Direct Lifetime Measurements Research Articles

Evaluation of electron lifetime for Te inclusions free CdZnTe

Te secondary phase defects are known as major obstacle for improving charge carriers transport properties of CdTe compounds material. The enhanced detector performance was reported for Te inclusions free CZT detector implemented through two-step annealing (i.e., first in Cd and second in Te). We applied the time-of-flight (TOF) technique to measure the electron lifetime in as-grown and two-step annealed CZT material. TOF has several advantages over Hecht equation fitting such as independence of the electric field distribution, direct measurement of carrier lifetime, and high accuracy for high mobility-lifetime product CZT material. The detector performance improved drastically for the two-step annealed CZT detector except which containing inordinate number and size of prismatic punching defects. The average electron lifetime increased more than 10 times after successful two-step annealing.

Quantum limits to resolution and discrimination of spontaneous emission lifetimes

In this work we investigate the quantum information theoretical limits to several tasks related to lifetime estimation and discrimination of a two-level spontaneous optical emitter. We focus in particular on the model problem of resolving two mutually incoherent exponential decays with highly overlapping temporal probability profiles. Mirroring recent work on quantum-inspired super-resolution of point emitters, we find that direct lifetime measurement suffers from an analogue of "Rayleigh's Curse" when the time constants of the two decay channels approach one another. We propose alternative measurement schemes that circumvent this limit, and also demonstrate superiority to direct measurement for a related binary hypothesis test. Our findings add to a growing list of examples in which a quantum analysis uncovers significant information gains for certain tasks in opto-molecular metrology that do not rely on multiphoton interference, but evidently do benefit from a more thorough exploitation of the coherence properties of single photons.

On the long decay time of the 7F5 level of Tb3+

The Tb3+7F5 level has been shown to play an important role in the energy transfer involving this ion. This is due to the unusually long lifetime of this level which is commonly disregarded when treating energy transfer involving this ion. In this work, we give a rationalized explanation for this phenomenon. It is discussed that the 7F5 level can be fed by an energy transfer process and the population is trapped due to a low decay rate, which is related to the energy gap to the 7F6 ground level in the far infrared and the correspondingly low photon density of states. This is in agreement with experimental data from direct measurements of the total decay lifetimes of the 7F5 level and the emission quantum yields when this level is considered as an energy acceptor in Tb3+ compounds.

Nature of seniority symmetry breaking in the semimagic nucleus Ru94

Direct lifetime measurements via γ−γ coincidences using a fast timing detector array consisting of LaBr3(Ce) scintillators has been applied to determine the lifetime of low-lying states in the semimagic (N=50) nucleus Ru94. The experiment was carried out as the first in a series of “FAIR-0” experiments with the DESPEC experimental setup at the Facility for Antiproton and Ion Research (FAIR). Excited states in Ru94 were populated primarily via the β-delayed proton emission of Pd95 nuclei, produced in the projectile fragmentation of an 850 MeV/nucleon Xe124 beam impinging on a 4 g/cm2Be9 target. While the deduced E2 strength for the 2+→0+ transition in the yrast cascade follows the expected behavior for conserved seniority symmetry, the intermediate 4+→2+ transition exhibits a drastic enhancement of transition strength in comparison with pure-seniority model predictions as well as standard shell model predictions in the fpg proton hole space with respect to doubly magic Sn100. The anomalous behavior is ascribed to a subtle interference between the wave function of the lowest seniority ν=2, Iπ=4+ state and that of a close-lying ν=4 state that exhibits partial dynamic symmetry. In addition, the observed strongly prohibitive 6+→4+ transition can be attributed to the same mechanism but with a destructive interference. It is noted that such effects may provide stringent tests of the nucleon-nucleon interactions employed in state-of-the-art theoretical model calculations.Received 17 October 2021Revised 17 January 2022Accepted 11 March 2022DOI:https://doi.org/10.1103/PhysRevC.105.L031304Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI. Funded by Bibsam.Published by the American Physical SocietyPhysics Subject Headings (PhySH)Research AreasIsomer decaysProton emissionProperties90 ≤ A ≤ 149Nuclear bindingTechniquesGamma ray spectroscopyNuclear structure & decaysRadiation detectorsRadioactive beamsSpectrometers & spectroscopic techniquesNuclear PhysicsAccelerators & Beams

Observation of 2D semiconductor P-type dark-exciton lifetime using two-photon ultrafast spectroscopy.

We report direct measurements of intrinsic lifetimes of P-type dark-excitons in MoS2 monolayers. Using sub-gap excitation, we demonstrate two-photon excited direct population of P-type dark excitons, observe their scattering to bright states and decay with femtosecond resolution. In contrast to one-photon excitation schemes, non-monotonic density variation in bright exciton population observed under two-photon excitation shows the indirect nature of its population and competing decay pathways. Detailed modeling of different recombination pathways of bright and dark excitons allows experimental measurement of 2P dark → 1S bright exciton scattering rates. These insights into the dark states in a MoS2 monolayer pave the way for novel devices such as quantum memories and computing.

Analysis of Optical and Electrical Responses of $\boldsymbol{\mu}$ -OLED With Metallized ITO Coplanar Waveguide Electrodes Submitted to Nanosecond Electrical Pulses

In this paper, the optical and electrical pulse responses of an optimized high-speed organic light-emitting diode (OLED) is investigated as a function of the pulse duration. The original design is based on the coplanar waveguide electrodes that are implemented on a transparent and conductive oxide thin film. The designed electrodes with reduced serial resistances (13 $\Omega $ ) allow to maximize the pulse energy delivery and to feed the organic device with short electrical pulses of few nanoseconds for the first time. This is achieved by designing the electrodes to have 50- $\Omega $ characteristic impedance, thanks to microwave techniques, and by implementing small values of capacitance (4.5 pF). The experimental results demonstrate $\boldsymbol \mu $ -OLED electrical and optical responses to electrical excitation pulses as short as 2.5 ns, for the first time, and state-of-the-art current densities above 1.7 kA/cm2. Moreover, and rather unexpectedly, the developed characterization procedure to extract the reported results demonstrated the first direct measurement of the electroluminescence lifetime of organic materials in the nanosecond time scale.

Direct measurement of CO2S-branch Raman linewidths broadened by O2, Ar, and C2H4.

Direct measurements of CO2S-branch Raman coherence-decay lifetimes resulting from CO2-O2, CO2-Ar, and CO2-C2H4 collisions by employing time-resolved picosecond rotational coherent anti-Stokes Raman scattering (CARS) spectroscopy are reported. Based on the measured Raman coherence dephasing rates, the corresponding Raman linewidths of various J levels are obtained. Our measured linewidth data will aid CO2 CARS fitting, which is applied to the high-accuracy extraction of temperature and species concentration information from CARS spectra.

Shockley–Read–Hall Lifetime Study and Implication in HgCdTe Photodiodes for IR Detection

The Shockley–Read–Hall (SRH) mechanism might be a limiting factor of an infrared (IR) photodiode's dark current. This limitation is twofold. SRH generation might occur in the depletion region of the photodiode. In that case, the corresponding current is usually limiting the low-temperature dark current. Moreover, SRH generation might also occur in the diffusion volume, close to the space charge region, resulting in an increase of the diffusion dark current, usually limiting the high-temperature behavior of the photodiode. Hence, the determination of the SRH lifetime of IR materials is of first importance and has to be measured (or at least estimated) to define upcoming trends in future high-performance IR detectors. During the last few years, a lot of papers have been published about SRH lifetime in III–V materials (InSb, superlattices, InAsSb) and a few other communications have been more focused on comparing different material systems including III–V and II–VI materials. Those latter communications proposed very long SRH lifetimes (longer than ms) for HgCdTe, instead of the classical 10–100 μs usually admitted until now. This paper aims at investigating this SRH lifetime in HgCdTe based on experimental measurements carried out at the Laboratoire d’electronique des technologies de l’information (LETI) on HgCdTe grown in-house. Direct lifetime measurement (photoconductive or photoluminescence decay) as well as indirect estimations from photodiode dark currents are discussed in order to clarify this question of SRH lifetime and its consequences in upcoming advanced IR detection structures. In the end, it appeared that except for p/n extrinsic heterojunctions (for which the narrow gap depleted volume is not well known), most of the devices tested seemed limited by SRH lifetimes in the 10–100-μs range.

Giant Phonon Tuning Effect via Pressure-Manipulated Polar Rotation in Perovskite MAPbI3.

Perovskite MAPbI3 that exhibits unique optoelectronic properties has emerged as a promising semiconductor material with a potential to revolutionize the photovoltaic industry. Inadequate understanding of the thermal instability and lattice dynamics of MAPbI3, however, hinders its practical applications. Herein, combing molecular dynamics with a first-principles-based interatomic potential and inelastic neutron scattering measurements, we have performed an in-depth study of the lattice dynamics of MAPbI3. The extremely large line widths of the optical phonons in the tetragonal phase, which prevent direct experimental measurement of the phonon lifetimes, have been obtained for the first time. Our atomic-level study also reveals a giant pressure tuning effect on phonon scattering, which is related to the four-fold rotation of the MA+ cations around the C-N axis. A hydrostatic pressure as low as 6 kbar can alter the phonon lifetime by more than 1 order of magnitude. This work is expected to pave the way for further phonon engineering and thermal optimization of MAPbI3 and related perovskites.

Electron Correlation in the Ionization Continuum of Molecules: Photoionization of N2 in the Vicinity of the Hopfield Series of Autoionizing States.

Direct measurement of autoionization lifetimes by using time-resolved experimental techniques is a promising approach when energy-resolved spectroscopic methods do not work. Attosecond time-resolved experiments have recently provided the first quantitative determination of autoionization lifetimes of the lowest members of the well-known Hopfield series of resonances in N2. In this work, we have used the recently developed XCHEM approach to study photoionization of the N2 molecule in the vicinity of these resonances. The XCHEM approach allows us to describe electron correlation in the molecular electronic continuum at a level similar to that provided by multireference configuration interaction methods in bound state calculations, a necessary condition to accurately describe autoionization, shakeup, and interchannel couplings occurring in this range of photon energies. Our results show that electron correlation leading to interchannel mixing is the main factor that determines the magnitude and shape of the N2 photoionization cross sections, as well as the lifetimes of the Hopfield resonances. At variance with recent speculations, nonadiabatic effects do not seem to play a significant role. These conclusions are supported by the very good agreement between the calculated cross sections and those determined in synchrotron radiation and attosecond experiments.

Direct measurement of individual phonon lifetimes in the clathrate compound Ba7.81Ge40.67Au5.33

Engineering lattice thermal conductivity requires to control the heat carried by atomic vibration waves, the phonons. The key parameter for quantifying it is the phonon lifetime, limiting the travelling distance, whose determination is however at the limits of instrumental capabilities. Here, we show the achievement of a direct quantitative measurement of phonon lifetimes in a single crystal of the clathrate Ba7.81Ge40.67Au5.33, renowned for its puzzling ‘glass-like’ thermal conductivity. Surprisingly, thermal transport is dominated by acoustic phonons with long lifetimes, travelling over distances of 10 to 100 nm as their wave-vector goes from 0.3 to 0.1 Å−1. Considering only low-energy acoustic phonons, and their observed lifetime, leads to a calculated thermal conductivity very close to the experimental one. Our results challenge the current picture of thermal transport in clathrates, underlining the inability of state-of-the-art simulations to reproduce the experimental data, thus representing a crucial experimental input for theoretical developments.

Molecular engineering to improve carrier lifetimes for organic photovoltaic devices with thick active layers

The morphology of the bulk heterojunction absorber layer in an organic photovoltaic (OPV) device has a profound effect on the electrical properties and efficiency of the device. Previous work has consistently demonstrated that the solubilizing side-chains of the donor material affect these properties and device performance in a non-trivial way. Here, using Time-Resolved Microwave Conductivity (TRMC), we show by direct measurements of carrier lifetimes that the choice of side chains can also make a substantial difference in photocarrier dynamics. We have previously demonstrated a correlation between peak photoconductance measured by TRMC and device efficiencies; here, we demonstrate that TRMC photocarrier dynamics have an important bearing on device performance in a case study of devices made from donor materials with linear vs. branched side-chains and with variable active layer thicknesses. We use Grazing-Incidence Wide Angle X-ray Scattering to elucidate the cause of the different carrier lifetimes as a function of different aggregation behavior in the polymers. Ultimately, the results help establish TRMC as a technique for screening OPV donor materials whose devices maintain performance in thick active layers (>250 nm) designed to improve light harvesting, film reproducibility, and ease of processing.

Direct confocal lifetime measurements on rare-earth-doped media exhibiting radiation trapping

Radiation trapping occurs in rare-earth-doped active media with strong spectral overlap of luminescence and ground-state absorption. It is demonstrated experimentally that a confocal measurement mitigates the influence of radiation trapping on the measured luminescence lifetime, hence allowing for direct extraction of the lifetime from the measured decay curves. The radiation trapping effect is largely suppressed by probing a small sample volume and rejecting the photons reemitted from the unpumped region. This non-destructive measurement method is applied to ytterbium (Yb3+) activated potassium double tungstate crystalline layers with Yb3+ concentrations ranging from 1.2 at.% up to 76 at.% (~8 × 1019 – 5 × 1021 cm−3). The measured lifetime values are comparable to the results reported for Yb3+-doped potassium double tungstate powder diluted in liquid.

Two wavelength operation of an acousto-optically tuned quantum cascade laser and direct measurements of quantum cascade laser level lifetimes

We report simultaneous two wavelength operation of an acousto-optically tuned quantum cascade laser (QCL). The two wavelengths can be independently tuned as well as independently switched, retaining the submicrosecond switching capability. In addition, we have used the two wavelength operation as a tool for the direct measure of the lifetimes of the lasing states in a practical QCL. The lifetime measurements in an operational QCL are facilitated by our ability to vary the frequency separation between two simultaneously lasing wavelengths. The measured lifetime is 0.6 ps ± 0.2 ps for our quantum cascade laser. The two wavelength operation of QCLs paves the way for time resolved pump/probe studies of infrared phenomena and provides direct insight into the effectiveness of various QCL structure designs.

Diffusing Colloidal Probes of kT-Scale Biomaterial-Cell Interactions.

In the optimization of applied biomaterials, measurements of their interactions with cell surfaces are important to understand their influence on specific and nonspecific cell surface adhesion, internalization pathways, and toxicity. In this study, a novel approach using dark field video microscopy with combined real-time particle and cell tracking allows the trajectories of biomaterial-coated colloids to be monitored in relation to their distance from cell perimeters. Dynamic and statistical mechanical analyses enable direct measurement of colloid-cell surface association lifetimes and interaction potentials mediated by biomaterials. Our analyses of colloidal transport showed polyethylene glycol (PEG) and bovine serum albumin (BSA) lead to net repulsive interactions with cell surfaces, while dextran and hyaluronic acid (HA) lead to reversible and irreversible association to the cell surface, respectively. Our results demonstrate how diffusing colloidal probes can be used for nonobtrusive, sensitive measurements of biomaterial-cell surface interactions important to therapeutics, diagnostics, and tissue engineering.

Direct Lifetime Measurements of the Excited States in (72)Ni.

The lifetimes of the first excited 2^{+} and 4^{+} states in ^{72}Ni were measured at the National Superconducting Cyclotron Laboratory with the recoil-distance Doppler-shift method, a model-independent probe to obtain the reduced transition probability. Excited states in ^{72}Ni were populated by the one-proton knockout reaction of an intermediate energy ^{73}Cu beam. γ-ray-recoil coincidences were detected with the γ-ray tracking array GRETINA and the S800 spectrograph. Our results provide evidence of enhanced transition probability B(E2;2^{+}→0^{+}) as compared to ^{68}Ni, but do not confirm the trend of large B(E2) values reported in the neighboring isotope ^{70}Ni obtained from Coulomb excitation measurement. The results are compared to shell model calculations. The lifetime obtained for the excited 4_{1}^{+} state is consistent with models showing decay of a seniority ν=4, 4^{+} state, which is consistent with the disappearance of the 8^{+} isomer in ^{72}Ni.

Impact of Macular Pigment on Fundus Autofluorescence Lifetimes.

To characterize the macular region and to investigate the influence of the macular pigment (MP) on fundus autofluorescence (FAF) lifetimes in vivo. Forty-eight healthy subjects with a mean age of 24.1 ± 3.6 years (range, 20-37 years) were included. A 30° retinal field was investigated using the fluorescence lifetime imaging ophthalmoscope (FLIO), based on a Heidelberg Engineering Spectralis system, detecting FAF decays in a short (498-560 nm; ch1)- and a long (560-720 nm; ch2)-wavelength channel. The mean fluorescence lifetime τm was calculated from a 3-exponential approximation of the FAF decays. Macular pigment optical density (MPOD) was measured by one-wavelength reflectometry, and macular optical coherence tomogram (OCT) scans were recorded. Correlations between τm and MPOD were analyzed. The τm showed shortest values at the macular region with a mean of 82 ps (ch1) and 126 ps (ch2). We found a strong correlation of τm to the MPOD (ch1: r = -0.760; ch2: r = -0.663; P < 0.001), as well as a topologic agreement of shortest τm with highest MPOD. Macular pigment, which is known to have very short fluorescence decays, considerably contributes to the macular autofluorescence (AF). This study gives indirect evidence for a strong impact of MP on macular τm, although no direct measurement of MP autofluorescence lifetimes in vivo is possible at this point. Potentially, imaging the FAF lifetimes could lead to a novel methodology for the detection of macular pigment properties and pathology-induced changes in the living human retina.

Lifetime of inner-shell hole states of Ar (2p) and Kr (3d) using equation-of-motion coupled cluster method.

Auger decay is an efficient ultrafast relaxation process of core-shell or inner-shell excited atom or molecule. Generally, it occurs in femto-second or even atto-second time domain. Direct measurement of lifetimes of Auger process of single ionized and double ionized inner-shell state of an atom or molecule is an extremely difficult task. In this paper, we have applied the highly correlated complex absorbing potential-equation-of-motion coupled cluster (CAP-EOMCC) approach which is a combination of CAP and EOMCC approach to calculate the lifetime of the states arising from 2p inner-shell ionization of an Ar atom and 3d inner-shell ionization of Kr atom. We have also calculated the lifetime of Ar(2+)(2p(-1)3p(-1)) (1)D, Ar(2+)(2p(-1)3p(-1)) (1)S, and Ar(2+)(2p(-1)3s(-1)) (1)P double ionized states. The predicted results are compared with the other theoretical results as well as experimental results available in the literature.

Microscopic studies of nonlocal spin dynamics and spin transport (invited)

Understanding the behavior of spins coupling across interfaces in the study of spin current generation and transport is a fundamental challenge that is important for spintronics applications. The transfer of spin angular momentum from a ferromagnet into an adjacent normal material as a consequence of the precession of the magnetization of the ferromagnet is a process known as spin pumping. We find that, in certain circumstances, the insertion of an intervening normal metal can enhance spin pumping between an excited ferromagnetic magnetization and a normal metal layer as a consequence of improved spin conductance matching. We have studied this using inverse spin Hall effect and enhanced damping measurements. Scanned probe magnetic resonance techniques are a complementary tool in this context offering high resolution magnetic resonance imaging, localized spin excitation, and direct measurement of spin lifetimes or damping. Localized magnetic resonance studies of size-dependent spin dynamics in the absence of lithographic confinement in both ferromagnets and paramagnets reveal the close relationship between spin transport and spin lifetime at microscopic length scales. Finally, detection of ferromagnetic resonance of a ferromagnetic film using the photoluminescence of nitrogen vacancy spins in neighboring nanodiamonds demonstrates long-range spin transport between insulating materials, indicating the complexity and generality of spin transport in diverse, spatially separated, material systems.

Development of an Optical Dissolved Oxygen Sensor for Aquaculture Based on Direct Measurement of Fluorescence Lifetime

Development of an Optical Dissolved Oxygen Sensor for Aquaculture Based on Direct Measurement of Fluorescence Lifetime