Femtosecond laser spectroscopy of In0.53Ga0.47As/InP multiple quantum wells: interfacial roughness and photoexcited carrier relaxation

Interfacial properties and relaxation dynamics of photoexcited carriers in In_0.53Ga_0.47As/InP multiple quantum wells (MQWs) have been investigated by means of cross-sectional scanning tunneling spectroscopy and optical spectroscopy methods (luminescence, absorption and pump–probe experiments). The MQW structure consists of 125 periods of 10-nm-wide well layers and 40-nm-wide barrier layers on an InP(0 0 1) substrate. The observed interfacial roughness of the InGaAs-on-InP is 1–2 monolayers (ML), while that of the InP-on-InGaAs is 3–4 ML. The Stokes shift observed in luminescence and absorption spectra at 77 K corresponds well to the well-width distribution observed by the cross-sectional STM. Differential absorption spectra measured by pump–probe spectroscopy show that relaxation of hot carriers in conduction and valence bands followed by exciton formation takes place in 17–30 ps depending on the excitation photon energy. The excitons formed at the band bottom are localized at thicker areas within a quantum well in 500 ps.     

The photoluminescence excitation spectra of multicomponent media

With no restrictions on the value of optical density, we derive an equation that describes the photoluminescence excitation spectra of separate components with overlapping absorption bands in a multicomponent medium. Based on the equation obtained, we propose methods for measuring the ratios of absorption optical densities of the components and quantum yields of their luminescence. The applicability of the proposed methods is demonstrated by measuring the characteristics of coumarin and porphyrin dissolved in different proportions in ethanol. We have also measured the quantum yield and luminescence decay time of the radiationinduced color centers F ₃ ⁺ in the lithium fluoride crystal and calculated probabilities of radiative and nonradiative transitions from the first excited singlet state of these centers.     

用巯基乙酸作稳定剂制备CdSe纳米晶的光学性质

以巯基乙酸为稳定剂制备了CdSe纳米晶，通过尺寸选择沉淀得到2nm到3nm之间不同尺寸的纳米晶，利用室温光吸收，光致发光（PL）和光致发光激发（PLE）谱来研究了CdSe纳米团簇的光学性质。紫外－可见吸收谱给了具有清晰激光特征的尖锐吸收边，这表明样品的尺寸分布很窄。光致发光研究表明，样品有两个发射带，一个具有较高能量位于吸收边，来自电子－空穴对从最低激发态能级弛豫后的辐射复合，另一个低能发射带归属于基质与纳米晶界面存在的俘获中心。PLE谱中有2个吸收带，分别是S－S和P－P跃迁。最后还给出了不同激发能量下的发光特性。     

Tunable Infrared Luminescence and Optical Amplification in PbS Doped Glasses

PbS-doped glasses are prepared. Absorption and luminescence spectra show that both the absorption and infrared emission can be tuned widely by thermal treatment conditions. Optical amplification at 1300 nm is observed, and amplified spontaneous emission （ASE） spectrum is also measured to confirm the optical gain from PbS quantum dots.     

Calibration of the spectral sensitivity of instruments for the near infrared region

We present an analysis of methods for calibration of the spectral sensitivity of instruments in the near IR region of the spectrum (0.90–2.05 μm), using as an example recording of the luminescence spectra of PbS semiconductor quantum dots using a diffraction monochromator and an InGaAs photodiode as the detector. We show that when high-sensitivity detectors are employed for calibration using the emission spectrum of an ideal black body, the problem of attenuation of the radiation flux is still important. Instead of neutral density glass and mesh light filters for attenuation of the radiation, we propose using UFS ultraviolet optical glasses (together with PS purple glasses), the maximum optical density of which is within the region of maximum spectral sensitivity of InGaAs photodiodes. We give examples of spectral calibration, taking into account instrumental characteristics and the effect of absorption by water vapor in the air, and also corrections of the luminescence spectra of quantum dots.     

BiI3层状半导体超微粒子的光学性质

本文研究了BiI3半导体溶胶的光学性质.进一步证实,在BiI3胶体样品中,真实的BiI3半导体微晶粒予的吸收被强的I3-离子吸收掩盖了.通过测量激发光谱,确定了BiI3微晶的吸收位置.用光谱数据计算得到的尺寸分布与电镜结果和理论分析符合得很好.得到的结果表明,BiI3胶体中的BiI3微晶与体材料相比。存在着显著的量子尺寸效应.     

Femtosecond quantum dynamics of diatomic molecules in optically dense gaseous media

A consistent quantum theory of a two-pulse pump-probe experiment in the femto-and picosecond spectroscopy of diatomic molecules is developed. The theory aims at the use of weak quantum femtosecond light pulses to excite molecular coherence. It is suggested that the experiment be realized using a double-frequency excitation scheme that is feasible for Na₂ molecules. On the basis of the theory developed, the luminescence signals are calculated at different temperatures and different optical densities of the medium for the time range from 100 fs to ~ 100 ps. The results obtained show the presence of a strong dependence of the time and frequency spectra of a luminescence signal on the optical density of the medium at temperatures from 50 to 300 K. The proposed approach makes it possible to use the quantum coherence properties of optically dense media for more detailed study of the vibronic dynamics of diatomic molecules, in particular, detection of weak optical transitions.     

ZnSe/SiO2半导体量子点玻璃的光谱特性

对采用溶胶凝胶法制备的ZnSe/SiO2半导体量子点玻璃的光谱性质进行了测试分析.UV-Vis透射光谱中观察到光吸收边相对于体相半导体有明显蓝移.稳态发射光谱(PL)中观察到ZnSe纳米晶体的位于蓝区的基本呈高斯分布的弱的最低激子发射峰、强而宽的表面态发光带以及对应杂质能级的三个锐峰发光.时间分辨荧光光谱(TRPL)中观察到发光效率高的最低激子发射峰,并测量其荧光衰减寿命,经尾部拟合为28.5 ps.同时,结合有效质量近似(EMA)模型,估计ZnSe纳米晶体的平均粒径介于2.45~3.60 nm之间,尺寸分布基本呈高斯型.     

Morphology and optical spectra of metal iodate microcrystals in porous matrices

Microcrystals of iodates of mercury, lead, thallium, and bismuth were grown in pores of glass and polymer matrices from solutions or through sublimation in vacuum. Images of these microcrystals embedded in matrices were obtained with an electron microscope. Exciton absorption and luminescence spectra of the microcrystals revealed a strong difference in the temperature regions of stability of the various structural modfications between bulk crystals and microcrystals of some iodates. The absorption and luminescence spectra are broadened inhomogeneously because of considerable size dispersion of the microcrystals and exhibit quantum confinement effects. The exciton emission spectra show that exciton interaction in microcrystals becomes significant at very low optical pumping levels because of efficient excitation transfer from the matrix.     

Coherent Interband and Intersubband Dynamics in Terahertz-Driven GaAs Quantum Wells

We theoretically investigate the optical absorption spectra and charge density by subjecting a GaAs quantum well to both an intense terahertz (THz)-frequency driving field and an optical pulse within the theory of density matrix. In presence of a strong THz field, the optical transitions in quantum well subbands are altered by the THz field. The alteration has a direct impact on the optical absorption and the charge density. The excitonic peak splitting and THz optical sideband in the absorption spectra show up when changing the THz field intensity and/or frequency. The Autler-Towns splitting is a result from the THz nonlinear dynamics of confined excitons. On the other hand, the carrier charge density is created as wave packets formed by coherent superposition of several eigenstates. The charge density exhibitsquantum beats for short pulses and/or wider wells and is modulated by the THz field.     

Optical absorption and electromagnetically induced transparency in semiconductor quantum well driven by intense terahertz field

An approach for solving the excitonic absorption in a semiconductor quantum well driven by an intense terahertz field is presented.The formalism relies on the stationary single-photon Schro¨dinger equation in the full quantum mechanical framework.The optical absorption dynamics in both weak and strong couplings are discussed and compared.The excitonic absorption spectra show the Autler-Townes doublets for the resonance terahertz field,a replica peak for the non-resonance terahertz field,and the electromagnetically induced transparency phenomenon for modulating the decay rate of the second electron state in the weak coupling.In particular,the electromagnetically induced transparency phenomenon window range is discussed.In the strong coupling region,the multi-order energy level resonance splitting due to the strong optical field is found.There are three(non-resonance terahertz field) or four(resonance terahertz field) peaks in the optical absorption spectra.This work provides a simple and convenient approach to deal with the optical absorption in the exciton system.     

Optical spectroscopy of Yb in the Cs2NaYF6 single crystal

Results of the optical spectroscopy investigation of the cubic paramagnetic center Yb³⁺ ion in the Cs₂NaYF₆ single crystal are presented. The Stark level energies of the Yb³⁺ multiplets are established from absorption, luminescence and excitation luminescence spectra and the crystal field parameters are calculated. Information about the phonon spectra of Cs₂NaYF₆ crystals is obtained from the electron-vibrational structure of the optical absorption and luminescence spectra.     

Optical absorption of 1-phenyl-3-methyl-1H-pyrazolo[3,4-b]quinoline derivatives: Molecular dynamics modeling

Paper deals with quantum chemical modeling of the optical absorption spectra of 6-fluoro, 7-trifluoromethyl, 6-cyano, 6-carboethoxy and 6-tert-butyl derivatives of 1-phenyl-3-methyl-1H-pyrazolo[3,4-b]quinoline. The calculations are performed by means of the semiempirical quantum chemical methods (AM1 or PM3) applied to the equilibrium molecular conformation in vacuo (T = 0 K) or molecular dynamic (MD) trajectories as obtained within fragmental or total MD simulations at T = 300 K. The results of these calculations are compared with the measured spectra of optical absorption. The quantum chemical analysis show that the dynamics of the methyl, trifluoromethyl, carboethoxy and tert-butyl groups practically does not influence the absorption spectra whereas the strongest their modifications are found to be related with dynamics of the aromatic group. The semiempirical method AM1 in combination with MD simulations gives for all dyes the best agreement between the calculated and measured spectral positions of absorption bands. In most cases the quantum chemical calculations describe properly the trends of their changes depending on the lateral substituent.     

Intraband absorption and emission of light in quantum wells and quantum dots

High-resolution spectroscopy in the mid-infrared spectral range is used to study electronic transitions between size-quantization subbands in stepped quantum wells under picosecond interband excitation. The contributions from intersubband and intrasubband absorption of light are separated by using the difference in time profiles of the absorption coefficient for these cases. For stepped quantum wells, spontaneous interband luminescence and superluminescence are studied for different excitation levels. For structures with quantum dots, the intraband absorption spectra for n-and p-type structures and the spectra of photoinduced intraband absorption and emission (for polarized radiation) for undoped structures are studied.     

Energy transfer in associates of semiconductor quantum dots with tetrapyridinoporphyrazine molecules

The interaction of CdSe/ZnS quantum dots (QDs) with metal-free tetrapyridinoporphyrazine (TPPA) molecules in chloroform has been investigated. It was found that, at QD concentrations lower than ～3 × 10^?7 M, QD luminescence is quenched in the presence of TPPA and characteristic changes occur in the absorption and luminescence spectra of TPPA, which reflect the interaction of TPPA molecules with the QD surface. Along with the QD luminescence quenching, sensitized luminescence of TPPA molecules adsorbed on QDs was observed. The luminescence excitation spectra of adsorbed TPPA molecules unambiguously indicate the presence of energy transfer from QDs to TPPA. The efficiency of energy transfer from QDs to TPPA is estimated from the quantum yield of sensitized TPPA luminescence.     

CdSe/CdS核/壳型纳米晶的光谱特性

以巯基乙酸为稳定剂制备了CdSe/CdS核／壳型纳米晶。用光吸收谱（Abs)、光致发光谱（PL）及光致发光激发谱（PLE）研究了CdS壳层对CdSe纳米晶电子结构，从而对其吸收和发光性能的影响。根据PL和PLE的结果以及带边激子精细结构的计算结果，我们用尺寸很小的纳米晶中所形成的基激缔合物解释了PL光谱与吸收边之间较大的Stokes位移。     

Photophysics of the analogs of pyrromethene PM 567

The spectral and luminescence properties of a number of pyrromethene (PM) dyes have been investigated. The absorption and luminescence spectra of PM molecules in different solvents are measured. The electronic structure and electronic excited states are calculated by the method of intermediate neglect of differential overlap with special spectroscopic parameterization. The rate constants of photophysical processes are estimated, and the fluorescence quantum yields are calculated. The fluorescence quantum yields of PM I and PM II molecules are found to decrease upon their excitation to the second short-wavelength absorption band. This phenomenon is interpreted.     

Emission characteristics of Dy3+ ions in lead antimony borate glasses

Glasses with the composition 30PbO–25Sb₂O₃–(45?x)B₂O₃–xDy₂O₃ for x=0 to 1 were prepared in steps of 0.2 by the melt-quenching method. Various physical parameters, viz., density, molar volume, and oxygen packing density, were evaluated. Optical absorption and luminescence spectra of all the glasses were recorded at room temperature. From the observed absorption edges optical band gap, the Urbach energies are calculated; the optical band gap is found to decrease with the concentration of Dy₂O₃. The Judd–Ofelt theory was applied to characterize the absorption and luminescence spectra of Dy³⁺ ions in these glasses. Following the luminescence spectra, various radiative properties, like transition probability A, branching ratio β and the radiative life time τ for different emission levels of Dy³⁺ ions, have been evaluated. The radiative lifetime for the ⁴F_9/2 multiplet has also been evaluated from the recorded life time decay curves, and the quantum efficiencies were estimated for all the glasses. The quantum efficiency is found to increase with the concentration of Dy₂O₃.     

C_（60）固体的光学性质

本文综述了有关Ｃ＿（６０）固体的光学性质最近的研究进展。其中包括Ｃ＿（６０）分子及其固体的非线性光学性质、各种吸收光谱及电子结构,光电导及光电子能谱等方面。     

Optical spectra of aqueous solutions of glutamine-tryptophan associates

The optical density and luminescence ability of aqueous solutions of glutamine-tryptophan depend on the degree of oxidation of the initial dry substances of dipeptide. Glutamine-tryptophan has a high associating ability, which increases if stored. The general form of the optical absorption and luminescence spectra of the associates differs little from the spectra of monomers. Among the spectral-optical symptoms of association of a substance in a solution for glutamine-tryptophan, we discovered the hypochromism and narrowing of the absorption spectra and shortening of the fluorescence lifetime. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 67, No. 4, pp. 436–439, July–August, 2000.