Photoinduced Spin Polarization of a Gadolinium Complex

This paper explores the interaction between a photoexcited organic chromophore and a gadolinium(III) ion in a complex, which exhibits an intriguing time evolution of the spin polarization in its electron paramagnetic resonance (EPR) signature. Time-resolved EPR, transient absorption, and photoluminescence spectroscopies combine with results from density functional theory and spectral simulations to allow elucidation of the photochemical mechanism and its impact on the complex's magnetic properties. We show that perturbation of the polarization of a gadolinium(III) ion is possible via photoexcitation of a neighboring, organic chromophore, reflected in the inversion of the lanthanide ion's EPR signal. We, therefore, suggest a new avenue to initialize and manipulate lanthanide-based qudits with potential applications in quantum information science.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-03-11
DOI
https://doi.org/10.1021/jacs.5c20047
Primary Topic
Lanthanide and Transition Metal Complexes
Type
article
Field-Weighted Citation Impact
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article

Photoinduced Spin Polarization of a Gadolinium Complex

Kevin B. Henbest, Christiane R. Timmel, Ashley J. Redman, Stephen Faulkner et al.
Journal of the American Chemical Society
Lanthanide and Transition Metal Complexes
article

Photoinduced Spin Polarization of a Gadolinium Complex

Kevin B. Henbest, Christiane R. Timmel, Ashley J. Redman, Stephen Faulkner, Dániel Kovács, Jonathon Clark, Damyan Frantzov, Ana Štuhec
article en

Abstract

This paper explores the interaction between a photoexcited organic chromophore and a gadolinium(III) ion in a complex, which exhibits an intriguing time evolution of the spin polarization in its electron paramagnetic resonance (EPR) signature. Time-resolved EPR, transient absorption, and photoluminescence spectroscopies combine with results from density functional theory and spectral simulations to allow elucidation of the photochemical mechanism and its impact on the complex's magnetic properties. We show that perturbation of the polarization of a gadolinium(III) ion is possible via photoexcitation of a neighboring, organic chromophore, reflected in the inversion of the lanthanide ion's EPR signal. We, therefore, suggest a new avenue to initialize and manipulate lanthanide-based qudits with potential applications in quantum information science.

Journal of the American Chemical SocietyVol. 148(11)
University of Oxford (GB), Canadian Sleep & Circadian Network (CA)
Openalex Percentile: Top 28%
Lanthanide and Transition Metal Complexes
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