In the year 1933, Herzberg and Teller realized that the potential energy surface of a triatomic, linear molecule splits into two as soon as the molecule is bent. The phenomenon, later dubbed the Renner-Teller effect due to the detailed follow-up work of Renner on the subject, describes the coupling of a symmetry-reducing molecular vibration with degenerate electronic states. In this article, we show that a very similar type of nonadiabatic coupling can occur for certain translational degrees of freedom of diatomic, electronically degenerate molecules when trapped in a nearly spherical or cylindrical quantum confinement, e.g., realized through electromagnetic fields or molecular encapsulation. We illustrate this on the example of fullerene-encapsulated nitric oxide, and provide a prediction of its interesting, perturbed vibronic spectrum.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935370 | PMC |
http://dx.doi.org/10.1021/acs.jpca.1c10970 | DOI Listing |
Sci Adv
December 2024
Department of Physics and Astronomy, Rice University, Houston, TX 77005, USA.
Electron transfer is at the heart of many fundamental physical, chemical, and biochemical processes essential for life. The exact simulation of these reactions is often hindered by the large number of degrees of freedom and by the essential role of quantum effects. Here, we experimentally simulate a paradigmatic model of molecular electron transfer using a multispecies trapped-ion crystal, where the donor-acceptor gap, the electronic and vibronic couplings, and the bath relaxation dynamics can all be controlled independently.
View Article and Find Full Text PDFNanomaterials (Basel)
November 2024
Physics Department, State Key Laboratory of Surface Physics, Key Laboratory of Micro and Nano Photonic Structures [Ministry of Education (MOE)], Fudan University, Shanghai 200433, China.
The hybrid heterostructures formed between two-dimensional (2D) materials and organic molecules have gained great interest for their potential applications in advanced photonic and optoelectronic devices, such as solar cells and biosensors. Characterizing the interfacial structure and dynamic properties at the molecular level is essential for realizing such applications. Here, we report a time-resolved sum-frequency generation (TR-SFG) approach to investigate the hybrid structure of polymethyl methacrylate (PMMA) molecules and 2D transition metal dichalcogenides (TMDCs).
View Article and Find Full Text PDFNano Lett
December 2024
School of Engineering, ANU College of Engineering, Computing and Cybernetics, The Australian National University, Canberra, ACT 2601, Australia.
The tightly bound excitons and strong dipole-dipole interactions in two-dimensional molecular crystals enable rich physics. Among them, superradiance (SR), the spontaneous coherent emission from bright excitons, has sparked considerable interest in quantum-information applications. In addition, optically forbidden states (dark exciton states) have potential to both achieve Bose-Einstein condensation and modulate exciton dynamics.
View Article and Find Full Text PDFNanophotonics
June 2024
Materials Structural Dynamics Laboratory, Department of Chemistry, Wayne State University, 48202, Detroit, MI, USA.
It remains unclear how the collective strong coupling of cavity-confined photons to the electronic transitions of molecular chromophore leverages the distinct properties of the polaritonic constituents for future technologies. In this study, we design, fabricate, and characterize multiple types of Fabry-Pérot (FP) mirco-resonators containing copper(II) tetraphenyl porphyrin (CuTPP) to show how cavity polariton formation affects radiative relaxation processes in the presence of substantial non-Condon vibronic coupling between two of this molecule's excited electronic states. Unlike the prototypical enhancement of Q state radiative relaxation of CuTPP in a FP resonator incapable of forming polaritons, we find the light emission processes in multimode cavity polariton samples become enhanced for cavity-exciton energy differences near those of vibrations known to mediate non-Condon vibronic coupling.
View Article and Find Full Text PDFLocalized symmetry has been shown to significantly impact the luminescence behavior of Mn ions through the electron-phonon coupling process. Building on this characteristic, three types of inverse spinel structure oxides (MgXO, where X = Ti, Ti/Ge, Ge) doped with Mn were developed, exhibiting strong red emission when exposed to UV and blue light. A thorough examination reveals that the symmetric improvement of the Mn sites within the octahedral environment leads to significant changes in their luminescence behavior, including a suppression of zero-phonon-line (ZPL) emission, a blueshift, and an extension of the luminescence lifetime.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!