arXiv subjects

Joachim Galiana

Publications and source records attributed to Joachim Galiana.

3 recordsLinked to original sources

arXiv2025

Wavepacket and Reduced-Density Approaches for High-Dimensional Quantum Dynamics: Application to the Nonlinear Spectroscopy of Asymmetrical Light-Harvesting Building Blocks

Excitation-energy transfer (EET) and relaxation in an optically excited building block of poly(phenylene ethynylene) (PPE) dendrimers are simulated using wavepackets with the multilayer multiconfiguration time-dependent Hartree (ML-MCTDH) method and reduced-density matrices with the hierachical equations of motion (HEOM) approach. The dynamics of the ultrafast electronic funneling between the first two excited electronic states in the asymmetrically meta-substituted PPE oligomer with two rings on one branch and three rings on the other side, with a shared ring in between, is treated with 93-dimensional ab initio vibronic-coupling Hamiltonian (VCH) models, either linear or with bilinear and quadratic terms. The linear VCH model is also used to calibrate an open quantum system that falls in a computationally demanding non-perturbative non-Markovian regime. The linear-response absorption and emission spectra are simulated with both the ML-MCTDH and HEOM methods. The latter is further used to explore the nonlinear regime towards two-dimensional (2D) spectroscopy. We illustrate how a minimal VCH model with the two main active bright states and the impulsive-pulse limit in third-order response theory may provide at lower cost polarization-sensitive time-resolved signals that monitor the early EET dynamics. We also confirm the essential role played by the high-frequency acetylenic and quinoidal vibrational modes.

physics.chem-ph↗

arXiv2024

Excitation-Energy Transfer and Vibronic Relaxation through Light-Harvesting Dendrimer Building Blocks: a Nonadiabatic Perspective

The light-harvesting excitonic properties of poly(phenylene ethynylene) (PPE) extended dendrimers (tree-like π-conjugated macromolecules) involve a directional cascade of local excitation-energy transfer (EET) processes occurring from the "leaves" (shortest branches) to the "trunk" (longest branch), which can be viewed from a vibronic perspective as a sequence of internal conversions occurring among a connected graph of nonadiabatically coupled locally-excited (LE) electronic states via conical intersections. The smallest PPE building block able to exhibit EET, the asymmetrically meta-substituted PPE oligomer with one acetylenic bond on one side and two parallel ones on the other side (2-ring and 3-ring para-substituted pseudo-fragments), is a prototype and the focus of the present work. From time-dependent density-functional theory (TD-DFT) electronic-structure calculations of the molecule as regards its first two nonadiabatically coupled, optically active, singlet excited states, we built a (1+2)-state-8-dimensional vibronic-coupling Hamiltonian (VCH) model for running multiconfiguration time-dependent Hartree (MCTDH) wavepacket relaxations and propagations, yielding both steady-state absorption and emission spectra, as well as real-time dynamics. The EET process from the shortest branch to the longest one occurs quite efficiently (about 80% quantum yield) within the first 25 fs after light excitation and is mediated vibrationally through acetylenic and quinoidal bond-stretching modes together with a particular role given to the central-ring anti-quinoidal rock-bending mode. Electronic and vibrational energy relaxations, together with redistributions of quantum populations and coherences, are interpreted through the lens of a nonadiabatic perspective, showing some interesting segregation among the foremost photoactive degrees of freedom as regards spectroscopy and reactivity.

physics.chem-ph↗

arXiv2023

On the unusual Stokes shift in the smallest PPE dendrimer building block: Role of the vibronic symmetry on the band origin?

1,3-bis(phenylethynyl)benzene is the primary chromophore of light-harvesting polyphenylene ethynylene (PPE) dendrimers. It is experimentally known to share the same absorption spectrum as its pair of diphenylacetylene (aka. tolane) meta-substituted branches, yet exhibits an unusual Stokes shift of about 2000 cm$^{-1}$ with respect to its band origin (corresponding to the loss of one vibrational quantum within the antisymmetric acetylenic stretching) in its emission spectrum. We suggest in the present work the unusual but plausible involvement of molecular symmetry selection rules in a situation where the Born-Oppenheimer approximation is far to be valid. Our hypothesis is comforted with quantum dynamics (MCTDH) simulations of absorption and emission UV-visible spectra based on quantum chemistry (TD-DFT) data and a diabatic vibronic coupling Hamiltonian model.

physics.chem-ph↗