RESUMEN
The orthorhombic polymorph of Cu2ZnGeS4 (CZGS) is a metastable wurtzite-derived phase that can only be prepared in the bulk form by extensive heating at high temperatures (≥790 °C) when using the conventional solid-state reaction route. By employing a facile solution-based synthetic strategy, we were able to obtain phase-pure orthorhombic CZGS in nanocrystalline form at a much lower reaction temperature. Prior to this work, the colloidal synthesis of single-phase orthorhombic CZGS on the nanoscale has never been reported. We find that the use of an appropriate combination of coordinating solvents and precursors is crucial to the sole formation of this metastable phase in solution. A possible formation mechanism is proposed on the basis of our experimental results. Because CZGS consists of environmentally benign metal components, it is regarded as a promising alternative material to the technologically useful yet toxic cadmium-containing semiconductors. The orthorhombic CZGS nanocrystals display strong photon absorption in the visible spectrum and are photocatalytically active in dye degradation under visible-light illumination.
RESUMEN
AgGaS2 (AGS) nanocrystals that exist in the orthorhombic phase were successfully prepared for the first time through a one-pot colloidal synthetic strategy using suitable coordinating solvents. These orthorhombic AGS nanocrystals were found to display great potential in visible-light-driven photocatalysis.
RESUMEN
Direct fabrication of core-shell or yolk-shell functional nanomaterials via a facile template-free method remains a challenge. In this work, we present a novel approach that involves straightforward chemical transformation and thermal treatment of the infinite coordination polymer particles to obtain composition-tunable CeO(2) yolk-shell structures. Uniform CeO(2) yolk-shell hollow spheres with a high surface area are promising support materials for tiny gold nanoparticles (ca. 4 nm), forming Au-CeO(2) nanocomposites which exhibit a remarkable catalytic activity and high stability for the reduction of p-nitrophenol. A possible mechanism for the formation of CeO(2) yolk-shell microspheres is also proposed.