No Arabic abstract
Quantum random number generation (QRNG) harnesses the intrinsic randomness of quantum mechanical phenomena. Demonstrations of such processes have, however, been limited to probabilistic sources, for instance, spontaneous parametric down-conversion or faint lasers, which cannot be triggered deterministically. Here, we demonstrate QRNG with a quantum emitter in hexagonal boron nitride; an emerging solid-state quantum source that can generate single photons on demand and operates at room temperature. We achieve true random number generation through the measurement of single photons exiting one of four integrated photonic waveguides, and subsequently, verify the randomness of the sequences in accordance with the National Institute of Standards and Technology benchmark suite. Our results open a new avenue to the fabrication of on-chip deterministic random number generators and other solid-state-based quantum-optical devices.
Sources of quantum light, in particular correlated photon pairs that are indistinguishable in all degrees of freedom, are the fundamental resource that enables continuous-variable quantum computation and paradigms such as Gaussian boson sampling. Nanophotonic systems offer a scalable platform for implementing sources of indistinguishable correlated photon pairs. However, such sources have so far relied on the use of a single component, such as a single waveguide or a ring resonator, which offers limited ability to tune the spectral and temporal correlations between photons. Here, we demonstrate the use of a topological photonic system comprising a two-dimensional array of ring resonators to generate indistinguishable photon pairs with dynamically tunable spectral and temporal correlations. Specifically, we realize dual-pump spontaneous four-wave mixing in this array of silicon ring resonators that exhibits topological edge states. We show that the linear dispersion of the edge states over a broad bandwidth allows us to tune the correlations, and therefore, quantum interference between photons by simply tuning the two pump frequencies in the edge band. Furthermore, we demonstrate energy-time entanglement between generated photons. We also show that our topological source is inherently protected against fabrication disorders. Our results pave the way for scalable and tunable sources of squeezed light that are indispensable for quantum information processing using continuous variables.
Apparatus for fluorescence-based single photon generation includes collection optics and various setups for characterization. Managing this system often reveals complexity in such a way that adjusting in a small region changes optimal alignments of others. We suggest here a modular system, where the optimal alignment is given to each compartment and tested independently. Based on this concept, we built a system for single photon generation with fluorescence center in hexagonal boron nitride nano-flake, advantageous for scaling up the number of single mode fiber output and a high degree of stability. The system allowed for a practical use of single photon stream extended over an hour with a uniform count rate of small fluctuation levels.
Single photons are fundamental elements for quantum information technologies such as quantum cryptography, quantum information storage and optical quantum computing. Colour centres in diamond have proven to be stable single photon sources and thus essential components for reliable and integrated quantum information technology. A key requirement for such applications is a large photon flux and a high efficiency. Paying tribute to various attempts to maximise the single photon flux we show that collection efficiencies of photons from colour centres can be increased with a rather simple experimental setup. To do so we spin-coated nanodiamonds containing single nitrogen-vacancy colour centres on the flat surface of a ZrO2 solid immersion lens. We found stable single photon count rates of up to 853 kcts/s at saturation under continuous wave excitation while having excess to more than 100 defect centres with count rates from 400 kcts/s to 500 kcts/s. For a blinking defect centre we found count rates up to 2.4 Mcts/s for time intervals of several ten seconds. It seems to be a general feature that very high rates are accompanied by a blinking behaviour. The overall collection efficiency of our setup of up to 4.2% is the highest yet reported for N-V defect centres in diamond. Under pulsed excitation of a stable emitter of 10 MHz, 2.2% of all pulses caused a click on the detector adding to 221 kcts/s thus opening the way towards diamond based on-demand single photon sources for quantum applications.
The ability to generate complex optical photon states involving entanglement between multiple optical modes is not only critical to advancing our understanding of quantum mechanics but will play a key role in generating many applications in quantum technologies. These include quantum communications, computation, imaging, microscopy and many other novel technologies that are constantly being proposed. However, approaches to generating parallel multiple, customisable bi- and multi-entangled quantum bits (qubits) on a chip are still in the early stages of development. Here, we review recent developments in the realisation of integrated sources of photonic quantum states, focusing on approaches based on nonlinear optics that are compatible with contemporary optical fibre telecommunications and quantum memory infrastructures as well as with chip-scale semiconductor technology. These new and exciting platforms hold the promise of compact, low-cost, scalable and practical implementations of sources for the generation and manipulation of complex quantum optical states on a chip, which will play a major role in bringing quantum technologies out of the laboratory and into the real world.
Single photon sources with high brightness and subnanosecond lifetimes are key components for quantum technologies. Optical nanoantennas can enhance the emission properties of single quantum emitters, but this approach requires accurate nanoscale positioning of the source at the plasmonic hotspot. Here, we use plasmonic nanoantennas to simultaneously trap single colloidal quantum dots and enhance their photoluminescence. The nano-optical trapping automatically locates the quantum emitter at the nanoantenna hotspot without further processing. Our dedicated nanoantenna design achieves a high trap stiffness of 0.6 fN/nm/mW for quantum dot trapping, together with a relatively low trapping power of 2 mW/$mu$m$^2$. The emission from the nanoantenna-trapped single quantum dot shows 7x increased brightness, 50x reduced blinking, 2x shortened lifetime and a clear antibunching below 0.5 demonstrating true single photon emission. Combining nano-optical tweezers with plasmonic enhancement is a promising route for quantum technologies and spectroscopy of single nano-objects.