Increasing Excitation Power Research Articles

Simulation of the electromagnetic scattering characteristics in inductively coupled plasma array for aircraft stealth

Abstract In this paper, an electromagnetic model of an inductively coupled plasma (ICP) array is developed to investigate its electromagnetic transmission characteristics under varying discharge conditions. The reliability of the model is enhanced by basing plasma parameters on simulation results from a fluid dynamics model. Electromagnetic simulations analyze the reflection spectrum of the inductively coupled plasma array, revealing the modulation mechanism of the plasma array. Findings indicate that as excitation power increases, the attenuation peak of the ICP array shifts to higher frequencies, and the attenuation bandwidth widens. By employing different power levels for the two layers in the Inductively Coupled Plasma (ICP) process, the array can achieve effective stealth performance with lower power consumption. Adjusting plasma discharge parameters to match specific scenarios enables the proposed plasma array to achieve varied modulation effects, expanding its potential applications in aircraft stealth.

Chromatic tuning of upconversion emission upon dual infrared wavelength co-excitation in Er3+ doped Ba3Lu4O9 phosphor

Emission color change of the upconversion luminescence materials is often required for applications in optical anti-counterfeiting, laser lighting, and 3D displays. In this work, we developed a new route for chromatic tuning of upconversion emission upon two wavelength co-excitation by changing excitation power density. The proposed route was used for Er3+ single-doped Ba3Lu4O9 phosphor which was derived from a traditional solid-state reaction. The crystal structure of the obtained Ba3Lu4O9:Er3+ phosphor was characterized by X-ray diffraction and Rietveld refinement modeling. Under individual excitation of 980 or 1550 nm, it was found that the luminescence intensity ratio of red to green changes slightly with respectively increasing excitation power density (working current of the laser) of 980 or 1550 nm laser. However, upon both 980 and 1550 nm co-excitation at the same time and by adjusting the excitation power density of one laser amongst the two lasers, the luminescence intensity ratio of red to green changes greatly with increasing excitation power density. The change of luminescence intensity ratio of red to green implies the upconversion emission color tuning. The mechanism for the color tuning was discovered. It was found that with changing excitation power density the ratio of red to green changed greatly when the phosphor was irradiated by 980 and 1550 together, but the ratio of red to green changed slightly when the phosphor was irradiated individually by 980 or 1550. It is proved that it is feasible to turn color by the method of two infrared wavelengths excitation.

Explaining the correlation between subharmonic amplitude and ambient pressure for subharmonic-aided pressure estimation (SHAPE)

BackgroundSubharmonic aided pressure estimation (SHAPE) is an innovative non-invasive technique that leverages ultrasound subharmonic imaging to estimate pressure. This method exploits the “negative correlation between subharmonic amplitude and ambient pressure” observed in experimental settings. Despite extensive experimental validation and some promising results in clinical studies, the underlying mechanism of SHAPE remains incompletely understood. Although some studies have attempted to provide theoretical explanations, definitive conclusions have yet to be reached. In addition, theoretical investigations have mainly focused on the steady oscillation of bubbles under long pulse excitation, which contrasts with the short pulse excitation required for clinical SHAPE applications. An understanding of the SHAPE principle under short pulse excitation is needed. MethodsThe exponential elasticity model (EEM) was used to simulate Sonazoid bubbles, and a probe-to-probe acoustic propagation model was introduced to mimic a practical SHAPE scenario. The simulated acoustic signals in response to three-cycle sinusoidal pulse excitations were analyzed for spectral composition. The relationship between microbubble oscillation patterns and subharmonic characteristics was identified through detailed investigation. ResultsFor the excitation pulse of 2.5 MHz frequency and 350 kPa magnitude, bubbles larger than the resonance radius (2.29 μm) exhibited significant subharmonics in the magnitude spectrum, while bubbles smaller than the subharmonic resonance radius (3.85 μm) showed the activity of scattering subharmonic energy and the sensitivity to ambient pressure. The emergence of subharmonics when increasing excitation power was related to the increasing amplification of the bubble self-oscillation and the period-doubling features in the acoustically forced oscillation. The negative correlation between subharmonic amplitude and ambient pressure was attributed to the reduced self-oscillation caused by increasing ambient pressure and hence bubble size reduction. Microbubbles falling between 2 and 3 μm showed the desired subharmonic sensitivity to ambient pressure under the specified excitation conditions. ConclusionThe transient oscillatory behavior of microbubbles in response to short pulse excitation, characterized by a ringing down self-oscillation after the acoustic forcing effect has ceased, is crucial for understanding the subharmonic emergence and the observed negative correlation between subharmonic amplitude and ambient pressure. The proposed concepts of subharmonic resonance radius, subharmonic-significant bubbles, and subharmonic-active bubbles provide valuable insights into the diverse subharmonic behavior of microbubbles. The theoretical explanation of this negative correlation highlights the importance of using subharmonic-significant-and-active bubbles for SHAPE applications.

Novel transparent glass-ceramics of NaLu2F7:Yb3+, Er3+ for accurate temperature sensing and anti-counterfeiting

The development of up-conversion materials with strong emission and low thermal effect is crucial for achieving higher temperature sensing accuracy. In this work, novel transparent NaLu2F7:xYb3+, 0.02Er3+ (x = 0, 0.2, 0.4, 0.6, 0.8, 1) glass-ceramics (GCs) were manufactured by melt-quenching technique. The temperature sensing capabilities of GC20 based on thermally coupled energy levels (TCELs) and non-thermally coupled energy levels (nTCELs) were studied, which enable self-calibration. Our findings reveal that the maximum relative sensitivity (SRmax) of TCELs and nTCELs are 1.19% K−1 and 0.89% K−1 at 313 K, respectively. More importantly, the UC luminescence color of GC20 varies from yellow to green as the excitation power increases. The unique phenomenon can be utilized for anti-counterfeiting purposes without any background interference. Overall, our results demonstrate that these novel GCs possess significant potential in accurate temperature sensing and anti-counterfeiting fields.

Space–Charge‐Limited Photocurrent as a Possible Cause for Low Power Conversion Efficiency in GaInN/GaN‐Based Optoelectronic Semiconductors

This study attempts to understand the cause of low power conversion efficiency (PCE) in III‐nitride optoelectronic semiconductors under optical operation. For this purpose, a GaInN/GaN heterojunction semiconductor is fabricated, and the photoexcited current–voltage (PEJV) curves are carefully measured depending on the optical excitation power and temperature. The results show unexpected excitation power‐ and temperature‐dependent behaviors, that is, the PCE decreases with increasing excitation power and increases with increasing temperature. To understand this, the space–charge‐limited photocurrent (JPh,SCL) theory (also referred to as Goodman and Rose theory) is employed, where the accumulated charge carriers in the active layer play a significant role. The conduction of JPh,SCL is ascertained by analyzing the PEJV curves. The conduction of JPh,SCL is investigated as a possible cause of the low PCE, revealing that the conduction of JPh,SCL could limit the high‐power operation of the device.

Photoluminescence modal splitting via strong coupling in hybrid Au/WS2/GaP nanoparticle-on-mirror cavities.

By integrating dielectric and metallic components, hybrid nanophotonic devices present promising opportunities for manipulating nanoscale light-matter interactions. Here, we investigate hybrid nanoparticle-on-mirror optical cavities, where semiconductor WS2 monolayers are positioned between gallium phosphide (GaP) nanoantennas and a gold mirror, thereby establishing extreme confinement of optical fields. Prior to integration of the mirror, we observe an intermediate coupling regime from GaP nanoantennas covered with WS2 monolayers. Upon introduction of the mirror, enhanced interactions lead to modal splitting in the exciton photoluminescence spectra, spatially localized within the dielectric-metallic gap. Using a coupled harmonic oscillator model, we extract an average Rabi splitting energy of 22.6 meV at room temperature, at the onset of the strong coupling regime. Moreover, the characteristics of polaritonic emission are revealed by the increasing Lorentzian linewidth and energy blueshift with increasing excitation power. Our findings highlight hybrid nanophotonic structures as novel platforms for controlling light-matter coupling with atomically thin materials.

Effect of Zn2+, S2−, Mo4+ and V5+ single doped BiTa7O19:Er3+/Yb3+ on upconversion luminescence intensity under 980 nm laser excitation

On the basis of BiTa7O19 (BTO):0.1Er3+/0.4 Yb3+, Zn2+, S2−, Mo4+ and V5+ single doped upconversion phosphors (UCP) were successfully prepared by solid phase sintering. The lattice structure, particle size and diffuse reflectance spectra were measured by X-ray diffraction, scanning electron microscope and spectrophotometer. Upconversion luminescence (UCL) spectra of these UCP were investigated under 980 nm laser excitation with power density from 1.82 to 124.99 W/cm2. Zn2+ doped UCP can obtain the highest UCL intensity when excitation power density is less than 56.91 W/cm2, and Mo4+ doped UCP can obtain the highest UCL intensity when excitation power density is from 56.91 to 124.99 W/cm2. The UCL intensity of all samples increases first and then decreases with the increase of excitation power. By measuring UCL intensity changes with the excitation power of the UCP mixing with BN and UCP in vacuum and atmosphere, the experimental results show that the increase of temperature caused by laser excitation is the reason for the decrease of UCL intensity under high power excitation. Utilizing LIR technology, it is proven that at high power 90.95 W/cm2, Mo4+ and Zn2+ single doped can decrease and increase the UCP temperature under the same power density excitation compared with BTO:0.1Er3+/0.4 Yb3+, respectively. The maximum relative temperature sensitivity of all UCP is calculated in the range of 0.00767–0.00854 K−1 at 303 K. All experiments show that Zn2+ and Mo4+ single-doped UCP are suitable for temperature sensing and luminescence imaging under low and high-power excitation, respectively.

Observation of aligned dipoles and angular chromism of exciplexes in organic molecular heterostructures

The dipole characteristics of Frenkel excitons and charge-transfer excitons between donor and acceptor molecules in organic heterostructures such as exciplexes are important in organic photonics and optoelectronics. For the bilayer of the organic donor 4,4′,4′′-tris[(3-methylphenyl)phenylamino]triphenylamine and acceptor 2,4,6-tris(biphenyl-3-yl)-1,3,5-triazine molecules, the exciplexes form aligned dipoles perpendicular to the Frenkel excitons, as observed in back focal plane photoluminescence images. The angular chromism of exciplexes observed in the 100 meV range indicates possible delocalization and angle-sensing photonic applications. The blue shift of the peak position and increase in the linewidth of photoluminescene spectra with increasing excitation power are caused by the repulsive aligned exciplex dipole moments with a long lifetime (4.65 μs). Electroluminescence spectra of the exciplex from organic light-emitting diodes using the bilayer are blue-shifted with increasing bias, suggesting unidirectional alignment of the exciplex dipole moments. The observation of exciplex dipole moment alignments across molecular interfaces can facilitate the controlled coupling of exciton species and increase efficiency of organic light-emitting diodes.

Broad Luminescence Generated by IR Laser Excitation from CsPbBr3:Yb3+ Perovskite Ceramics.

This paper demonstrates the generation of broadband emission in the visible and infrared ranges induced by a concentrated beam of infrared radiation from CsPbBr3 ceramics doped with Yb3+ ions. The sample was obtained by the conventional solid-state reaction method, and XRD measurements confirmed the phase purity of the material crystallizing in the orthorhombic system. Spectroscopic measurements required further sample preparation in the form of ceramics using a high-pressure press. The research showed that as the excitation power increases, the emission intensity does not increase linearly from the beginning of the experiment. Irradiation of the material results in the accumulation of the delivered energy. Absorption of a sufficient number of photons triggers avalanche emission. It was found that the most intense luminescence is produced in a vacuum. Changes in conductivity were also observed, where the excitation was able to lower the resistivity of the material and it was highly dependent on the excitation power. The mechanism responsible for the generation of the observed phenomenon involving intervalence charge transfer (IVCT) transitions has been postulated.

Effect of Doping Concentration and Excitation Power on Upconversion and Temperature Sensitivity of Gd3Ga5O12:Yb3+/Er3+ Phosphors

Yb/Er codoped Gd3Ga5O12 nanocrystalline upconverting phosphors were produced by the sol-gel pechini method at 1000 °C annealing temperature. The phosphor structure, morphological features, and luminescent properties of the fabricated material were studied using X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HR-TEM), and photoluminescence measurements (PL). Upconversion luminescence characteristics were investigated in the range of 450-850 nm by a 975 nm laser source. Emission, optical, and theoretical thermal behaviors were analyzed with respect to Er3+ ion content and the increasing excitation power. Temperature sensitivity calculations based on the fluorescence intensity ratio were performed by employing the thermally-coupled levels of Er3+. The maximum sensitivity was calculated with the optimal value of 0.83x10-2 K-1 for Gd3Ga5O12:2%Yb3+,0.5%Er3+ nanophosphor. The results pointed out that Yb/Er codoped Gd3Ga5O12 may be a potential candidate for optical temperature sensors and lighting.

Interfacial-Water-Modulated Photoluminescence of Single-Layer WS2 on Mica.

Because of their bandgap tunability and strong light-matter interactions, two-dimensional (2D) semiconductors are considered promising candidates for next-generation optoelectronic devices. However, their photophysical properties are greatly affected by their surrounding environment because of their 2D nature. In this work, we report that the photoluminescence (PL) of single-layer WS2 is substantially affected by interfacial water that is inevitably present between it and the supporting mica substrates. Using PL spectroscopy and wide-field imaging, we show that the emission signals from A excitons and their negative trions decreased at distinctively different rates with increasing excitation power, which could be attributed to the more efficient annihilation between excitons than between trions. By gas-controlled PL imaging, we also prove that the interfacial water converted the trions into excitons by depleting native negative charges through an oxygen reduction reaction, which rendered the excited WS2 more susceptible to nonradiative decay via exciton-exciton annihilation. Understanding the role of nanoscopic water in complex low-dimensional materials will eventually contribute to devising their novel functions and related devices.

Power dependent photoacoustic and photoluminescence studies on a Ho3+/Yb3+ doped Y2O3 phosphor.

The Ho3+/Yb3+ doped Y2O3 phosphor samples were synthesized through a combustion method and then were annealed at 800 °C, 1000 °C, and 1200 °C. The cubic phase of the synthesized samples was confirmed by XRD analysis. The upconversion (UC) & photoacoustic (PA) spectroscopic studies were done on prepared samples and both spectra are compared. The samples have shown intense green upconversion emission at 551 nm due to the 5S2 → 5I8 transition of Ho3+ ion along with other bands. The maximum emission intensity is obtained for the sample annealed at 1000 °C for 2 hours. The authors have also measured the lifetime corresponding to 5S2 → 5I8 transition and found that lifetime values follow the trend of upconversion intensity. The maximum lifetime of 224 μs is observed for the sample annealed at 1000 °C. A photoacoustic cell & a pre-amplifier was fabricated and optimized for maximum sensitivity of the system. The PA signal was found to increase with increase of excitation power within the studied range, while UC emission was found to saturate after a certain pump power. The increase in PA signal is due to the increase in non-radiative transitions in the sample. The wavelength-dependent photoacoustic spectrum of sample has shown absorption bands around 445, 536, 649 and 945 (970) nm with maximum absorption at 945 (970) nm. This indicates its potential for photo-thermal therapy using infrared excitation.

Achieving excitation wavelength-power-dependent colorful luminescence via multiplexing of dual lanthanides in fluorine oxide particles for multilevel anticounterfeiting.

The optical characteristics of multimode luminescent materials like multimode luminescence (photoluminescence, afterglow, thermoluminescence) and a multi-excitation source (light, thermal, mechanical force) play crucial roles in optical data storage and readout, document security and anticounterfeiting. A higher level of advanced anticounterfeiting may rely on multimode anticounterfeiting materials that can realize multicolor luminescence. Here, a highly integrated multimode and multicolor Y7O6F9:Er3+,Eu3+ material is developed through multiplexing of dual lanthanides in fluorine oxide particles. In photoluminescence and photoluminescence/up-conversion luminescence modes, the material Y7O6F9:Er3+,Eu3+ has the characteristic of excitation wavelength and power dependence. In the photoluminescence mode, under excitation at 254 nm and 365 nm, Y7O6F9:Er3+ and Y7O6F9:Eu3+ showed bright red and green emissions, respectively. In the photoluminescence/up-conversion mode, under the increased excitation power from 0.2 to 2.0 W cm-2, the color of luminescence emission can be finely tuned from red to orange, yellow and green. Taking this unique excitation wavelength-power-dependent luminescence property into account, a multilevel anticounterfeiting device with the Lily pattern was designed. The device readily integrates the advantages of the excitation wavelength-dependent photoluminescence emissions and excitation power-dependent photoluminescence emissions in one overall device. These findings offer unique insight for designing highly integrated multimode, multicolor luminescence materials and advanced anticounterfeiting technology toward a wide variety of applications, particularly multilevel anticounterfeiting devices.

SILAR ve Dönel Kaplama Yöntemleri Kullanılarak Büyütülen ZnO İnce Filmlerin Yapısal, Yüzeysel ve Optik Karakterizasyonu

In this study, ZnO thin films were deposited on (1 1 1) oriented n-type and (1 0 0) oriented p-type Si substrates using SILAR and spin-coating methods, respectively. The XRD, SEM, and PL measurements of the samples were performed. The XRD results showed the presence of ZnO peaks. The SEM results showed that the surfaces were homogeneous in both methods, and nanorods were present in the samples grown by the SILAR method. The PL results showed that the samples emitted light at different wavelengths. The PL results under different powers were interpreted from the samples, and it was determined that this sample reached a higher emission intensity with increasing excitation power.

Limitation of room temperature phosphorescence efficiency in metal organic frameworks due to triplet-triplet annihilation.

The effect of triplet-triplet annihilation (TTA) on the room-temperature phosphorescence (RTP) in metal-organic frameworks (MOFs) is studied in benchmark RTP MOFs based on Zn metal centers and isophthalic or terephthalic acid linkers (ZnIPA and ZnTPA). The ratio of RTP to singlet fluorescence is observed to decrease with increasing excitation power density. Explicitly, in ZnIPA the ratio of the RTP to fluorescence is 0.58at 1.04mWcm-2, but only 0.42at (the still modest) 52.6mWcm-2. The decrease in ratio is due to the reduction of RTP efficiency at higher excitation due to TTA. The density of triplet states increases at higher excitation power densities, allowing triplets to diffuse far enough during their long lifetime to meet another triplet and annihilate. On the other hand, the shorter-lived singlet species can never meet an annihilate. Therefore, the singlet fluorescence scales linearly with excitation power density whereas the RTP scales sub-linearly. Equivalently, the efficiency of fluorescence is unaffected by excitation power density but the efficiency of RTP is significantly reduced at higher excitation power density due to TTA. Interestingly, in time-resolved measurements, the fraction of fast decay increases but the lifetime of long tail of the RTP remains unaffected by excitation power density. This may be due to the confinement of triplets to individual grains, leading decay to be faster until there is only one triplet per grain left. Subsequently, the remaining "lone triplets" decay with the unchanging rate expressed by the long tail. These results increase the understanding of RTP in MOFs by explicitly showing the importance of TTA in determining the (excitation power density dependent) efficiency of RTP. Also, for applications in optical sensing, these results suggest that a method based on long tail lifetime of the RTP is preferable to a ratiometric approach as the former will not be affected by variation in excitation power density whereas the latter will be.

Theoretical insight on the saturated stimulated emission intensity of a squaraine dye for STED nanoscopy

Stimulated emission depletion nanoscopy (STED) is increasingly applied for the insights into the ultra-structures of organelles in live cells because of the bypassing of the Abbe’s optical diffraction limit. Theoretically, with the increase of excitation and depletion laser power, the imaging resolution can be accordingly enhanced and even close to the infinity. Unfortunately, powerful laser illuminations usually produce severe phototoxicity and photobleaching, which will lead to more extra-interference with biological events in live cells and accelerate the decomposition of the fluorescent probes. In view of the trade-off of cell viability and imaging resolution, excellent probes with superior photophysical properties are great in demand. For a qualified STED probes, the saturated stimulated emission intensity (Isat) is considered as a key evaluating factor. According to the formula, Isat is inversely proportional to the stimulated emission cross section (σsti) of the fluorescent probe. However, the relationship between the σsti and chemical structure of the STED probe remain to be unclear. In this work, we explore the influence factors by theoretical calculations on a squaraine dye (MitoEsq-635) and a commercial dye (Atto647N). The results indicate that the increase of transition dipole moment (μ) are beneficial for the increase of σsti, thereafter reducing Isat. Furthermore, we firstly proposed that stimulated emission depletion was qualitatively interpreted by the investigation on the potential energy surfaces of ground states (S0) and the first excited states (S1) of the dyes.

Effect of Diode Field on Time-Resolved Photoluminescence of CdTe-Based Solar Cells

Time-resolved photoluminescence (TRPL) measurements with externally applied voltage bias were performed on a variety of thin-film CdTe-based solar cells. These measurements revealed a substantial variation in luminescence decays with the application of external voltage bias in many of the samples. Experimental results were replicated with a MATLAB-based modeling tool. Decay variations are attributed to the changing strength of internal p-n junction electric fields as bias is modulated; this exercise, therefore, illustrates whether or not field effects influence a particular TRPL measurement and how. It is found via modeling that the field influence on TRPL decays is dependent on the cell's bulk minority carrier lifetime, mobility, and carrier concentration, as well as the laser excitation power during a measurement. While nearly insignificant in poorer quality legacy cells, the field effects are substantial in state-of-the-art CdTe cells with high lifetime, mobility, and doping, complicating determination of bulk lifetime. It is found that forward bias is effective in eliminating junction fields. It is also shown that fields can be effectively suppressed by increasing excitation power, but doing so is imprecise and can also introduce additional errors unrelated to fields. It is therefore concluded that lifetime is most accurately measured in completed cells under forward bias at low excitation intensity.

Temperature and power characteristics of quarter-wavelength superconducting coplanar waveguide resonator

A quarter wavelength superconducting aluminum film coplanar waveguide resonator with a high-quality factor was designed and fabricated. Furthermore, its resonant frequency and quality as a function of temperatures and exciting powers were investigated. The experimental results showed that the resonance frequency decreases about 1% with the increase of temperature from 50 mk to 1 K, and the load quality factor of the resonator also decreases. The resonant frequency decreases with power from − 120 to − 70 dBm. The quality factor increases with increased excitation power due to the loss decreases and nonlinearity. The results are consistent with the theoretical analysis of the surface impedance model.

Dynamic Response of Bridge-Landslide Parallel System under Earthquake

In order to further understand the instability mechanism and geohazard causation when the main sliding path of the slope body is parallel to the path of the bridge, the corresponding bridge-landslide parallel system is constructed for shaking table tests. This paper summarizes the combination forms of bridge-landslide model under different position and focused on the slope body located above the bridge deck. Firstly, based on the shaking table test results of El Centro (1940), the failure behavior of bridge-landslide parallel system was evaluated, and the changes of acceleration and deformation of bridge pile were subsequently analyzed. Then, the interaction bridge structure and sliding body were explained by the spectral features. The main conclusions are as follows. First, in the model test, the landslide belongs to the thrust-type landslide. Due to the barrier function of the bridge, the main failure site of landslide occurs in the middle and trailing edge of slope body. At the same time, the acceleration value of earthquake waves is 0.3 g, which is the key to this variation. Second, the acceleration response of the measuring points on the bridge pile and landslide increases with the increase of ground elevation. If the slope structure is damaged severely, the deformation response of weak interlayer is inconsistent with the surrounding soil structure. Third, with the increase of excitation power, the dominant frequency of bridge-landslide parallel system gradually transitions from low to high frequency rate, and the interaction of the parallel system weakens the influence of river direction on frequency. Finally, under the same working condition, the dynamic response of the measuring points has obvious regularity with the change of situation. But the response of the same points is not regular due to the different earthquake excitation intensity.

Reverse Intersystem Crossing of Single Deuterated Perylene Molecules in a Dibenzothiophene Matrix.

Intersystem crossing to the long‐lived metastable triplet state is often a strong limitation on fluorescence brightness of single molecules, particularly for perylene in various matrices. In this paper, we report on a strong excitation‐induced reverse intersystem crossing (rISC), a process where single perylene molecules in a dibenzothiophene matrix recover faster from the triplet state, turning into bright emitters at saturated excitation powers. With a detailed study of single‐molecule fluorescence autocorrelations, we quantify the effect of rISC. The intrinsic lifetimes found for the two effective triplet states (8.5±0.4 ms and 64±12 ms) become significantly shorter, into the sub‐millisecond range, as the excitation power increases and fluorescence brightness is ultimately enhanced at least fourfold. Our results are relevant for the understanding of triplet state manipulation of single‐molecule quantum emitters and for markedly improving their brightness.