Stacking-Order-Driven Optical Properties and Carrier Dynamics in ReS2

Two distinct stacking orders in ReS₂ are identified without ambiguity and their influence on vibrational, optical properties and carrier dynamics are investigated. With atomic resolution scanning transmission electron microscopy (STEM), two stacking orders are determined as AA stacking with negligible displacement across layers, and AB stacking with about a one-unit cell displacement along the a axis. First-principles calculations confirm that these two stacking orders correspond to two local energy minima. Raman spectra inform a consistent difference of modes I & III, about 13 cm⁻¹ for AA stacking, and 20 cm⁻¹ for AB stacking, making a simple tool for determining the stacking orders in ReS₂. Polarized photoluminescence (PL) reveals that AB stacking possesses blueshifted PL peak positions, and broader peak widths, compared with AA stacking, indicating stronger interlayer interaction. Transient transmission measured with femtosecond pump–probe spectroscopy suggests exciton dynamics being more anisotropic in AB stacking, where excited state absorption related to Exc. III mode disappears when probe polarization aligns perpendicular to b axis. The findings underscore the stacking-order driven optical properties and carrier dynamics of ReS₂, mediate many seemingly contradictory results in the literature, and open up an opportunity to engineer electronic devices with new functionalities by manipulating the stacking order.     

Ultrafast Carrier Dynamics and Bandgap Renormalization in Layered PtSe2

Carrier interactions in 2D nanostructures are of central importance not only in condensed‐matter physics but also for a wide range of optoelectronic and photonic applications. Here, new insights into the behavior of photoinduced carriers in layered platinum diselenide (PtSe₂) through ultrafast time‐resolved pump–probe and nonlinear optical measurements are presented. The measurements reveal the temporal evolution of carrier relaxation, chemical potential and bandgap renormalization in PtSe₂. These results imply that few‐layer PtSe₂ has a semiconductor‐like carrier relaxation instead of a metal‐like one. The relaxation follows a triple‐exponential decay process and exhibits thickness‐dependent relaxation times. This occurs along with a band‐filling effect, which can be controlled based on the number of layers and may be applied in saturable absorption for generating ultrafast laser pulses. The findings may provide means to study many‐body physics in 2D materials as well as potentially leading to applications in the field of optoelectronics and ultrafast photonics.     

Transient SHG Imaging on Ultrafast Carrier Dynamics of MoS2 Nanosheets

Understanding the collaborative behaviors of the excitons and phonons that result from light–matter interactions is important for interpreting and optimizing the underlying fundamental physics at work in devices made from atomically thin materials. In this study, the generation of exciton‐coupled phonon vibration from molybdenum disulfide (MoS₂) nanosheets in a pre‐excitonic resonance condition is reported. A strong rise‐to‐decay profile for the transient second‐harmonic generation (TSHG) of the probe pulse is achieved by applying substantial (20%) beam polarization normal to the nanosheet plane, and tuning the wavelength of the pump beam to the absorption of the A‐exciton. The time‐dependent TSHG signals clearly exhibit acoustic phonon generation at vibration modes below 10 cm^?1 (close to the Γ point) after the photoinduced energy is transferred from exciton to phonon in a nonradiative fashion. Interestingly, by observing the TSHG signal oscillation period from MoS₂ samples of varying thicknesses, the speed of the supersonic waves generated in the out‐of‐plane direction (Mach 8.6) is generated. Additionally, TSHG microscopy reveals critical information about the phase and amplitude of the acoustic phonons from different edge chiralities (armchair and zigzag) of the MoS₂ monolayers. This suggests that the technique could be used more broadly to study ultrafast physics and chemistry in low‐dimensional materials and their hybrids with ultrahigh fidelity.     

Pump- and Probe-polarization Analyses of Ultrafast Carrier Dynamics in Organic Superconductors

We investigated photo-excited carrier relaxation dynamics in the strongly correlated organic superconductors κ-(BEDT-TTF)₂Cu(NCS)₂ and κ-(BEDT-TTF)₂Cu[N(CN)₂]Br, using different polarizations of pump and probe pulses. Below the glasslike transition temperature (T _g) anisotropic responses for probe polarization were observed in both compounds. Decomposing the data into anisotropic and isotropic components, we found the anisotropic component shows no pump polarization dependence, meaning that dissipative excitation process was dominant for the anisotropic carrier relaxation. This behavior indicates that the appearance of anisotropic responses can be associated with spatial symmetry breaking due to structural change of BEDT-TTF molecules.     

Direct Observation and Interpretation of Carrier Dynamics of Molecular Magnetic Superconductors

The temperature-dependent time-resolved reflectance spectra of the organic superconductors (OSs) κ- and λ-(BETS)₂MCl₄ (M=Fe, Ga) and κ-(ET)₂Cu[N(CN)₂]Br are reported. The π electrons of the organic molecules (BETS or ET) are responsible for the electrical conduction in these salts, while only the Fe-containing salts have localized spins on the d electrons in the Fe atoms (S=5/2) with π–d interaction. Analysis of the spectra provided the relaxation time τ of the carriers, as well as information concerning the number of carriers at the Fermi energy N(E _F). The carrier dynamics were classified in terms of high-T _C and low-T _C OSs. In these salts, the results indicate that (1) the electron-phonon interaction is important in the occurrence and stability of the superconducting phase, and (2) electron correlation can be related to the enhancement of T _C.     

Nonequilibrium Carrier Dynamics Studied in Underdoped Bi2212 by Polarized Optical Pump-Probe Spectroscopy

We investigate nonequilibrium quasiparticle dynamics measured by ultrafast optical spectroscopy on underdoped Bi2212 crystals, which provide direct evidence that superconducting (SC) and pseudogap (PG) quasiparticles coexist below T _c . We verify that the ratio of signals from SC and PG quasiparticles depends on both excitation energy and polarization of the probe beam due to the anisotropy of the probe transition matrix elements and the interband transition probability. Based on this property, we successfully separate the SC or PG component and precisely evaluate the temperature dependence of them across T _c .     

Sub-Picosecond Carrier Dynamics Explored using Automated High-Throughput Studies of Doping Inhomogeneity within a Bayesian Framework

Bottom–up production of semiconductor nanomaterials is often accompanied by inhomogeneity resulting in a spread in electronic properties which may be influenced by the nanoparticle geometry, crystal quality, stoichiometry, or doping. Using photoluminescence spectroscopy of a population of more than 11 000 individual zinc-doped gallium arsenide nanowires, inhomogeneity is revealed in, and correlation between doping and nanowire diameter by use of a Bayesian statistical approach. Recombination of hot-carriers is shown to be responsible for the photoluminescence lineshape; by exploiting lifetime variation across the population, hot-carrier dynamics is revealed at the sub-picosecond timescale showing interband electronic dynamics. High-throughput spectroscopy together with a Bayesian approach are shown to provide unique insight in an inhomogeneous nanomaterial population, and can reveal electronic dynamics otherwise requiring complex pump-probe experiments in highly non-equilibrium conditions.     

Morphology-Dependent Charge Carrier Dynamics and Ion Migration Behavior of CsPbBr3 Halide Perovskite Quantum Dot Films

Exceptional electronic, optoelectronic, and sensing properties of inorganic Cs-based perovskites are significantly influenced by the defect chemistry of the material. Although organic halide perovskites that have a polycrystalline structure are heavily studied, understanding of the defect properties at the grain boundaries (GB) of inorganic Cs-based perovskite quantum dots (QDs) is still limited. Here, morphology-dependent charge carrier dynamics of CsPbBr₃ quantum dots at the nanoscale by performing scanning probe microscopy of thermally treated samples are investigated. The grain boundaries of defect-engineered samples show higher surface potential than the grain interiors under light illumination, suggesting an effective role of GBs as charge collection and transport channels. The lower density of crystallographic defects and lower trap density at GBs specifically of heat-treated samples cause insignificant dark current, lower local current hysteresis, and higher photocurrent, than the control samples. It is also shown that the decay rate of surface photovoltage of the heated sample is quicker than the control sample, which implies a considerable impact of ion migration on the relaxation dynamic of photogenerated charge carriers. These findings reveal that the annealing process is an effective strategy to control not only the morphology but also the optoelectrical properties of GB defects, and the dynamic of ion migration. Understanding the origin of photoelectric activity in this material allows for designing and engineering optoelectronic QD devices with enhanced functionality.     

High‐Temperature Ionic Epitaxy of Halide Perovskite Thin Film and the Hidden Carrier Dynamics

High‐temperature vapor phase epitaxy (VPE) has been proved ubiquitously powerful in enabling high‐performance electro‐optic devices in III–V semiconductor field. A typical example is the successful growth of p‐type GaN by VPE for blue light‐emitting diodes. VPE excels as it controls film defects such as point/interface defects and grain boundary, thanks to its high‐temperature processing condition and controllable deposition rate. For the first time, single‐crystalline high‐temperature VPE halide perovskite thin film has been demonstrated—a unique platform on unveiling previously uncovered carrier dynamics in inorganic halide perovskites. Toward wafer‐scale epitaxial and grain boundary‐free film is grown with alkali halides as substrates. It is shown the metal alkali halides could be used as universal substrates for VPE growth of perovskite due to their similar material chemistry and lattice constant. With VPE, hot photoluminescence and nanosecond photo‐Dember effect are revealed in inorganic halide perovskite. These two phenomena suggest that inorganic halide perovskite could be as compelling as its organic–inorganic counterpart regarding optoelectronic properties and help explain the long carrier lifetime in halide perovskite. The findings suggest a new avenue on developing high‐quality large‐scale single‐crystalline halide perovskite films requiring precise control of defects and morphology.     

The Role of Excitation Photons Energy in the Photoinduced Carrier Dynamics in InGaAs/InAlAs Superlattice Heterostructures

Technical Physics Letters - The influence of excitation photons energy on the relaxation times of photoexcited carriers is studied. The involved relaxation mechanisms are evaluated and the...     

Carrier Diffusivity Measurement in Silicon Wafers Using Free Carrier Absorption

In this article, it has been shown that the modulated free carrier absorption method (MFCA) can be used to determine unambiguously and without contact the carrier diffusivity of semiconductor wafers. The linear dependence of the phase on the distance of pump and probe beams are investigated with computer simulation, and then it has been found that at high frequency the slope of the MFCA phase versus distance depends solely on the carrier diffusivity. Hence, the carrier diffusivity can be extracted from the slope of the phase versus distance. Experiments were carried out on an $n$ -type Si wafer with 7 $\Omega \, \cdot $  cm to 10 $\Omega \, \cdot $  cm resistivity and (525 $\pm $ 20) $\mu $ m thickness. Comparing the experimental fitted results to those by fitting the MFCA amplitude and phase on the pump-probe-beam separation measured at several modulation frequencies to the rigorous three-dimensional carrier diffusion model, the fitted results by both methods agreed well. This shows that the simplified model can be used to determine the carrier diffusivity with high precision.     

Regulation of Charge Carrier Dynamics in ZnO Microarchitecture‐Based UV/Visible Photodetector via Photonic‐Strain Induced Effects

A feasible, morphological influence on photoresponse behavior of ZnO microarchitectures such as microwire (MW), coral‐like microstrip (CMS), fibril‐like clustered microwire (F‐MW) grown by one‐step carrier gas/metal catalyst “free” vapor transport technique is reported. Among them, ZnO F‐MW exhibits higher photocurrent (I_Ph) response, i.e., I_{Ph/ZnO F‐MW} > I_{Ph/ZnO CMS} > I_{Ph/ZnO MW}. The unique structural alignment of ZnO F‐MW has enhanced the I_Ph from 14.2 to 186, 221, 290 µA upon various light intensities such as 0 to 6, 11, 17 mW cm^?2 at λ_{405 nm}. Herein, the nature of the as‐fabricated ZnO photodetector (PD) is also demonstrated modulated by tuning the inner crystals piezoelectric potential through the piezo‐phototronic effect. The I_Ph response of PD decreases monotonically by introducing compressive strain along the length of the device, which is due to the synergistic effect between the induced piezoelectric polarization and photogenerated charge carriers across the metal–semiconductor interface. The current behavior observed at the two interfaces acting as the source (S) and drain (D) is carefully investigated by analyzing the Schottky barrier heights (Φ_SB). This work can pave the way for the development of geometrically modified strain induced performances of PD to promote next generation self‐powered optoelectronic integrated devices and switches.     

Chitosan-Alginate Microparticles as a Protein Carrier

The oral administration of peptidic drugs requires their protection from degradation in the gastric environment and the improvement of their absorption in the intestinal tract. For these requirements, a microsystem based on cross-linked alginate as the carrier of bovine serum albumin (BSA), used as a model protein, was proposed. A spray-drying technique was applied to BSA/sodium alginate solutions to obtain spherical particles having a mean diameter less than 10 μm. The microparticles were hardened using first a solution of calcium chloride and then a solution of chitosan (CS) to obtain stable microsystems. The cross-linking process was carried out at different CS concentrations and pH values of the cross-linking medium. The CS concentration affected the BSA loading in the microparticles prepared at a pH value less than the protein isoelectric point (pI). Moreover, the BSA loading at a pH value less than the pI was higher than that at a pH similar to the pI regardless of the CS concentration. This finding could be attributable to the formation of a BSA/alginate complex. The evaluation of the interaction between BSA and alginate at different pH values by means rheological measurements confirmed this hypothesis. This approach may represent a promising way to devise a microcarrier system with appropriate size for targeting the Peyer's patches, with appropriate immobilization capacity, and suitable for the oral administration of peptidic drugs.     

琼脂糖-透明质酸共聚物作为胰岛素载体

本文主要研究了一种新型的多肽药物载体材料的制备方法及其释药特征。首先氧化降解成小分子量、低凝胶温度的琼脂糖,用环氧氯丙烷活化后,与透明质酸共混接枝制备成琼脂糖-透明质酸共聚物,再用该共聚物包载胰岛素,并观察所形成微粒的形态及其释药行为。红外光谱及元素分析结果显示成功制备了琼脂糖接枝透明质酸共聚物;释药实验表明包载的胰岛素有缓释行为。因此,琼脂糖接枝透明质酸有望成为胰岛素的缓释载体。     

Chitosan-Alginate Microparticles as a Protein Carrier

The oral administration of peptidic drugs requires their protection from degradation in the gastric environment and the improvement of their absorption in the intestinal tract. For these requirements, a microsystem based on cross-linked alginate as the carrier of bovine serum albumin (BSA), used as a model protein, was proposed. A spray-drying technique was applied to BSA/sodium alginate solutions to obtain spherical particles having a mean diameter less than 10 μm. The microparticles were hardened using first a solution of calcium chloride and then a solution of chitosan (CS) to obtain stable microsystems. The cross-linking process was carried out at different CS concentrations and pH values of the cross-linking medium. The CS concentration affected the BSA loading in the microparticles prepared at a pH value less than the protein isoelectric point (pI). Moreover, the BSA loading at a pH value less than the pI was higher than that at a pH similar to the pI regardless of the CS concentration. This finding could be attributable to the formation of a BSA/alginate complex. The evaluation of the interaction between BSA and alginate at different pH values by means rheological measurements confirmed this hypothesis. This approach may represent a promising way to devise a microcarrier system with appropriate size for targeting the Peyer's patches, with appropriate immobilization capacity, and suitable for the oral administration of peptidic drugs.     

Simulation Model of a Carrier Standard

A model is described for simulating the functioning process of a carrier standard in a system for transferring the sizes of units of physical quantities. The model is intended for obtaining values of a probability series characterizing the carrier standard being located at different stages of a standard functioning cycle.     

整体式载体的分形研究

整体式Al2O3载体结构实测结果表明,虽然不同组分、不同条件下形成的块体具有不同的结构,但孔隙尺寸均满足分形标度律,是一种分形.本文构造了整体式载体分形体,提出了整体式载体的一种分形模型--蜂窝分形体,导出了关联表面积和体积增量的分形表达式,并分析了表面分维数的几何意义.本文在测得载体孔径分布的基础上,利用该模型的表面积与体积增量分形表达式,从压汞法的实验数据,研究了整体式载体分维数:实验得到的比表面积、体积增量及样品制备条件、孔隙尺寸等性能与分维数的关系,与模型提出的结论符合得很好,此方法对优化制备条件与块状载体的性能有重要意义.