4.6 Article

Engineering local strain for single-atom nuclear acoustic resonance in silicon

Journal

APPLIED PHYSICS LETTERS
Volume 119, Issue 17, Pages -

Publisher

AIP Publishing
DOI: 10.1063/5.0069305

Keywords

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Funding

  1. Australian Research Council [DP180100969, DP210103769]
  2. U.S. Army Research Office [W911NF-17-1-0200]
  3. Australian Department of Industry, Innovation, and Science [AUSMURI000002]
  4. U.S. Department of Energy, Office of Science, National Quantum Information Science Research Centers (Quantum Systems Accelerator)
  5. Sandia National Laboratories' Laboratory Directed Research and Development program [213048]
  6. DOE's National Nuclear Security Administration [DE-NA0003525]

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The research describes the design of a nanoelectronic device that coherently controls a single nuclear spin through nuclear acoustic resonance using dynamical strain. The strain modulates nuclear quadrupole interaction to drive spin transitions and optimize the NAR drive. By using an AlN piezoelectric actuator and optimizing device layout, NAR Rabi frequencies of order 200 Hz for a single nucleus are predicted in a wide region of the device.
Mechanical strain plays a key role in the physics and operation of nanoscale semiconductor systems, including quantum dots and single-dopant devices. Here, we describe the design of a nanoelectronic device, where a single nuclear spin is coherently controlled via nuclear acoustic resonance (NAR) through the local application of dynamical strain. The strain drives spin transitions by modulating the nuclear quadrupole interaction. We adopt an AlN piezoelectric actuator compatible with standard silicon metal-oxide-semiconductor processing and optimize the device layout to maximize the NAR drive. We predict NAR Rabi frequencies of order 200 Hz for a single Sb-123 nucleus in a wide region of the device. Spin transitions driven directly by electric fields are suppressed in the center of the device, allowing the observation of pure NAR. Using electric field gradient-elastic tensors calculated by the density-functional theory, we extend our predictions to other high-spin group-V donors in silicon and to the isoelectronic Ge-73 atom.

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