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A diamond nanowire single- photon source IIDA Atsushi Miyasaka lab. nature nanotechnology, 2010, 5, 195-199
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Single-molecule detection Single-molecule detection can provide the information which cannot be obtained by ensemble measurements Dye molecule Quencher( 消光剤 ) Direct observation of dynamical state changes Fluctuation Single-molecule detection Ensemble measurement
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Single-photon source Only one photon can be detected at one time. Time Photon number 1 0 0 We consider that a single molecule is a single photon emitter. The high secure communication such as Quantum cryptography ( 量子暗号 ) Application Radiation process
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Requirement 1. Emission efficiency should be high. kfkf knkn k f : radiation rate k n : nonradiation rate k f >> k n quantum dots, fluorescence dyes 2. Detection efficiency should be high. Free-space Waveguide, Nanowire Photons are emitted to all directions. Only two directions Using a detector positioned above optical structure
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Motivation Fabrication of a free-standing diamond nanowire including nitrogen vacancy Comparison of the efficiency between diamond nanowire and bulk diamond crystal. To realize highly efficient single photon emitting source at room temperature
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Contents Introduction Single-molecule spectroscopy Single-photon source Requirement for single photon source Motivation Experiment Nitrogen vacancy (N-V) center Sample Result & Discussion Confocal microscopy Photon anti-bunching Photon correlation Comparison between nanowire and bulk diamond crystal Conclusion
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Nitrogen-vacancy (N-V) center High photostability No-photobleach( 光退色 ) Quantum efficiency ( 量子収率) ≈ 1 Short decay time at excited state Room temperature operation !! Most of the artificial diamond are this type. Diamond: Ⅰ a, Ⅰ b, Ⅱ a, Ⅱ b yellow A two point defect in the diamond lattice 1. Substitutional nitrogen atom 2. Vacancy (missing carbon atom)
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FDTD calculation Finite Difference Time Domain method ( 時間領域差分法 ) Maxwell’s equation Nanowire geometry provides an order of magnitude improvement. low collection efficiency The rate of the leaks to the substrate is large
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Sample Reactive-ion etching O2O2 + ++ prasma negative electrode positive electrode E-beam lithography provide ordered arrays. Etching direction is only perpendicular.
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Sample Straight, smooth sidewall Diameter=260 nm Height=1.9 μ m
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Confocal microscopy 5μm5μm
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12 Photon anti-bunching Beam splitter (50:50) Detector 1 Detector 2 A molecule emits one photon from its one excited state. If you detect photons from a single molecule, there is no possibility to detect two photons by the detector 1 and 2 at the same time. One photon can not be divided. Phenomenon that multiple photons do not exist at the same time.
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Photon correlation Cross-correlation function ( 相関関数 ) Photodetector 1 Photodetector 2 τ1τ1 τ2τ2 τ3τ3 τ4τ4 τ5τ5 τ6τ6 delay time τ 0 τ1τ1 τ2τ2 τ3τ3 τ4τ4 τ5τ5 τ6τ6 Coincidence counts 1 τ=0
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Photon correlation N-V center in diamond nanowire can operate as “single-photon source”. Anti-bunching The fitting function of decay rate; exp(-(r+ Γ)|τ| ) r; excitation rate excited power (P) Γ ; decay rate from excited state = 1/ lifetime 14.6±1.9ns The value in the limit of zero excited power Life-time
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Photon correlation High excitation power metastable state (dark state) ・ Probability of exciting a molecule again The molecule in the metastable state cannot be excited.
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Comparison between nanowire and bulk diamond crystal I Sat (kcps) P Sat ( μW ) nanowire168±3758±37 bulk21±2990±540 nanowire bulk I; number of photon counts per second (cps) P; the power used to saturate the N-V center response In the case of nanowire; The collection efficiency is the order of magnitude larger.
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Conclusion Large number of ordered arrays of diamond nanowire can be fabricated. Photon correlation establishes N-V center embedded in nanowire is considered as single-photon source. The detection efficiency of nanowire is much higher than that of bulk crystal.
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