Time dependence of the luminescence excited by rectangular pulses

The theory of the time dependence of luminescence, during and after excitation by rectangular pulse, is discussed. Some phenomena, which cannot be described as direct excited luminescence, will be mentioned. In order to explain these phenomena, the model for energy transfer between two monomolecular centres has been used. On the basis of this model, the theoretical time dependence of the luminescence is obtained. The theoretical formula describe qualitatively very well the experimental observations in ZnSMn and other compounds.     

Lanthanide-Sensitized Luminescence as a Promising Tool in Clinical Analysis

Abstract

The recent applications and novelties of lanthanide-sensitized luminescence (LSL) as a detection technique in clinical analysis are here reviewed. In LSL, lanthanide ions form complexes with organic compounds; in these complexes, the energy absorbed by the organic chromophore (usually the analyte) at its characteristic excitation wavelength is transferred to a triplet state of the molecule and then transferred to a resonance level of the lanthanide ion, which finally emits luminescence at its particular emission wavelength. The characteristics of this process will be reviewed and particular attention will be paid to the development of automatic methods of analysis, fluorescence probes, or flow-through optosensors, due to their potential applications in clinical analysis. A critical discussion of the advantages and handicaps of each analytical method is done and the trends of analytical chemistry in this research field are also presented.     

Optical detection of spin relaxation processes in the triplet state of the self trapped exciton in alkali halides

The transient response of the triplet self trapped exciton luminescence intensity to a pulsed microwave excitation has been measured for 1.3 K < T < 4.2 K in NaCl, KCl, RbCl, KBr, RbBr and CsBr. The results are quantitatively explained with a theoretical model describing the spin relaxation phenomena as one phonon direct processes. Good agreement is obtained as a function of temperature and magnetic field.     

Silicon–germanium nanostructures for on-chip optical interconnects

Silicon–germanium epitaxially grown on silicon in the form of two-dimensional (quantum wells) and three-dimensional (quantum dots) nanostructures exhibits photoluminescence and electroluminescence in the technologically important spectral range of 1.3–1.6 μm. Until recently, the major roadblocks for practical applications of these devices were strong thermal quenching of the luminescence quantum efficiency, and a long carrier radiative lifetime. This paper summarizes recent progress in the understanding of carrier recombination in Si/SiGe nanostructures and presents a potential new route toward CMOS compatible light emitters for on-chip optical interconnects.     

Exciton dispersion in silicon nanostructures formed by intense,ultra-fast electronic excitation

The intense, ultra-fast electronic excitation of clean silicon (100)–(2×1) surfaces leads to the formation of silicon nanostructures embedded in silicon, which photoluminesce in the yellow-green (∼2-eV band gap). The silicon surfaces were irradiated with slow, highly charged ions (e.g. Xe⁴⁴⁺ and Au⁵³⁺) to produce the ultra-fast electronic excitation. The observation of excitonic features in the luminescence from these nanostructures has recently been reported. In this paper we report the dispersion of the excitonic features with laser excitation energy. A phonon-scattering process is proposed to explain the observed dispersion. Received: 2 October 2001 / Accepted: 18 July 2002 / Published online: 25 October 2002 RID="*" ID="*"Corresponding author. Fax: +1-925/423-7040, E-mail: Hamza1@llnl.gov RID="**" ID="**"Present address: University of California, Lawrence Berkeley National Laboratory, Berkeley, CA 94 720, USA     

表面等离激元研究新进展

随着理论研究的深入和现代微加工技术的进步,对支持表面等离激元的金属微纳结构体系的研究已形成了一门新兴学科方向,即表面等离激元光子学。由于表面等离激元具有独特的光学特性,在数据存储、超分辨成像、光准直、太阳能电池、生物传感器以及负折射材料等方面有着重要的应用前景,成为当前广受国内外学者重视的热点研究领域之一。本文对表面等离激元的特点、基本现象,以及其带来的新颖效应及其应用研究前景的最新发展进行了介绍。     

Study of electrical field distribution of gold-capped nanoparticle for excitation of localized surface plasmon resonance

The specific optical characteristics which can be observed from noble metal nanostructured materials such as nanoparticles and nanoislands have wide variety of applications such as biosensors, solar cells, and optical circuit. Because, these noble metal nanostructures induce the increment of light absorption efficiency by the enhancing effect of electrical field from localized surface plasmon resonance (LSPR) excitation. However, the enhancing effects of electrical field from LSPR using simple structured noble metal nanostructures for several applications are not satisfactory. To realize the more effective light absorption efficiency by the enhancing effect of electrical field, quite different noble metal nanostructures have been desired for applying to several applications using LSPR. In this study, to obtain the more effective enhancing effect of electrical field, conditions for LSPR excitation using a gold-capped nanoparticle layer substrate are computationally analyzed using finite-difference time-domain (FDTD) method. From the previous research, LSPR excitation using such gold-capped nanoparticle layer substrates has a great potential for application to high-sensitive label-free monitoring of biomolecular interactions. For understanding of detailed LSPR excitation mechanism, LSPR excitation conditions were investigated by analyzing the electrical field distribution using simulation software and comparing the results obtained with experimental results. As a result of computational analysis, LSPR excitation was found to depend on the particle alignment, interparticle distance, and excitation wavelength. Furthermore, the LSPR optical characteristics obtained from the simulation analysis were consistent with experimentally approximated LSPR optical characteristics. Using this gold-capped nanoparticle layer substrate, LSPR can be excited easily more than conventional noble metal nanoparticle-based LSPR excitation without noble metal nanoparticle synthesis. Hence, this structure is detectable a small change of refractive index such as biomolecular interactions for biosensing applications.     

Dynamics of a quantum phase transition and relaxation to a steady state

We review recent theoretical work on two closely related issues: excitation of an isolated quantum condensed matter system driven adiabatically across a continuous quantum phase transition or a gapless phase, and apparent relaxation of an excited system after a sudden quench of a parameter in its Hamiltonian. Accordingly, the review is divided into two parts. The first part revolves around a quantum version of the Kibble–Zurek mechanism including also phenomena that go beyond this simple paradigm. What they have in common is that excitation of a gapless many-body system scales with a power of the driving rate. The second part attempts a systematic presentation of recent results and conjectures on apparent relaxation of a pure state of an isolated quantum many-body system after its excitation by a sudden quench. This research is motivated in part by recent experimental developments in the physics of ultracold atoms with potential applications in the adiabatic quantum state preparation and quantum computation.     

Physical Manipulation of Lanthanide‐Activated Photoluminescence

Versatile manipulation of lanthanide photoluminescence not only enables a more thorough understanding of the luminescent mechanism, but also promotes their widespread applications including advanced display and security, bioimaging and biotherapy, and sensors. The traditional chemical methods, engineering of composition, concentration, size, morphology, and surface defects, can easily tune the excitation, energy transfer and emission processes and have been frequently used. Despite the powerful ability to control luminescence intensity and selectivity, these chemical approaches suffer from cumbersome synthesis processes and are usually time consuming and irreversible. Recently, there have been numerous examples of physical approaches realizing in situ, real time, and reversible luminescence manipulation for certain materials under a given excitation. Herein, the existing physical strategies comprising temperature, magnetic field, electric field, and mechanical stress are summarized. For each approach, the action mechanism, material design, applications, as well as current challenges are discussed, and possible development directions and broadening of the potential application areas are considered.     

Persistent hole burning in semiconductor nanocrystals

The persistent spectral hole burning (PSHB) phenomenon was found to occur in many kinds of nanocrystalline semiconductors, such as CdSe, CdS, CuCl, CuBr and CuI, embedded in crystals, glass or polymers. In inhomogeneously broadened exciton absorption spectra of these nanocrystals, the spectral hole and its associated structure were created by the narrow-band laser excitation and were conserved for more than several hours at 2 K. Hole depth grew in proportion to the logarithm of the burning fluence. Thermally-annealing and light-induced hole-filling phenomena were observed. The hole burning takes place by the tunneling process through potential barriers with broadly distributed barrier height and thickness. Unusual luminescence behaviors related to the PSHB phenomena were also observed. They are luminescence elongation with increase of the light exposure and hole burning in the luminescence spectrum. The observed PSHB phenomena are explained by the exciton localization and the succeeding ionization of nanocrystals. The energy of the photoionized nanocrystal is released from the original energy and the new energies depend on the spatial arrangement of the trapped carriers. Quantum confinement of carriers and resulting strong Coulomb interaction between confined carriers and trapped carriers are essential for the energy change. Possible applications of the PSHB phenomenon is discussed.     

Ultraviolet and visible upconversion dynamics in Er^3＋：YAlO3 under ^2H11/2 excitation

The luminescence of Er^3＋：YAlO3 in ultraviolet visible and infrared ranges under the 518 nm excitation of the multiples ^2H11/2 have been investigated. Ultraviolet （275 nm and 318 nm）, violet （405 nm and 413 nm） and blue （474 nm） upconversion and infrared downconversion luminescence has been observed. By means of measuring the fluorescence decay curves and using the theory of rate equations, the luminescence kinetics was studied in detail and the processes of energy transfer upconversion （ETU） and excitation state absorption （ESA） were proposed to explain the upconversion phenomena.     

Optical nonlinearity of CdS

The discovery and investigation of optically nonlinear behavior of CdS is reviewed. The development is described from nonlinear anti-Stokes excitation via the characterization of inelastic light scattering processes and the identification of high-density phenomena like biexciton creation, excitonic collisions, and electron-hole plasma generation towards very recent time-resolved gain, light-induced grating, and in particular optical bistability experiments. CdS is thus shown to allow for an extremely wide variety of different optically nonlinear processes and may be regarded as a model material for this field. Possible applications show up for several of the described phenomena.     

Synthesis of aligned carbon nanotubes

Carbon nanomaterials seem to be most attractive because of their fascinating features. Carbon nanotubes emerged recently as unique nanostructures with remarkable mechanical and electronic properties. Future applications will require a fabrication method capable of producing uniform carbon nanotubes with well-defined and controllable reproducibility of their properties. In this review, recent results addressing rational and efficient methods to obtain aligned arrays of these one-dimensional carbon nanomaterials will be discussed. Received: 3 November 2000 / Accepted: 30 May 2001 / Published online: 30 August 2001     

Preparation and luminescence of water soluble poly (N-vinyl-2-pyrrolidone)/LaF3:Eu nanocrystals

Lanthanide-doped luminescent nanocrystals have great potential as biological luminescent labels, but their use has been limited because of most of these nanocrystals are hydrophobic. In this work, water soluble LaF₃:Eu³⁺ down-conversion nanocrystals were prepared by encapsulated individual nanocrystals with polyvinylpyrrolidone (PVP). Their morphology, surface structure and luminescence properties were explored in detail. The results indicate that these nanocrystals can be readily dispersed in water, forming a stable and transparent colloidal solution. The colloidal solution displayed unique red luminescence with high emission intensity under ultraviolet excitation. These results suggest that these nanocrystals have great potential as luminescent labeling materials for biological applications.     

Modulation of electronic properties with external fields in silicene-based nanostructures

This work reviews our recent works about the density functional theory(DFT) calculational aspects of electronic properties in silicene-based nanostructures with the modulation of external fields, such as electric field, strain, etc. For the two-dimensional(2D) silicene-based nonostructures, the magnetic moment of Fe-doped silicene shows a sharp jump at a threshold electric field, which indicates a good switching effect, implying potential applications as a magnetoelectric(ME) diode. With the electric field, the good controllability and sharp switching of the magnetism may offer a potential applications in the ME devices. For the one-dimensional(1D) nanostructures, the silicene nanoribbons with sawtooth edges(SSi NRs) are more stable than the zigzag silicene nanoribbons(ZSiNRs) and show spin-semiconducting features. Under external electric field or uniaxial compressive strain, the gapless spin-semiconductors are gained, which is significant in designing qubits for quantum computing in spintronics. The superlattice structures of silicene-based armchair nanoribbons(ASiSLs) is another example for 1D silicene nanostructures. The band structures of ASi SLs can be modulated by the size and strain of the superlattices. With the stain increased, the related energy gaps of ASi SLs will change, which are significantly different with that of the constituent nanoribbons. The results suggest potential applications in designing quantum wells.     

Super broadband reddish emitting glass with Eu2+ doped for warm-white light-emitting diodes

We present our recent achievements of glasses able to produce ultra-broadband visible fluorescence. The luminescence system was Eu²⁺ doped low silica calcium aluminosilica (LSCAS) glass excited by blue light. The LSCAS glass has the superior properties of oxide glasses and the low phonon energy property of non-oxide glasses. The large Stokes-shift (12163 cm^?1) and smoothing broadband emission (from 450 nm to 800 nm) were explained by the strong electron–phonon interaction and a remarkable nephelauxetic effect. Besides, given the broad excitation band in blue range, the commercialized blue LED will be a good excitation source. Therefore, these glasses have large potential to be used as warm-white light phosphor material.     

Kinetic effects in recombination of optical excitations in disordered quantum heterostructures: Theory and experiment

An overview of recent experimental and theoretical results on stationary and time-dependent photoluminescence spectra in disordered semiconductor heterostructures is presented. In particular, temperature-dependent peak position and linewidth of the luminescence spectra, as well as the luminescence intensity are considered along with the time evolution of the luminescence intensity after pulsed excitation. Emphasis is given on the comparison between experimental and theoretical results aiming at a characterization of disorder in the underlying structures.     

Single ion induced surface nanostructures: a comparison between slow highly charged and swift heavy ions

This topical review focuses on recent advances in the understanding of the formation of surface nanostructures, an intriguing phenomenon in ion-surface interaction due to the impact of individual ions. In many solid targets, swift heavy ions produce narrow cylindrical tracks accompanied by the formation of a surface nanostructure. More recently, a similar nanometric surface effect has been revealed for the impact of individual, very slow but highly charged ions. While swift ions transfer their large kinetic energy to the target via ionization and electronic excitation processes (electronic stopping), slow highly charged ions produce surface structures due to potential energy deposited at the top surface layers. Despite the differences in primary excitation, the similarity between the nanostructures is striking and strongly points to a common mechanism related to the energy transfer from the electronic to the lattice system of the target. A comparison of surface structures induced by swift heavy ions and slow highly charged ions provides a valuable insight to better understand the formation mechanisms.     

Up-conversion luminescence tuning in Er~(3+) -doped ceramic glass by femtosecond laser pulse at different laser powers

The up-conversion luminescence tuning of rare-earth ions is an important research topic for understanding luminescence mechanisms and promoting related applications. In this paper, we experimentally study the up-conversion luminescence tuning of Er~(3+)-doped ceramic glass excited by the unshaped, V-shaped and cosine-shaped femtosecond laser field with different laser powers. The results show that green and red up-conversion luminescence can be effectively tuned by varying the power or spectral phase of the femtosecond laser field. We further analyze the up-conversion luminescence tuning mechanism by considering different excitation processes, including single-photon absorption(SPA), two-photon absorption(TPA), excited state absorption(ESA), and energy transfer up-conversion(ETU). The relative weight of TPA in the whole excitation process can increase with the increase of the laser power, thereby enhancing the intensity ratio between green and red luminescence(I_(547)/I_(656)). However, the second ETU(ETU2) process can generate red luminescence and reduce the green and red luminescence intensity ratio I_(547)/I_(656), while the third ESA(ESA3) process can produce green luminescence and enhance its control efficiency. Moreover, the up-conversion luminescence tuning mechanism is further validated by observing the up-conversion luminescence intensity, depending on the laser power and the down-conversion luminescence spectrum under the excitation of 400-nm femtosecond laser pulse. These studies can present a clear physical picture that enables us to understand the up-conversion luminescence tuning mechanism in rare-earth ions, and can also provide an opportunity to tune up-conversion luminescence to promote its related applications.