Estudio de interfases metal-tiol en superficies planas y nanopartículas

Las nanopartículas (NPs) de metales nobles presentan gran interés tanto por sus propiedades básicas como por la amplia variedad de aplicaciones en las que se utilizan activamente. Para obtener NPs estables y evitar su aglomeración, es necesario utilizaragentes estabilizantes durante la síntesis. Estas moléculas se adsorben sobre la superficie de las NPs y evitan que estas interaccionen directamente con las partículas vecinas. Si bien existen diversas moléculas que pueden ser utilizadas para este fin, uno de los únicos tipos de NPs metálicas cuya distribución de tamaños es estrecha, son estables a lo largo del tiempo y pueden ser obtenidas en forma de polvo, lavadas, y utilizadas como si se tratase de un compuesto químico tradicional, son las NPs cubiertas por tioles. La gran estabilidad de estas partículas está dada por la alta energía del enlace que se forma entre el azufre del grupo tiol y el metal. Resulta, entonces, particularmente interesante estudiar la interfase entre la superficie metálica y las moléculas adsorbidas. En este trabajo se presenta un estudio de la interfase Au-tiol y Pd-tiol en diferentes sistemas que van desde monocapas autoensambladas (SAMs) de tioles sobre superficies planas hasta compuestos poliméricos de tiolatos metálicos, con especial énfasis en las NPs metálicas cubiertas por tioles. El estudio de estos sistemas fue realizado mediante la utilización de diversas técnicas. En todos los experimentos se controlaron las condiciones de medida de manera tal de minimizar los daños producidos sobre las muestras. En los casos en que esto no fue posible, se intentó elucidar qué tipo de daño se estaba produciendo para realizar el análisis de los resultados teniendo en cuenta estos efectos o bien descartar los datos que hayan sido afectados por los mismos.Facultad de Ciencias Exacta

A portable and affordable aligner for the assembly of microfluidic devices

The incorporation of sophisticated capabilities within microfluidic devices often requires the assembly of different layers in a correct arrangement. For example, when it is desired to include electrodes inside microfluidic channels or to create 3D microfluidic structures. However, the alignment between different substrates at the microscale requires expensive equipment not available for all research groups. In this work, we present an affordable, compact and portable aligner for assembling multilayered composite microfluidic chips. The instrument is composed of aluminum machined pieces combined with precision stages and includes a digital microscope with a LED illumination system for monitoring the alignment process. An interchangeable holder was created for substrate fixing, allowing the bonding of PDMS with other materials. Microscopic visualization is achieved through any device with internet access, avoiding the need of a computer attached to the aligner. To test the performance of the aligner, the center of an indium tin oxide microelectrode on a glass substrate was aligned with the center of a microchannel in a PDMS chip. The accuracy and precision of the instrument are suited for many microfluidic applications. The small and inexpensive design of the aligner makes it a cost-effective option for small groups working in microfluidics.Fil: Guglielmotti, Victoria. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Saffioti, Nicolas Andres. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Tohmé, Ana Laura. Universidad Nacional de San Martin. Instituto de Nanosistemas; ArgentinaFil: Gambarotta, Martín. Universidad Nacional de San Martin. Instituto de Nanosistemas; ArgentinaFil: Corthey, Gastón. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Pallarola, Diego Andres. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentin

New insights into the chemistry of thiolate-protected palladium nanoparticles

This paper establishes the chemical nature of Pd nanoparticles protected by alkanethiolates that were prepared through a ligand place-exchange approach and the two-phase method, first developed for Au nanoparticles by Brust and Schiffrin. After 10 years since the first study on this kind of Pd nanoparticles was published, the surface composition of the particles is a matter of debate in the literature and it has not been unambiguously assessed. The nanoparticles were studied by means of several techniques: UV-visible spectroscopy, scanning transmission electron microscopy, Fourier-transform infrared spectroscopy, extended X-ray absorption fine structure, and X-ray photoelectron spectroscopy. The experimental data, obtained for the 3 nm diameter Pd particles, prepared by both synthetic routes, are consistent with nanoparticles composed by Pd(0) cores surrounded by a submonolayer of sulfide species, which are protected by alkanethiolates. Also, we unambiguously demonstrate that the chemical nature of these particles is very similar to that experimentally found for alkanethiolate-modified bulk Pd. The results from this paper are important not only for handling thiolate-protected Pd nanoparticles in catalysis and sensing, but also for the basic comprehension of metallic nanoparticles and the relation of their surface structure with the synthesis method.Fil: Corthey, Gastón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Rubert, Aldo Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Picone, Andrea Lorena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Amaya, Edgar Gilberto. University of Texas at San Antonio; Estados UnidosFil: Giovanetti, Lisandro Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Ramallo Lopez, Jose Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Zelaya, Maria Eugenia. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Benitez, Guillermo Alfredo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Requejo, Felix Gregorio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Yacamán, Miguel Jose. University of Texas at San Antonio; Estados UnidosFil: Salvarezza, Roberto Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Fonticelli, Mariano Hernan. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentin

The Complex Thiol-Palladium Interface: A Theoretical and Experimental Study

This paper presents a theoretical study of the surface structures and thermodynamic stability of different thiol and sulfide structures present on the palladium surface as a function of the chemical potential of the thiol species. It has been found that as the chemical potential of the thiol is increased, the initially clean palladium surface is covered by a ( √ 3 x √ 3)R30º sulfur lattice. Further increase in the thiol pressure or concentration leads to the formation of a denser ( √ 7 x √ 7)R19.1º sulfur lattice, which finally undergoes a phase transition to form a complex ( √ 7 x √ 7)R19.1º sulfurþ thiol adlayer (3/7 sulfur þ 2/7 thiol coverage). This transition is accompanied by a strong reconstruction of the Pd(111) surface. The formation of these surface structures has been explained in terms of the catalytic properties of the palladium surface. These results have been compared with X-ray photoelectron spectroscopy results obtained for thiols adsorbed on different palladium surfaces.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

‘‘Naked’’ gold nanoparticles supported on HOPG: melanin functionalization and catalytic activity

Reductive electrodesorption has been used to produce ‘‘naked’’ gold nanoparticles (AuNPs) 3 nm in size on HOPG from different thiolate-capped AuNPs. The clean AuNPs transform the electrocatalytic inert HOPG into an active surface for hydrogen peroxide electroreduction, causing a lowering of the cathodic overpotential of 0.25 V with respect to the Au(111) surface. Compared to the plain gold substrates, the nanostructures promote only a slight increase in the hydrogen evolution reaction. In a second modification step a 1 nm thick melanin–iron coating is electrochemically formed around the AuNPs. This ultrathin melanin–iron coating largely improves the catalytic activity of the bare AuNPs for both hydrogen peroxide electroreduction and hydrogen evolution reaction. This strategy, which integrates electrochemistry and nanotechnology, can be applied to the preparation of efficient ‘‘naked’’ AuNPs and organic-iron capped AuNPs catalysts.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Self-assembled monolayers of thiolates on metals: A review article on sulfur-metal chemistry and surface structures

A review article on fundamental aspects of thiolate self-assembled monolayers (SAMs) on the (111) and (100) surfaces of the Cu and Ni groups is presented. In particular this work is focused on two important points that remain poorly understood in most of these metals: the chemistry of the S-metal interface, which strongly depends on the nature of the metallic surface, and the role of the interaction forces that not only guide the self-assembly process but also influence the surface structure of SAMs. In addition to recent experimental and theoretical data on these issues we present new density functional calculations including van der Waals forces for an important number of known thiolate surface structures as a function of the hydrocarbon chain length.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Synthesis and Characterization of Gold@Gold(I)-Thiomalate Core@Shell Nanoparticles

In this paper, the synthesis of gold@gold(I)−thiolate core@shell nanoparticles is described for the first time. The chemical nature and structure of these nanoparticles were characterized by a multi-technique approach. The prepared particles consist of gold metallic cores, about 1 nm in size, surrounded by stable gold(I)−thiomalate shells (Au@Au(I)−TM). These nanoparticles could be useful in medicine due to the interesting properties that gold(I)−thiomalate has against rheumatoid arthritis. Furthermore, the described results give new insights in the synthesis and characterization of metallic and core@shell nanoparticles.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Influence of capping on the atomistic arrangement in palladium nanoparticles at room temperature

The role that protecting molecules have on the way that palladium atoms arrange themselves in nanoparticles prepared at room temperature was studied by the analysis of aberration-corrected scanning transmission electron microscopy images and atomistic Langevin dynamics simulations. It was found that the arrangement of Pd atoms is less ordered in thiolate-protected nanoparticles than in amine-protected ones. The experimental and theoretical data showed that the disorder in ∼3 nm thiolate-protected particles is promoted by the strong S–Pd bond in the sulfide layer that surrounds the nanoparticles.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

New insights into the chemistry of thiolate-protected palladium nanoparticles

This paper establishes the chemical nature of Pd nanoparticles protected by alkanethiolates that were prepared through a ligand place-exchange approach and the two-phase method, first developed for Au nanoparticles by Brust and Schiffrin. After 10 years since the first study on this kind of Pd nanoparticles was published, the surface composition of the particles is a matter of debate in the literature and it has not been unambiguously assessed. The nanoparticles were studied by means of several techniques: UV–visible spectroscopy, scanning transmission electron microscopy, Fourier-transform infrared spectroscopy, extended X-ray absorption fine structure, and X-ray photoelectron spectroscopy. The experimental data, obtained for the 3 nm diameter Pd particles, prepared by both synthetic routes, are consistent with nanoparticles composed by Pd(0) cores surrounded by a submonolayer of sulfide species, which are protected by alkanethiolates. Also, we unambiguously demonstrate that the chemical nature of these particles is very similar to that experimentally found for alkanethiolate-modified bulk Pd. The results from this paper are important not only for handling thiolate-protected Pd nanoparticles in catalysis and sensing, but also for the basic comprehension of metallic nanoparticles and the relation of their surface structure with the synthesis method.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada