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Article

Single- and Twin-Photons Emitted from Fiber-Coupled Quantum Dots in a Distributed Bragg Reflector Cavity

1
State Key Laboratory for Superlattices and Microstructures, Institute of Semiconductors, Chinese Academy of Sciences, Beijing 100083, China
2
Beijing Academy of Quantum Information Sciences, Beijing 100193, China
3
Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, China
*
Author to whom correspondence should be addressed.
Nanomaterials 2022, 12(7), 1219; https://doi.org/10.3390/nano12071219
Submission received: 30 December 2021 / Revised: 9 March 2022 / Accepted: 27 March 2022 / Published: 5 April 2022
(This article belongs to the Special Issue Low-Dimensional Nanomaterials and Their Applications)

Abstract

:
In this work, we develop single-mode fiber devices of an InAs/GaAs quantum dot (QD) by bonding a fiber array with large smooth facet, small core, and small numerical aperture to QDs in a distributed Bragg reflector planar cavity with vertical light extraction that prove mode overlap and efficient output for plug-and-play stable use and extensive study. Modulated Si doping as electron reservoir builds electric field and level tunnel coupling to reduce fine-structure splitting (FSS) and populate dominant XX and higher excitons XX+ and XXX. Epoxy package thermal stress induces light hole (lh) with various behaviors related to the donor field: lh h1 confined with more anisotropy shows an additional XZ line (its space to the traditional X lines reflects the field intensity) and larger FSS; lh h2 delocalized to wetting layer shows a fast h2–h1 decay; lh h2 confined shows D3h symmetric higher excitons with slow h2–h1 decay and more confined h1 to raise h1–h1 Coulomb interaction.

1. Introduction

Semiconductor quantum dots (QDs) have been identified as a promising solid-state quantum emitter with feasible integration of micro-cavities and enhanced coupling to light as compared to real atoms. At stronger pump, several excited carriers presented in a QD lead to multi-exciton states with sharp spectral lines separated energetically by the confinement potentials and Coulomb configuration interactions. Each can be used as a single-photon emitter, and a definite photon-pair emission is built in them. However, QD light extraction relies on microscope optics with fine tuning; its coupling in single-mode (SM) fiber with core diameter (DM) of 2–9 μm [1] for practical use—e.g., time-modulated two-photon interference [2] or inter-QD interference [3]—is usually made by aspheric lens. A direct near-field fiber bond realizes integrated single-QD emitters for a plug-and-play stable use for extensive study. Instead of tapered fiber evanescent lateral coupling [4,5] or cleaved fiber facet vertical coupling [6,7,8] with QD host precisely positioned to the fiber core, an efficient vertical coupling of a QD at wavelength (λ) ~0.9 μm is proved by random bond of V-groove fiber array with large smooth facet and no bend (i.e., angle self-aligned) to QD chip with large-area low-density InAs/GaAs QDs in a distributed Bragg reflector (DBR) cavity for vertical light extraction [9], with coupling efficiency mainly dependent on the cavity; a >3-fold enhancement of fiber-output single-photons has been achieved in an optimal pillar cavity with an intrinsic radiative lifetime < 0.2 ns (Purcell factor > 3) [10]. This work presents our resent study on fiber devices: (1) a planar DBR cavity with only fundamental cavity mode (CM) is bonded to Nurfern 780HP SM fiber (numerical aperture (NA) ~0.13, DM ~4.4 μm) for optical mode overlap (Figure 1a), with single QD selected by small DM and NA, enabling flexible SM-fiber selection (especially DM ~2 μm); (2) modulated Si doping as electron reservoir [11] builds electric field and level tunnel coupling [12] to reduce fine-structure splitting (FSS) and populate dominant X and XX (in pair rate ~12 Mcps) and higher excitons XX+ (2e12h11h2), XXX (2e12h11e21h2), XXX+ (2e12h11e22h2) and XXXX (2e12h12e22h2); (3) epoxy thermal stress induces light hole (lh) h1 and h2 with various distribution in the donor field to affect exciton symmetry, FSS, Coulomb interaction and inter-level decay. The fiber-output XX-X pairs are promising for polarization correlation.

2. Materials and Methods

Dilute InAs QDs are grown in epitaxy on semi-insulating GaAs (001) substrates with a gradient indium flux and subcritical deposition amount [13] and integrated in a planar GaAs/Al0.9Ga0.1As DBR cavity with CM at 910~920 nm (Q~1300). As Figure 1f indicates, QDs with no donor show a dominant X+ from background p-impurity; hole traps induce a secondary X by a slow tunnel capture [14]; delicate modulated Si doping added above QDs populate dominant X and XX. Single-QD region on chip is pre-selected by temperature (T) ~5 K micro-photoluminescence (PL) spectroscopy [15]; the fibers with single-QDs are post-selected by T < 20 K PL spectroscopy by a fused SM fiber 650/980-nm wavelength division multiplexer (WDM, SM28e). For no-space bond, a pressure is added (Figure 1b) during the ultraviolet adhesive (Norland61) curing; bond separation is avoided by epoxy package in copper mount (Figure 1c,d) that remains thermal stress (see Table 1, thermal expansion coefficient, very large for cured epoxy); cured ultraviolet adhesive acts a stress buffer to QD chip. PL spectroscopy is by spectrograph with a low-noise CCD under HeNe laser continuous-wave (cw) pump, power tuned by density filter (DF). Figure 1e illustrates the Hanbury-Brown and Twiss (HBT) setup to measure correlations: fiber device PL output connects a non-polarized 50:50 beamsplitter (BS) after λ > 900 nm longpass (LP) set (optical density, OD > 12 at the laser 633 nm and >4 at the matrix PL, 800~870 nm); exciton lines are filtered by narrowline bandpass (BP) (window λ < 930 nm, tunable by tilt angle, Δλ < 0.5 nm); multi-mode fiber (MMF) with collimator for collection and Si-avalanched photodiode (APD) detectors for photon count; auto/cross-correlations g2(t) between the two detectors are fitted with convolution of the HBT system response function (Gaussian, approximately [16]) for decay time analysis; polarization is selected by a half-wave plane (HWP) or quarter-wave plane (QWP) and a linear polarizer (P), also used to observe FSS oscillation deduced from time-integrated PL spectra [11] and unaffected by bi-refraction in fiber. For pulsed pump, a 640 nm diode laser with repeat rate ~80 MHz and pulse width ~70 ps is used. The radiative lifetime and extraction efficiency are usually measured/estimated under pulsed pump for QDs in flat band. For QD coupled to electron reservoir, the tunnel population is different under cw and pulsed pumps: as seen below, under pulsed pump, higher excitons are populated with XX and X emission efficiency reduced; under cw pump, dominant X and XX populated can be considered as a pure three-level ladder system to study the radiative lifetime and extraction efficiency. Under above-band pump, QD emission includes population and radiation. The exciton intrinsic radiative lifetime is estimated by the decay time in photon correlation under saturation with dense carriers in the barrier for a rapid population. XX with 2e12h1 and independent transitions of two e-h pairs shows an intrinsic radiative lifetime near half that of X, while X+ has the same one as X. As our previous measure of auto-correlations of a dominant X+ shows [12], X+ decay time under saturation is 0.25 ns, reflecting X+ (X) intrinsic radiative lifetime in a DBR cavity with >3-fold Purcell enhancement. Here, QD-fiber device, QD0 undoped, in Figure 1g also shows a dominant X+ with saturated decay time ~0.22 ns and g2(0) ~0.02 (i.e., pure single photon). For QDs coupled to donor levels, the tunnel population is usually dependent on the pump power [12], i.e., electron density in the coupled level. A half-filled coupled level under cw pump shows XX (2e) population time nearly twice that of X (1e) while under pulsed pump with electron reservoir temporally saturated and the coupled level full-filled; X (1e) and XX (2e) tunnel population show nearly the same time. Under saturation with XX and X in comparable intensity, X and XX decay times in auto-correlations are used to estimate their intrinsic radiative lifetimes; the decay time of bunching peak in their cross-correlation reflects the difference of their radiative lifetimes. The fiber extraction efficiency is estimated with dominant XX and X spectral lines under cw pump. This work presents three single-QD fiber devices, QD1~3 with donor fields and level coupling, for illustration. A well selection of single QD (i.e., multi-excitons from the same QD) is reflected. The donor field intensity is well characterized by lh h1 and h2 formed in epoxy package thermal stress; their various distribution in the donor field show lh excitons with different FSS, symmetry, h–h Coulomb interaction and inter-level decay with physical understanding.

3. Results

3.1. Electron Level Coupling and Stress-Induced lh Levels

Figure 2 presents QD2. The auto-correlations show nearly the same decay times for X (0.8 ns) and XX (0.7 ns) under cw pump, while 0.4 ns corresponds to XX under pulsed pump with photoelectrons temporally saturated in reservoir (which is half that of X—0.7 ns); as the decay time of the bunching peak reflects, the difference of X and XX radiative lifetimes is 0.3 ns, so X and XX show intrinsic radiative lifetimes of 0.6 ns and 0.3 ns, respectively, with the remaining 0.2 ns and 0.4 ns representing 1e and 2e tunnel population time under cw pump with the coupled level half-filled, while 0.1 ns corresponds to 1e and 2e tunnel under pulsed pump with the coupled level full-filled. X intrinsic radiative lifetime ~0.6 ns, longer than X+ ~0.25 ns in a DBR cavity, reflects delocalized wave function in the coupled level for slow e-h transition. By fitting experimental data under pulsed pump with double exponential functions, the higher auto-correlation g2(0) (multi-photon probability)—0.3 for X and 0.55 for XX—are obtained, nearly the same under cw pump, due to recapture from reservoir [17], in contrast to near zero g2(0) for a dominant X+ in flat band (QD0 in Figure 1g). In the non-pulse region of auto-correlation, the higher background count in X also reflects a fluent 1e recapture. In fact, QDs here (include QD3 and QD1 in Figure 3) show a prior X appearance under weak pump in power dependence slope of 1.0 and XX in slope of 1.7 (i.e., 1e filling in the coupled level), unlike a prior X in [11] (i.e., 2e filling due to Fermi level pin by a closer donor); the donor field is a little higher to get the minimal FSS: QD3 in a lower field has FSS ~4 μeV while QD2 and QD1 in higher fields show higher FSS. There is an additional X line, XZ, from lh h1 polarized in z-axis coexisting with the traditional X lines (power-dependent spectra in Figure 2c and that of QD3 and QD1 in Figure 3), similar to a strain-tuned GaAs QD [18]; the energy offset between XZ and the traditional X lines reflects e-h separation, Stark shift and donor field intensity: 0.18 meV in QD3 (Figure 3a) in a lower field and 1.68 meV in QD2 (Figure 2) and 1.89 meV in QD1 (Figure 3b) in a higher field, consistent with monolithic increase of FSS from ~4 μeV in QD3 to ~6–12 μeV in QD2 and 35 μeV in QD1, due to lh h1 more confined with more anisotropy in the donor field. In contrast, lh h2 is more delocalized: in QD3 in a lower field with lh h2 coupled to wetting layer, a fast h2–h1 decay is expected and XXī1 (2e11h11h2) shows considerable intensity in a broad linewidth from a fast h2–h1 decay of its transition target X01 (1e11h2); QD1 in a much stronger field with lh h2 decoupled from wetting layer and confined in QD shows higher excitons related to h2 such as X1ī+, Xī1+ (1e11h21h2), X0ī, XXī1, and XX1ī [19]—located around XX [11] with D3h symmetric spectral features and slow h2–h1 decay, unlike C2v featured X and XX with large FSS ~35 μeV; the slow h2–h1 decay is likely from their spatial distribution as the model in Figure 3b inset indicates: the stress at QD base with large strain distribution [20] forms lh h2 strongly confined there in the donor field and leads to lh h1 being more confined (from h2 repulsion) for larger Vhh and slower h2–h1 decay; the more confined h1 contains more anisotropy for larger FSS in XX and X; in QD2 in a high field with lh h2 gradually decoupled from wetting layer by epoxy thermal stress during cryogen circles (see spectra under 2nd and N-th cryogen circles, Figure 2a inset), lh h1 gets more confined to show increased e1–h1 overlap for shaper XZ, FSS raising from 6 to 12 μeV (i.e., e1–h1 overlap increased), X2+, XX+ and XXX blue-shift slightly (i.e., an increased h1–h2 Coulomb interaction). In QD1 in a stronger field with lh h1 more confined, a shape XZ, a large FSS and an increased h1-h1 Coulomb interaction Vhh to enlarge negative XX binding energy EB(XX) = 2Veh − Vee − Vhh [21] as compared to the spectrum before epoxy package (Figure 3b inset, with a slightly negative EB(XX) from the field-reduced Veh, e1–h1 Coulomb interaction) are shown. In QD2, under pulsed pump, XX+, XXX, and XXX+ get relatively stronger (Figure 2a inset), due to rapid tunnel capture of 2e or 3e from reservoir being temporally saturated. In comparison, QD3 shows the highest exciton of XX+, small FSS ~4 μeV, and lower auto-correlation g2(0)—0.18 for X and 0.35 for XX—due to lower donor reservoir, field, and recapture with nearly the same decay time (XX ~0.45 ns and X ~0.4 ns) under cw pump, shorter than QD2, reflecting excitons with less e–h separation in the lower field and shorter radiative lifetimes—X ~0.25 ns and XX ~0.13 ns—with Purcell enhancement kept; the remaining 0.15 ns and 0.32 ns represent 1e and 2e tunnel times. In QD1 in a stronger electric field, the near zero auto-correlation g2(0) for X and XX and their decay times under saturation (X ~0.5 ns and XX ~0.25 ns) reflecting their intrinsic radiative lifetimes, longer than the usual (X ~0.25 ns in a DBR cavity, e.g., QD3 in a lower field) from e–h separation in the field, but smaller than QD2 (X ~0.6 ns), with no tunnel population or recapture due to a large stress field to confine e1 and h1 and improve their overlap (model in Figure 3b inset). In all, the donor field and level tunnel coupling reduce FSS to ~4 μeV, compared to the usual 20~30 μeV in C2v QDs; unlike lh-heavy hole mixing of h1 in a donor field [11], a pure lh h1 is formed in the stress field. The donor and stress field modulate lh h1 and h2 distribution to tune exciton symmetry, FSS, Vhh, and inter-level decay.

3.2. High-Rate Photon Pairs and Polarization Correlation

The fiber devices prove efficient output. The high-rate XX-X pairs are obtained under cw pump with moderate tunnel population when QD can be considered as a pure 3-level ladder system for efficient quantum-pair emission. To estimate the overall fiber-output photon-pair rate under cw pump, the optical route efficiency is estimated by PL spectral peak intensity of an exciton line in QD2. As shown in Figure 4a, it is 12%, including efficiencies of BP (83%), LP (80%), and MMF collection (18%). When XX and X are saturated with comparable intensity (i.e., ~40,000 cts per 0.1 s of its PL peak intensity), XX is filtered and its single-photon rate is measured at Si-APDs, 240 kcps, corresponding to an overall XX-X pair rate ~12 Mcps, taking into account Si-APD efficiency (33% at λ~900 nm) and the optical route efficiency. As shown in Figure 2c, XX becomes dominant under higher pump, with single-photon rate ~21 Mcps as estimated by PL intensity, the same level as a pillar cavity before 1st lens (20~40 Mcps [22]), reflecting QD at the fiber core center with coupling efficiency > 50%, consistent with simulation [23]. For QD with a dominant X+ and radiative lifetime ~0.2 ns (QD0 in Figure 1g), the optimal fiber-output single-photon rate will be the same ~20 Mcps. Figure 4b presents polarization-resolved XX-X correlations in QD2 (FSS ~12 μeV): most clear in HH basis; high in HV, DD and DA from cross-dephasing, carrier scattering or fiber bi-refraction that projects single-photon polarization in H or V to reduce polarization correlation, and nearly zero in RR and RL, reflecting independent HH and VV emissions with little superposition for R and L. The correlations are lower under pulsed pump with the barrier carriers temporally saturated for scattering. For QD3 (FSS ~4 μeV), similarly, the most clear polarization correlation is shown in HH basis; the theoretically predicted entanglement degree is >0.5 [24], but ~0.38 under low pump with fewer barrier carriers for scattering, reflecting fiber bi-refraction to project single-photon polarizations and degrade their polarization correlation, understood through math (α is the phase between H and V):
DD = (H + eV)(H + eV)/2 = (HH + ei2αVV)/2 + eHV
DA = (H + eV)(H − eV)/2 = (HH − ei2αVV)/2
The noisy correlation could be improved by reducing ‘cross-talk’ in HBT setup and back reflection in fibers. To use the fiber-output photon pairs for detection, a post-selection of polarization and time bin is used to recover the HH/VV correlation (see Figure 4c). More desired, H and V polarizations can be kept in polarization-maintaining fiber, PM780HP, for entanglement usage or resonant excitation. The fiber coupling efficiency can be further improved by using SM fibers with tapered facet [25] or high NA [26].

4. Conclusions

In this work, we optimize the fabrication of single quantum dot (QD) fiber devices and achieve XX-X pair rate ~12 Mcps for plug-and-play stable use and study. QDs coupled to the donor electric field show smaller FSS and higher exciton population. Epoxy stress-induced light hole (lh) h1 confined in QD raises FSS; lh h2 delocalized fastens h2–h1 decay; lh h2 confined shows D3h symmetric excitons and more confined h1 with slow h2–h1 decay and large h1–h1 Coulomb interaction. The combined donor field and stress field to tune lh h1 and h2 distribution to affect QD exciton behaviors, e.g., FSS, is promising for a physical understanding and a proper design of the hybrid QD structure.

Author Contributions

X.S. (Xiangjun Shang), H.H., D.D, X.L., Y.L. and Y.G. took part in the fabrication of the QD fiber devices. S.L., H.L., X.S. (Xiangbin Su) and H.N. took part in the sample growth. X.S. (Xiangjun Shang), H.L. and D.D. took part in the optical measurements. X.S. (Xiangjun Shang) wrote the manuscript. X.D. and H.N. participated in the discussions. H.N. and Z.N. supervised the writing of manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research work is supported by the National Key Technologies R&D Program of China (Grant No. 2018YFB2200504), the Science and Technology Program of Guangzhou (Grant No. 202103030001), the Key-Area Research and Development Program of Guangdong Province (Grant No. 2018B030329001), the National Natural Science Foundation of China (Grant Nos. 62035017, 61505196), the Scientific Instrument Developing Project of Chinese Academy of Sciences (Grant No. YJKYYQ20170032), and the Program of Beijing Academy of Quantum Information Sciences (Grant No. Y18G01).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. (a) Schematic fiber coupling of a QD in a planar DBR cavity; (b) spring pressure at QD chip backside for bond; (c) model and (d) real image of epoxy package (dark blue) and copper mount (yellow), cured ultraviolet adhesive (light blue) as a stress buffer, and a ceramic ferrule as fiber interface; (e) setup for PL spectroscopy and photon correlations, inset: fused SM fiber BS (780HP, Thorlabs) sometimes used; (f) PL spectra of single-QDs on sample: (left): intrinsic, (middle): near hole defects, (right): near Si donors; (g) PL spectrum of fiber-coupled single QD, QD0 with a dominant X+ and higher XX+ and X2+; inset: X+ auto-correlation with theoretical (red) and convoluted (blue) fitting.
Figure 1. (a) Schematic fiber coupling of a QD in a planar DBR cavity; (b) spring pressure at QD chip backside for bond; (c) model and (d) real image of epoxy package (dark blue) and copper mount (yellow), cured ultraviolet adhesive (light blue) as a stress buffer, and a ceramic ferrule as fiber interface; (e) setup for PL spectroscopy and photon correlations, inset: fused SM fiber BS (780HP, Thorlabs) sometimes used; (f) PL spectra of single-QDs on sample: (left): intrinsic, (middle): near hole defects, (right): near Si donors; (g) PL spectrum of fiber-coupled single QD, QD0 with a dominant X+ and higher XX+ and X2+; inset: X+ auto-correlation with theoretical (red) and convoluted (blue) fitting.
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Figure 2. (a) PL spectra of single-QD fiber, QD2 in donor field with level coupling. Insets: spectrum under pulsed pump; spectra in 2nd (red) and N-th (black) cryogen circles with shift of X2+, XX+, and XXX; sharper XZ and raising FSS from 6 to 12 μeV; intensity pump power dependence. (b) Photon auto-/cross-correlations under cw and pulsed pumps with theoretical (red) and convoluted (blue) fitting, decay times given; FSS oscillation of XX and X. (c) Cw pump power-dependent spectra.
Figure 2. (a) PL spectra of single-QD fiber, QD2 in donor field with level coupling. Insets: spectrum under pulsed pump; spectra in 2nd (red) and N-th (black) cryogen circles with shift of X2+, XX+, and XXX; sharper XZ and raising FSS from 6 to 12 μeV; intensity pump power dependence. (b) Photon auto-/cross-correlations under cw and pulsed pumps with theoretical (red) and convoluted (blue) fitting, decay times given; FSS oscillation of XX and X. (c) Cw pump power-dependent spectra.
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Figure 3. PL spectra of single-QD fibers, (a) QD3 in lower donor field with small FSS and (b) QD1 in stronger field with large FSS and negative EB enlarged by stress. (c) Schematic e and h distribution. QD1 in stress field with e and h confined for more overlap shows X and XX with shorter decay time and higher excitons in D3h symmetry (confined lh h1 and h2, model in inset). Insets: FSS oscillation, photon correlations with similar fitting, QD1 spectrum before epoxy coverage.
Figure 3. PL spectra of single-QD fibers, (a) QD3 in lower donor field with small FSS and (b) QD1 in stronger field with large FSS and negative EB enlarged by stress. (c) Schematic e and h distribution. QD1 in stress field with e and h confined for more overlap shows X and XX with shorter decay time and higher excitons in D3h symmetry (confined lh h1 and h2, model in inset). Insets: FSS oscillation, photon correlations with similar fitting, QD1 spectrum before epoxy coverage.
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Figure 4. (a) PL spectra of QD2 to stimate optical route efficiency. The intensity ratio for integrated time 0.1 s and 1 s is estimated by X peak intensity under low pump p350, i.e., 52,357/7570 = 6.9 (less than 10 due to CCD processing time), which has been checked for many QDs, so the direct unfiltered spectrum for integrated time of 0.1 s with peak intensity of 41,391 will be 41,391 × 6.9 = 286,276 at peak intensity for integrated time of 1 s. The optical route efficiency is estimated by the filtered XX peak intensity of 17,649 (one beam) and the direct unfiltered one of 286,276, 17,649 × 2/286,276 = 12%. BP efficiency is estimated by BP filtered and unfiltered XX peak intensity: 17,649/21,308 = 83%. LP efficiency is estimated by its filtered and unfiltered XX peak intensity: 21,308/26,511 = 80%. The filtered XX line (inset: semi-log plot) shows photon count rate ~240k cps at APDs, so the overall fiber-output single-photon rate is 240k/17,649 × 286,276/0.33 = 12 Mcps for XX and X in comparable intensity, taking into account Si-APD efficiency. (b) Polarization-resolved XX-X cross-correlations under cw and pulsed pumps. (c) Post-selection to prepare HH/VV correlation. (pink region) Setup: a 2 × 2 fused fiber BS to split light, a SM fiber for delay in one beam, two P orthogonal polarized to select HH (VV) polarized photon pairs in each beam, a BS to group them and separate XX and X for output, filtered by BPs. (bottom right) Measurement results of polarization-resolved XX-X correlations with polarization in each output selected by a P. HH and VV show bunching at zero delay while HV and VH show bunching at large delays defined by the delay fiber length, which can be as long as ~km and neglected in time bin selection (dashed rectangular).
Figure 4. (a) PL spectra of QD2 to stimate optical route efficiency. The intensity ratio for integrated time 0.1 s and 1 s is estimated by X peak intensity under low pump p350, i.e., 52,357/7570 = 6.9 (less than 10 due to CCD processing time), which has been checked for many QDs, so the direct unfiltered spectrum for integrated time of 0.1 s with peak intensity of 41,391 will be 41,391 × 6.9 = 286,276 at peak intensity for integrated time of 1 s. The optical route efficiency is estimated by the filtered XX peak intensity of 17,649 (one beam) and the direct unfiltered one of 286,276, 17,649 × 2/286,276 = 12%. BP efficiency is estimated by BP filtered and unfiltered XX peak intensity: 17,649/21,308 = 83%. LP efficiency is estimated by its filtered and unfiltered XX peak intensity: 21,308/26,511 = 80%. The filtered XX line (inset: semi-log plot) shows photon count rate ~240k cps at APDs, so the overall fiber-output single-photon rate is 240k/17,649 × 286,276/0.33 = 12 Mcps for XX and X in comparable intensity, taking into account Si-APD efficiency. (b) Polarization-resolved XX-X cross-correlations under cw and pulsed pumps. (c) Post-selection to prepare HH/VV correlation. (pink region) Setup: a 2 × 2 fused fiber BS to split light, a SM fiber for delay in one beam, two P orthogonal polarized to select HH (VV) polarized photon pairs in each beam, a BS to group them and separate XX and X for output, filtered by BPs. (bottom right) Measurement results of polarization-resolved XX-X correlations with polarization in each output selected by a P. HH and VV show bunching at zero delay while HV and VH show bunching at large delays defined by the delay fiber length, which can be as long as ~km and neglected in time bin selection (dashed rectangular).
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Table 1. Thermal expansion coefficient (α) of materials used in fiber bond.
Table 1. Thermal expansion coefficient (α) of materials used in fiber bond.
MaterialsGaAsInAsAl0.9Ga0.1AsSilicaCured EpoxyCopper
α (10−6/K)5.74.55.20.55718
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MDPI and ACS Style

Shang, X.; Li, S.; Liu, H.; Su, X.; Hao, H.; Dai, D.; Li, X.; Li, Y.; Gao, Y.; Dou, X.; et al. Single- and Twin-Photons Emitted from Fiber-Coupled Quantum Dots in a Distributed Bragg Reflector Cavity. Nanomaterials 2022, 12, 1219. https://doi.org/10.3390/nano12071219

AMA Style

Shang X, Li S, Liu H, Su X, Hao H, Dai D, Li X, Li Y, Gao Y, Dou X, et al. Single- and Twin-Photons Emitted from Fiber-Coupled Quantum Dots in a Distributed Bragg Reflector Cavity. Nanomaterials. 2022; 12(7):1219. https://doi.org/10.3390/nano12071219

Chicago/Turabian Style

Shang, Xiangjun, Shulun Li, Hanqing Liu, Xiangbin Su, Huiming Hao, Deyan Dai, Xiaoming Li, Yuanyuan Li, Yuanfei Gao, Xiuming Dou, and et al. 2022. "Single- and Twin-Photons Emitted from Fiber-Coupled Quantum Dots in a Distributed Bragg Reflector Cavity" Nanomaterials 12, no. 7: 1219. https://doi.org/10.3390/nano12071219

APA Style

Shang, X., Li, S., Liu, H., Su, X., Hao, H., Dai, D., Li, X., Li, Y., Gao, Y., Dou, X., Ni, H., & Niu, Z. (2022). Single- and Twin-Photons Emitted from Fiber-Coupled Quantum Dots in a Distributed Bragg Reflector Cavity. Nanomaterials, 12(7), 1219. https://doi.org/10.3390/nano12071219

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