Abstract

In this paper, we demonstrate an active control of the charge state of a single nitrogen-vacancy (NV) centre by using in-plane Schottky-diode geometries with aluminium on hydrogen-terminated diamond surface. A switching between NV+, NV0 and NV− can be performed with the Al-gates which apply electric fields in the hole depletion region of the Schottky junction that induces a band bending modulation, thereby shifting the Fermi-level over NV charge transition levels. We simulated the in-plane band structure of the Schottky junction with the Software ATLAS by solving the drift-diffusion model and the Poisson-equation self-consistently. We simulated the IV-characteristics, calculated the width of the hole depletion region, the position of the Fermi-level intersection with the NV charge transition levels for different reverse bias voltages applied on the Al-gate. We can show that the field-induced band bending modulation in the depletion region causes a shifting of the Fermi-level over NV charge transition levels in such a way that the charge state of a single NV centre and thus its electrical and optical properties is tuned. In addition, the NV centre should be approx. 1–2 μm away from the Al-edge in order to be switched with moderate bias voltages.

Highlights

  • Our confocal microscope set-up is equipped with a diode-pumped and frequency-doubled Nd:YAG-laser operating at a wavelength of 532 nm with an output power of 5 mW and a commercial confocal microscope (LabRam BX41, Horiba Jobin Yvon)

  • The process parameters used were 210 mbar gas pressure at a gas flow of 290 sccm H2 and 10 sccm CH4 and a microwave power of 2.1 kW

  • The laser beam is passed to the microscope through an optical fibre and focused onto the sample by the microscope objective

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Summary

Introduction

Our confocal microscope set-up is equipped with a diode-pumped and frequency-doubled Nd:YAG-laser operating at a wavelength of 532 nm with an output power of 5 mW and a commercial confocal microscope (LabRam BX41, Horiba Jobin Yvon). The laser beam is passed to the microscope through an optical fibre and focused onto the sample by the microscope objective. The laser power illuminating the sample is 1 mW due to losses in the optical path of the microscope setup. The resulting photoluminescence signal is collected by the same objective and the excitation wavelength is spectrally filtered out using notch filter. The light beam is subsequently focused onto a pinhole for spatial filtering and routed via a fibre to a monochromator (iHR-320, Horiba Jobin Yvon). As detector a Peltier-cooled CCD-Camera (SYNAPSE, Horiba Jobin Yvon) was us

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