Abstract

A surfactant-free strategy for controllable growth of various hierarchical CuO nanostructures was successfully achieved through a facile, one-pot solution-phase transformation of CuxMy(OH)z (M = SO42−, Cl−, NO3− and CH3COO−) precursors method without extra heat treatment in air. The formation of CuO nanostructures here is essentially determined by the species of CuxMy(OH)z precursors. The nanoparticle aggregation with controllable shapes can be formed under different concentrations of reactants. Hierarchical CuO nanoflowers with different branched building blocks were prepared by the transformation of Cu4(SO4)(OH)6 precursors. Hierarchical CuO nanospindles and nanoplates were fabricated by the transformation of Cu2(OH)3NO3 precursors. Hierarchical CuO nanoplate assemblies and nanoplates were synthesized by the transformation of Cu7Cl4(OH)10H2O and C8H6Cu3O104H2O precursors, respectively. Structural and morphological evolutions were investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and field-emission scanning electron microscopy (FESEM). This study is of great importance in controllable synthesis of surfactant-free CuO nanostructures, because it not only enriches the family of CuO architectures but also offers a good chance to understand the nature of the solution-phase precursor transformation method for synthesizing CuO nanostructures. Significantly, it is believed that this surfactant-free solution-phase precursor-driven synthesis of nanostructures presented here might provide a green approach to design and growth other well-defined metal oxide nanostructures.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.