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Title: Synthesis of porous and nonporous ZnO nanobelt, multipod, and hierarchical nanostructure from Zn-HDS

Journal Article · · Journal of Solid State Chemistry
 [1];  [2];  [3];  [1];  [4]
  1. Molecular Imaging Program at Stanford (MIPS) and Bio-X Program, Department of Radiology, Stanford University, 1201 Welch Road, Stanford, CA 94305 (United States)
  2. Hygiene Application Team, LG Household and Health Care, Daejeon 305-343 (Korea, Republic of)
  3. School of Materials Science and Engineering, Seoul National University, Seoul 151-744 (Korea, Republic of)
  4. Center for Intelligent Nano-Bio Materials (CINBM), Division of Nanosciences and Department of Chemistry, Ewha Womans University, Seoul 120-750 (Korea, Republic of)

Zn based hydroxide double salts (Zn-HDS) with an interlayer spacing of 20 A was produced by dissolving dumbbell-like ZnO crystal. The resulting Zn-HDS with a ribbon-like shape has a suitable morphology to explore the remarkably mild procedure for synthesis of ZnO nanobelts. We found that the intercalated water molecules into the Zn-HDS could play a key role in the ZnO nanobelts porosity. The nonporous ZnO nanobelts were successfully synthesized from the Zn-HDS by soft-solution process at 95 {sup o}C through mild dehydration agent as Na{sub 2}CO{sub 3}. As-synthesized ZnO nanobelts were grown along not only the [0 1 -1 0], but also the [2 -1 -1 0]. On the other hand, the porous ZnO nanobelts were obtained from the Zn-HDS by calcinations at 200 and 400 {sup o}C. In addition, flower-like ZnO multipod and hierarchical nanostructures were produced from the Zn-HDS by using of strong dehydration agent (NaOH) through hydrothermal reaction at 150 and 230 {sup o}C. - Graphical abstract: Porous and nonporous ZnO nanobelts, multipod, and hierarchical nanostructure were successfully synthesized from Zn based hydroxyl double salts by hydrothermal reaction.

OSTI ID:
21421582
Journal Information:
Journal of Solid State Chemistry, Vol. 183, Issue 8; Other Information: DOI: 10.1016/j.jssc.2010.05.025; PII: S0022-4596(10)00228-8; Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; ISSN 0022-4596
Country of Publication:
United States
Language:
English