We present a 1 Mpixel single-photon avalanche diode camera featuring 3.8 ns time gating and 24 kfps frame rate, fabricated in 180 nm CMOS image sensor technology. We designed two pixels with a pitch of 9.4 µm in 7 T and 5.75 T configurations respectively, achieving a maximum fill factor of 13.4%. The maximum photon detection probability is 27%, median dark count rate is 2.0 cps, variation in gating length is 120 ps, position skew is 410 ps, and rise/fall time is , all FWHM at 3.3 V excess bias. The sensor was used to capture 2D/3D scenes over 2 m with resolution (least significant bit) of 5.4 mm and precision better than 7.8 mm (rms). We demonstrate extended dynamic range in dual exposure operation mode and show spatially overlapped multi-object detection in single-photon time-gated time-of-flight experiments.
We present a novel guard-ring-sharing technique to push the limit of SPAD pixel miniaturization, and to demonstrate the operation of SPAD arrays with a 2.2 µm-pitch, the smallest ever reported. Device simulation and preliminary tests suggest that the optimized device design ensures the electrical isolation of SPADs with guard-ring sharing. 4×4 SPAD arrays with two parallel selective readout circuits are designed in 180 nm CMOS technology. SPAD characteristics for the pixel pitch of 2.2, 3, and 4 µm are systematically measured as a function of an active diameter, active-to-active distance, and excess bias. For a 4 µm-pitch, the fill factor is 42.4%, the maximum PDP 33.5%, the median DCR 2.5 cps, the timing jitter 88 ps, and the crosstalk probability is 3.57%, while the afterpulsing probability is 0.21%. Finally, we verified the feasibility of the proposed technique towards compact multi-megapixel 3D-stacked SPAD arrays.
With ionic liquid (IL) gating in electric-double-layer transistors (EDLTs), we report field effect operation and electronic state modulation in a layered material of , demonstrating that the EDLT is applicable to modifying the electronic properties of metal dichalcogenides. The IL-gated EDLTs allow us to realize high performance transistor operation and to achieve interfacial carrier accumulation to a level as high as , as quantitatively estimated from the Hall effect. A considerable decrease of the activation energy in temperature-dependent sheet resistance implies that liquid gating is an effective way to tune the electronic states of metal dichalcogenides at EDL interfaces.
Gate-defined quantum dots (QDs) are such a highly-tunable quantum system in which single spins can be electrically coupled, manipulated, and measured. However, the spins in gate-defined QDs are lacking its interface to free-space photons. Here, we verify that a circularly-polarized single photon can excite a single electron spin via the transfer of angular momentum, measured using Pauli spin blockade (PSB) in a double QD. We monitor the inter-dot charge tunneling which only occur when the photo-electron spin in one QD is anti-parallel to the electron spin in the other. This allows us to detect single photo-electrons in the spin-up/down basis using PSB. The photon polarization dependence of the excited spin state was finally confirmed for the heavy-hole exciton excitation. The angular momentum transfer observed here is a fundamental step providing a route to instant injection of spins, distributing single spin information, and possibly towards extending quantum communication.
We detect in real time interdot tunneling events in a weakly coupled two-electron double quantum dot in GaAs. At finite magnetic fields, we observe two characteristic tunneling times and , belonging to, respectively, a direct and a blocked (spin-flip-assisted) tunneling. The latter corresponds to the lifting of a Pauli spin blockade, and the tunneling times ratio characterizes the blockade efficiency. We find pronounced changes in the behavior of upon increasing the magnetic field, with increasing, saturating, and increasing again. We explain this behavior as due to the crossover of the dominant blockade-lifting mechanism from the hyperfine to spin-orbit interactions and due to a change in the contribution of the charge decoherence.