Observation of Binary Spectral Jumps in Color Centers in Diamond
Optical “blinking” normally refers to a switching behavior of fluorescence for quantum emissions between “ON” and “OFF” state. For quantum dots, single molecules, and nitrogen‐vacancy centers in diamond, it usually stems from conversions between two different charge states, with one emitting strong...
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Veröffentlicht in: | Advanced optical materials 2020-10, Vol.8 (19), p.n/a |
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Sprache: | eng |
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Zusammenfassung: | Optical “blinking” normally refers to a switching behavior of fluorescence for quantum emissions between “ON” and “OFF” state. For quantum dots, single molecules, and nitrogen‐vacancy centers in diamond, it usually stems from conversions between two different charge states, with one emitting strong and bright fluorescence while the other scattering weak or no fluorescence. Here, a different type of blinking from single emitters in ion implanted diamond is reported, with both blinking states exhibiting detectable photoluminescence under nonresonant excitation. Thanks to the low jumping rates, the dynamics of the emission can be directly monitored. The quadratic power dependence of the conversion rates suggests the possibility of two‐photon ionization process in quantum jumps. This work provides extra insights into the photodynamics of the spectral jumps on defect‐based single‐photon emitters hosted in wide‐bandgap semiconductors.
Blinking is reported for both quantum dots and defects in nanodiamonds, which is linked to a bright and a dark state. In this work, binary spectral jumps between two bright states are observed from single color centers in diamond under nonresonant excitation. The jumps can be speeded up by increasing excitation power. |
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ISSN: | 2195-1071 2195-1071 |
DOI: | 10.1002/adom.202000495 |