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Fabrication of ultrathin CuO nanowires augmenting oriented attachment crystal growth directed self-assembly of Cu(OH)(2) colloidal nanocrystals

Augmenting the oriented attachment (OA) crystal growth phenomena, herein, we demonstrate fabrication of ultrathin CuO nanowires from self-assembled one-dimensional (1D) nanowires of Cu(OH)(2) nanocrystals. A facile environmentally benign sol–gel approach, which utilizes base-catalyzed hydrolysis fol...

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Detalles Bibliográficos
Autores principales: Pathiraja, Gayani, Yarbrough, Ryan, Rathnayake, Hemali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419473/
https://www.ncbi.nlm.nih.gov/pubmed/36132408
http://dx.doi.org/10.1039/d0na00308e
Descripción
Sumario:Augmenting the oriented attachment (OA) crystal growth phenomena, herein, we demonstrate fabrication of ultrathin CuO nanowires from self-assembled one-dimensional (1D) nanowires of Cu(OH)(2) nanocrystals. A facile environmentally benign sol–gel approach, which utilizes base-catalyzed hydrolysis followed by directed self-assembly and crystal growth of nanocrystals, is developed to prepare Cu(OH)(2) nanowires. The sol of Cu(OH)(2) nanocrystals shows aggregative self-assembly guided by the OA crystal growth process to form ultrathin Cu(OH)(2) nanowires, with an average length of 675 ± 4 nm and diameter of 6 ± 2 nm. The time-dependent UV-visible spectral traces, along with real-time imaging of nanocrystals self-assembly and growth under the transmission electron microscope, are evidenced the concept of the OA crystal growth directed self-assembly, yielding 1D colloidal nanoarrays of Cu(OH)(2). The powder XRD traces collected during the self-assembly and crystal growth process reveal the directional aggregative crystal growth along the facet of [001], confirming the OA directed crystal growth and fusion of nanocrystals to yield 1D nanostructures. The gradual blue-shift in optical absorption maxima from 770 nm in initial precursor solution, to 670 nm for Cu(OH)(2) nanocrystals sol, and finally to 647 nm for self-assembled 1D Cu(OH)(2) nanowires have further evidenced the formation of Cu(OH)(2) nanowires. Upon subjecting self-assembled Cu(OH)(2) nanowires for post-annealing treatment, ultrathin CuO nanowires with average length of 7 ± 0.50 μm and diameter of 27 ± 2 nm is obtained in high purity. The experimental powder XRD patterns of Cu(OH)(2) and CuO nanowires match the simulated XRD patterns, indexing the crystal unit cell structures to orthorhombic and monoclinic, respectively. The tailored narrow optical band gaps for Cu(OH)(2) and CuO nanowires are found to be 1.51 eV and 1.10 eV. The theoretical band gap predicted for Cu(OH)(2) nanowires is 1.52 eV and is in good agreement with its optical band gap, whereas theoretical band computed for CuO nanowires is 0.13 eV lower than from its optical band gap.