RESUMEN
Finding simple, easily controlled, and flexible synthetic routes for the preparation of ternary and hybrid nanostructured semiconductors is always highly desirable, especially to fulfill the requirements for mass production to enable application to many fields such as optoelectronics, thermoelectricity, and catalysis. Moreover, understanding the underlying reaction mechanisms is equally important, offering a starting point for its extrapolation from one system to another. In this work, we developed a new and more straightforward colloidal synthetic way to form hybrid Au-Ag2X (X = S, Se) nanoparticles under mild conditions through the reaction of Au and Ag2X nanostructured precursors in solution. At the solid-solid interface between metallic domains and the binary chalcogenide domains, a small fraction of a ternary AuAg3X2 phase was observed to have grown as a consequence of a solid-state electrochemical reaction, as confirmed by computational studies. Thus, the formation of stable ternary phases drives the selective hetero-attachment of Au and Ag2X nanoparticles in solution, consolidates the interface between their domains, and stabilizes the whole hybrid Au-Ag2X systems.
RESUMEN
The tuning of the chemical composition in nanostructures is a key aspect to control for the preparation of new multifunctional and highly performing materials. The modification of Cu2-xSe nanocrystals with Pt could provide a good way to tune both optical and catalytic properties of the structure. Although the heterogeneous nucleation of metallic Pt domains on semiconductor chalcogenides has been frequently reported, the insertion of Pt into chalcogenide materials has not been conceived so far. In this work we have explored the experimental conditions to facilitate and enhance the insertion of Pt into the Cu2-xSe nanocrystalline lattice, forming novel ternary phases that show a high degree of miscibility and compositional variability. Our results show that Pt is mainly found as a pure metal or a CuPt alloy at high Pt loads (Pt : Cu atomic ratio in reaction medium >1). However, two main ternary CuPtSe phases with cubic and monoclinic symmetry can be identified when working at lower Pt : Cu atomic ratios. Their structure and chemical composition have been studied by local STEM-EDS and HRTEM analyses. The samples containing ternary domains have been loaded on graphite-like C3N4 (g-C3N4) semiconductor layers, and the resulting nanocomposite materials have been tested as promising photocatalysts for the production of H2 from aqueous ethanolic solutions.
RESUMEN
Different gold microstructures have been synthesized by using supramolecular gold(i) organometallic compounds as templates and Ag nanoparticles as reducing agents. The use of fibers resulting from supramolecular assemblies of neutral gold(i) compounds gives rise to the formation of microrods. The use of supramolecular assemblies from ionic molecules results in spherical or square-based prism gold microstructures, depending on the shape of the supramolecular gold(i) precursor assembly. In addition to temperature and reaction time, solvents exert a strong influence on the formation and morphology of gold structures, as borne out by the example that well-defined star-like morphologies have been obtained in chloroform.
RESUMEN
A new antimonato polyoxovanadate {Zn(en)3 }3 [V15 Sb6 O42 (H2 O)]â 3 enâ 10 H2 O (en=ethylenediamine) synthesized under hydrothermal conditions exhibits remarkable solubility in water. Electrospray ionization mass spectrometry (ESI-MS) investigations on an aqueous solution demonstrate that the cluster core remains fully intact for 72â h. At longer times, slow transformation into a {V14 Sb8 O42 } cluster is observed. The conversion reaches 50 % after 14â days and is complete after approximately 20â days. The rate of this {V15 Sb6 }â{V14 Sb8 } cluster transformation is significantly increased in the presence of ammonium acetate. Applying the new compound as a synthon in the presence of 1,10-phenanthroline (phen) led to crystallization of {Zn(phen)3 }2 [Zn(en)2 V15 Sb6 O42 (H2 O)]â 23 H2 O after a short reaction time, whereas addition of Sb2 O3 led to fast crystallization of {(Zn(en)2 (H2 O)2 )(Zn(en)2 )}[Zn(en)2 V15 Sb6 O42 (H2 O)] â 8.5 H2 O. In the crystal structure of {Zn(en)3 }3 [V15 Sb6 O42 (H2 O)]â 3 enâ 10 H2 O, the en molecules are seen to be attached to the cluster anion through Sb-N bonds. In the structures of the two new compounds obtained, the [V15 Sb6 O42 (H2 O)]6- anions are expanded by Zn2+ -centered complexes through Zn-O-V bond formation.
RESUMEN
Both long-term native language experience and immediate linguistic expectations can affect listeners' use of acoustic information when making a phonetic decision. In this study, a Garner selective attention task was used to investigate differences in attention to consonants and tones by American English-speaking listeners (N = 20) and Mandarin Chinese-speaking listeners hearing speech in either American English (N = 17) or Mandarin Chinese (N = 20). To minimize the effects of lexical differences and differences in the linguistic status of pitch across the two languages, stimuli and response conditions were selected such that all tokens constitute legitimate words in both languages and all responses required listeners to make decisions that were linguistically meaningful in their native language. Results showed that regardless of ambient language, Chinese listeners processed consonant and tone in a combined manner, consistent with previous research. In contrast, English listeners treated tones and consonants as perceptually separable. Results are discussed in terms of the role of sub-phonemic differences in acoustic cues across language, and the linguistic status of consonants and pitch contours in the two languages.