Evaporative electron cooling in asymmetric double barrier semiconductor heterostructures

International audienceRapid progress in high-speed, densely packed electronic/photonic devices has brought unprecedented benefits to our society. However, this technology trend has in reverse led to a tremendous increase in heat dissipation, which degrades device performance and lifetimes. The scientific and technological challenge henceforth lies in efficient cooling of such high-performance devices. Here, we report on evaporative electron cooling in asymmetric Aluminum Gallium Arsenide/Gallium Arsenide (AlGaAs/GaAs) double barrier heterostructures. Electron temperature, T e , in the quantum well (QW) and that in the electrodes are determined from photoluminescence measurements. At 300 K, T e in the QW is gradually decreased down to 250 K as the bias voltage is increased up to the maximum resonant tunneling condition, whereas T e in the electrode remains unchanged. This behavior is explained in term of the evaporative cooling process and is quantitatively described by the quantum transport theory

Phosphor Thermometry of Alumina-Forming High-Temperature Alloys Using Luminescent Rare-Earth Ions in YAG: Proof of Concept Using a Dispersion of Ce3+ -Doped YAG Particles in a FeCrAl Alloy

Most high-temperature processes require monitoring and controlling temperature, preferably with high precision and good lateral resolution. Here we evaluate the use of the technique commonly known as phosphor thermometry, which exploits the temperature dependent photoluminescence from an inorganic phosphor, for the determination of the temperature of a composite material consisting of the metallic alloy FeCrAl dispersed with phosphor particles of yttrium aluminum garnet (Y3Al5O12, YAG) doped with a small amount of luminescent Ce3+ ions (YAG:Ce3+). The results show that with some optimization and by changing the dopant ion, YAG based phosphor particles offer a unique opportunity to measure the surface temperature of metal alloys with high precision and high lateral resolution, all the way up to the maximum working temperature of alumina-forming high temperature alloys at ca. 1300 \ub0C

Photoluminescence Mapping over Laser Pulse Fluence and Repetition Rate as a Fingerprint of Charge and Defect Dynamics in Perovskites

Defects in metal halide perovskites (MHP) are photosensitive, making the observer effect unavoidable when laser spectroscopy methods are applied. Photoluminescence (PL) bleaching and enhancement under light soaking and recovery in dark are examples of the transient phenomena that are consequent to the creation and healing of defects. Depending on the initial sample composition, environment, and other factors, the defect nature and evolution can strongly vary, making spectroscopic data analysis prone to misinterpretations. Herein, the use of an automatically acquired dependence of PL quantum yield (PLQY) on the laser pulse repetition rate and pulse fluence as a unique fingerprint of both charge carrier dynamics and defect evolution is demonstrated. A simple visual comparison of such fingerprints allows for assessment of similarities and differences between MHP samples. The study illustrates this by examining methylammonium lead triiodide (MAPbI3) films with altered stoichiometry that just after preparation showed very pronounced defect dynamics at time scale from milliseconds to seconds, clearly distorting the PLQY fingerprint. Upon weeks of storage, the sample fingerprints evolve toward the standard stoichiometric MAPbI3 in terms of both charge carrier dynamics and defect stability. Automatic PLQY mapping can be used as a universal method for assessment of perovskite sample quality

Are Shockley-Read-Hall and ABC models valid for lead halide perovskites?

Metal halide perovskites are an important class of emerging semiconductors. Their charge dynamics is poorly understood due to limited knowledge of defect physics and charge recombination mechanisms. Nevertheless, classical ABC and Shockley-Read-Hall (SRH) models are ubiquitously applied to perovskites without considering their validity. Herein, an advanced technique mapping photoluminescence quantum yield (PLQY) as a function of both the excitation pulse energy and repetition frequency is developed and employed to examine the validity of these models. While ABC and SRH fail to explain the charge dynamics in a broad range of conditions, the addition of Auger recombination and trapping to the SRH model enables a quantitative fitting of PLQY maps and low-power PL decay kinetics, and extracting trap concentrations and efficacies. Higher-power PL kinetics requires the inclusion of additional non-linear processes. The PLQY mapping developed herein is suitable for a comprehensive testing of theories and is applicable to any semiconductor.Comment: Supplementary Information available at https://cloudstore.zih.tu-dresden.de/index.php/s/t5gBPJgwZiwfRR

Remarkable performance recovery in highly defective perovskite solar cells by photo-oxidation

Exposure to environmental factors is generally expected to cause degradation in perovskite films and solar cells. Herein, we show that films with certain defect profiles can display the opposite effect, healing upon exposure to oxygen under illumination. We tune the iodine content of methylammonium lead triiodide perovskite from understoichiometric to overstoichiometric and expose them to oxygen and light prior to the addition of the top layers of the device, thereby examining the defect dependence of their photooxidative response in the absence of storage-related chemical processes. The contrast between the photovoltaic properties of the cells with different defects is stark. Understoichiometric samples indeed degrade, demonstrating performance at 33% of their untreated counterparts, while stoichiometric samples maintain their performance levels. Surprisingly, overstoichiometric samples, which show low current density and strong reverse hysteresis when untreated, heal to maximum performance levels (the same as untreated, stoichiometric samples) upon the photooxidative treatment. A similar, albeit smaller-scale, effect is observed for triple cation and methylammonium-free compositions, demonstrating the general application of this treatment to state-of-the-art compositions. We examine the reasons behind this response by a suite of characterization techniques, finding that the performance changes coincide with microstructural decay at the crystal surface, reorientation of the bulk crystal structure for the understoichiometric cells, and a decrease in the iodine-to-lead ratio of all films. These results indicate that defect engineering is a powerful tool to manipulate the stability of perovskite solar cells

Etude des propriétés optiques et structurales des matériaux hybrides organiques-inorganiques à base de Plomb : émission de lumière blanche

Inorganic organic hybrid materials have attracted a great attention do to their special structure and important optical such as the high luminescence, even at room temperature. This relatively new research on this family of materials, offers a variety of technological opportunities. In this context, we are interested in the study of optical properties of both inorganic and organic hybrid materials (C6H11NH3)2[PbI4] and (C6H11NH3)2[PbBr4], and mainly their luminescence properties. The results shows that under ultraviolet excitation, (C6H11NH3)2[PbBr4] show a strong white light emission, even at room temperature, which open a great interest in the use of these materials as a source of the white light emission. The origin of this large emission has been studied by different techniques such as the time resolved photoluminescence measurements .Les matériaux hybrides organiques inorganiques ont attirés l'attention vue qu'ils présentent des propriétés optiques et optoélectroniques fascinantes comme la forte photoluminescence même à température ambiante. Cet axe de recherche relativement nouveau, sur cette famille de matériaux, offre une variété d’opportunités technologiques. Dans ce contexte, nous nous sommes intéressés par l'étude des propriétés optiques des deux matériaux hybrides organiques inorganiques (C6H11NH3)2[PbI4] et (C6H11NH3)2[PbBr4], et principalement leurs propriétés de luminescence. Les résultats montre que sous excitation dans l'ultraviolet, (C6H11NH3)2[PbBr4] émet de la lumière blanche, même à température ambiante, ce qui présente un grand intérêt de l'utilisation de ces matériaux comme source d'émission de la lumière blanche. L'origine de cette émission a été étudié par différentes techniques comme la photoluminescence résolution en temps

Optical and structural study of organic-inorganic hybrid materials based on lead halides : white-light emission

Les matériaux hybrides organiques inorganiques ont attirés l'attention vue qu'ils présentent des propriétés optiques et optoélectroniques fascinantes comme la forte photoluminescence même à température ambiante. Cet axe de recherche relativement nouveau, sur cette famille de matériaux, offre une variété d’opportunités technologiques. Dans ce contexte, nous nous sommes intéressés par l'étude des propriétés optiques des deux matériaux hybrides organiques inorganiques (C6H11NH3)2[PbI4] et (C6H11NH3)2[PbBr4], et principalement leurs propriétés de luminescence. Les résultats montre que sous excitation dans l'ultraviolet, (C6H11NH3)2[PbBr4] émet de la lumière blanche, même à température ambiante, ce qui présente un grand intérêt de l'utilisation de ces matériaux comme source d'émission de la lumière blanche. L'origine de cette émission a été étudié par différentes techniques comme la photoluminescence résolution en temps.Inorganic organic hybrid materials have attracted a great attention do to their special structure and important optical such as the high luminescence, even at room temperature. This relatively new research on this family of materials, offers a variety of technological opportunities. In this context, we are interested in the study of optical properties of both inorganic and organic hybrid materials (C6H11NH3)2[PbI4] and (C6H11NH3)2[PbBr4], and mainly their luminescence properties. The results shows that under ultraviolet excitation, (C6H11NH3)2[PbBr4] show a strong white light emission, even at room temperature, which open a great interest in the use of these materials as a source of the white light emission. The origin of this large emission has been studied by different techniques such as the time resolved photoluminescence measurements

READ-IoT: Reliable Event and Anomaly Detection Framework for the Internet of Things

International audienceInternet of Things (IoT) enables a myriad of applications by interconnecting software to physical objects. The objects range from wireless sensors to robots and include surveillance cameras. The applications are often critical (e.g. physical intrusion detection, fire fighting) and latency-sensitive. On the one hand, such applications rely on specific protocols (e.g. MQTT, COAP) and the network to communicate with the objects under very tight timeframe. On the other hand, anomalies (e.g. communication noise, sensors' failures, security attacks) are likely to occur in open IoT systems and can result by sending false alerts or the failure to properly detect critical events. To address that, IoT systems have to be equipped with anomaly detection processing in addition to the required event detection capability. This is a key feature that enables reliability and efficiency in IoT. However, anomaly detection systems can be themselves object of failures and attacks, and then can easily fall short to accomplish their mission. This paper introduces a Reliable Event and Anomaly Detection Framework for the Internet of Things (READ-IoT for short). The designed framework integrates events and anomalies detection into a single and common system that centralizes the management of both concepts. To enforce its reliability, the system relies on a reputationaware provisioning of detection capabilities that takes into account the vulnerability of the deployment hosts. As for validation, READ-IoT was implemented and evaluated using two real life applications, i.e. a fire detection and an unauthorized person detection applications. Several scenarios of anomalies and events were conducted using NSL-KDD public dataset, as well as, generated data to simulate routing attacks. The obtained results and performance measurements show the efficiency of READ-IoT in terms of event detection accuracy and real-time processing

Bis[tris(propane-1,3-diamine-κ2N,N′)nickel(II)] diaquabis(propane-1,3-diamine-κ2N,N′)nickel(II) hexabromide dihydrate

In the title compound, [Ni(C3H10N2)3]2[Ni(C3H10N2)2(H2O)2]Br6·2H2O, one Ni2+ cation, located on an inversion centre, is coordinated by four N atoms from two ligands and by two water O atoms. The other Ni2+ cation, located in a general position, is coordinated by six N atoms from three ligands. In both cases, the Ni2+ cation has an octahedral coordination environment. The overall structural cohesion is ensured by three types of hydrogen bonds, N—H...Br, O—H...Br and O—H...O, which connect the two types of complex cations, the bromide counter-anions and the lattice water molecules into a three-dimensional network

Yellowish White-Light Emission Involving Resonant Energy Transfer in a New One-Dimensional Hybrid Material: (C 9 H 10 N 2 )PbCl 4

International audienceThe present work deals with a new one-dimensional (1D) organic-inorganic hybrid material namely (C9H10N2)PbCl4 (abbreviated as AQPbCl4). Its crystal structure is built up from infinite 1D chain of edge-sharing PbCl6 octahedra surrounded by 3-aminoquinoline (abbreviated as AQ) organic molecules. Contrary to the most organic-inorganic hybrid materials, where the organic moieties act as barriers and the inorganic parts play the role of quantum wells, both inorganic and organic parts in AQPbCl4 are optically active, giving rise to optical properties involving the competition and the interaction of two organic and inorganic emitting entities. Under UV excitation, this hybrid compound shows a strong yellowish white-light emission that can be seen even with the naked eye and at room temperature. Photoluminescence spectrum is composed from a strong and broad yellow band at 538 nm associated with π-π* transition localized within AQ organic molecule and a less intense band in the UV region at 340nm associated with inorganic Wannier exciton confined in the PbCl4 inorganic wires. These attributions were made possible thanks to comparisons with homologous materials and it was supported by theoretical band structure calculations. In addition, both theoretical and experimental results suggest that the emission involves resonant energy transfer mechanism in which the inorganic PbCl4 wires act as a donor and the organic molecules act as an acceptor. Moreover, the temperature dependence study of the photoluminescence led to an estimation of the binding energies of interacting excitons and showed that the energy transfer mechanism is characterized by a remarkable enhancement of the emission band intensity