RESUMEN
The unsaturated "dangling" bonds on the surface of nanomaterials are extremely sensitive to the external environment, which gives nanomaterials a dual nature, i.e., high reactivity and poor stability. However, studies on the long-term effects of stability and reactivity of nanomaterials under practical conditions are rarely found in the literature and lag far behind other research. Furthermore, the long-term effects on the stability and reactivity of a nanomaterial without coating under practical conditions are seriously long-neglected. Herein, by choosing copper nanowire as an example, we systematically study the stability of copper nanowires (CuNWs) in the liquid and gas phase by monitoring the change of morphology, phase, and valence state of CuNWs during storage. CuNWs exhibit good dispersibility and durable chemical stability in polar organic solvents, while CuNWs stored in water or nonpolar organic solvents evolve into a mace-like structure. Additionally, fresh CuNWs are oxidized into CuO nanotubes with thin shells by heating in air. The activation energies of oxidation of CuNWs in the gas phase are determined by the Kissinger method. More importantly, the different oxidation pathways have significant effects on the final morphology, surface area, phase, optical absorption, band gap, and vibrational property of the oxidation products. Understanding the stability and reactivity of Cu nanostructures will add value to their storage and applications. This work emphasizes the significant issue on the stability of nanostructures, which should be taken into account from the viewpoint of their practical application.
RESUMEN
Two-dimensional inorganic nanomaterials have drawn much attention due to their excellent properties and wide applications associated with unique 2D structures. However, an efficient and versatile chemical synthesis method using ambient conditions for 2D nanomaterials, especially with secondary structures (e.g. mesopores), has still not been reported. Herein, we report a versatile method to synthesize a family of ultrathin and mesoporous nanosheets of metal selenides based on a precursor so-called "red Se remaining Zn" (RSRZ). The principle of our synthesis is based on a template-assisted chemical transformation process via acidification of inorganic-organic hybrid ZnSe(DETA)0.5 nanosheets (DETA: diethylenetriamine). An appropriate amount of acid was added into an aqueous dispersion of ZnSe(DETA)0.5 nanosheets under air for activation. The acidification induced chemical transformation mechanism was studied by tracking the acidification process. This acid controlled reactivity of lamellar hybrids allows it to be possible to capture the highly reactive intermediates, which will provide a new platform for the synthesis of various mesoporous metal selenides.