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Extending the Large Molecule Limit: The Role of Fermi Resonance in Developing a Quantum Functional Group.
Zhu, Guo-Zhu; Lao, Guanming; Dickerson, Claire E; Caram, Justin R; Campbell, Wesley C; Alexandrova, Anastassia N; Hudson, Eric R.
Afiliación
  • Zhu GZ; Department of Physics and Astronomy, University of California, Los Angeles, California 90095, United States.
  • Lao G; Department of Physics and Astronomy, University of California, Los Angeles, California 90095, United States.
  • Dickerson CE; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.
  • Caram JR; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.
  • Campbell WC; Center for Quantum Science and Engineering, University of California, Los Angeles, California 90095, United States.
  • Alexandrova AN; Department of Physics and Astronomy, University of California, Los Angeles, California 90095, United States.
  • Hudson ER; Center for Quantum Science and Engineering, University of California, Los Angeles, California 90095, United States.
J Phys Chem Lett ; 15(2): 590-597, 2024 Jan 18.
Article en En | MEDLINE | ID: mdl-38198595
ABSTRACT
Polyatomic molecules equipped with optical cycling centers (OCCs), enabling continuous photon scattering during optical excitation, are exciting candidates for advancing quantum information science. However, as these molecules grow in size and complexity, the interplay of complex vibronic couplings on optical cycling becomes a critical but relatively unexplored consideration. Here, we present an extensive exploration of Fermi resonances in large-scale OCC-containing molecules using high-resolution dispersed laser-induced fluorescence and excitation spectroscopy. These resonances manifest as vibrational coupling leading to intensity borrowing by combination bands near optically active harmonic bands, which require additional repumping lasers for effective optical cycling. To mitigate these effects, we explore altering the vibrational energy level spacing through substitutions on the phenyl ring or changes in the OCC itself. While the complete elimination of vibrational coupling in complex molecules remains challenging, our findings highlight significant mitigation possibilities, opening new avenues for optimizing optical cycling in large polyatomic molecules.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Phys Chem Lett Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Phys Chem Lett Año: 2024 Tipo del documento: Article