Abstract
Photonic integrated circuits (PICs) are attractive platforms to perform large-scale quantum information processing. While highly functional PICs (e.g., silicon-based photonic circuits) and high-performance single-photon sources [SPSs, e.g., compound-semiconductor quantum dots (QDs)] have been independently demonstrated, their combination for single-photon-based applications has still been limited. This is largely due to the complexities of introducing SPSs into existing PIC platforms, which are generally realized with different materials and using distinct fabrication protocols. Here, we report a novel approach to combine SPSs and PICs prepared independently. We employ transfer printing, by which multiple desired SPSs can be integrated in a simple pick-and-place manner with a theoretical waveguide coupling efficiency , fulfilling the demanding requirements of large-scale quantum applications. Experimentally, we demonstrated QD-based SPSs with high waveguide coupling efficiencies, together with the integration of two SPSs into a waveguide. Our approach will accelerate scalable fusion between modern PICs and cutting-edge quantum technologies.
© 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
The rapid evolution of photonic integrated circuit (PIC) technologies, as represented by the current flourish of silicon photonics [1], is a basis for modern information technologies. State-of-the-art PICs are being used for an expanding array of applications [2], such as photonics-based artificial neural networks [3] with laser light inputs. Introducing quantum light into PICs [4,5] will allow for advanced PIC-based optical information processing, such as linear optical quantum computation [6].
To that end, it is vital to use near-ideal quantum light sources [7]: e.g., it is required that single-photon sources (SPSs) provide single photons with near-unity efficiency, indistinguishability, and purity. Even after the long-term development of diverse SPS technologies [8–10], only a few solid-state materials, including InAs/GaAs semiconductor quantum dots (QDs) [11–15], have currently been proven to potentially fulfill these demanding requirements [7]. As such, the combination of such SPSs with existing high-end PIC platforms is an immediate route for the realization of large-scale quantum PICs.
In this context, the hybrid integration of SPSs into PICs is very promising. In previous demonstrations [16–18], photonic structures for the SPSs and the waveguides have been jointly processed on single wafers made, e.g., by conventional wafer bonding [16]. Such a joint-fabrication process of hybridized material platforms could hinder the highly optimized fabrication of each element: indeed, experimental waveguide coupling efficiencies of so-far demonstrated hybrid SPSs have been limited to around 10% to 40%. The necessary complicated process flows will also hamper the straightforward use of existing PIC platforms that are in general fabricated in specially customized facilities [such as complementally metal-oxide (CMOS) process foundries]. Very recently, the hybrid integration of QD SPSs on silicon waveguides by using a micro manipulator has been reported [19], succeeding in the independent preparation of the SPS and the waveguide for high-quality fabrication. However, the demonstrated waveguide coupling efficiency is still far less than the unity.
In this Letter, we propose and demonstrate an alternative approach based on transfer printing [20–24], by which SPSs and PICs can be prepared independently and integrated easily in a pick-and-place manner. The SPS is based on a QD in a nanocavity and is placed above a waveguide buried in glass, supporting near-perfect theoretical coupling of single-photon emission into the waveguide. Transfer printing largely simplifies the required three-dimensional integration of the optical elements, allowing for the demonstration of QD-based SPSs with high experimental coupling efficiencies as well as the dense integration of two SPSs into a waveguide.
Figure 1 shows the basic flow of the proposed hybrid integration process (see Supplement 1 for more details). First, we prepare a QD wafer [Fig. 1(a)] for the fabrication of nanocavity-based air-bridge SPSs [Fig. 1(b)]. We also use another wafer [Fig. 1(d)] to separately fabricate wire waveguides buried in glass cladding [Fig. 1(e)], which, if necessary, can be prepared by CMOS process foundries [25]. Then, we use transfer printing to pick up a suitable SPS from the processed QD substrate using a transparent rubber stamp [Fig. 1(c)]. We transfer the SPS onto the waveguide under an optical microscope: the SPS can be released on the waveguide by slowly peeling the stamp off [Fig. 1(f)]. A schematic of the completed waveguide-coupled SPS is shown in Fig. 1(g). This structure enables near-unity coupling of QD emission into the waveguide, as discussed later. By pre-selecting suitable SPS candidates prior to the transfer (with appropriate emitter linewidths, positions, and wavelengths), as well as by co-integrating post-tuning functionalities (such as heaters and stressors), the transfer-printing approach may solve major difficulties for incorporating multiple solid-state SPSs, which are often inherently random in their spatial locations and emission wavelengths [7,26].
Our design of the SPS structure allows near-unity coupling of QD radiation into the waveguide. Figures 2(a) and 2(b), respectively, show top-view and cross-sectional schematics of the waveguide-coupled SPS. The nanocavity is based on a one-dimensional photonic crystal (PhC) with local lattice deformation [27–29]. Here we utilize the fundamental cavity mode, which resonates at around 900 nm and possesses a high -factor of and a small mode volume of when located solely on a glass clad without the waveguide. When introducing the waveguide underneath [30], the cavity -factor exhibits an exponential dependence on the cavity–waveguide distance, , as shown in Fig. 2(c). The sharp reduction in stems predominantly from the coupling of light into the waveguide, characterized with a cavity–waveguide coupling efficiency of over 99% for . Further reduction of leads to a degradation of , as the waveguide becomes too close to the cavity and starts to scatter cavity photons into free space. In the design presented here, we tuned the cavity/waveguide parameters to minimize the free space scattering for a given (see Supplement 1).
The emitter–cavity coupling efficiency, , reduces when decreasing cavity due to the reduction of the Purcell effect, which scales with . Nevertheless, even when (), the maximum possible is as large as 99.9%, thanks to the very small . Overall, the theoretical maximum single photon coupling efficiency from the QD into the waveguide, , is deduced to be a near-unity value of 99.7% for (see Supplement 1). We note that such near-unity can be obtained even in different material combinations (see Supplement 1). It is also noteworthy that the SPS design can maintain high efficiencies even under the presence of the misalignment between the cavity and waveguide (see Supplement 1), which is inherent to the transfer printing approach.
Figure 3(a) shows an optical microscope image of a fabricated sample. For the waveguide, we fabricated a glass-clad GaAs structure using transfer printing and spin-on-glass coating (see Supplement 1). From the microscope image, a good alignment between the top nanobeam cavity and the underlying waveguide can be seen. Indeed, there is less than 100 nm position deviation between the nanobeam and the waveguide in the direction (see Supplement 1). This high alignment accuracy was reproducibly obtained in our manual printing process relying on a high-magnification optical microscope. The waveguide is terminated by two exit ports, which are composed of diffraction gratings to direct the single photons into free space [31]. In order to optically characterize this structure, we performed low-temperature photoluminescence (PL) measurements (see Supplement 1). As an initial experiment, we focused a pump laser beam onto the center of the nanocavity and measured a sample image, as displayed in Fig. 3(b). We observed bright light out-coupling from the exit ports, indicating efficient waveguiding of the cavity mode emission.
Then, with low optical pumping to the cavity center, we measured emission spectra of the radiation from one of the exit ports, as shown in Fig. 3(c). In the upper red curve, an intense cavity mode emission at 902.5 nm, together with cavity-coupled QD emission is clearly seen. The measured cavity was 3600, which is 3.6 times smaller than those measured for the nanocavities placed on flat glass. This significant reduction of the -factor suggests a large experimental cavity–waveguide coupling efficiency () of 72% [30]. The estimation is based on the assumption that the -factor reduction here occurs solely by the waveguide coupling (see Supplement 1 for the validity of the assumption and the details of the estimation). The lower, green, spectrum in Fig. 3(c) is of the emission measured above the cavity center. This spectrum does not show the cavity peak, implying that the leakage into free space is largely suppressed, and that the emission occurs predominantly into the waveguide. Here, the largest perturbation to the cavity is provided by the waveguide, which drains the predominant cavity photon leakage and in turn suppresses the radiation into free space. We note that a more direct measurement of will be possible by measuring the transmission spectra of the waveguide–cavity system [30].
We performed further detailed optical characterization of the fabricated sample. Figure 4(a) shows a color plot of the temperature-dependent emission spectra measured through the exit port. We observed an enhancement of the QD emission near the cavity resonance [13,14], suggesting that the increase of is due to the Purcell effect. We also performed time-resolved PL measurements under the QD-cavity resonance, as shown in Fig. 4(b). A rapid decay of the emission with a rate of is observed, which is 3.9 times faster than that of unprocessed QDs (as shown by the gray curve). The estimated emitter–cavity coupling efficiency from these measurements () is 87% (see Supplement 1). Given , the total single-photon coupling efficiency, , is estimated to be 63%. We primarily attribute this non-ideal to the fabrication imperfection of the nanocavity (degrading ) and the non-maximum Purcell effect on the QD presumably due to its position deviation from the field maximum (degrading ). We estimated that, by increasing the intrinsic cavity (without the waveguide coupling) to 50,000, the maximum possible will reach 98.4% (see Supplement 1).
Next we performed second-order correlation measurements based on a Hanbury Brown–Twiss setup when the QD is slightly detuned from the cavity resonance by 0.43 nm. Figure 4(c) shows a measured intensity correlation histogram, exhibiting a clear anti-bunching with a zero delay time value of the second-order coherence function of , demonstrating single-photon generation from the QD. We consider that the relatively large value originates primarily from the intrusion of the background cavity emission supplied by other off-resonant QDs embedded in the cavity and possibly from multiple pump-and-emission processes in the QD within an excitation pulse.
Finally, we extended our method to integrate multiple SPSs into a waveguide, which will be required for the realization of large-scale quantum PICs. For this demonstration, we used the same waveguide platform and were able to integrate two different SPSs by repeating the transfer printing process. A microscope image of the completed sample is shown in Fig. 5(a). The nanocavities are designed to resonate at different wavelengths, such that any disturbance on the transport of single photons by the other cavity is largely suppressed (see Supplement 1). We characterized the optical performance of the two SPSs using PL measurements through the waveguide exit ports, as shown in Figs. 5(b)–5(g). For both SPSs, strong QD emission peaks are observed [Figs. 5(b) and 5(c)]. These peaks show fast radiative decay rates, as can be seen in time-resolved PL spectra for each emission line [Figs. 5(d) and 5(e)], indicating their Purcell-enhanced emission into the cavity modes. From these results, we deduced high efficiencies of 71% and 54% for the left and right SPSs, respectively. In addition, we confirmed that the QD emission peaks exhibit strong anti-bunching, as shown in Figs. 5(f) and 5(g), suggesting the successful integration of two Purcell-enhanced, efficient SPSs into the individual waveguide.
In summary, we have demonstrated the transfer-printing-based integration of QD SPSs into wire waveguides. We have shown that our strategy allows near-unity total single-photon coupling efficiencies into the waveguide, while largely relaxing the difficulties in the hybrid integration of SPSs into PICs. Experimentally, we demonstrated high efficiencies of up to , which we expect will be further improved by elaborating the nanofabrication. We believe that our approach will be a key technology for the fusions between the state-of-the-art SPSs and modern PICs, irrespective of material choice.
Funding
Japan Society for the Promotion of Science (JSPS) (15H05700, 16K06294); New Energy and Industrial Technology Development Organization (NEDO).
Acknowledgment
The authors thank M. Holmes, C. F. Fong, S. Ishida, K. Watanabe, A. Osada, K. Kuruma, A. Tamada, and M. Fuwa for fruitful discussions.
See Supplement 1 for supporting content.
REFERENCES
1. R. Soref, IEEE J. Sel. Top. Quantum Electron. 12, 1678 (2006). [CrossRef]
2. K. Vandoorne, P. Mechet, T. Van Vaerenbergh, M. Fiers, G. Morthier, D. Verstraeten, B. Schrauwen, J. Dambre, and P. Bienstman, Nat. Commun. 5, 3541 (2014). [CrossRef]
3. Y. Shen, N. C. Harris, S. Skirlo, M. Prabhu, T. Baehr-Jones, M. Hochberg, X. Sun, S. Zhao, H. Larochelle, D. Englund, and M. Soljačić, Nat. Photonics 11, 441 (2017). [CrossRef]
4. J. W. Silverstone, D. Bonneau, J. L. O’Brien, and M. G. Thompson, IEEE J. Sel. Top. Quantum Electron. 22, 390 (2016). [CrossRef]
5. J. L. O’Brien, A. Furusawa, J. Vučković, J. L. O. Brien, A. Furusawa, and J. Vučković, Nat. Photonics 3, 687 (2009). [CrossRef]
6. E. Knill, R. Laflamme, and G. J. Milburn, Nature 409, 46 (2001). [CrossRef]
7. I. Aharonovich, D. Englund, and M. Toth, Nat. Photonics 10, 631 (2016). [CrossRef]
8. C. Kurtsiefer, S. Mayer, P. Zarda, and H. Weinfurter, Phys. Rev. Lett. 85, 290 (2000). [CrossRef]
9. X. Ma, N. F. Hartmann, J. K. S. Baldwin, S. K. Doorn, and H. Htoon, Nat. Nanotechnol. 10, 671 (2015). [CrossRef]
10. K. F. Mak and J. Shan, Nat. Photonics 10, 216 (2016). [CrossRef]
11. P. Senellart, G. Solomon, and A. White, Nat. Nanotechnol. 12, 1026 (2017). [CrossRef]
12. J. Claudon, J. Bleuse, N. S. Malik, M. Bazin, P. Jaffrennou, N. Gregersen, C. Sauvan, P. Lalanne, and J.-M. Gérard, Nat. Photonics 4, 174 (2010).
13. X. Ding, Y. He, Z.-C. Duan, N. Gregersen, M.-C. Chen, S. Unsleber, S. Maier, C. Schneider, M. Kamp, S. Höfling, C.-Y. Lu, and J.-W. Pan, Phys. Rev. Lett. 116, 020401 (2016). [CrossRef]
14. N. Somaschi, V. Giesz, L. De Santis, J. C. Loredo, M. P. Almeida, G. Hornecker, S. L. Portalupi, T. Grange, C. Antón, J. Demory, C. Gómez, I. Sagnes, N. D. Lanzillotti-Kimura, A. Lemaítre, A. Auffeves, A. G. White, L. Lanco, and P. Senellart, Nat. Photonics 10, 340 (2016). [CrossRef]
15. M. Arcari, I. Söllner, A. Javadi, S. Lindskov Hansen, S. Mahmoodian, J. Liu, H. Thyrrestrup, E. H. Lee, J. D. Song, S. Stobbe, and P. Lodahl, Phys. Rev. Lett. 113, 093603 (2014). [CrossRef]
16. M. Davanco, J. Liu, L. Sapienza, C.-Z. Zhang, J. V. De Miranda Cardoso, V. Verma, R. Mirin, S. W. Nam, L. Liu, and K. Srinivasan, Nat. Commun. 8, 889 (2017). [CrossRef]
17. I. E. Zadeh, A. W. Elshaari, K. D. Jöns, A. Fognini, D. Dalacu, P. J. Poole, M. E. Reimer, and V. Zwiller, Nano Lett. 16, 2289 (2016). [CrossRef]
18. A. W. Elshaari, I. E. Zadeh, A. Fognini, M. E. Reimer, D. Dalacu, P. J. Poole, V. Zwiller, and K. D. Jöns, Nat. Commun. 8, 379 (2017). [CrossRef]
19. J.-H. Kim, S. Aghaeimeibodi, C. J. K. Richardson, R. P. Leavitt, D. Englund, and E. Waks, Nano Lett. 17, 7394 (2017). [CrossRef]
20. E. Menard, K. J. Lee, D. Y. Khang, R. G. Nuzzo, and J. A. Rogers, Appl. Phys. Lett. 84, 5398 (2004). [CrossRef]
21. A. De Groote, P. Cardile, A. Z. Subramanian, A. M. Fecioru, C. Bower, D. Delbeke, R. Baets, and G. Roelkens, Opt. Express 24, 13754 (2016). [CrossRef]
22. J. Justice, C. Bower, M. Meitl, M. B. Mooney, M. A. Gubbins, and B. Corbett, Nat. Photonics 6, 610 (2012). [CrossRef]
23. H. Yang, D. Zhao, S. Chuwongin, J. Seo, W. Yang, Y. Shuai, J. Berggren, M. Hammar, Z. Ma, and W. Zhou, Nat. Photonics 6, 615 (2012). [CrossRef]
24. J. Lee, I. Karnadi, J. T. Kim, Y.-H. Lee, and M.-K. Kim, ACS Photon. 4, 2117 (2017). [CrossRef]
25. M. Hochberg and T. Baehr-Jones, Nat. Photonics 4, 492 (2010). [CrossRef]
26. C. P. Dietrich, A. Fiore, M. G. Thompson, M. Kamp, and S. Höfling, Laser Photon. Rev. 10, 870 (2016). [CrossRef]
27. P. B. Deotare, M. W. McCutcheon, I. W. Frank, M. Khan, and M. Lončar, Appl. Phys. Lett. 94, 121106 (2009). [CrossRef]
28. R. Ohta, Y. Ota, M. Nomura, N. Kumagai, S. Ishida, S. Iwamoto, and Y. Arakawa, Appl. Phys. Lett. 98, 173104 (2011). [CrossRef]
29. E. Kuramochi, H. Taniyama, T. Tanabe, K. Kawasaki, Y.-G. Roh, and M. Notomi, Opt. Express 18, 15859 (2010). [CrossRef]
30. Y. Halioua, A. Bazin, P. Monnier, T. J. Karle, G. Roelkens, I. Sagnes, R. Raj, and F. Raineri, Opt. Express 19, 9221 (2011). [CrossRef]
31. A. Faraon, I. Fushman, D. Englund, N. Stoltz, P. Petroff, and J. Vuckovic, Opt. Express 16, 12154 (2008). [CrossRef]