Photoinduced charge transfer between CdSe nanocrystal quantum dots and Ru-polypyridine complexes

In this communication, we demonstrate a new approach to sensitization of Ru-polypyridine complexes by using semiconductor nanocrystal quantum dots (NQDs). When mixed in solution, the complexes functionalized by carboxylic groups adsorb onto the surface of the NQDs. Excitation of NQDs by 400 nm light leads to fast, 5 ps hole transfer from the photoexcited NQDs to the surface-adsorbed complexes. This result indicates that Ru complexes can be sensitized by CdSe NQDs, which opens interesting opportunities for designing new types of photocatalytic materials for solar energy conversion applications. These materials will take advantage of broad size-controlled absorption spectra and large extinction coefficients of NQDs as well as the unique property of NQDs to respond to absorption of a single photon by producing multiple electron-hole pairs.     

Photo-gated charge transfer of organized assemblies of CdSe quantum dots

The electronic conductivity of tri-n-octylphosphineoxide (TOPO)-protected CdSe quantum dots (QDs) was studied at the air-water interface using the Langmuir technique within the context of photochemical and photophysical excitation. It was found that, upon photoirradiation with photon energies higher than that of the absorption threshold, the voltammetric currents increased rather substantially with a pair of voltammetric peaks at positive potentials. However, the photoconductivity profiles exhibited a dynamic transition, which was ascribed to the strong affinity of oxygen onto the CdSe surface and the consequent trapping of the photogenerated electrons. The resulting excess of holes led to photocorrosion of the particle cores. The oxygen adsorption and photoetching processes were found to be reversible upon cessation of the photoexcitation. In contrast, only featureless voltammetric responses were observed when the particle monolayers were deposited onto the electrode surface and the film conductance was measured in a vacuum (the overall profiles were analogous to that of a Coulomb blockade). A comparative study was also carried out with a CdSe dropcast thick film immersed in acetonitrile, where the photoconductivity profiles were reversible and almost linear. The latter was attributed to the separation of photogenerated electrons and holes which were subsequently collected at the electrodes under voltammetric control. In the dropcast system, the oxygen effects were minimal which was ascribed to the acetontrile medium that limited the access to oxygen and thus the particles were chemically intact. These studies suggest that chemical environment plays an important role in the determination of the chemical stability and electronic conductivity of CdSe QD thin films.     

Energy transfer between CdS quantum dots and Au nanoparticles in photoelectrochemical detection

This work is the first report on the energy transfer between CdS quantum dots and Au nanoparticles for photoelectrochemical biosensing applications.     

Synthesis of carbohydrate-conjugated nanoparticles and quantum dots

Nanoparticle-based probes are emerging as alternatives to molecular probes due to their various advantages, such as bright and tunable optical property, enhanced chemical and photochemical stability, and ease of introduction of multifunctionality. This work presents a simple and general approach for functionalizing various nanoparticle systems for use as glycobiological probes. Silica-coated nanoparticles of Ag, Fe3O4, and ZnS-CdSe were synthesized and functionalized with dextran. The resulting 10-40-nm-sized particles were robust, water-soluble, colloidally stable, and biochemically active.     

Electrochemical properties of CdSe and CdTe quantum dots

Semiconductor nanocrystal quantum dots (QDs), owing to their unique opto-electronic properties determined by quantum confinement effects, have been the subject of extensive investigations in different areas of science and technology in the past two decades. The electrochemical behaviour of QDs, particularly for CdSe and CdTe nanocrystals, has also been explored, although to a lesser extent compared to the optical properties. Voltammetric measurements can be used to probe the redox levels available for the nanocrystals, which is an invaluable piece of information if these systems are involved in electron transfer processes. Electrochemical data can also foster the interpretation of the spectroscopic properties of QDs, and give insightful information on their chemical composition, dimension, and surface properties. Hence, electrochemical methods constitute in principle an effective tool to probe the quality of QD samples in terms of purity, size dispersion, and surface defects. The scope of this critical review is to discuss the results of electrochemical studies carried out on CdSe and CdTe core and core-shell semiconductor nanocrystals of spherical shape. Examples of emerging or potential applications that exploit electroactive quantum dot-based systems will also be illustrated.     

Semiconductor quantum dots and metal nanoparticles: syntheses,optical properties,and biological applications

We review the syntheses, optical properties, and biological applications of cadmium selenide (CdSe) and cadmium selenide–zinc sulfide (CdSe–ZnS) quantum dots (QDs) and gold (Au) and silver (Ag) nanoparticles (NPs). Specifically, we selected the syntheses of QDs and Au and Ag NPs in aqueous and organic phases, size- and shape-dependent photoluminescence (PL) of QDs and plasmon of metal NPs, and their bioimaging applications. The PL properties of QDs are discussed with reference to their band gap structure and various electronic transitions, relations of PL and photoactivated PL with surface defects, and blinking of single QDs. Optical properties of Ag and Au NPs are discussed with reference to their size- and shape-dependent surface plasmon bands, electron dynamics and relaxation, and surface-enhanced Raman scattering (SERS). The bioimaging applications are discussed with reference to in vitro and in vivo imaging of live cells, and in vivo imaging of cancers, tumor vasculature, and lymph nodes. Other aspects of the review are in vivo deep tissue imaging, multiphoton excitation, NIR fluorescence and SERS imaging, and toxic effects of NPs and their clearance from the body. Figure Semiconductor quantum dots and metal nanoparticles have extensive applications, e.g., in vitro and in vivo bioimaging Tamitake Itoh and Abdulaziz Anas contributed equally to this article.     

Photoinduced charge transfer mediated by DNA-wrapped carbon nanotubes

We report our observation of solution photochemical reactions catalyzed by carbon nanotubes. Addition of sub-millimolar Ag+ ions into a solution of DNA-wrapped carbon nanotubes (DNA-CNT) leads to a strong charge-transfer band in the UV region of the optical absorption spectrum. Light irradiation of the Ag+/DNA-CNT mixture results in reduction of Ag+ to Ag nanoparticles and concomitant oxidation of water.     

A perspective on bioconjugated nanoparticles and quantum dots

Bioconjugated nanoparticles and quantum dots are among the most exciting nanomaterials with promising application potentials in nanomedicine field. These applications include biosensing, bioimaging, bioassay, targeted drug delivery and new therapeutic agents or method development. Although most of these applications are based on the optical properties of nanoparticle materials such as surface plasmon resonance, surface enhanced Raman scattering and strong photoluminescence, other aspects of nanoparticles such as the catalytic effect and amplification effect associated with the nanoscale dimension have also been explored. This review presents a narrative summary on the use of bioconjugated nanoparticles and quantum dots for biological applications, along with a discussion on some critical challenges existing in the field and possible solutions that have been or are being developed to overcome these challenges.     

Silica-coated nanocomposites of magnetic nanoparticles and quantum dots

Quantum dots (QDs) and magnetic nanoparticles (MPs) are of interest for biological imaging, drug targeting, and bioconjugation because of their unique optoelectronic and magnetic properties, respectively. To provide for water solubility and biocompatibility, QDs and MPs were encapsulated within a silica shell using a reverse microemulsion synthesis. The resulting SiO2/MP-QD nanocomposite particles present a unique combination of magnetic and optical properties. Their nonporous silica shell allows them to be surface modified for bioconjugation in various biomedical applications.     

Electrochemical detection of quantum dots by stabilization of electrogenerated copper species

The determination of quantum dots is of particular interest as they are frequently used as labels in electrochemical biosensors. In this paper, we describe a method for the detection of very low concentrations of quantum dots using the voltammetric response of copper in ammonia solution. Copper species electrogenerated on the electrode surface are stabilized by the nanoparticles, preventing their oxidation by dissolved oxygen, and a relationship between the concentration of the nanoparticles and the copper voltammetric response can thus be obtained. The reported method shows a linear range between 0.05 and 2 nM of quantum dots, with a limit of detection in the order of 9 × 10⁷ nanoparticles. This method could be employed to improve the detection limit of electrochemical biosensors using quantum dots as labels.     

Influence of gold nanoparticles on nonradiative energy transfer in nanoclusters of colloidal quantum dots InP@ZnS

The influence of gold nanoparticles on the efficiency of nonradiative resonance energy transfer between InP@ZnS quantum dots composed of nanoclusters, a new type of organized structures consisting of hydrophobic quantum dots and gold nanoparticles, has been experimentally studied.     

Detection of DNA damage by exploiting the distance dependence of the electrochemiluminescence energy transfer between quantum dots and gold nanoparticles

Microchimica Acta - We have developed a platform to detect DNA damage induced by perfluorooctanoic acid (PFOA) by measuring the electrochemiluminescence (ECL) of a layer-by-layer electrostatic...     

Light-emitting charge transfer species promoted by metal ion coordination

The coordinative interaction between zinc(II) and naphthalene-labeled diiminopyridine ligands induces the formation of light-emitting intracomplex charge transfer species.     

Photoelectrochemical determination of inorganic mercury ions based on energy transfer between CdS quantum dots and Au nanoparticles

A novel photoelectrochemical (PEC) sensor for mercury ions (Hg^2 +) was fabricated based on the energy transfer (ET) between CdS quantum dots (QDs) and Au nanoparticles (NPs) with the formation of T–Hg^2 +–T pairs. In the presence of Hg^2 + ions, a T-rich single-strand (ss) DNA labeled with Au NPs could hybridize with another T-rich ssDNA anchored on the CdS QDs modified electrode, through T–Hg^2 +–T interactions, rendering the Au NPs in close proximity with the CdS QDs and hence the photocurrent decrease due to the ET between the CdS QDs and the Au NPs. Under the optimal condition, the photocurrent decrease was proportional to the Hg^2 + concentration, ranging from 3.0 × 10^− 9 to 1.0 × 10^− 7 M, with the detection limit of 6.0 × 10^− 10 M.     

Electron and hole transfer from indium phosphide quantum dots

Electron- and hole-transfer reactions are studied in colloidal InP quantum dots (QDs). Photoluminescence quenching and time-resolved transient absorption (TA) measurements are utilized to examine hole transfer from photoexcited InP QDs to the hole acceptor N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD) and electron transfer to nanocrystalline titanium dioxide (TiO2) films. Core-confined holes are effectively quenched by TMPD, resulting in a new approximately 4-ps component in the TA decay. It is found that electron transfer to TiO2 is primarily mediated through surface-localized states on the InP QDs.     

The quenching of CdSe quantum dots photoluminescence by gold nanoparticles in solution

The photoluminescence (PL) of CdSe quantum dots (QD) in aqueous media has been studied in the presence of gold nanoparticles (NP) with different shapes. The steady state PL intensity of CdSe QD (1.5-2 nm in size) is quenched in the presence of gold NP. Picosecond bleach recovery and nanosecond time-resolved luminescence measurements show a faster bleach recovery and decrease in the lifetime of the emitting states of CdSe QD in the presence of quenchers. Surfactant-capped gold nanorods (NR) with aspect ratio of 3 and surfactant-capped and citrate-capped nanospheres (NS) of 12 nm diameter were used as quenchers in order to study the effect of shape and surface charge on the quenching rates. The Stern-Volmer kinetics model is used to examine the observed quenching behavior as a function of the quencher concentration. It was found that the quenching rate of NR is more than 1000 times stronger than that of NS with the same capping material. We also found that the quenching rate decreases as the length of the NR decreases, although the overlap between the CdSe emission and the NR absorption increases. This suggests that the quenching is a result of electron transfer rather than long-range (Forster-type) energy transfer processes. The quenching was attributed to the transfer of electron with energies below the Fermi level of gold to the trap holes of CdSe QD. The observed large difference between NR and NS quenching efficiencies was attributed to the presence of the [110] facets only in the NR, which have higher surface energy.     

Synthesis and electronic properties of semiconductor nanoparticles/quantum dots

This review examines recent work on the synthesis, characterisation and potential applications of semiconductor nanoparticles (quantum dots). Recent advances in single quatum dot spectroscopy is also reviewed.     

Electrochemical sensors based on metal and semiconductor nanoparticles

Metal and semiconductor nanoparticles exhibit unique optical, electrical, thermal and catalytic properties. Therefore, they have attracted considerable interest and have been employed for construction of various electrochemical sensors. This minireview gives a general view of recent advances in electrochemical sensor development based on metal and semiconductor nanoparticles covering genosensors, protein and enzyme-based sensors, gas sensors and sensor for other organic and inorganic substances. Different assay strategies based on metal and semiconductor nanoparticles for biosensor and bioelectronic applications are presented, including electrochemical, electrical, and magnetic signal transduction techniques. Electrochemical transduction principles provide signal changes in conductance, charge, potential and current. We have paid much attention to the potential-based and current-based sensors herein. Lastly, a brief introduction is given into advances concerning the role of nanoparticles, quantum dots and nanowires for nanomedicine, such as drug delivery and discovery.     

Electrochemical biosensing for dsDNA damage induced by PbSe quantum dots under UV irradiation

<正>An electrochemical sensor for the detection of the natural double-stranded DNA(dsDNA) damage induced by PbSe quantum dots(QDs) under UV irradiation was developed.The biosensing membranes were prepared by successively assembling 3- mercaptopropionic acid,polycationic poly(diallyldimethyl ammonium) and dsDNA on the surface of the gold electrode.Damage of dsDNA was fulfilled by immersing the sensing membrane electrode in PbSe QDs suspension and illuminating it with an UV lamp. Cyclic voltammetry was utilized to detect dsDNA damage with Co(phen)_3~(3+) as the electroactive probe.The UV irradiation,Pb~(2+) ions liberated from the PbSe QDs under the UV irradiation and the reactive oxygen species(ROS) generated in the presence of the PbSe QDs also under the UV irradiation were the three factors of inducing the dsDNA damage.The synergistic effect of the three factors might dramatically enhance the damage of dsDNA.This electrochemical sensor provided a simple method for detecting DNA damage,and may be used for investigating the DNA damage induced by other QDs.