Nonvolatile Multilevel Photomemory Based on Lead-Free Double Perovskite Cs2AgBiBr6 Nanocrystals Wrapped Within SiO2 as a Charge Trapping Layer.

Floating gate transistor photomemory (FGTPM) has been regarded as one of the most prospective nonvolatile photomemory devices because of its compatibility with transistor-based circuits, nondestructive reading, and multilevel storage. Until now, owing to the excellent photoelectric properties, lead-based perovskite nanocrystals (PNCs) have been applied in most of the perovskite-based FGTPM devices and embedded in the polymer matrix as the charge trapping layer. However, the polymer matrix and its solvent would degrade the structure of the PNCs, resulting in the loss of their unique photoresponse ability. In addition, lead-based perovskites have environmental unfriendliness and poor stability. Hence, a novel nonvolatile FGTPM based on oligomeric silica (OS) wrapped lead-free double perovskite Cs2AgBiBr6 NCs was demonstrated for the first time. Acting synchronously as the protection layer for the discrete Cs2AgBiBr6 NCs and charge tunneling layer for the FGTPM device, the OS layer can achieve controllable thickness by adjusting the process parameters, leading to an adjustment of storage properties with a larger memory window (58 V). Owing to the excellent photoresponse ability of the Cs2AgBiBr6@OS composite layer, the FGTPM device exhibited high-performance with repeatable multilevel nonvolatile photomemory and precise photoresponse ability of wavelength/time/power-dependent photoirradiation without extra gate biasing.

Synaptic Transistor Capable of Accelerated Learning Induced by Temperature-Facilitated Modulation of Synaptic Plasticity.

Neuromorphic computation, which emulates the signal process of the human brain, is considered to be a feasible way for future computation. Realization of dynamic modulation of synaptic plasticity and accelerated learning, which could improve the processing capacity and learning ability of artificial synaptic devices, is considered to further improve energy efficiency of neuromorphic computation. Nevertheless, realization of dynamic regulation of synaptic weight without an external regular terminal and the method that could endow artificial synaptic devices with the ability to modulate learning speed have rarely been reported. Furthermore, finding suitable materials to fully mimic the response of photoelectric stimulation is still challenging for photoelectric synapses. Here, a floating gate synaptic transistor based on an L-type ligand-modified all-inorganic CsPbBr3 perovskite quantum dots is demonstrated. This work provides first clear experimental evidence that the synaptic plasticity can be dynamically regulated by changing the waveforms of action potential and the environment temperature and both of these parameters originate from and are crucial in higher organisms. Moreover, benefiting from the excellent photoelectric properties and stability of quantum dots, a temperature-facilitated learning process is illustrated by the classical conditioning experiment with and without illumination, and the mechanism of synaptic plasticity is also demonstrated. This work offers a feasible way to realize dynamic modulation of synaptic weight and accelerating the learning process of artificial synapses, which showed great potential in the reduction of energy consumption and improvement of efficiency of future neuromorphic computing.

Ultrastable Quantum Dot Composite Films under Severe Environments.

Semiconductor quantum dots (QDs) have attracted extensive attention because of their remarkable optical and electrical characteristics. However, the practical application of QDs and further the QD composite films have greatly been hindered mainly owing to their essential drawbacks of extreme unstability under oxygen and water environments. Herein, one simple method has been employed to enhance enormously the stability of Cd xZn1- xSe yS1- y QD composite films by a combination of Cd xZn1- xSe yS1- y QDs and poly(vinylidene) fluoride (PVDF), which is characteristic of closely arranged molecular chains and strong hydrogen bonds. There are many particular advantages in using QD/PVDF composite films such as easy processing, low cost, large-area fabrication, and especially extreme stability even in the boiling water for more than 240 min. By employing K2SiF6:Mn4+ as a red phosphor, a prototype white light-emitting diode (WLED) with color coordinates of (0.3307, 0.3387), Tc of 5568 K, and color gamut 112.1NTSC(1931)% at 20 mA has been fabricated, and there is little variation under different excitation currents, indicating that the QD/PVDF composite films fabricated by this simple blade-coating process make them ideal candidates for liquid-crystal display backlight utilization via assembling a WLED on a large scale owing to its ultrahigh stability under severe environments.

Fluorescence Polarization Switching from a Single Silicon Vacancy Colour Centre in Diamond.

Single-photon emitters with stable and uniform photoluminescence properties are important for quantum technology. However, in many cases, colour centres in diamond exhibit spectral diffusion and photoluminescence intensity fluctuation. It is therefore essential to investigate the dynamics of colour centres at the single defect level in order to enable the on-demand manipulation and improved applications in quantum technology. Here we report the polarization switching, intensity jumps and spectral shifting observed on a negatively charged single silicon-vacancy colour centre in diamond. The observed phenomena elucidate the single emitter dynamics induced by photoionization of nearby electron donors in the diamond.

Magnetic-based Fano resonance of hybrid silicon-gold nanocavities in the near-infrared region.

Direct interference between the orthogonal electric and magnetic modes in a hybrid silicon-gold nanocavity is demonstrated to induce a pronounced asymmetric magnetic-based Fano resonance in the total scattering spectrum at near-infrared frequencies. Differing from the previously reported magnetic-based Fano resonances in metal nanoparticle clusters, the narrow discrete mode provided by the silicon magnetic dipole resonance can be directly excited by external illumination, and greatly enhanced electric and magnetic fields are simultaneously obtained at the Fano dip.

Controllable Synthesis and Peculiar Optical Properties of Lanthanide-Doped Fluoride Nanocrystals.

Yb3+ /Tm3+ -codoped NaYF4 nanocrystals with different phases (cubic α and hexagonal ß) and morphologies (nanoparticles, nanorods, nanoplates) have been controllably fabricated by a convenient hydrothermal synthesis technique. Up-conversion emission peaks were observed at λ=450, 475, 645, and 700 nm, which were assigned to the 1 D2 -3 F4 , 1 G4 -3 H6 , 1 G4 -3 F4 , and 3 F2 -3 H6 transitions of Tm3+ ions, respectively. By using a homemade detection system, the anisotropic polarized emission properties of individual NaYF4 :Yb, Tm nanorods and nanoplates were investigated. The results indicated that the polarization emission ratio, ρ, of the 1 G4 -3 F4 emission of individual NaYF4 :Yb,Tm nanorods was 0.18, whereas the anisotropic polarization emission of individual NaYF4 :Yb,Tm nanoplates could be neglected; this indicated that the size and morphology of the nanocrystal played an important role in the polarized emission properties. Investigation into the mechanism indicated that the dielectric mismatch was not the predominant mechanism for the polarized emission of individual NaYF4 :Yb,Tm nanorods. The as-prepared NaYF4 :Yb,Tm nanocrystals, with controllable morphology and anisotropic polarized emission properties, are expected to be widely applied as polarized light resources, bio-labels, photodetectors, and so forth.

Fabrication of nitrogen vacancy color centers by femtosecond pulse laser illumination.

We report on a novel method to fabricate single, multiple and large-area high-density ensembles of nitrogen vacancy (NV) color centers in synthetic type Ib bulk diamond by femtosecond laser illumination. Electron beams generated in propagation of intense infrared laser pulses in air sputtered on a diamond sample under high temperature aroused by the laser illumination, creating NV color centers. Typical photoluminescence (PL) spectra of NV centers could be observed on the illuminated spots. Photon streams from individual photoluminescent points exhibited anti-bunching effect by the second-order correlation measurement, evidencing single and multiple photon-emitters around the laser illuminated spots.

Ultrasensitive polarized up-conversion of Tm(3+)-Yb3+ doped ß-NaYF4 single nanorod.

Up-conversion luminescence in rare earth ions (REs) doped nanoparticles has attracted considerable research attention for the promising applications in solid-state lasers, three-dimensional displays, solar cells, biological imaging, and so forth. However, there have been no reports on REs doped nanoparticles to investigate their polarized energy transfer up-conversion, especially for single particle. Herein, the polarized energy transfer up-conversion from REs doped fluoride nanorods is demonstrated in a single particle spectroscopy mode for the first time. Unique luminescent phenomena, for example, sharp energy level split and singlet-to-triplet transitions at room temperature, multiple discrete luminescence intensity periodic variation with polarization direction, are observed upon excitation with 980 nm linearly polarized laser. Furthermore, nanorods with the controllable aspect ratio and symmetry are fabricated for analysis of the mechanism of polarization anisotropy. The comparative experiments suggest that intraions transition properties and crystal local symmetry dominate the polarization anisotropy, which is also confirmed by density functional theory calculations. Taking advantage of the REs based up-conversion, potential application in polarized microscopic multi-information transportation is suggested for the polarization anisotropy from REs doped fluoride single nanorod or nanorod array.

Polarization properties of surface plasmon enhanced photoluminescence from a single Ag nanowire.

Metallic nanowires are of great research interest due to their applications in surface plasmon polariton coupling of light. The efficiency is much dependent on the polarization of the light due to the phase matching requirement in the light-surface plasmon polariton coupling. By scanning confocal microscope, the photoluminescence from a single Ag nanowire was demonstrated strongly dependent on the excitation laser polarization, showing good consistency with the theoretical simulation. Meanwhile strong avalanche photoluminescence from a single Ag nanowire was observed when the excitation laser was polarized along the long axis of the Ag nanowire. The photoluminescence emission exhibited a polarization-sensitive spatial distribution. This may stimulate promising applications in designing polarization-controllable nanoscale plasmonic devices.