Self-aligned nanocrystalline ZnO hexagons by facile solid-state and co-precipitation route

  • J. H. Thorat
  • K. G. Kanade
  • L. K. Nikam
  • P. D. Chaudhari
  • R. P. Panmand
  • B. B. Kale
Research Paper


In this study, we report the synthesis of well-aligned nanocrystalline hexagonal zinc oxide (ZnO) nanoparticles by facile solid-state and co-precipitation method. The co-precipitation reactions were performed using aqueous and ethylene glycol (EG) medium using zinc acetate and adipic acid to obtain zinc adipate and further decomposition at 450 °C to confer nanocrystalline ZnO hexagons. XRD shows the hexagonal wurtzite structure of the ZnO. Thermal study reveals complete formation of ZnO at 430 °C in case of solid-state method, whereas in case of co-precipitation method complete formation was observed at 400 °C. Field emission scanning electron microscope shows spherical morphology for ZnO synthesized by solid-state method. The aqueous-mediated ZnO by co-precipitation method shows rod-like morphology. These rods are formed via self assembling of spherical nanoparticles, however, uniformly dispersed spherical crystallites were seen in EG-mediated ZnO. Transmission electron microscope (TEM) investigations clearly show well aligned and highly crystalline transparent and thin hexagonal ZnO. The particle size was measured using TEM and was observed to be 50–60 nm in case of solid-state method and aqueous-mediated co-precipitation method, while 25–50 nm in case of EG-mediated co-precipitation method. UV absorption spectra showed sharp absorption peaks with a blue shift for EG-mediated ZnO, which demonstrate the mono-dispersed lower particle size. The band gap of the ZnO was observed to be 3.4 eV which is higher than the bulk, implies nanocrystalline nature of the ZnO. The photoluminescence studies clearly indicate the strong violet and weak blue emission in ZnO nanoparticles which is quite unique. The process investigated may be useful to synthesize other oxide semiconductors and transition metal oxides.


ZnO Hexagonal Nanostructured Semiconductor 



The authors were grateful to University of Pune and UGC, Government of India for the financial assistance and Dr. Arun Andhale, Principal, Mahatama Phule Mavidyalaya, Pimpri Pune-411017 for providing facilities to carry out the above research. The authors also thank staff of Nanocrystalline Material laboratory of C-MET, Pune for many stimulating discussions and providing characterization facilities.


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Copyright information

© Springer Science+Business Media B.V. 2012

Authors and Affiliations

  • J. H. Thorat
    • 2
  • K. G. Kanade
    • 3
  • L. K. Nikam
    • 4
  • P. D. Chaudhari
    • 1
  • R. P. Panmand
    • 1
  • B. B. Kale
    • 1
  1. 1.Center for Materials for Electronics Technology (C-MET)PuneIndia
  2. 2.Department of ChemistryMahatma Phule CollegePuneIndia
  3. 3.Annasaheb Awate CollegePuneIndia
  4. 4.B.G. CollegePuneIndia

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