scholarly journals Vibronic Coupling in a Molecular 4f Qubit

Author(s):  
Jonathan Marbey ◽  
Jon G. C. Kragskow ◽  
Christian Dirk Buch ◽  
Joscha Nehrkorn ◽  
Mykhaylo Ozerov ◽  
...  

<p><b>Vibronic coupling, the interaction between molecular vibrations and electronic states, is a pervasive effect that profoundly affects chemical processes. In the case of molecular magnetic materials, vibronic, or spin-phonon, coupling leads to magnetic relaxation, which equates to loss of magnetic memory and loss of phase coherence in molecular magnets and qubits, respectively. The study of vibronic coupling is challenging, and most experimental evidence is indirect. Here we employ far-infrared magnetospectroscopy to probe vibronic transitions in a Yb<sup>III</sup> molecular qubit directly. We find intense signals near electronic states, which we show arise due to an “envelope effect” in the vibronic coupling Hamiltonian, and we calculate the vibronic coupling fully <i>ab initio</i> to simulate the spectra. We subsequently show that vibronic coupling is strongest for vibrational modes that simultaneously distort the first coordination sphere and break the C<sub>3</sub> symmetry of the molecule. With this knowledge, vibrational modes could be identified and engineered to shift their energy towards or away from particular electronic states to alter their impact. Hence, these findings provide new insights towards developing general guidelines for the control of vibronic coupling in molecules.</b></p>

2021 ◽  
Author(s):  
Jonathan Marbey ◽  
Jon G. C. Kragskow ◽  
Christian Dirk Buch ◽  
Joscha Nehrkorn ◽  
Mykhaylo Ozerov ◽  
...  

<p><b>Vibronic coupling, the interaction between molecular vibrations and electronic states, is a pervasive effect that profoundly affects chemical processes. In the case of molecular magnetic materials, vibronic, or spin-phonon, coupling leads to magnetic relaxation, which equates to loss of magnetic memory and loss of phase coherence in molecular magnets and qubits, respectively. The study of vibronic coupling is challenging, and most experimental evidence is indirect. Here we employ far-infrared magnetospectroscopy to probe vibronic transitions in a Yb<sup>III</sup> molecular qubit directly. We find intense signals near electronic states, which we show arise due to an “envelope effect” in the vibronic coupling Hamiltonian, and we calculate the vibronic coupling fully <i>ab initio</i> to simulate the spectra. We subsequently show that vibronic coupling is strongest for vibrational modes that simultaneously distort the first coordination sphere and break the C<sub>3</sub> symmetry of the molecule. With this knowledge, vibrational modes could be identified and engineered to shift their energy towards or away from particular electronic states to alter their impact. Hence, these findings provide new insights towards developing general guidelines for the control of vibronic coupling in molecules.</b></p>


2021 ◽  
Author(s):  
Jon G. C. Kragskow ◽  
Jonathan Marbey ◽  
Christian Dirk Buch ◽  
Joscha Nehrkorn ◽  
Mykhaylo Ozerov ◽  
...  

<p><b>Vibronic coupling, the interaction between molecular vibrations and electronic states, is a pervasive effect that profoundly affects chemical processes. In the case of molecular magnetic materials, vibronic, or spin-phonon, coupling leads to magnetic relaxation, which equates to loss of magnetic memory and loss of phase coherence in molecular magnets and qubits, respectively. The study of vibronic coupling is challenging, and most experimental evidence is indirect. Here we employ far-infrared magnetospectroscopy to probe vibronic transitions in in [Yb(trensal)] (where H<sub>3</sub>trensal = 2,2,2-tris(salicylideneimino)trimethylamine). We find intense signals near electronic states, which we show arise due to an “envelope effect” in the vibronic coupling Hamiltonian, and we calculate the vibronic coupling fully <i>ab initio</i> to simulate the spectra. We subsequently show that vibronic coupling is strongest for vibrational modes that simultaneously distort the first coordination sphere and break the C<sub>3</sub> symmetry of the molecule. With this knowledge, vibrational modes could be identified and engineered to shift their energy towards or away from particular electronic states to alter their impact. Hence, these findings provide new insights towards developing general guidelines for the control of vibronic coupling in molecules.</b></p>


2014 ◽  
Vol 53 (9) ◽  
pp. 4340-4349 ◽  
Author(s):  
Trystan Bennett ◽  
Rohul H. Adnan ◽  
Jason F. Alvino ◽  
Vladimir Golovko ◽  
Gunther G. Andersson ◽  
...  

2007 ◽  
Vol 76 (17) ◽  
Author(s):  
T. Rudolf ◽  
Ch. Kant ◽  
F. Mayr ◽  
J. Hemberger ◽  
V. Tsurkan ◽  
...  

2019 ◽  
Vol 55 (4) ◽  
pp. 541-544 ◽  
Author(s):  
Shuji Ye ◽  
Junjun Tan ◽  
Kangzhen Tian ◽  
Chuanzhao Li ◽  
Jiahui Zhang ◽  
...  

Coherent degenerate infrared-infrared-visible sum frequency generation vibrational spectroscopy provides a powerful label-free probe for identifying the vibrational modes that are coupled through the electronic states in situ and in real time.


2020 ◽  
Vol 56 (75) ◽  
pp. 11062-11065
Author(s):  
Stephanie A. Beach ◽  
Jesse L. Guillet ◽  
Sydney P. Lagueux ◽  
Mauro Perfetti ◽  
Brooke N. Livesay ◽  
...  

PtVO(SOCR)4 lantern complexes and Ce(OAr)3 or Nd(OAr)3 form heterotrimetallic [Ln(OAr)3{PtVO(SOCR)4}] with linear Ln–OVPt linkages; all four exhibit slow magnetic relaxation and likely antiferromagnetic coupling.


1961 ◽  
Vol 35 (3) ◽  
pp. 1059-1071 ◽  
Author(s):  
Robert L. Fulton ◽  
Martin Gouterman

Polyhedron ◽  
1986 ◽  
Vol 5 (3) ◽  
pp. 833-838 ◽  
Author(s):  
J.O. Dziȩgielewski ◽  
B. Jeżowska-Trzebiatowska ◽  
R. Gil-Bortnowska ◽  
R. Grzybek

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