ABSTRACT
The development of multi-level anti-counterfeiting techniques is of great significance for economics and security issues, particularly the newly emerged temporal-domain techniques based on lifetime coding. However, the intricate reading methods required to obtain temporal-level information are inevitably cumbersome and expensive, which greatly limits the practical applications of these techniques. Herein, we report a novel, unclonable time-domain anti-counterfeiting strategy for the first time, which is achieved using photo-responsive ZnSe:Mn/ZnS quantum dots (QDs) with dynamic luminescence and can be authenticated by the naked eye. Through introducing electron traps and constructing cascade electron channels in the QDs, the binary temporary photo-response is tailored and manifested as distinctive response rates between the band-edge and Mn 4T1-6A1 transition emissions. Impressively, the generated photo-response is instantaneous, is capable of delayed recovery, and can be visibly detected under UV irradiation. The prospective use of colorless, nontoxic aqueous-phase ZnSe:Mn/ZnS QDs provides a new idea and important guidance for developing the next generation of multi-level anti-counterfeiting techniques without the need for complex time-gated decoding instrumentation.
ABSTRACT
Assembling thermoelectric modules into fabric to harvest energy from body heat could one day power multitudinous wearable electronics. However, the invalid 2D architecture of fabric limits the application in thermoelectrics. Here, we make the valid thermoelectric fabric woven out of thermoelectric fibers producing an unobtrusive working thermoelectric module. Alternately doped carbon nanotube fibers wrapped with acrylic fibers are woven into π-type thermoelectric modules. Utilizing elasticity originating from interlocked thermoelectric modules, stretchable 3D thermoelectric generators without substrate can be made to enable sufficient alignment with the heat flow direction. The textile generator shows a peak power density of 70 mWm-2 for a temperature difference of 44 K and excellent stretchability (~80% strain) with no output degradation. The compatibility between body movement and sustained power supply is further displayed. The generators described here are true textiles, proving active thermoelectrics can be woven into various fabric architectures for sensing, energy harvesting, or thermal management.
ABSTRACT
Replacing traditional luminous silicone or resins with phosphor in ceramics (PiCs) as color converters has been proposed as an efficient way to improve thermal stability of high-power white light-emitting diodes (WLEDs). However, excessive light scattering in existing PiCs results in enormous phosphor-converted light losses, which makes the luminosity of current PiCs color converters less efficient and means that they can only be used in devices working in reflective mode. By introducing nano wave plate structuring and Rayleigh scattering, luminous hydroxyapatite (HA)-YAG: Ce ceramics are prepared from mesoporous HA nanorods and YAG: Ce phosphors at 850 °C, enabling for the first time WLEDs equipped with PiC color converters in transmission mode. With low-temperature sintering and a highly transparent matrix, the quantum yield of HA-YAG: Ce retains ≈90% of the raw phosphor, and WLEDs with the color converters exhibit a record luminous efficiency of 170 lm W-1 and a correlated color temperature below 4500 K. A facile and practical strategy of using nano structural modulation to eliminate birefringence-induced light scattering for fabricating high-performance ceramic converters suitable for multiple mode luminaires is demonstrated.
ABSTRACT
Narrowband ultraviolet (UV) photodetectors are highly desired in multiple areas. Photodetectors based on organic-inorganic nanocomposites offer high sensitivity, widely adjustable response range, light weight, and low-temperature solution processibility. However, the broad absorption range of organic and inorganic semiconductor materials makes it difficult to achieve a narrowband detection feature for nanocomposite photodetectors. In this work, nanocomposite thin films containing the wide band gap conjugated polymer poly[(9,9-dioctylfluorenyl-2,7-diyl)- alt- co-(bithiophene)] (F8T2) blended with wide band gap ZnO nanoparticles (NPs) serve as the active layers of the photodetectors. Narrowband UV photodetectors with high gain and low driving voltage are demonstrated by adopting a symmetric device structure, controlling the active layer composition and microstructure, and manipulating the light penetration depth in the active layer. The fabricated photodetector exhibits a high external quantum efficiency of 782% at 358 nm under a low forward bias of 3 V with the full-width at half-maximum of 16 nm. Combined with a low dark current, a high specific detectivity of 8.45 × 1012 Jones is achieved. The impacts of the F8T2:ZnO NPs weight ratio and the device structure on the UV-selectivity and the device performance are investigated and discussed. Our method offers a pathway to design and fabricate narrowband UV photodetectors.
ABSTRACT
A facile and economical one-pot strategy has been developed for the synthesis of water-solute CdTe and CdTe/ZnS core/shell quantum dots (QDs) using tellurium dioxide (TeO2) as a tellurium precursor and thioglycolic acid (TGA) as stabilizer without any pre-treatment and inert atmosphere protection. As-synthesized QDs were characterized by transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), electron diffraction spectroscopy (EDS), X-ray powder diffraction (XRD), UV-vis and photoluminescence (PL). The spherical particles were uniformly distributed with the average diameters of 3.2 nm (CdTe QDs) and -5 nm (CdTe/ZnS QDs). By altering the reaction conditions, the emission wavelengths of the CdTe core QDs and CdTe/ZnS core/shell QDs could be tuned from 508 to 574 nm and 526 to 600 nm with narrow full widths at half maximum (FWHM) of 33 to 58 nm, respectively. Meanwhile, on the optimum condition, the luminescence efficiency of CdTe/ZnS QDs can achieve to 74%, which was higher than that of CdTe core QDs (24%).
