Long spin coherence times of nitrogen vacancy centers in milled nanodiamonds
Long spin coherence times of nitrogen vacancy centers in milled nanodiamonds
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DOI:
10.1103/physrevb.105.205401
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发表时间:
2021-12
影响因子:
3.7
通讯作者:
B. D. Wood;G. Stimpson;J. March;Y. Lekhai;C. Stephen;B. Green;A. Frangeskou;L. Gin'es;S. Mandal;O. Williams;Gavin W. Morley
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文献类型:
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作者:
B. D. Wood;G. Stimpson;J. March;Y. Lekhai;C. Stephen;B. Green;A. Frangeskou;L. Gin'es;S. Mandal;O. Williams;Gavin W. Morley
Nanodiamonds containing negatively charged nitrogen vacancy centres (${\text{NV}}^{-}$) have applications as localized sensors in biological material and have been proposed as a platform to probe the macroscopic limits of spatial superposition and the quantum nature of gravity. A key requirement for these applications is to obtain nanodiamonds containing ${\text{NV}}^{-}$ with long spin coherence times. Using milling to fabricate nanodiamonds processes the full 3D volume of the bulk material at once, unlike etching, but has, up to now, limited ${\text{NV}}^{-}$ spin coherence times. Here, we use natural isotopic abundance nanodiamonds produced by ${\text{Si}}_{3}{\text{N}}_{4}$ ball milling of bulk diamond grown by chemical vapour deposition with an average single substitutional nitrogen concentration of $121 ~\text{ppb}$. We show that the electron spin coherence times of ${\text{NV}}^{-}$ centres in these nanodiamonds can exceed $400 ~\mu\text{s}$ at room temperature with dynamical decoupling. Scanning electron microscopy provides images of the specific nanodiamonds containing ${\text{NV}}^{-}$ for which a spin coherence time was measured.