Polarized light detection can effectively identify the difference between the polarization information on the target and the background, which is of great significance for detection in complex natural environments and/or extreme weather. Generally, polarized light detection inevitably relies on anisotropic structures of photodetector devices, while organic-inorganic hybrid perovskites are ideal for anisotropic patterning due to their simple and efficient preparation by solution method. Compared to patterned thin films, patterned arrays of aligned one-dimensional (1D) perovskite nanowires (PNWAs) have fewer grain boundaries and lower defect densities, making them well suited for high-performance polarization-sensitive photodetectors. Here, we fabricated PNWAs crystallographically aligned with variable line widths and alignment densities employing CD-ROM and DVD-ROM grating pattern template-confined growth (TCG) methods. The photodetectors constructed from MAPbI3 PNWAs achieved responsivity of 35.01 A/W, detectivity of 6.85 × 1013 Jones, and fast response with a rise time of 172 µs and fall time of 114 µs. They were successfully applied to high-performance polarization detection with a polarization ratio of 1.81, potentially applicable in polarized light detection systems.
Organic-inorganic halide perovskites (HPs) have attracted respectable interests as active layers in solar cells, light-emitting diodes, photodetectors, etc. Besides the promising optoelectronic properties and solution-processed preparation, the soft lattice in HPs leads to flexible and versatile compositions and structures, providing an effective platform to regulate the bandgaps and optoelectronic properties. However, conventional solution-processed HPs are homogeneous in composition. Therefore, it often requires the cooperation of multiple devices in order to achieve multi-band detection or emission, which increases the complexity of the detection/emission system. In light of this, the construction of a multi-component compositional gradient in a single active layer has promising prospects. In this review, we summarize the gradient engineering methods for different forms of HPs. The advantages and limitations of these methods are compared. Moreover, the entropy-driven ion diffusion favors compositional homogeneity, thus the stability issue of the gradient is also discussed for long-term applications. Furthermore, applications based on these compositional gradient HPs will also be presented, where the gradient bandgap introduced therein can facilitate carrier extraction, and the multi-components on one device facilitate functional integration. It is expected that this review can provide guidance for the further development of gradient HPs and their applications.
Various spectral bands provide different types of information, and information enhancement could be achieved by selective fusion of different spectral bands. The fused solar-blind Ultraviolet (UV)/Visible (VIS) bi-spectral sensing and imaging can provide the precise location of UV targets in virtue of VIS background, which has been increasingly promoted. However, most reported UV/VIS bi-spectral photodetectors (PDs) only have one single channel towards a broadband spectrum of both UV and VIS light, which cannot distinguish two kinds of signals, hindering the image fusion of bi-spectral signals. This work demonstrates the solar-blind UV/VIS bi-spectral PD based on vertically stacking perovskite of MAPbI3and ternary oxide of ZnGa2O4with independent and distinct response toward solar-blind UV and VIS light in a single pixel. The PD exhibits excellent sensing properties with anIon/Ioffratio of >107and 102, detectivity of >1010and 108Jones, and response decay time of 90µs and 16 ms for VIS and UV channels, respectively. The successful fusion of VIS and UV images suggests that our bi-spectral PD can be applied in the accurate identification of corona discharge and fire detection.
Quantum dots (QDs) are important frontier luminescent materials for future technology in flexible ultrahigh-definition display, optical information internet, and bioimaging due to their outstanding luminescence efficiency and high color purity. I-III-VI QDs and derivatives demonstrate characteristics of composition-dependent band gap, full visible light coverage, high efficiency, excellent stability, and nontoxicity, and hence are expected to be ideal candidates for environmentally friendly materials replacing traditional Cd and Pb-based QDs. In particular, their compositional flexibility is highly conducive to precise control energy band structure and microstructure. Furthermore, the quantum dot light-emitting diodes (QLEDs) exhibits superior prospects in monochrome display and white illumination. This review summarizes the recent progress of I-III-VI QDs and their application in LEDs. First, the luminescence mechanism is illustrated based on their electronic-band structural characteristics. Second, focusing on the latest progress of I-III-VI QDs, the preparation mechanism, and the regulation of photophysical properties, the corresponding application progress particularly in light-emitting diodes is summarized as well. Finally, we provide perspectives on the overall current status and challenges propose performance improvement strategies in promoting the evolution of QDs and QLEDs, indicating the future directions in this field.
Anion-exchange reactions are recognized as a vital and facile post-synthesis method to precisely manipulate the emission spectra of perovskite quantum dots (QDs). However, the anion-exchange process often induces adverse structural evolution and trap-mediated mechanisms, so mixed-halide perovskite QDs suffer inefficient anion exchange and poor spectra-stability issues, which limits access to high-quality primary color perovskite QDs for display applications. Here we report an Al3+ bonding-doping synergistic strategy for manufacturing stable mixed Br/Cl deep-blue perovskite QDs. By doping Al3+ into perovskite QDs, highly-efficient Cl- anion exchange and a large-range blue shift of the PL spectrum (â¼62 nm with only 0.1 mmol of Cl feed) can be easily achieved. Notably, the Al3+-mediated deep-blue emission sample exhibits superior stability against moisture and electric fields. It also shows an elevated valence band maximum level. Based on the anion-exchanged QDs, a spectrum-stable deep-blue QLED with an EQE of 1.38% at 463 nm is achieved. Our findings demonstrate a feasible and promising strategy for developing high-performance deep-blue perovskite materials and optoelectronic devices.
Multispectral sensing is extremely desired in intelligent systems, e.g., autonomous vehicles, encrypted information communication, and health biometric monitoring, due to its highly sensitive spectral discrimination ability. Nevertheless, rigid bulky optics and delicate optical paths in devices significantly increase their complexity and size, which subsequently impede their integration in smart optoelectronic chips for universal applications. In this work, a filterless miniaturized multispectral photodetector is realized with an organic narrowband response unit array. With the manipulation of Frenkel exciton dissociation in active layers, a series of narrowband organic sensing units with full-width-at-half-maximum (fwhm) narrowing to â¼50 nm are achieved from 700 to 1050 nm with a laudable performance of responsivity of over 60 mA/W, -3 dB bandwidth over 10 kHz, linear dynamic range (LDR) reaching â¼120 dB, and a low noise current of less than 4 × 10-14 A·Hz-0.5. Furthermore, a 6 × 8 multispectral sensing array on a flexible substrate was fabricated with blade-coating. Assisted by a computational process, we successfully demonstrate the spectral recognition with a resolution of â¼50 nm and a mismatch of â¼10 nm. Finally, the function of matter identification is successfully achieved with our multispectral detector array.
The multispectral fusion of near-infrared (NIR) and visible red-green-blue (RGB) photons can enhance target identification under weak light conditions. Nevertheless, the crosstalk between NIR and RGB photons in a traditional pixelated sensor impedes their practical application, while using complex algorithms and optical filters would significantly increase the cost, form factor, and frame latency. In this work, a delicate monolithic RGBN (RGB-NIR) multispectral photodetector (PD) is proposed on the basis of perovskite materials without complicated algorithms or optical filters. The multispectral response toward selective RGBN signals in this monolithic PD pixels can be achieved by switching the polarity of the applied bias, affording the following benefits: Ion/Ioff ratio of >104, detectivity of >1010 Jones, crosstalk of -74 dB, and fast response with -3 dB > 103 Hz. Moreover, proof-of-concept imaging of the iris and periocular with successful recognition in multispectral fusion further confirms its potential for identity authentication.
Terahertz (THz) detection technology is getting increasing attention from scientists and industries alike due to its superiority in imaging, communication, and defense. Unfortunately, the detection of THz electromagnetic waves under room temperature requires a complicated device architecture design or additional cryogenic cooling units, which increase the cost and complexity of devices, subsequently imposing an impediment in its universal application. In this work, THz detectors operated under room temperature are designed based on the thermoelectric effect with MAPbI3 single crystals (SCs) as active layers. With solution-processed molecular growth engineering, the anti-reflection 2D perovskite layers were constructed on SCs' surfaces to suppress THz reflection loss. Simultaneously, by finely regulating the main carrier types and the direction of the applied bias across the inclined energy level, the thermoelectric effect is further promoted. As a result, THz-induced ΔT in MAPbI3 SCs reaches 4.6 °C, while the enhancement in the bolometric and photothermoelectric effects reach â¼4.8 times and â¼16.9 times, respectively. Finally, the devices achieve responsivity of 88.8 µA W-1 at 0.1 THz under 60 V cm-1, noise equivalent power (NEP) less than 2.16 × 10-9 W Hz-1/2, and specific detectivity (D*) of 1.5 × 108 Jones, which even surpasses the performance of state-of-the-art graphene-based room-temperature THz thermoelectric devices. More importantly, proof-of-concept imaging gives direct evidence of perovskite-based THz sensing in practical applications.
Halide perovskite (HP) single crystals (SCs) are garnering extensive attention as active materials to substitute polycrystalline counterparts in solar cells, photodiodes, and photodetectors, etc. Nevertheless, the large thickness and defect-rich surface results in severe carrier recombination and becomes the major bottleneck for augmented performance. In this perspective, we are looking forward to explaining in detail why the SCs hardly unleash their engrossing potential and introduce two parallel paths for further advancement. First is the modification of thick SCs by reducing the prepared thickness or surface passivation. Second is the large thickness that is conducive to the sufficient absorption of high-energy rays with strong penetrating ability and is beneficial to the thermoelectric effect due to the ultralow thermal conductivity of HPs. These applications provide a roundabout strategy to exploit freestanding SCs with a large thickness. Herein, direct modification and application of thick SCs are systematically introduced, expecting to give rise to the prosperity of HP SCs.
Miniaturized multispectral detectors are urgently desired given the unprecedented prosperity of smart optoelectronic chips for integrated functions including communication, imaging, scientific analysis, etc. However, multispectral detectors require complicated prism optics or interference/interferometric filters for spectral recognition, which hampers the miniaturization and their subsequent integration in photonic integrated circuits. In this work, inspired by the advance of computational imaging, optical-component-free miniaturized multispectral detector on 4 mm gradient bandgap MAPbX3 microwire with a diameter of 30 µm, is reported. With accurate composition engineering, halide ions in MAPbX3 microwire vary from Cl to I giving in the gradual variation of optical bandgap from 2.96 to 1.68 eV along axis. The sensing units on MAPbX3 microwire offer the response edge ranging from 450 to 790 nm with the responsivity over 20 mA W-1 , -3dB width over 450 Hz, LDR of ≈60 dB, and a noise current less than ≈1.4 × 10-12 A Hz-0.5 . As a result, the derived miniaturized detector achieves the function of multispectral sensing and discrimination with spectral resolution of ≈25 nm and mismatch of ≈10 nm. Finally, the proof-of-concept colorful imaging is successfully conducted with the miniaturized multispectral detector to further confirm its application in spectral recognition.
Photodetectors selective to the polarization empower breakthroughs in sensing technology for target identification. However, the realization of polarization-sensitive photodetectors based on intrinsically anisotropic crystal structure or extrinsically anisotropic device pattern requires complicated epitaxy and etching processes, which limit scalable production and application. Here, solution-processed PEA2 MA4 (Sn0.5 Pb0.5 )5 I16 (PEA= phenylethylammonium, MA= methylammonium) polycrystalline film is probed as photoactive layer toward sensing polarized photon from 300 to 1050 nm. The growth of the PEA2 MA4 (Sn0.5 Pb0.5 )5 I16 crystal occurs in confined crystallographic orientation of the (202) facet upon the assistance of NH4 SCN and NH4 Cl, enhancing anisotropic photoelectric properties. Therefore, the photodetector achieves a polarization ratio of 0.41 and dichroism ratio (Imax /Imin ) of 2.4 at 900 nm. At 520 nm, the Imax /Imin even surpasses the one of the perovskite crystalline films, 1.8 and ≈1.2, respectively. It is worth noting that the superior figure-of-merits possess a response width of 900 kHz, Ion /Ioff ratio of ≈3 × 108 , linear dynamic range from 0.15 nW to 12 mW, noise current of 8.28 × 10-13 A × Hz-0.5 , and specific detectivity of 1.53 × 1012 Jones, which demonstrate high resolution and high speed for weak signal sensing and imaging. The proof of concept in polarized imaging confirms that the polarization-sensitive photodetector meets the requirements for practical application in target recognition.
Light fidelity (LiFi), which is emerging as a compelling technology paradigm shifting the common means of high-capacity wireless communication technologies, requires wearable and full-duplex compact design because of its great significance in smart wearables as well as the 'Internet of Things'. However, the construction of the key component of wearable full-duplex LiFi, light-emitting/detecting bifunctional fibres, is still challenging because of the conflicting process between carrier separation and recombination, as well as the highly dynamic film-forming process. Here, we demonstrate light-emitting/detecting bifunctional fibres enabled by perovskite QDs with hybrid components. The hybrid perovskite inks endow fibres with super-smooth QD films. This, combined with the small exciton binding energy and high carrier mobility of perovskite QDs, enables successful integration of electroluminescence and photodetection into monofilaments. The bifunctional fibres possess the narrowest electroluminescence full width at half maximum of ~19 nm and, more importantly, the capability for simultaneously transmitting and receiving information. The successful fabrication of narrow emission full-duplex LiFi fibres paves the way for the fabrication and integration of low crosstalk interoperable smart wearables.
Multispectral detection and imaging facilitate advances in target identification; for example, the switchable functionality of sensing visible photons and sensing near-infrared photons in the eyes of some vertebrate species provide visual sensitivity beyond the range of human vision. In this work, a single sensor device is constructed with stacking solution-processed MAPbI3 and MA0.5FA0.5Pb0.5Sn0.5I3 in opposite polarity for the multispectral detection of visible and NIR photons. With applied bias modulating built-in potential, the sensing response is tunable, while the good ambipolar carrier transport and high trap tolerance in perovskite films ensure high performance. As a result, the selective sensing toward visible photons from 350-800 nm and NIR photons from 700-1000 nm is achieved in a single photodetector under -0.3V and 0.5 V, respectively, with a high on/off ratio of â¼104, a relatively low optical crosstalk of -70 dB, and specific detectivity of over 1012 Jones. Moreover, the high mode-switching rate of 1000 Hz in altering the visible and NIR sensing mode and the high -3 dB bandwidth of â¼50 kHz enable our solution-processed perovskite-based multispectral photodetector to be recognized as an advanced technique for the fast and sensitive target multispectral imaging and identification.
Due to the rapid development of smart technology infusion, visible light communication (VLC) has been promising as a connection belt among real estates due to the appealing features including fast speed of data transmission and high bandwidth. Unfortunately, the issues of crosstalk, interference, or data leakage in the VLC impose rigorous requests for the receiver terminal, photodetector, including fast and accurate signal recognition, rapid decoding, etc. In pursuit of distinctive merits, a dual-band photodetector is proposed as an efficient receiver terminal for VLC in this work. With MAPbBr3 and MAPbI3 as photoactive layers, a device by stacking two photodiodes in opposite polarity is constructed to sense the signals at two different wavelengths from a commercial white light-emitting diode (LED) transmitter. By manipulating the applied bias direction, the response of a single device can be controllably switched between 300-570 and 630-800 nm with an optical crosstalk of less than -30 dB. The performance with an Ion/Ioff ratio of about 108, a response bandwidth (f-3dB) of â¼33 kHz, a response switching rate approaching 1000 Hz, and a detectivity of 1.75 × 1010 Jones ensures its application as an efficient data receiver. We believe that this work will provide the motivation to explore novel functional perovskite optoelectronic devices and put them to practical applications in the special field.
Radiative cooling, a passive cooling technique, has shown great potentials in recent years to lower the power consumption of air conditioning. With the ever-increasing cooling power being reported, the theoretical cooling limit of such a technique is still unclear. In this work, we proposed a theoretical limit imposing an upper bound for the attainable cooling power. To approach this limit, we exploited the localized surface plasmon resonance (LSPR) of self-doped In2O3 nanoparticles, which enhance the emissivity in both primary and secondary atmospheric windows. The measured cooling power of poly(methyl methacrylate) (PMMA) films containing 4.5% In2O3 nanoparticles is very close to the limit with the closest value only about 0.4 W/m2 below the limit. Hopefully, this work may help the researchers better evaluating the performance of their device in the future and pave the way for achieving even higher radiative cooling powers during the daytime operations with the help of LSPR.
Ensuring nuclear safety has become of great significance as nuclear power is playing an increasingly important role in supplying worldwide electricity. ß-ray monitoring is a crucial method, but commercial organic scintillators for ß-ray detection suffer from high temperature failure and irradiation damage. Here, we report a type of ß-ray scintillator with good thermotolerance and irradiation hardness based on a two-dimensional halide perovskite. Comprehensive composition engineering and doping are carried out with the rationale elaborated. Consequently, effective ß-ray scintillation is obtained, the scintillator shows satisfactory thermal quenching and high decomposition temperature, no functionality decay or hysteresis is observed after an accumulated radiation dose of 10 kGy (dose rate 0.67 kGy h-1). Besides, the two-dimensional halide perovskite ß-ray scintillator also overcomes the notorious intrinsic water instability, and benefits from low-cost aqueous synthesis along with superior waterproofness, thus paving the way towards practical application.
Fully-inorganic halide perovskites (HPs) have realized respectable progress in multiple optoelectronic applications. However, Cl-based fully-inorganic HPs that are ideal for ultraviolet (UV) photodetection applications in high demand still remain rarely explored mainly due to the poor solution processability compared with other counterparts. Here we propose a facile solution method to fabricate CsPbCl3 with not only high crystallinity but also a two dimensional (2D) morphology for efficient UV photodetection. 2D Ruddlesden-Popper perovskites (RPPs) are firstly prepared as the intermediate phase, which habitually grow into microplates owing to an intrinsic 2D structure. Then Cs+ was introduced in the form of highly soluble cesium acetate to exchange with the organic cations in the RPPs to produce 2D CsPbCl3 with preserved morphology and micron scale size. By this chemical route, the poor solubility issue can be addressed. All the procedures are conducted at room temperature in open air. The perfect band gap, high crystallinity and 2D morphology promise superior UV light sensing capability, one of the best overall performances featuring high responsivity, fast response speed, low driving voltages and good stability is obtained. This work is believed to fill in the "Cl-gap" for this promising class of material.
Benefiting from morphology-/size-tunable optical features, nanocrystals have been considered promising candidates for display or lighting applications. To achieve selective characteristic emission, precise control in size and morphology is thus a prerequisite. Herein, we report that the nanosecond-pulsed laser irradiation induces CsPbBr3 reshaping, yielding precise control of size and morphology. Under 532 and 355 nm laser irradiation, polydisperse CsPbBr3 nanocrystals or raw micron powders can be reshaped into uniform sizes of 12 and 6 nm, respectively. Moreover, by tuning ligand composition, the morphology of reshaped nanocrystals can be manipulated, such as nanocubes, nanorods, or nanosheets. Results reveal that the reshaping process relies on striving for a delicate balance between energy deposition and heat dissipation under irradiation. A low dissipation rate leads to temperature rising and lattice breaking, which turn out to be the driving forces for reshaping. This feasible method provides a reliable, and scalable route toward preparation of perovskite functional nanocrystals.
Flexible and wearable electrical devices have attracted extensive research attention in recent years. In the device fabrication process, the low-cost and compatibility with industrialized mass production are of great importance. Herein, membrane-based flexible photodetectors (PDs) based on Polyvinylidene Fluoride filter membrane with the structure of Ag nanowires (NWs)/ZnO NWs/graphene were fabricated by a full-solution method. The built-in electric field due to the ZnO/graphene Schottky junction is in favor of the separation and transport of photo-generated carriers, leading to enhanced device performance. The I light/I dark ratio was as high as â¼102, which is far superior to that of the reported ZnO-based fiber-shaped PDs. The PDs with remarkable flexibility can be easily attached to the human body and even can work steadily under serious bending conditions. Particularly, the photocurrent can keep 95% of the maximum value after the PD was bent 1000 times. In addition to the wearable applications, the membrane-based PD arrays can also be applied for imaging application.
Image sensor arrays are widely used in digital cameras, smartphones, and biorobots. However, most commercial image arrays rely on the dichroic prisms or a set of interference filters to distinguish characteristic color spectrum, which significantly increases the cost and fabrication processing complexity. In this work, an ultranarrow response photodetector with full-width at half-maximum being â¼12 nm and specific detectivity over 1011 Jones at 545 nm are successfully achieved in CsPbBr3 polycrystalline films using freeze-drying casting method to adjust the surface-charge recombination. To our best knowledge, this is the narrowest spectrum response for perovskite photodetectors in the visible light waveband. More importantly, a series of narrowband photodetectors are developed to enhance diverse selectivity for target signals covering from blue light to red light via bandgap tuning in CsPbX3 by tailoring the halide component. Finally, an integrated sensing array with CsPbX3 (X = Cl, Br, I) narrowband photodetectors acting as color recognition cones is constructed, which presents clear color and shape recognition paving the way for commercialization of perovskite photodetector in artificial vision.
Cesium/chemistry , Lead/chemistry , Nanostructures/chemistry , Bionics , Calcium Compounds/chemistry , Crystallization , Freeze Drying , Halogenation , Humans , Light , Oxides/chemistry , Titanium/chemistry , Vision, Ocular
