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Volume 2012 (2012), Article ID 372505, 6 pages
Synthesis, Characterization, and Spectroscopic Properties of ZnO Nanoparticles
1Department of Electronics and Instrumentation Engineering, Lakireddy Bali Reddy College of Engineering (Autonomous), Mylavaram 521230, India
2Department of Chemistry, C.S.T.S. Government Kalasala, Jangareddygudem 534 447, India
Received 1 February 2012; Accepted 4 March 2012
Academic Editor: Z. Crnjak Orel
Copyright © 2012 Satyanarayana Talam et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
ZnO nanoparticles have been synthesized by precipitation method from Zinc nitrate. The powder was characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, selected-area electron diffraction, UV-vis optical absorption, and photoluminescence spectroscopy analyses. XRD patterns showed that ZnO nanoparticles have hexagonal unit cell structure. SEM and TEM pictures reveal the morphology and particle size of prepared ZnO nanoparticles. The UV-vis absorption spectrum shows an absorption band at 355 nm due to ZnO nanoparticles. The photoluminescence spectrum exhibits two emission peaks one at 392 nm corresponding to band gap excitonic emission and another located at 520 nm due to the presence of singly ionized oxygen vacancies. The synthesis method has potential for application in manufacturing units due to ease processing and more economical reagents.
Nowadays, there has been an increasing demand for the development of nanosized semiconductors due to their significant electrical and optical properties which are highly useful in fabricating nanoscaled optoelectronic and electronic devices with multifunctionality [1–3]. Among various semiconducting materials, zinc oxide (ZnO) is a distinctive electronic and photonic wurtzite n-type semiconductor with a wide direct band gap of 3.37 eV and a high exciton binding energy (60 meV) at room temperature [4, 5]. The high exciton binding energy of ZnO would allow for excitonic transitions even at room temperature, which could mean high radiative recombination efficiency for spontaneous emission as well as a lower threshold voltage for laser emission. The lack of a centre of symmetry in wurtzite, combined with a large electromechanical coupling, results in strong piezoelectric and pyroelectric properties and hence the use of ZnO in mechanical actuators and piezoelectric sensors [6, 7]. ZnO is potential candidate for optoelectronic applications in the short wavelength range (green, blue, UV), information storage, and sensors as it exhibits similar properties to GaN [8–10]. ZnO nanoparticles are promising candidates for various applications, such as nanogenerators , gas sensors , biosensors , solar cells , varistors , photodetectors , and photocatalysts . From the literature survey, it was found that various approaches for the preparation of ZnO nanopowders have been developed, namely, sol-gel, microemulsion, thermal decomposition of organic precursor, spray pyrolysis, electrodeposition, ultrasonic, microwave-assisted techniques, chemical vapor deposition, and hydrothermal and precipitation methods [18–27]. Most of these techniques were not extensively used on a large scale, but chemical synthesis has been widely used due to its simplicity and less expensive. In the present study, we report the synthesis of ZnO nanoparticles using chemical method and the characterization of ZnO nanoparticles using X-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), UV-vis absorbance, and photoluminescence spectra is discussed.
2. Experimental Methods
Zinc nitrate, sodium hydroxide, and ethanol were purchased and used without further purification. Zinc oxide nanoparticles were synthesized by wet chemical method using zinc nitrate and sodium hydroxide precursors. In this experiment, a 0.5 M aqueous ethanol solution of zinc nitrate (Zn(NO3)2·4H2O) was kept under constant stirring using magnetic stirrer to completely dissolve the zinc nitrate for one hour and 0.9 M aqueous ethanol solution of sodium hydroxide (NaOH) was also prepared in the same way with stirring of one hour. After complete dissolution of zinc nitrate, 0.9 M NaOH aqueous solution was added under high speed constant stirring, drop by drop (slowly for 45 min) touching the walls of the vessel. The reaction was allowed to proceed for 2 hrs after complete addition of sodium hydroxide. The beaker was sealed at this condition for 2 h. After the completion of reaction, the solution was allowed to settle for overnight and further, the supernatant solution was separated carefully. The remaining solution was centrifuged for 10 min, and the precipitate was removed. Thus, precipitated ZnO NPs were cleaned three times with deionized water and ethanol to remove the byproducts which were bound with the nanoparticles and then dried in air atmosphere at about 60°C. During drying, Zn(OH)2 is completely converted in to ZnO. The prepared ZnO nanoparticles were characterized for their optical and nanostructural properties. X-ray diffraction pattern for the ZnO NPs was recorded using an X-ray diffractometer (PANLYTICAL) using Cu Kα radiation of wavelength nm in the scan range . Morphology of the sample was investigated using scanning electron microscope (SEM with EDXA, Sirion) which also has been used for compositional analysis of the prepared ZnO nanoparticles. The optical transmission/absorption spectra of ZnO dispersed in water were recorded using a UV-VIS spectrophotometer (Hitachi, U-3010). The photoluminescence (PL) spectrum of the ZnO nanoparticles dispersed in water has been measured using a spectrofluorimeter (F-2500 FL Spectrophotometer, Hitachi).
3. Results and Discussion
As part of our research programme, we synthesize nanoparticles with enhanced particle properties using chemical routes that help in controlling the surface energy. The functionalized particles were characterized by the following techniques.
3.1. X-Ray Diffraction (XRD)
Figure 1 represents the X-ray diffraction pattern of ZnO nanopowder. A definite line broadening of the XRD peaks indicates that the prepared material consist of particles in nanoscale range. From this XRD patterns analysis, we determined peak intensity, position and width, full-width at half-maximum (FWHM) data. The diffraction peaks located at 31.84°, 34.52°, 36.33°, 47.63°, 56.71°, 62.96°, 68.13°, and 69.18° have been keenly indexed as hexagonal wurtzite phase of ZnO [28, 29] with lattice constants nm and nm (JPCDS card number: 36-1451) , and further it also confirms the synthesized nanopowder was free of impurities as it does not contain any characteristics XRD peaks other than ZnO peaks. The synthesized ZnO nanoparticle diameter was calculated using Debye-Scherrer formula  where 0.89 is Scherrer’s constant, is the wavelength of X-rays, is the Bragg diffraction angle, and is the full width at half-maximum (FWHM) of the diffraction peak corresponding to plane . The average particle size of the sample was found to be 16.21 nm which is derived from the FWHM of more intense peak corresponding to 101 plane located at 36.33° using Scherrer’s formula.
3.2. SEM/TEM Pictures
Figure 2 represents the SEM pictures of ZnO nanoparticles at different magnifications. These pictures confirm the formation of ZnO nanoparticles. These pictures substantiate the approximate spherical shape to the nanoparticles, and most of the particles exhibit some faceting. From the pictures, it also can be seen that the size of the nanoparticle is less than 10 nm which was in good agreement with the particle sizes (8.32 nm) calculated from the Debye-Scherrer formula. The selected area electron diffraction (SAED) pattern (Figure 3) shows distinct bright rings which confirm the preferential orientation of nanocrystals instead of irregular [29, 32]. Transmission electron microscopic pictures (Figures 4(a), 4(b), and 4(c)) have also revealed the ZnO nanoparticles formation produced at different magnifications by confirming the hexagonal plane to the prepared nanoparticles.
3.3. UV-Vis Absorption Spectrum
The size of the nanoparticles plays an important role in changing the entire properties of materials. Thus, size evolution of semiconducting nanoparticles becomes very essential to explore the properties of the materials. UV-visible absorption spectroscopy is widely being used technique to examine the optical properties of nanosized particles. The absorption spectrum of ZnO nanopowder is shown in Figure 4. It exhibits a strong absorption band at about 355 nm . An excitonic absorption peak is found at about 258 nm due to the ZnO nanoparticles which lie much below the band gap wavelength of 358 nm ( eV). It is also evident that significant sharp absorption of ZnO indicates the monodispersed nature of the nanoparticle distribution .
The average particle size in a nanocolloid can be calculated from the absorption onset from UV-vis absorption spectra by using effective mass model (Figure 5) [34, 35] where the band gap can be approximated by where is the bulk band gap expressed in eV, is Plank’s constant, is the particle radius, is the electron effective mass, is the hole effective mass, is free electron mass, is the charge on the electron, is the relative permittivity, and is the permittivity of free space. Due to the relatively small effective masses for ZnO (, ), band gap enlargement is expected for particle radii less than about 4 nm [34, 35]. The following equation was derived from the effective mass model given above with small mathematical simplification  which is used to find the size of the particle from the absorbance spectra, where is peak absorbance wavelength in nm. The prepared ZnO nanoparticles exhibit an absorbance peak at about 258 nm which corresponds to the particle size of 2.07 nm. This result has also been confirmed by the SEM pictures.
3.4. Photoluminescence Spectrum
It is worth mentioning that the physical properties of semiconducting materials undergo changes when their dimensions get down to nanometer scale known as the “quantum size effects.” For example, quantum confinement increases the band gap energy of ZnO, which has been observed from photoluminescence . The photoluminescence originates from the recombination of surface states. The strong PL implies that the surface states remain very shallow, as it is reported that quantum yields of band edge will decrease exponentially with increasing depth of surface state energy levels [38, 39]. Figure 6 shows the photoluminescence spectrum of ZnO nanopowder with excitation wavelength 320 nm at room temperature. The spectrum exhibits two emission peaks, one is located at around 392 nm (UV region) corresponding to the near band gap excitonic emission  and the other is located at around 520 nm attributed to the presence of singly ionized oxygen vacancies . The emission is caused by the radiative recombination of a photogenerated hole with an electron occupying the oxygen vacancy [28, 40]. Further, the spectrum also reveals the narrow size distribution of nanoparticles in the powder as the luminescence peak full-width half-maximum (FWHM) is only in few nanometers .
ZnO nanoparticles have been prepared using wet chemical synthesis method and were characterized by XRD, SEM, SAED, UV-vis absorption, and photoluminescence spectroscopy. XRD and SEM studies confirmed the nanostructures for the prepared ZnO nanoparticles. SAED pattern consists of bright uniform rings confirming preferential orientation for nanocrystals instead of random orientation. From UV-vis absorption spectrum, the calculated average size of the prepared ZnO nanoparticles is found to be 2.2 nm for peak absorbance wavelength. The prepared ZnO nanoparticles exhibit ( nm) sharp UV band corresponding to near band gap excitonic emission and broad green emission band due to the oxygen vacancy at room temperature. These ZnO nanoparticles can be used in different industrial applications, namely, luminescent material for fluorescent tubes, active medium for lasers, sensors, and so forth.
The authors would like to thank the management and the director of Lakireddy Bali Reddy College of Engineering for their constant encouragement and financial support to carry out this work.
- M. S. Tokumoto, V. Briois, C. V. Santilli, and S. H. Pulcinelli, “Preparation of ZnO nanoparticles: structural study of the molecular precursor,” Journal of Sol-Gel Science and Technology, vol. 26, no. 1–3, pp. 547–551, 2003.
- P. Kumar, L. S. Panchakarla, S. V. Bhat, U. Maitra, K. S. Subrahmanyam, and C. N. R. Rao, “Photoluminescence, white light emitting properties and related aspects of ZnO nanoparticles admixed with graphene and GaN,” Nanotechnology, vol. 21, no. 38, Article ID 385701, 2010.
- G. Thomas, “Invisible circuits,” Nature, vol. 389, no. 6654, pp. 907–908, 1997.
- Z. L. Wang, “Nanostructures of zinc oxide,” Materials Today, vol. 7, no. 6, pp. 26–33, 2004.
- C. N. R. Rao and A. Govindaraj, in Nanotubes and Nanowires, H. Kroto, P. O’Brien, and H. Craighead, Eds., The RSC Nanoscience and Nanotechnology Series, Royal Society of Chemistry, London, UK, 2005.
- S. C. Ko, Y. C. Kim, S. S. Lee, S. H. Choi, and S. R. Kim, “Micromachined piezoelectric membrane acoustic device,” Sensors and Actuators, A, vol. 103, no. 1-2, pp. 130–134, 2003.
- D. Zaouk, Y. Zaatar, R. Asmar, and J. Jabbour, “Piezoelectric zinc oxide by electrostatic spray pyrolysis,” Microelectronics Journal, vol. 37, no. 11, pp. 1276–1279, 2006.
- D. H. Zhang, Z. Y. Xue, and Q. P. Wang, “Formation of ZnO nanoparticles by the reaction of zinc metal with aliphatic alcohols,” Journal of Physics D, vol. 35, no. 21, pp. 2837–2840, 2002.
- H. Hayashi, A. Ishizaka, M. Haemori, and H. Koinuma, “Bright blue phosphors in ZnO-WO3 binary system discovered through combinatorial methodology,” Applied Physics Letters, vol. 82, no. 9, pp. 1365–1367, 2003.
- H. T. Ng, B. Chen, J. Li et al., “Optical properties of single-crystalline ZnO nanowires on m-sapphire,” Applied Physics Letters, vol. 82, no. 13, pp. 2023–2025, 2003.
- P. X. Gao, Y. Ding, W. Mai, W. L. Hughes, C. Lao, and Z. L. Wang, “Materials science: conversion of zinc oxide nanobelts into superlattice-structured nanohelices,” Science, vol. 309, no. 5741, pp. 1700–1704, 2005.
- X. L. Cheng, H. Zhao, L. H. Huo, S. Gao, and J. G. Zhao, “ZnO nanoparticulate thin film: preparation, characterization and gas-sensing property,” Sensors and Actuators, B, vol. 102, no. 2, pp. 248–252, 2004.
- E. Topoglidis, A. E. G. Cass, B. O'Regan, and J. R. Durrant, “Immobilisation and bioelectrochemistry of proteins on nanoporous TiO2 and ZnO films,” Journal of Electroanalytical Chemistry, vol. 517, no. 1-2, pp. 20–27, 2001.
- Y. Hames, Z. Alpaslan, A. Kösemen, S. E. San, and Y. Yerli, “Electrochemically grown ZnO nanorods for hybrid solar cell applications,” Solar Energy, vol. 84, no. 3, pp. 426–431, 2010.
- W. Jun, X. Changsheng, B. Zikui, Z. Bailin, H. Kaijin, and W. Run, “Preparation of ZnO-glass varistor from tetrapod ZnO nanopowders,” Materials Science and Engineering B, vol. 95, no. 2, pp. 157–161, 2002.
- P. Sharma, K. Sreenivas, and K. V. Rao, “Analysis of ultraviolet photoconductivity in ZnO films prepared by unbalanced magnetron sputtering,” Journal of Applied Physics, vol. 93, no. 7, pp. 3963–3970, 2003.
- P. V. Kamat, R. Huehn, and R. Nicolaescu, “A “sense and shoot” approach for photocatalytic degradation of organic contaminants in water,” Journal of Physical Chemistry B, vol. 106, no. 4, pp. 788–794, 2002.
- M. S. Takumoto, , S. H. Pulcinelli, C. V. Santilli, and V. Briois, Journal of Physical Chemistry B, vol. 107, p. 568, 2003.
- M. Singhal, V. Chhabra, P. Kang, and D. O. Shah, “Synthesis of ZnO nanoparticles for varistor application using Zn-substituted aerosol OT microemulsion,” Materials Research Bulletin, vol. 32, no. 2, pp. 239–247, 1997.
- F. Rataboul, C. Nayral, M. J. Casanove, A. Maisonnat, and B. Chaudret, “Synthesis and characterization of monodisperse zinc and zinc oxide nanoparticles from the organometallic precursor [Zn(C6H11)2],” Journal of Organometalic Chemistry, vol. 643-644, pp. 307–312, 2002.
- K. Okuyama and W. W. Lenggoro, “Preparation of nanoparticles via spray route,” Chemical Engineering Science, vol. 58, no. 3–6, pp. 537–547, 2003.
- A. B. Moghaddam, T. Nazari, J. Badraghi, and M. Kazemzad, “Synthesis of ZnO nanoparticles and electrodeposition of polypyrrole/ZnO nanocomposite film,” International Journal of Electrochemical Science, vol. 4, no. 2, pp. 247–257, 2009.
- Y.-L. Wei and P.-C. Chang, “Characteristics of nano zinc oxide synthesized under ultrasonic condition,” Journal of Physics and Chemistry of Solids, vol. 69, no. 2-3, pp. 688–692, 2008.
- X.-L. Hu, Y.-J. Zhu, and S.-W. Wang, “Sonochemical and microwave-assisted synthesis of linked single-crystalline ZnO rods,” Materials Chemistry and Physics, vol. 88, no. 2-3, pp. 421–426, 2004.
- J.-J. Wu and S.-C. Liu, “Low-temperature growth of well-aligned ZnO nanorods by chemical vapor deposition,” Advanced Materials, vol. 14, no. 3, pp. 215–218, 2002.
- H. J. Zhai, W. H. Wu, F. Lu, H. -S. Wang, and C. Wang, “Effects of ammonia and cetyltrimethylammonium bromide (CTAB) on morphologies of ZnO nano- and micromaterials under solvothermal process,” Materials Chemistry and Physics, vol. 112, no. 3, pp. 1024–1028, 2008.
- M. Bitenc, M. Marinšek, and Z. Crnjak Orel, “Preparation and characterization of zinc hydroxide carbonate and porous zinc oxide particles,” Journal of the European Ceramic Society, vol. 28, no. 15, pp. 2915–2921, 2008.
- J. Zhou, F. Zhao, Y. Wang, Y. Zhang, and L. Yang, “Size-controlled synthesis of ZnO nanoparticles and their photoluminescence properties,” Journal of Luminescence, vol. 122-123, no. 1-2, pp. 195–197, 2007.
- Z. M. Khoshhesab, M. Sarfaraz, and M. A. Asadabad, “Preparation of ZnO nanostructures by chemical precipitation method,” Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry, vol. 41, no. 7, pp. 814–819, 2011.
- JCPDS, Powder Diffraction File, Alphabetical Index, Inorganic Compounds, International Centre for Diffraction Data, Newtown Square, Pa, USA, 1977.
- B. D. Cullity, Elements of X-Ray Diffraction, Addison-Wesley, Reading, Mass, USA, 3rd edition, 1967.
- A. Gupta, H. S. Bhatti, D. Kumar, N. K. Verma, and dan R. P. Tandon, “Nano and Bulk Crystals of ZnO: synthesis and Characterization,” Digest Journal of. Nanomaterials and Biostructures, vol. 1, no. 1, pp. 1–9, 2006.
- Y. D. Jin, J. P. Yang, P. L. Heremans et al., “Single-layer organic light-emitting diode with 2.0% external quantum efficiency prepared by spin-coating,” Chemical Physics Letters, vol. 320, no. 5-6, pp. 387–392, 2000.
- S. Shionoya and W. M. Yen, Eds., Phosphor Handbook, CRC Press, Boca Raton, Fla, USA, 1998.
- L. I. Berger, Semiconductor Materials, CRC Press, Boca Raton, Fla, USA, 1997.
- L. Brus, “Electronic wave functions in semiconductor clusters: experiment and theory,” Journal of Physical Chemistry, vol. 90, no. 12, pp. 2555–2560, 1986.
- X. Wang, Y. Ding, C. J. Summers, and Z. L. Wang, “Large-scale synthesis of six-nanometer-wide ZnO nanobelts,” Journal of Physical Chemistry B, vol. 108, no. 26, pp. 8773–8777, 2004.
- N. Chestnoy, T. D. Harris, R. Hull, and L. E. Brus, “Luminescence and photophysics of CdS semiconductor clusters: the nature of the emitting electronic state,” Journal of Physical Chemistry, vol. 90, no. 15, pp. 3393–3399, 1986.
- J. R. Heath and J. J. Shiang, “Covalency in semiconductor quantum dots,” Chemical Society Reviews, vol. 27, no. 1, pp. 65–71, 1998.
- M. H. Huang, Y. Wu, H. Feick, N. Tran, E. Weber, and P. Yang, “Catalytic growth of zinc oxide nanowires by vapor transport,” Advanced Materials, vol. 13, no. 2, pp. 113–116, 2001.
- G. Williams and P. V. Kamat, “Graphene-semiconductor nanocomposites: excited-state interactions between ZnO nanoparticles and graphene oxide,” Langmuir, vol. 25, no. 24, pp. 13869–13873, 2009.
- B. Srinivasa Rao, B. Rajesh Kumar, V. Rajagopal Reddy, and T. Subba Rao, “Preparation and characterization of CdS nanoparticles by chemical co-precipitation technique,” Chalcogenide Letters, vol. 8, no. 3, pp. 177–185, 2011.