Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Nature Physics

Vibrational and electronic dynamics of nitrogen–vacancy centres in diamond revealed by two-dimensional ultrafast spectroscopy

Vanessa M. Huxter, Thomas A. A. Oliver, Dmitry Budker, Graham R. Fleming

Published Sep 29, 2013• 81 citations
Publisher
DOI
10.1038/nphys2753

Related papers

Vibrational and electronic ultrafast relaxation of the nitrogen-vacancy centers in diamond

Vanessa M. Huxter, Thomas A. A. Oliver, Dmitry Budker +1 more

Two dimensional electronic spectroscopy and transient grating measurements were performed, for the first time, on nitrogen-vacancy centers in diamond. These measurements reveal energy transfer and vibrational pathways with consequences for spin coherence.

arXiv:1207.4251•Jul 18, 2012•0 citations

Charge state dynamics of the nitrogen vacancy center in diamond under near-infrared excitation

Ji Peng, Meenakshi Dutt

Bulletin of the American Physical Society•May 26, 2016•0 citations

Near-infrared induced charge dynamics of the nitrogen vacancy center in diamond

David A. Hopper, Richard R. Grote, Annemarie L. Exarhos +1 more

Bulletin of the American Physical Society•Mar 15, 2016•0 citations

Vibrational and electronic ultrafast relaxation of the nitrogen-vacancy centers in diamond

Vanessa M. Huxter, Thomas A. A. Oliver, Dmitry Budker +1 more

Two dimensional electronic spectroscopy and transient grating measurements were performed, for the first time, on nitrogen-vacancy centers in diamond. These measurements reveal energy transfer and vibrational pathways with consequences for spin coherence.

EPJ Web of Conferences•Jan 1, 2013•2 citations

Spectral broadening and ultrafast dynamics of a nitrogen-vacancy center ensemble in diamond

Albert Liu, Steven T. Cundiff, Diogo Burigo Almeida +1 more

Abstract Many applications of nitrogen-vacancy (NV) centers in diamond crucially rely on a spectrally narrow and stable optical zero-phonon line transition. Though many impressive proof-of-principle experiments have been demonstrated, much work remains in engineering NV centers with spectral properties that are sufficiently robust for practical implementation. To elucidate the mechanisms underlying their interactions with the environment, we apply multi-dimensional coherent spectroscopy to an NV center ensemble in bulk diamond at cryogenic temperatures. Our spectra reveal thermal dephasing due to quasi-localized vibrational modes as well as ultrafast spectral diffusion on the picosecond timescale. The intrinsic, ensemble-averaged homogeneous linewidth is found to be in the tens of GHz range by extrapolating to zero temperature. We also observe a temperature-dependent Stark splitting of the excited state manifold, relevant to NV sensing protocols.

arXiv:2011.00153•Materials for Quantum Technology•Mar 29, 2021•36 citations

Infrared Spectroscopy and Vibronic Structure of the Nitrogen-Vacancy Center in Diamond

Pauli Kehayias, Marcus W. Doherty, D. English +7 more

Bulletin of the American Physical Society•Jun 4, 2013•0 citations
Abstract Many applications of nitrogen-vacancy (NV) centers in diamond crucially rely on a spectrally narrow and stable optical zero-phonon line transition. Though many impressive proof-of-principle experiments have been demonstrated, much work remains in engineering NV centers with spectral properties that are sufficiently robust for practical implementation. To elucidate the mechanisms underlying their interactions with the environment, we apply multi-dimensional coherent spectroscopy to an NV center ensemble in bulk diamond at cryogenic temperatures. Our spectra reveal thermal dephasing due to quasi-localized vibrational modes as well as ultrafast spectral diffusion on the picosecond timescale. The intrinsic, ensemble-averaged homogeneous linewidth is found to be in the tens of GHz range by extrapolating to zero temperature. We also observe a temperature-dependent Stark splitting of the excited state manifold, relevant to NV sensing protocols.