Practical applications of quantum information technologies exploiting the quantum nature of light require efficient and bright true single-photon sources which operate under ambient conditions. Currently, point defects in the crystal lattice of diamond known as color centers have taken the lead in the race for the most promising quantum system for practical non-classical light sources. This work is focused on a different quantum optoelectronic material, namely a color center in silicon carbide, and reveals the physics behind the process of single-photon emission from color centers in SiC under electrical pumping. We show that color centers in silicon carbide can be far superior to any other quantum light emitter under electrical control at room temperature. Using a comprehensive theoretical approach and rigorous numerical simulations, we demonstrate that at room temperature, the photon emission rate from a p-in silicon carbide single-photon emitting diode can exceed 5 Gcounts/s, which is higher than what can be achieved with electrically driven color centers in diamond or epitaxial quantum dots. These findings lay the foundation for the development of practical photonic quantum devices which can be produced in a well-developed CMOS compatible process flow.
Low-power, high-speed and bright electrically driven true single-photon sources, which are able to operate at room temperature, are vital for the practical realization of quantum communication networks and optical quantum computations. Color centers in semiconductors are currently the best candidates, however, in spite of their intensive study in the past decade, the behavior of color centers in electrically controlled systems is poorly understood. Here we present a physical model and establish a theoretical approach to address single-photon emission dynamics of electrically pumped color centers, which interprets experimental results. We support our analysis with self-consistent numerical simulations of a single-photon emitting diode based on a single nitrogen-vacancy center in diamond and predict the second-order autocorrelation function and other emission characteristics. Our theoretical findings demonstrate remarkable agreement with the experimental results and pave the way to the understanding of single-electron/single-photon processes in semiconductors.
The silicon-vacancy (SiV) color center in diamond has recently emerged as a promising qubit for quantum photonics. However, the electrical control and excitation of the SiV centers are challenging due to the low density of free carriers in doped diamond. Here, we realize electrical excitation of SiV centers in a single-crystal diamond membrane, which is promising for scalable photonic architectures. We further demonstrate electrical switching of the charge states of the SiV centers by applying a forward bias voltage to the fabricated diamond-membrane devices and identify the position of the SiV−/SiV0 charge transition level. Our findings provide a perspective toward electrical triggering of color centers in diamond and accelerate the development of scalable quantum nanophotonic technologies.
Efficient generation of single photons on demand at a high repetition rate is a key to the practical realization of quantum-communication networks and optical quantum computations. Color centers in diamond and related wide-bandgap semiconductors are considered to be the most promising candidates for building such single-photon sources owing to the outstanding emission properties at room temperature. However, efficient electrical excitation of color centers in most materials remains a challenge due to the inability to create a high density of free carriers. Here, we predict a superinjection effect in diamond p-i-n diodes. By employing a comprehensive theoretical approach, we numerically demonstrate that one can overcome the doping problem in diamond and inject four orders of magnitude more electrons into the i-region of the diamond p-in diode than the doping of the n-region allows. This high density of free electrons can be efficiently used to boost the single-photon electroluminescence process and enhance the brightness of the diamond single-photon source by more than three orders of magnitude.Moreover, we show that such a high single-photon emission rate can be achieved at exceptionally low injection current densities of only 0.001 A/mm 2 , which creates the backbone for the development of low-power and cost-efficient diamond quantum optoelectronic devices for quantum information technologies.
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