Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond
Single-photon emission from the nitrogen-vacancy defect in diamond constitutes one of its many proposed applications. Owing to its doubly degenerate 3E electronic excited state, photons from this defect can be emitted by two optical transitions with perpendicular polarization. Previous measurements...
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sg-ntu-dr.10356-839032023-02-28T19:38:46Z Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond Ulbricht, Ronald Dong, Shuo Chang, I-Ya Mariserla, Bala Murali Krishna Dani, Keshav M. Hyeon-Deuk, Kim Loh, Zhi-Heng School of Physical and Mathematical Sciences Chemical Physics Optical Properties of Diamond Single-photon emission from the nitrogen-vacancy defect in diamond constitutes one of its many proposed applications. Owing to its doubly degenerate 3E electronic excited state, photons from this defect can be emitted by two optical transitions with perpendicular polarization. Previous measurements have indicated that orbital-selective photoexcitation does not, however, yield photoluminescence with well-defined polarizations, thus hinting at orbital-averaging dynamics even at cryogenic temperatures. Here we employ femtosecond polarization anisotropy spectroscopy to investigate the ultrafast electronic dynamics of the 3E state. We observe subpicosecond electronic dephasing dynamics even at cryogenic temperatures, up to five orders of magnitude faster than dephasing rates suggested by previous frequency- and time-domain measurements. Ab initio molecular dynamics simulations assign the ultrafast depolarization dynamics to nonadiabatic transitions and phonon-induced electronic dephasing between the two components of the 3E state. Our results provide an explanation for the ultrafast orbital averaging that exists even at cryogenic temperatures. ASTAR (Agency for Sci., Tech. and Research, S’pore) MOE (Min. of Education, S’pore) Published version 2017-07-14T05:08:54Z 2019-12-06T15:34:16Z 2017-07-14T05:08:54Z 2019-12-06T15:34:16Z 2016 Journal Article Ulbricht, R., Dong, S., Chang, I.-Y., Mariserla, B. M. K., Dani, K. M., Hyeon-Deuk, K., et al. (2016). Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond. Nature Communications, 7, 13510-. 2041-1723 https://hdl.handle.net/10356/83903 http://hdl.handle.net/10220/42864 10.1038/ncomms13510 en Nature Communications © 2016 The Author(s). This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ 6 p. application/pdf |
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Chemical Physics Optical Properties of Diamond Ulbricht, Ronald Dong, Shuo Chang, I-Ya Mariserla, Bala Murali Krishna Dani, Keshav M. Hyeon-Deuk, Kim Loh, Zhi-Heng Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond |
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Single-photon emission from the nitrogen-vacancy defect in diamond constitutes one of its many proposed applications. Owing to its doubly degenerate 3E electronic excited state, photons from this defect can be emitted by two optical transitions with perpendicular polarization. Previous measurements have indicated that orbital-selective photoexcitation does not, however, yield photoluminescence with well-defined polarizations, thus hinting at orbital-averaging dynamics even at cryogenic temperatures. Here we employ femtosecond polarization anisotropy spectroscopy to investigate the ultrafast electronic dynamics of the 3E state. We observe subpicosecond electronic dephasing dynamics even at cryogenic temperatures, up to five orders of magnitude faster than dephasing rates suggested by previous frequency- and time-domain measurements. Ab initio molecular dynamics simulations assign the ultrafast depolarization dynamics to nonadiabatic transitions and phonon-induced electronic dephasing between the two components of the 3E state. Our results provide an explanation for the ultrafast orbital averaging that exists even at cryogenic temperatures. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Ulbricht, Ronald Dong, Shuo Chang, I-Ya Mariserla, Bala Murali Krishna Dani, Keshav M. Hyeon-Deuk, Kim Loh, Zhi-Heng |
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Article |
author |
Ulbricht, Ronald Dong, Shuo Chang, I-Ya Mariserla, Bala Murali Krishna Dani, Keshav M. Hyeon-Deuk, Kim Loh, Zhi-Heng |
author_sort |
Ulbricht, Ronald |
title |
Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond |
title_short |
Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond |
title_full |
Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond |
title_fullStr |
Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond |
title_full_unstemmed |
Jahn-Teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond |
title_sort |
jahn-teller-induced femtosecond electronic depolarization dynamics of the nitrogen-vacancy defect in diamond |
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2017 |
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https://hdl.handle.net/10356/83903 http://hdl.handle.net/10220/42864 |
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1759853910284042240 |