Visible fluorescence induced by the metal semiconductor transition in composites of carbon nanotubes with noble metal nanoparticles

We show that single-walled carbon nanotube (SWNT) bundles emit visible fluorescence in the presence of noble metal nanoparticles and nanorods in the solid state. Conductivity measurements with metallic nanotubes, isolated from pristine SWNTs, show that they become semiconducting in the presence of the metal nanoparticles. Nanoparticle binding increases the defects in the nanotube structures which is evident in the Raman spectra. The metal-semiconductor transition removes the nonradiative decay channels of the excited states enabling visible fluorescence. Nanotube structures are imaged using this emission with resolution below the classical limits.     

Fluorescence Characteristics of Isolated Dye Molecules within Silicalite-1 Channels

Fluorescence characteristics of hemicyanine dye molecules isolated from neighboring molecules and strongly restricted inside nanosized pores of zeolite (silicalite-1) crystal were investigated. For samples in which the molecules were sufficiently far away from the others, the fluorescence decay lifetime of the molecules was about 2.2?ns. As the intermolecular distance was reduced, the steady-state fluorescence peak shifted toward the longer wavelength and the fluorescence efficiency decreased markedly. The fluorescence decay lifetime also decreased to 0.8?ns for a sample with the smallest intermolecular distance of 2.1?nm. These results were explained in terms of a dipole-dipole interaction between pairs of dye molecules. From the relation between the intermolecular distances and the fluorescence decay lifetimes of the molecules, the radius of energy transfer of hemicyanine donor-acceptor pair in zeolite matrix was determined to be 2.2?nm, in fair agreement with the calculated F?rster radius between dye molecules of the same species.     

Interactions between individual carbon nanotubes studied by Rayleigh scattering spectroscopy

The electronic properties of single-walled carbon nanotubes (SWNTs) are altered by intertube coupling whenever bundles are formed. These effects are examined experimentally by applying Rayleigh scattering spectroscopy to probe the optical transitions of given individual SWNTs in their isolated and bundled forms. The transition energies of SWNTs are observed to undergo redshifts of tens of meVs upon bundling with other SWNTs. These intertube coupling effects can be understood as arising from the mutual dielectric screening of SWNTs in a bundle.     

Diameter-dependent relaxation dynamics of 1D excitons in single-walled carbon nanotubes

We have studied 1D exciton relaxation dynamics in semiconducting single-walled carbon nanotubes (SWNTs) by femtosecond pump–probe experiments. The time evolution of change in transmittance ΔT/T induced by photo-excitation varies depending on the tube diameter. The decay time decreases with a decrease in the tube diameter. Pressure measurements have been conducted to explore the relaxation mechanism. The deformation potential estimated from the pressure dependence of photoluminescence spectra increases with decreasing tube diameter. This means that the exciton–phonon interaction becomes stronger in the smaller diameter tubes. The diameter dependences of decay time and deformation potential suggest that the exciton–phonon interaction plays an important role in exciton nonradiative relaxation process in semiconducting SWNTs.     

High temperature vibrational fluorescence of CN- ions in alkali halides

Infrared fluorescence from vibrational levels of matrix isolated CN^- ions has been studied in the temperature range of 300 K to 600 K. At 300 K the variation in the fluorescence lifetime from host to host is compatible with a multiphonon decay mechanism, but the measured temperature dependence does not agree with thermally induced multiphonon decay.     

Visible and near-infrared excited-state dynamics of single-walled carbon nanotubes

Excited-state lifetimes of isolated single-walled semiconducting carbon nanotubes (SWNTs) have been measured for the first time; these excited states, observed over the 400- to 1800-nm spectral domain, possess lifetimes that range from several ps to more than 100 ps. Sub-ps to ps decay components are assigned to relaxation in SWNT bundles. Interrogation of the samples with different SWNT mean diameters further confirms the dependence of the excited-state lifetime on roll-up vector. The ratio of fast and slow decaying component contributions in the first van Hove band can be viewed as a measure of the bundle content. PACS 78.67.Ch; 78.47.+p; 61.46.+w; 73.22.-f     

Selection of isolated and individual single-walled carbon nanotube from a film and its usage in nanodevices

Individual and isolated single-walled carbon nanotubes (SWNTs) are important for fabricating relevant nanode- vices and studying the properties of the SWNT devices. In this work, we demonstrate that individual and isolated SWNT can be selected and obtained from a film containing a huge number of SWNTs. By using both the polymethyl-methacrylate (PMMA) as a negative resist and the electron beam lithography, the selected SWNT can be fixed on a substrate, while the other SWNTs in the film can lift off. The selected SWNT can be used to fabricate nanodevice and a gas sensor of oxygen is demonstrated in this work.     

Effect of purification on the electron structure and field emission characteristics of a carbonaceous material containing single-wall carbon nanotubes

A carbonaceous material containing single-wall carbon nanotubes (SWNTs) has been synthesized by arc-discharge evaporation of graphite with a catalytic additive of nickel and cobalt powders. The synthesized SWNTs were purified from an amorphous carbon component (soot) and the catalyst particles by boiling in nitric acid. A comparison of the X-ray fluorescence spectra measured before and after this treatment showed that acid etching significantly decreased the content of soot in the material. The material enriched with SWNTs is characterized by a reduced threshold for the appearance of the field emission current, which is explained by a decrease in the screening effect of soot. The current-voltage characteristics of SWNTs exhibit a hysteresis, which is suggested to be due to the adsorption of molecules and radicals on the surface and at the ends of carbon nanotubes.     

Kinetics of annihilation of triplet excitationsand decay of delayed fluorescence for isolated 1,12-benzoperylene pairs

We studied the annihilation kinetics for triplet excitations in isolated pairs of organic molecules and their delayed fluorescence decay using a new mathematical model for the process. According to this model, the intensity of delayed annihilation fluorescence (DAF) for isolated pairs is directly proportional to the number of pairs in which both molecules are found in the excited triplet state. We show that the decrease in such pairs and the decay of their delayed annihilation fluorescence occur according to an exponential law in the absence of random scatter in the deactivation rate constants for the triplet excitations. The results of an experimental study of the DAF decay kinetics for 1,12-benzoperylene in n-hexane at 77 K, where triplet–triplet annihilation occurs in isolated pairs, confirm the validity of the theoretical conclusions.     

Kinetics study of ultrafast electron transfer from sensitized dyes to silver halide microcrystals

Spectral sensitization micromechanism of cyanine dyes J-aggregate adsorbed on the tabular and cubic AgBr microcrystals with different dye concentrations is studied by using picosecond time-resolved fluorescence spectroscopy, and the dependences of electron transfer and spectral efficiency sensitization on different conditions are analysed in detail. With the steady spectroscopy, the wavelengths of absorption and fluorescence of J-aggregate adsorbed on AgBr microcrystals are found to shift to red relative to dye monomer. The spectrum of fluorescence has a red shift relative to the absorption peak. With the time-resolved fluorescence spectroscopy, the fluorescence decay curves of cyanine dyes J-aggregate adsorbed on the tabular and cubic AgBr grains are found to be fitted well by a double-exponential decay function. The fitting curves consist of a fast and a slow component. Because of the large amplitude of the fast component, this fast decay should be attributable mainly to the electron transfer from J-aggregate of dye to a conduction band of AgBr.     

Subnanosecond fluorescence spectroscopy of human serum albumin as a method to estimate the efficiency of the depression therapy

The efficiency of the therapy of psychiatric diseases is estimated using the fluorescence measurements of the conformational changes of human serum albumin in the course of medical treatment. The fluorescence decay curves of the CAPIDAN probe (N-carboxyphenylimide of the dimethylaminonaphthalic acid) in the blood serum are measured. The probe is specifically bound to the albumin drug binding sites and exhibits fluorescence as a reporter ligand. A variation in the conformation of the albumin molecule substantially affects the CAPIDAN fluorescence decay curve on the subnanosecond time scale. A subnanosecond pulsed laser or a Pico-Quant LED excitation source and a fast photon detector with a time resolution of about 50 ps are used for the kinetic measurements. The blood sera of ten patients suffering from depression and treated at the Institute of Psychiatry were preliminary clinically tested. Blood for analysis was taken from each patient prior to the treatment and on the third week of treatment. For ten patients, the analysis of the fluorescence decay curves of the probe in the blood serum using the three-exponential fitting shows that the difference between the amplitudes of the decay function corresponding to the long-lived (9 ns) fluorescence of the probe prior to and after the therapeutic procedure reliably differs from zero at a significance level of 1% (p < 0.01).     

微孔对单壁纳米碳管储氢性能的影响

用巨正则蒙特卡罗分子模拟方法研究了单壁纳米碳管中的微孔即单壁纳米碳管基本孔-内管腔和管间孔对单壁纳米碳管储氢性能的影响.与低温下氮气吸附实验结果的比较发现单壁纳米碳管的内管腔是吸附的主要位置.分析单壁纳米碳管内管腔中吸附势的叠加和利用效率，发现管径为2nm左右时单壁纳米碳管内管腔的储氢容量最高.当单壁纳米碳管阵列的管间距增加时，单壁纳米碳管的管间孔也会成为有效的氢吸附位. 关键词： Monte Carlo方法 单壁纳米碳管 储氢 微孔     

Dynamics of individual single-walled carbon nanotubes in water by real-time visualization

Individual single-walled carbon nanotubes (SWNTs) in aqueous suspension are visualized directly by fluorescence video microscopy. The fluorescent tagging is simple, biocompatible, and does not modify the SWNTs. The dynamics of individual SWNTs in water are observed and quantified for the first time. We measure the confined rotational diffusion coefficient and find it in reasonable agreement with predictions based on confined diffusion of dilute Brownian rods. We determine the critical concentration at which SWNTs in suspensions start interacting. By analyzing the fluctuating shape of SWNTs in the 3 to 5 microm range, we determine that their persistence length ranges between 32 and 174 microm, in agreement with theoretical estimates; thus, commonly available SWNTs in liquids can be considered as rigid Brownian rods in the absence of imposed external fields or self-attractive forces.     

Photophysics of polymer-wrapped single-walled carbon nanotubes

Single-walled carbon nanotubes (SWNTs) are successfully dispersed in two conjugated polymer poly(9,9-dioctylfluorenyl-2,7-diyl) (PFO) and poly[2-methoxy-5- (2’-ethyl-hexyloxy)-1,4-phenylene vinylene] (MEHPPV) solutions. Steady-state and time-resolved photoluminescence spectroscopy in the near-infrared and visible spectral regions are used to study the interaction of the dispersed carbon nanotube and the wrapped polymer in the nano-hybrids. The SWNTs infrared emission is the signatures of the separation of single semiconducting tubes, the lifetime of the photoluminescence of these tubes is bi-exponential with the first component varying from 6 ps (in MEHPPV wrapped SWNTs) to 14 ps (in PFO wrapped SWNTs), while the second component of the decay for all samples is in the range of 30-40 ps, revealing the intrinsic lifetime of the SWNTs. The study of the photoluminescence of the nano-hybrids in the visible spectral range shows, in the case of the PFO, a relatively strong quenching, the photoluminescence lifetime for the hybrid is more than 100 ps shorter than the one of the pristine polyfluorene solution. For the MEHPPV-SWNT hybrid an opposite behavior is revealed with the photoluminescence lifetime surprisingly longer than the polymer solution. The possible mechanism for the interaction of the two conjugated polymers and the SWNTs is discussed in terms of their electronic band structure.     

DMANS——一种新型荧光闪烁体染料的寿命与能量转移的研究

本工作对一种新型荧光闪烁体染料——4-二甲胺基—4''硝基芪(DMANS)在不同介质中的光谱行为和能量转移进行了研究,发现介质的极性大小以及介质和染料间的能量转移对该闪烁体染料的荧光量子产率和闪烁发光延迟具有重大影响。研究对选择基体材料和合理组成闪烁材料配方有一定的参考价值。     

Multi-functionalized single-walled carbon nanotubes as tumor cell targeting biological transporters

Multi-functionalized single walled carbon nanotubes (SWNTs) were prepared and applied as tumor cell targeting biological transporters. A positive charge was introduced on SWNTs to get high loading efficiency of fluorescein (FAM) labeled short double strands DNA (20 base pairs). The SWNTs were encapsulated with the folic acid modified phospholipids for active targeting into tumor cell. The tumor cell-targeting properties of these multi-functionalized SWNTs were investigated by active targeting into mouse ovarian surface epithelial cells. The experimental results show that these multi-functionalized SWNTs have good tumor cell targeting property.     

Resonance Raman spectra of carbon nanotubes by cross-polarized light

Resonance Raman studies on single wall carbon nanotubes (SWNTs) show that resonance with cross polarized light, i.e., with the E(mu,mu+/-1) van Hove singularities in the joint density of states needs to be taken into account when analyzing the Raman and optical absorption spectra from isolated SWNTs. This study is performed by analyzing the polarization, laser energy, and diameter dependence of two Raman features, the tangential modes (G band) and a second-order mode (G' band), at the isolated SWNT level.     

Single-Walled Carbon Nanotubes Acting as Controllable Transport Channels

The motion and equilibrium distribution of water molecules adsorbed inside neutral and negatively charged singlewalled carbon nanotubes (SWNTs) have been studied using molecular dynamics simulations (MDSs) at room temperature based on CHARMM (Chemistry at HARvard Molecular Mechanics) potential parameters. We find that water molecules have a conspicuous electropism phenomenon and regular tubule patterns inside and outside the charged tube wall. The analyses of the motion behaviour of water molecules in the radial and axial directions show that by charging the SWNT, the adsorption efficiency is greatly enhanced, and the electric field produced by the charged SWNTs prevents water molecules from flowing out of the nanotube. However, water molecules can travel through the neutral SWNT in a fluctuating manner. This indicates that by electrically charging and uncharging the SWNTs, one can control the adsorption and transport behaviour of polar molecules in SWNTs for using as a stable storage medium or long transport channels. The transport velocity can be tailored by changing the charge on the SWNTs, which may have a further application as modulatable transport channels.     

单光子调制频谱用于量子点荧光寿命动力学的研究

本文开展了基于单光子调制频谱测量量子点荧光寿命动力学特性的研究.在脉冲激光激发下,对探测到的量子点单光子荧光信号进行频谱分析以获得荧光调制频谱,研究发现特征频谱信号幅值与荧光寿命之间存在确定的非线性对应关系.这种单光子调制频谱方法能有效消除背景噪声和单光子探测器暗计数的影响,用于分析量子点荧光寿命动力学特性时在准确度以及时间分辨率方面都较目前普遍采用的荧光衰减曲线寿命拟合方法呈现出明显优势:当涨落误差为5%时,寿命测量准确度提高了一个数量级;当涨落误差和偏离误差均为5%时,对动力学测量效率以及时间分辨率提高了四倍以上.因此单光子调制频谱可以作为获取量子点在短时间尺度内激发态动力学信息的一种有效技术手段.     

Dielectric response of aligned semiconducting single-wall nanotubes

We report measurements of the full intrinsic optical anisotropy of isolated single-wall carbon nanotubes (SWNTs). By combining absorption spectroscopy with transmission ellipsometry and polarization-dependent resonant Raman scattering, we obtain the real and imaginary parts of the SWNT permittivity from aligned semiconducting SWNTs dispersed in stretched polymer films. Our results are in agreement with theoretical predictions, highlighting the limited polarizability of excitons in a quasi-1D system.