emitted field are experimentally accessible through techniques such as spectral interferometry and electro-optic sampling, the full field itself serves as a rich observable for characterizing nonlinear responses in atomic, molecular, and condensed-matter systems. Leveraging this, the simulations presented here uncover novel and largely unexplored physical phenomena encoded in these field observables. The second part turns to optical spectroscopy with quantum light. Although nonlinear optical processes are conventionally modeled within a semiclassical framework, treating the matter quantum mechanically while the driving ultrafast fields remain classical, the resulting signals can nonetheless exhibit intrinsically non-classical properties. Building on this insight, a framework for interpreting experimental data is introduced and used to show that four-wave mixing driven by ultrafast femtosecond laser pulses generates bright squeezed light. Beyond squeezed light, strong field-matter interactions can also produce attosecond entangled photons, a distinct form of quantum light. Several strategies are proposed to enhance the efficiency of their generation, with the developed theory predicting rates of energy-time entangled biphoton production orders of magnitude beyond those achievable with conventional spontaneous parametric down-conversion (SPDC) sources. The studies presented here are initial steps toward investigating quantum properties of these systems through quantum phynonlinear spectroscopy, which is not achievable with classical light.
It was first realized by Purcell (1) that the spontaneous emission rate of a quantum system can be enhanced or suppressed by placing it in a resonant radiofrequency cavity. Spontaneous emission as it was first theoretically described by Einstein (2) is not a pure property of matter. It is described by matter coupled to quantized radiation field modes, which can be manipulated in an artificial structure such as a cavity. Cavity quantum electrodynamics (QED) is used to describe such effects that intimately depend on the fact that light is made of photons. Cavity QED has been extensively studied in atoms and the experimental proof was awarded with the Nobel Prize in 2012 (3). It has been applied to cooling of single atoms and for the detection of single atoms and creating and studying states with few photons and few atoms (4). In more recent developments these ideas have been extended to manipulate electronic states (5) and vibrations in molecules (6, 7). In PNAS, Flick et al. (8) introduce recent theoretical developments for the application of cavity QED to molecules and suggest possible novel applications to photochemistry. These include nonadiabatic dynamics of molecules in cavities, the modification of molecular properties, and the integration of QED with density functional theory. A quantized electromagnetic field mode can be described as a harmonic oscillator whose coordinate is the electric field displacement (Fig. 1 A ). The zero point energy translates into a nonvanishing field intensity ⟨ e 2 ⟩ in the ground state | 0 ⟩ (vacuum fluctuations). The electric vacuum field increases for a small cavity volume e c = ℏ ω c V ϵ 0 , [1] Fig. 1. ( A ) Illustration of the standing wave cavity mode and the resulting field quantization (Fock states). ( B ) Combined matter-field states (dressed states, | ± , n ⟩ … [↵][1]1To whom correspondence should be addressed. Email: smukamel{at}uci.edu. [1]: #xref-corresp-1-1
Spectroscopy, the study of matter via its interactions with light, is a vast subject that includes many of humanity's principle means of probing the fundamental structure of matter. Though usually understood from the perspective of classical light, important effects arise due to the quantum nature of the electromagnetic field. Additionally, the quantum vacuum can serve as an effective couple between molecules in the system, generating many-body interactions and cooperative processes in the material. While many techniques are well-described classically, quantum-field corrections can dominate the desired signals in certain cases, such as cascading in higher-order n-wave mixing signals, and are key for experimental interpretation. Even spontaneous emission and light scattering are best understood from the perspective of quantum fields. In this thesis, we utilize a systematic procedure, based on the density matrix in Liouville space, to give a rigorous description of elementary quantum-field effects in nonlinear spectroscopy, with specific examples made to ultrafast x-ray and optical techniques.