pH-sensitive ligand for luminescent quantum dots

We developed a strategy to switch the luminescence of semiconductor quantum dots with chemical stimulations. It is based on the photoinduced transfer of either energy from CdSe-ZnS core-shell quantum dots to [1,3]oxazine ligands or electrons from the organic to the inorganic components. The organic ligands incorporate a dithiolane anchoring group, an electron-rich indole, and a 4-nitrophenylazophenoxy chromophore in their molecular skeleton. Their adsorption on the surface of the quantum dots results in partial luminescence quenching. Electron transfer from the indole fragment to the nanoparticles is mainly responsible for the decrease in luminescence intensity. Upon addition of base, the [1,3]oxazine ring of the ligands opens to generate a 4-nitrophenylazophenolate chromophore, which absorbs in the range of wavelengths where the quantum dots emit. This transformation activates an energy-transfer pathway from the excited nanoparticles to the ligands. In addition, the oxidation potential of the ligand shifts in the negative direction, improving the efficiency of electron transfer. The overall result is a decrease in the luminescence quantum yield of 83%. Addition of acid also opens the [1,3]oxazine ring of the ligands. However, the resulting 4-nitrophenylazophenol does not absorb in the visible region and cannot accept energy from the excited nanoparticles. Furthermore, the oxidation potential shifts in the positive direction, lowering the electron-transfer efficiency. In fact, the luminescence quantum yield increases by 33% as a result of this transformation. These changes are fully reversible and can be exploited to probe the pH of aqueous solutions from 3 to 11. Indeed, our sensitive quantum dots adjust their luminescence in response to variations in pH within this particular range of values. Thus, our general design strategy can eventually lead to the development of pH-sensitive luminescent probes for biomedical applications based on the unique photophysical properties of semiconductor quantum dots.     

Luminescent chemosensors based on semiconductor quantum dots

Semiconductor quantum dots are inorganic nanoparticles with unique photophysical properties. In particular, their huge one- and two-photon absorption cross sections, tunable emission bands and excellent photobleaching resistances are stimulating the development of luminescent probes for biomedical imaging and sensing applications. Indeed, electron and energy transfer processes can be designed to switch the luminescence of semiconductor quantum dots in response to molecular recognition events. On the basis of these operating principles, the presence of target analytes can be transduced into detectable luminescence signals. In fact, luminescent chemosensors based on semiconductor quantum dots are starting to be developed to detect small molecules, monitor DNA hybridization, assess protein-ligand complementarities, test enzymatic activity and probe pH distributions. Although fundamental research is still very much needed to understand further the fundamental factors regulating the behavior of these systems and refine their performance, it is becoming apparent that sensitive probes based on semiconductor quantum dots will become invaluable analytical tools for a diversity of applications in biomedical research.     

Photoinduced enhancement in the luminescence of hydrophilic quantum dots coated with photocleavable ligands

In search of strategies to photoactivate the luminescence of semiconductor quantum dots, we devised a synthetic approach to attach photocleavable 2-nitrobenzyl groups to CdSe-ZnS core-shell quantum dots coated with hydrophilic polymeric ligands. The emission intensity of the resulting nanostructured constructs increases by more than 60% with the photolysis of the 2-nitrobenzyl appendages. Indeed, the photoinduced separation of the organic chromophores from the inorganic nanoparticles suppresses an electron-transfer pathway from the latter to the former and is mostly responsible for the luminescence enhancement. However, the thiol groups anchoring the polymeric envelope to the ZnS shell also contribute to the photoinduced emission increase. Presumably, their photooxidation eliminates defects on the nanoparticle surface and promotes the radiative deactivation of the excited quantum dots. This effect is fully reversible but its magnitude is only a fraction of the change caused by the photocleavage of the 2-nitrobenzyl groups. In addition, these particular quantum dots can cross the membrane of model cells and their luminescence increases by ~80% after the intracellular photocleavage of the 2-nitrobenzyl quenchers. Thus, photoswitchable luminescent constructs with biocompatible character can be assembled combining the established photochemistry of the 2-nitrobenzyl photocage with the outstanding photophysical properties of semiconductor quantum dots and the hydrophilic character of appropriate polymeric ligands.     

Features of the influence of stabilizing ligands on luminescence properties of cadmium selenide colloidal quantum dots

It has been shown that immediately after the synthesis, the luminescence efficiency of CdSe quantum dots stabilized by n-octadecylphosphonic acid together with one of the auxiliary ligands decreases in the order: oleylamine, hexadecylamine, trioctylphosphine oxide, 1-octadecene, and stearic acid, which is due to combination of the energy of their binding with surface atoms of the nanoparticles and the packing density of the ligands in the shell. In the course of post-synthetic ripening of the quantum dots in a solution, changes in their luminescence quantum yield occur, depending on the solvent polarity and due to rearrangement of the ligands in the shells. The effect of dark recovery of trap luminescence from UV-irradiated quantum dots stabilized by octadecylphosphonic acid and a long-chain amine has been found.     

Highly luminescent Eu3+ chelate nanoparticles prepared by a reprecipitation-encapsulation method

Aqueous suspensions of highly luminescent Eu3+ chelate nanoparticles are prepared by a novel reprecipitation-encapsulation method. An alkyl alkoxysilane encapsulation agent is included during the nanoparticle formation process, forming a nanoparticle encapsulation layer that inhibits aggregation as evidenced by UV-vis spectroscopy and atomic force microscopy. In addition, the encapsulated nanoparticles exhibit a small size (10 nm), intense luminescence, and excellent photostability. We estimate that the molar extinction coefficients of the approximately 10 nm particles are approximately 5.0x10(7) M-1 cm-1 with a luminescence quantum yield of 6%, indicating a luminescence brightness many times larger than that of conventional fluorescent dyes and comparable to that of colloidal semiconductor quantum dots. The small size, high brightness, highly red-shifted luminescence, and long luminescence lifetimes of the nanoparticles are of interest for luminescence labeling and sensing applications.     

Hydrophilization of CdSe quantum dots with surfactants

A procedure has been developed for hydrophilization of CdSe semiconductor quantum dots with anionic, cationic, and nonionic surfactants. Depending on the type of a surfactant, these particles may carry positive, negative, or no charges. In spite of the universality of the proposed procedure, the hydrophilization with specific surfactants must be carried out at specific concentrations of reagents and medium pH values. Under optimum conditions, the transfer of the quantum dots to water substantially increases the quantum yield of their luminescence. Conditions have been found under which the luminescence properties of the hydrophilic particles remain almost unchanged for a long time period.     

Surface-modified CdSe quantum dots as luminescent probes for cyanide determination

Luminescent surface-modified CdSe semiconductor quantum dots (QDs), with nanoparticle (NP) size distribution in the order of 2-7 nm, have been synthesized for optical determination of cyanide ions. The nanoparticles have been functionalised with tert-butyl-N-(2-mercaptoethyl)-carbamate (BMC) groups and exhibit a strong fluorescent emission at about 580 nm with rather long fluorescence lifetimes (several hundred nanoseconds) in aerated methanolic solution. The observed luminescence emitted by the synthesized nanocrystals was tremendously increased by photo-activation under sunlight exposure. The functionalised QDs turned out to exhibit excellent long-term stability when stored in the dark (no significant changes in QDs luminescence emission intensity was observed even after two months from synthesis). The functionalisation of the NPs with carbamate ligand allowed a highly sensitive determination of free cyanide via analyte-induced changes in the photoluminescence (fluorescence quenching of intensity at 580 nm and lifetime changes) of the modified quantum dots (excited at 400 nm). A detection limit of 1.1 × 10⁻⁷ M (2.9 μg l⁻¹) of cyanide ions was obtained, while the interfering effect of other inorganic anions (including NO₃⁻, Cl⁻ or SCN⁻) was negligible even at 200-fold level concentrations in excess of cyanide.     

Fluorescent II-VI semiconductor quantum dots in living cells: nonlinear microspectroscopy in an optical tweezers system

In this work we used a setup consisting of an optical tweezers combined with a nonlinear microspectroscopy system to perform scanning microscopy and obtain emission spectra using two photon excited (TPE) luminescence of captured single living cells labeled with core-shell fluorescent semiconductor quantum dots (QDs). The QDs were obtained via colloidal synthesis in aqueous medium with an adequate physiological resulting pH. Sodium polyphosphate was used as the stabilizing agent. The results obtained show the potential presented by this system as well as by these II-VI fluorescent semiconductor quantum dots to perform spectroscopy in living trapped cells in any neighborhood and dynamically observe the cell chemical reactions in real time.     

Luminescent Sensing with Quantum Dots

Summary This review highlights recent advances in the use of quantum dots (QD’s) as luminescent sensors. The bulk of the study concentrates on systems that possess organic ligands bound to the surface of QD’s. These ligands vary from low molecular weight thiols to larger molecules such as maltose binding protein. All have one thing in common: when a target analyte binds to the ligand/receptor, a perturbation of the system occurs, that registers itself as a change in the luminescence intensity of the QD. Two main mechanisms are prevalent in controlling the luminescent intensity in such systems. The first is Photoinduced Electron Transfer (PET) and the second energy transfer. This review looks at current sensors that operate by using these mechanisms. Two component systems are also investigated where a quencher is first added to a solution of the QD, followed by addition of the target analyte that interacts with the quencher to influence the luminescence intensity.     

Fluorescent pH nanosensors: Design strategies and applications

Accurate measuring of pH is of great significance for various research areas ranging from environmental to chemical and biological sciences. In the past decades, there has been growing interest in the use of nanoparticles (NPs) for pH measurement, especially for intracellular pH sensing and imaging. In this regard, a number of different NP-based fluorescent pH sensors have been developed, which can be classified into three major categories including (I) fluorescent NPs with direct or indirect responses to pH, (II) nonfluorescent NPs that are used only as scaffold and carriers for pH-sensitive fluorescent dyes, and (III) nonfluorescent NPs whose pH-responsive structural change is converted into the fluorescence signal of their conjugated dyes. This review is a complete coverage of all NPs used so far for fluorescence pH sensing. The authors of this review invite readers to find all design strategies for employing semiconductor quantum dot, nanoclusters, carbon-based dots, polymer dots, upconversion NPs, fluorescent metal-organic frameworks, metallic NPs, silica NPs, polymer NPs, micellar NPs, nanogels, and protein NPs for this purpose.     

表面配体对CdSe量子点发光性质的影响

本文采用热注入法合成了以油胺/油酸为表面配体的、粒径均一的CdSe量子点(CdSe QDs)。调节表面配体交换中辛硫醇与CdSe QDs的比例,研究了表面配体对CdSe QDs光致发光及电致化学发光性质的影响,并提出了CdSe QDs的发光模型。结果表明,辛硫醇表面配体显著影响CdSe QDs的带边发射和深能级陷阱发射,因而导致CdSe QDs光致发光强度的显著降低,以及电致化学发光强度的增加。上述结果为进一步提高量子点的发光性能提供了依据。     

Photoluminescence of cadmium selenide quantum dots in polymer solutions

The effect of solvent on the photoluminescence of cadmium selenide quantum dots stabilized by oleic acid is examined with the example of two organic solvents: toluene and THF. It is found that THF favors desorption of ligands and formation of surface defects to a greater extent than toluene; as a result, the maximum of the photoluminescence band shifts to the red spectral region and its intensity decreases. The addition of polymers to the solution of quantum dots causes changes in the efficiency of photoluminescence and in the kinetics of its quenching. In the range of low concentrations (≤2 wt %) of quantum dots in polymer solutions, the intensity of luminescence first grows and then passes through a maximum and decreases. This effect may be explained both by the increasing number of surface defects and by quenching via energy transfer to polymers, especially in the case of polymers containing aromatic groups.     

Synthesis of surface-modified quantum dots

The review discusses the main methods used to obtain surface-modified quantum dots, specifically silicon, heavy metal chalcogenide and pnictide semiconductor nanoparticles. Examples of transformation processes of the grafted layer are considered. The importance of surface modification of A^IIB^VI- and A^IIIB^V-type semiconductor nanoparticles for the practical application of quantum dots is shown. It was determined that the most promising areas of their practical application are biology, medicine, and pharmacology. Special attention is paid to the hydrophilization of quantum dots, because only these materials can be used in biomedical applications. Modification of the quantum dot surface with amino acids is considered.

     

Observation of enhanced energy transfer in individual quantum dot-oligophenylene vinylene nanostructures

The temporal and spectral properties of luminescence from individual CdSe quantum dot-oligophenylene vinylene nanostructures (single quantum dots with conjugated organic ligands coordinated to the surface) are profoundly modified relative to blended films of the same components. These kinds of composite quantum dot-conjugated organic systems have attracted significant interest as a way to improve efficiency in photovoltaic device applications. By direct functionalization of the dot surface with the conjugated organic ligands, we realize a significant enhancement in energy transfer and luminescence stability.     

Fluorescence resonance energy transfer in doubly-quantum dot labeled IgG system

The mouse immunoglobulin G (mouse IgG) as a kind of bio-molecule was labeled with two different luminescent colloidal semiconductor quantum dots (QDs), green-emitting CdTe quantum dots and red-emitting CdTe quantum dots in this work. As a result of the fluorescence resonance energy transfer (FRET) between the two different sizes nanoparticles with mouse IgG as the binding bridge, a significant enhancement of the emission of the red-emitting CdTe quantum dots and the corresponding quenching of the emission of green-emitting CdTe quantum dots were observed. The relationship between the concentration of the mouse immunoglobulin G and the fluorescence intensity ratio (I_a/I_d) of acceptors and donors was studied also. Under optimal conditions, the calibration graph is linear over the range of 0.1–20.0 mg/L mouse IgG.     

Molecularly imprinted polymeric film on semiconductor nanoparticles analyte detection by quantum dot photoluminescence

Incorporation of semiconductor nanoparticles into molecularly imprinted polymer provides a sensor material which can be easily shaped and with better selectivity because the bound template would quench the photoluminescence (PL) emission of quantum dots significantly. In this work, artificial receptors of various templates were synthesized with functional monomers such as methacrylic acid (MAA), semiconductor like CdSe/ZnS core-shell derivatized with 4-vinylpyridine and ethylene glycol dimethacrylic acid as the cross-linker. The quenching of photoluminescence emissions is presumably due to the fluorescence resonance energy transfer between quantum dots and template molecules. The photoluminescence emission is unaffected upon incubation of analyte with the blank control polymer.     

Luminescence quenching in self-assembled adducts of [Ru(dpp)3]2+ complexes and CdTe nanocrystals

We have investigated chloroform solutions containing tris(4,7-diphenyl-1,10-phenanthroline) ruthenium(II) and CdTe nanocrystal quantum dots (5.6 nm diameter). The electronic levels of these two components are such that the Ru complex can act as an energy donor towards the quantum dot, which can thus behave as an energy acceptor. Steady-state and time-resolved spectroscopic experiments indicate that the Ru complexes and the CdTe nanocrystals self-assemble to give stable 1?:?1 adducts, in which the luminescence of the former units is strongly quenched. Such a quenching can be ascribed to either energy transfer to the CdTe quantum dot, or to electron transfer from the CdTe valence band to the excited Ru complex. However, no supporting evidence for the occurrence of photoinduced energy transfer in the adduct could be found. The CdTe luminescence is also slightly quenched in the presence of the ruthenium complex. The strong association of the metal complexes with the nanocrystals suggests that self-assembly strategies may be effectively employed to achieve surface functionalization of semiconductor quantum dots with molecular units.     

Observation of correlated emission intensity and polarization fluctuations in single CdSe/ZnS quantum dots

Time-resolved single-nanoparticle spectroscopy has been carried out to examine the luminescence characteristics of individual CdSe/ZnS core/shell quantum dots. In particular, the possible correlations between emission intensity, lifetime, spectrum, and polarization fluctuations have been investigated. The emission polarization was found to be correlated with the luminescence intensity in a nonlinear way. The low-emissive states were found to correlate with red-shifted spectrum, increased nonradiative decay, and low degree of emission polarization. The observations are consistent with the model that charged quantum dots can be emissive.     

Hydrophilic semiconductor quantum dots

Comparative analysis of recent literature data on hydrophilization of semiconductor quantum dots, which are actively used at present in various fields, has been performed. The main methods of preparation of hydrophilic quantum dots are considered: synthesis of the particles in aqueous solutions; replacement of hydrophobic ligands with hydrophilic ligands in the shells stabilizing the particles; creation of a second, water-soluble shell around the hydrophobic particles; and various methods of post-preparative treatment to improve photoluminescent properties of quantum dots.     

Luminescence of Hybrid Nanostructures of InP@ZnS Colloidal Quantum Dots and <Emphasis Type="Italic">meso</Emphasis>-Tetra(3-pyridyl)porphyrin Molecules

The formation of hybrid nanostructures consisting of InP@ZnS colloidal quantum dots and mesotetra(3-pyridyl)porphyrin molecules adsorbed on the quantum dots has been studied. In such nanostructures, strong quenching of quantum dot luminescence and an increase in the emission intensity of porphyrin are observed due to nonradiative resonance energy transfer from colloidal quantum dots to porphyrin.