A. N. Goldstein

Bio: A. N. Goldstein is an academic researcher. The author has contributed to research in topics: Self-assembled monolayer & Transmission electron microscopy. The author has an hindex of 1, co-authored 1 publications receiving 584 citations.

Semiconductor nanocrystals covalently bound to metal surfaces with self-assembled monolayers

Abstract: A method is described for attaching semiconductor nanocrystals to metal surfaces using self-assembled difunctional organic monolayers as bridge compounds. Three different techniques are presented. Two rely on the formation of self-assembled monolayers on gold and aluminum in which the exposed tail groups are thiols. When exposed to heptane solutions of cadmium-rich nanocrystals, these free thiols bind the cadmium and anchor it to the surface. The third technique attaches nanocrystals already coated with carboxylic acids to freshly cleaned aluminum. The nanocrystals, before deposition on the metals, were characterized by ultraviolet-visible spectroscopy, X-ray powder diffraction, resonance Raman scattering, transmission electron microscopy (TEM), and electron diffraction. Afterward, the nanocrystal films were characterized by resonance Raman scattering, Rutherford back scattering (RBS), contact angle measurements, and TEM. All techniques indicate the presence of quantum confined clusters on the metal surfaces with a coverage of approximately 0.5 monolayers. These samples represent the first step toward synthesis of an organized assembly of clusters as well as allow the first application of electron spectroscopies to be completed on this type of cluster. As an example of this, the first X-ray photoelectron spectra of semiconductor nanocrystals are presented. 51 refs., 17 figs.

Dye-Sensitized Solar Cells

Abstract: Dye-sensitized solar cells (DSCs) offer the possibilities to design solar cells with a large flexibility in shape, color, and transparency. DSC research groups have been established around the worl ...

A DNA-based Method for Rationally Assembling Nanoparticles Into Macroscopic Materials

Abstract: COLLOIDAL particles of metals and semiconductors have potentially useful optical, optoelectronic and material properties1–4 that derive from their small (nanoscopic) size. These properties might lead to applications including chemical sensors, spectro-scopic enhancers, quantum dot and nanostructure fabrication, and microimaging methods2–4. A great deal of control can now be exercised over the chemical composition, size and polydis-persity1,2 of colloidal particles, and many methods have been developed for assembling them into useful aggregates and materials. Here we describe a method for assembling colloidal gold nanoparticles rationally and reversibly into macroscopic aggregates. The method involves attaching to the surfaces of two batches of 13-nm gold particles non-complementary DNA oligo-nucleotides capped with thiol groups, which bind to gold. When we add to the solution an oligonucleotide duplex with 'sticky ends' that are complementary to the two grafted sequences, the nanoparticles self-assemble into aggregates. This assembly process can be reversed by thermal denaturation. This strategy should now make it possible to tailor the optical, electronic and structural properties of the colloidal aggregates by using the specificity of DNA interactions to direct the interactions between particles of different size and composition.

Magnetic nanoparticles: Synthesis, protection, functionalization, and application

Abstract: This review focuses on the synthesis, protection, functionalization, and application of magnetic nanoparticles, as well as the magnetic properties of nanostructured systems. Substantial progress in the size and shape control of magnetic nanoparticles has been made by developing methods such as co-precipitation, thermal decomposition and/or reduction, micelle synthesis, and hydrothermal synthesis. A major challenge still is protection against corrosion, and therefore suitable protection strategies will be emphasized, for example, surfactant/polymer coating, silica coating and carbon coating of magnetic nanoparticles or embedding them in a matrix/support. Properly protected magnetic nanoparticles can be used as building blocks for the fabrication of various functional systems, and their application in catalysis and biotechnology will be briefly reviewed. Finally, some future trends and perspectives in these research areas will be outlined.

Light-emitting diodes made from cadmium selenide nanocrystals and a semiconducting polymer

Abstract: ELECTROLUMINESCENT devices have been developed recently that are based on new materials such as porous silicon1 and semiconducting polymers2,3. By taking advantage of developments in the preparation and characterization of direct-gap semiconductor nanocrystals4–6, and of electroluminescent polymers7, we have now constructed a hybrid organic/inorganic electroluminescent device. Light emission arises from the recombination of holes injected into a layer of semiconducting p-paraphenylene vinylene (PPV)8–10 with electrons injected into a multilayer film of cadmium selenide nanocrystals. Close matching of the emitting layer of nanocrystals with the work function of the metal contact leads to an operating voltage11 of only 4V. At low voltages emission from the CdSe layer occurs. Because of the quantum size effect19–24 the colour of this emission can be varied from red to yellow by changing the nanocrystal size. At higher voltages green emission from the polymer layer predominates. Thus this device has a degree of voltage tunability of colour.

Light-emitting diodes made from cadmium selenide nanocrystals and a semiconducting polymer

Abstract: ELECTROLUMINESCENT devices have been developed recently that are based on new materials such as porous silicon' and semiconducting polymers 2,3 . By taking advantage of developments in the preparation and characterization of direct-gap semiconductor nanocrystals 4-6 , and of electroluminescent polymers7, we have now constructed a hybrid organic/inorganic electroluminescent device. Light emission arises from the recombination of holes injected into a layer of semiconducting p-paraphenylene vinylene (PPV) 2-10 with electrons injected into a multilayer film of cadmium selenide nanocrystals. Close matching of the emitting layer of nanocrystals with the work function of the metal contact leads to an operating voltage" of only 4 V. At low voltages emission from the CdSe layer occurs. Because of the quantum size effect 19-24 the colour of this emission can be varied from red to yellow by changing the nanocrystal size. At higher voltages green emission from the polymer layer predominates. Thus this device has a degree of voltage tunability of colour.