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Babinec, Thomas Michael

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Babinec

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Thomas Michael

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Babinec, Thomas Michael

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Now showing 1 - 4 of 4
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    Readout and Control of a Single Nuclear Spin with a Metastable Electron Spin Ancilla
    (Nature Publishing Group, 2013) Lee, Sang-Yun; Widmann, Matthias; Rendler, Torsten; Doherty, Marcus W.; Babinec, Thomas Michael; Yang, Sen; Eyer, Moritz; Siyushev, Petr; Hausmann, Birgit Judith Maria; Loncar, Marko; Bodrog, Zoltán; Gali, Adam; Manson, Neil B.; Fedder, Helmut; Wrachtrup, Jörg
    Electron and nuclear spins associated with point defects in insulators are promising systems for solid-state quantum technology1, 2, 3. The electron spin is usually used for readout and addressing, and nuclear spins are used as exquisite quantum bits4, 5 and memory systems3, 6. With these systems, single-shot readout of single nuclear spins5, 7 as well as entanglement4, 8, 9, aided by the electron spin, have been shown. Although the electron spin in this example is essential for readout, it usually limits the nuclear spin coherence10, leading to a quest for defects with spin-free ground states9, 11. Here, we isolate a hitherto unidentified defect in diamond and use it at room temperature to demonstrate optical spin polarization and readout with exceptionally high contrast (up to 45%), coherent manipulation of an individual excited triplet state spin, and coherent nuclear spin manipulation using the triplet electron spin as a metastable ancilla. We demonstrate nuclear magnetic resonance and Rabi oscillations of the uncoupled nuclear spin in the spin-free electronic ground state. Our study demonstrates that nuclei coupled to single metastable electron spins are useful quantum systems with long memory times, in spite of electronic relaxation processes.
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    Single-Color Centers Implanted in Diamond Nanostructures
    (Institute of Physics Publishing, 2011) Hausmann, Birgit Judith Maria; Babinec, Thomas Michael; Choy, Jennifer Tze-Heng; Hodges, Jonathan S.; Hong, Sungkun; Bulu, Irfan; Yacoby, Amir; Lukin, Mikhail; Loncar, Marko
    The development of material-processing techniques that can be used to generate optical diamond nanostructures containing a single-color center is an important problem in quantum science and technology. In this work, we present the combination of ion implantation and top-down diamond nanofabrication in two scenarios: diamond nanopillars and diamond nanowires. The first device consists of a 'shallow' implant (similar to 20 nm) to generate nitrogen-vacancy (NV) color centers near the top surface of the diamond crystal prior to device fabrication. Individual NV centers are then mechanically isolated by etching a regular array of nanopillars in the diamond surface. Photon anti-bunching measurements indicate that a high yield (> 10%) of the devices contain a single NV center. The second device demonstrates 'deep' (similar to \(1 \mu m\)) implantation of individual NV centers into diamond nanowires as a post-processing step. The high single-photon flux of the nanowire geometry, combined with the low background fluorescence of the ultrapure diamond, allowed us to observe sustained photon anti-bunching even at high pump powers.
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    Topics in Nanophotonic Devices for Nitrogen-Vacancy Color Centers in Diamond
    (2013-03-14) Babinec, Thomas Michael; Loncar, Marko; Capasso, Federico; Hu, Evelyn
    Recently, developments in novel and high-purity materials allow for the presence of a single, solitary crystalline defect to define the electronic, magnetic, and optical functionality of a device. The discrete nature of the active dopant, whose properties are defined by a quantum mechanical description of its structure, enables radically new quantum investigations and applications in these arenas. Finally,there has been significant development in large-scale device engineering due to mature semiconductor manufacturing techniques. The diverse set of photonic device architectures offering light confinement, guiding, and extraction is a prime example. These three paradigms – solitary dopant photonics and optoelectronics (solotronics), quantum science and technology, and device engineering – merge in the development of novel quantum photonic devices for the next generation of information processing systems. We present in this thesis a series of investigations of optical nanostructures for single optically active spins in single crystal diamond. Chapter 1 introduces the Nitrogen-Vacancy (NV) color center, summarizes its applications, and motivates the need for their integration into photonic structures. Chapter 2 describes two prototype nanobeam photonic crystal cavities for generating strong light-matter interactions with NV centers. The first device consists of a silicon nitride photonic crystal nanobeam cavity with high quality factor \(Q \sim 10^5\) and small mode volume \(V \sim 0.5*(\lambda/n)^3\). The second device consists of a monolithic diamond nanobeam cavity fabricated with the focused ion beam (FIB) directly in a single crystal diamond sample. Chapter 3 presents a high-efficiency source of single photons consisting of a single NV center in a photonic diamond nanowire. Early FIB prototypes are described, as is the first successful realization of the device achieved via reactive ion etching nanowires in a single crystal diamond containing NV centers, and finally a variation of this approach based on incorporation of NV centers in pure diamond via ion implantation. In chapter 4 we consider the optimal design of photonic devices offering both collection efficiency and cavity-enhancements and extend the model of the NV center to include photonic effects. In chapter 5 we briefly introduce a novel optically active spin discovered in a diamond nanowire. Finally, in chapter 6 we conclude with several proposals to extend this research program.
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    Enhanced Single-Photon Emission from a Diamond-Silver Aperture
    (Nature Publishing Group, 2011) Choy, Jennifer Tze-Heng; Hausmann, Birgit Judith Maria; Babinec, Thomas Michael; Bulu, Irfan; Khan, Mughees; Maletinsky, Patrick; Yacoby, Amir; Lončar, Marko
    Solid-state quantum emitters, such as the nitrogen-vacancy centre in diamond, are robust systems for practical realizations of various quantum information processing protocols and nanoscale magnetometry schemes at room temperature. Such applications benefit from the high emission efficiency and flux of single photons, which can be achieved by engineering the electromagnetic environment of the emitter. One attractive approach is based on plasmonic resonators, in which sub-wavelength confinement of optical fields can strongly modify the spontaneous emission of a suitably embedded dipole despite having only modest quality factors. Meanwhile, the scalability of solid-state quantum systems critically depends on the ability to control such emitter–cavity interaction in a number of devices arranged in parallel. Here, we demonstrate a method to enhance the radiative emission rate of single nitrogen-vacancy centres in ordered arrays of plasmonic apertures that promises greater scalability over the previously demonstrated bottom-up approaches for the realization of on-chip quantum networks.