Synthesis of Silver-Doped Zinc Oxide Nanocomposite by Pulse Mode Ultrasonication and Its Characterization Studies

Siva Vijayakumar, T.; Karthikeyeni, S.; Vasanth, S.; Ganesh, Arul; Bupesh, G.; Ramesh, R.; Manimegalai, M.; Subramanian, P.

doi:https://doi.org/10.1155/2013/785064

Journal of Nanoscience

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Abstract Introduction Materials and Methods Results and Discussion Conclusions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2013 | Article ID 785064 | https://doi.org/10.1155/2013/785064

Synthesis of Silver-Doped Zinc Oxide Nanocomposite by Pulse Mode Ultrasonication and Its Characterization Studies

T. Siva Vijayakumar,¹S. Karthikeyeni,¹S. Vasanth,¹Arul Ganesh,¹G. Bupesh,²R. Ramesh,¹M. Manimegalai,³and P. Subramanian¹

Academic Editor: Oleg I. Lupan

Received23 Apr 2013

Revised08 Jul 2013

Accepted30 Jul 2013

Published12 Sept 2013

Abstract

The synthesis of silver-doped zinc oxide (Ag:ZnO) nanocomposite material was achieved using a simple chemical coprecipitation method, in which 0.2 M zinc chloride and 0.001 M silver nitrate coprecipitated with 25% ammonia solution by pulse mode dispersion using ultrasonicator. The obtained silvery white precipitate was dried overnight at 110°C in hot air oven, and the powder was collected. The resulted Ag:ZnO nanocomposite was structurally and optically characterized using various techniques. The X-ray diffraction (XRD) pattern clearly showed the presence of crystalline Ag:ZnO particles. Further, UV-Vis spectrophotometer and fourier transform infrared spectroscopy (FT-IR) results showed the presence of Ag:ZnO nanocomposite at specific wavelengths. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analysis confirm that the synthesized Ag:ZnO nanocomposite material was truncated nanorod in shape and has 48 to 226 nm size in diameter.

1. Introduction

Zinc oxide (ZnO) is an important industrial material, because it has an inorganic and semiconducting material with inherent properties that share its structure as wurtzite [1]. ZnO nanocomposite has attracted interest because of its optical properties. These particles are transparent to visible light, but they absorb UV-light. ZnO has attracted intensive research effort for its unique properties and versatile applications in transparent electronics, chemical sensors, and spin electronics [2–8]. A variety of metal oxides like zinc oxide, titanium dioxide (TiO₂), and silicon dioxide (SiO₂) and different techniques such as chemical coprecipitation [9, 10], sol-gel process [11, 12] chemical vapour deposition [13], thermal decomposition [14, 15], hydrothermal synthesis [16, 17], solid-state reaction [18], spray pyrolysis [19], vapour-liquid-solid method [20], and microemulsion precipitation [21–23] have been used so far. Hingorani et al. also reported the synthesis of ZnO nanoparticles (NPs) and it was the first study using reverse microemulsion in the early 1990s [24, 25].

Synthesis process of Ag:ZnO nanocomposite plays a key role in governing size, morphology, and its properties of nanocomposite through dispersion method (pulse mode), using ultrasonication [26]. The main objective of synthesis is to produce particles only in nanorod structure for various toxicity and biological application studies. There are different doping agents like P [27], N [28], As [29], Li [30], Sb [31–34], and Ag [35]. Among these, we have taken Ag as doping agent. Because the nature of Ag ions is simple link matrices, their behaviour to surface states in nanomaterials where the surfaces of are becomes prime importance as the size decreases. The sonochemical synthesis of nanomaterial is extensively used to generate novel materials with different properties, because this method can produce similar truncated nanorods with smaller size than those reported by other methods [36–38]. The advantages of chemical coprecipitation method through sol-gel process for preparing nanocomposite materials are to get small average particle size and narrow size distribution, homogeneity, purity, and more possibility to obtain nanorods.

2. Materials and Methods

All chemicals used in this study (zinc chloride 98%, silver nitrate 99.8%, and ammonia 25%) were AR grade purchased from HiMedia, Mumbai, India. All reagents were prepared by using deionised water (18 MΩ resistivity).

2.1. Synthesis of Ag-Doped ZnO Nanocomposite

0.2 M zinc chloride (ZnCl₂) and 0.001 M silver nitrate (AgNO₃) were mixed to 50 mL of distilled water. A 2 mL of 25% ammonia solution was added dropwise until precipitation occurred, and then further 10 drops of ammonia solution (NH₄OH) were added to make the solution clear. Pulse mode sonication (PS) was operated at 112.5 W, and the frequency of the sonicator were maintained at 20 kHz ± 50 Hz. PS takes place for one second then stops for one second, and the total process took two hours to get precipitates. The initial pH of the solution was 10.2, whereas at the end, the pH was 8.2 and the solution became clear silvery white, and gradually solid suspension is settled. The formed precipitate was washed several times with deionised water and acetone followed by centrifugation at 3500 rpm for the complete elimination of chloride. The precipitate was then dried at room temperature and kept overnight inside an oven at 110°C in atmospheric pressure to obtain dry powder.

Ammonia solution (NH₄OH) was used as precipitating agent during synthesis between zinc chloride (ZnCl₂) and silver nitrate (AgNO₃) with water (H₂O) to form Zn(OH)₂, AgOH, NH₄Cl, NH₄NO₃, and H₂O. The product was washed with deionised water for several times to form Zn(OH)₂, AgOH, and H₂O, then again washed with acetone by centrifuging in order to form Zn(OH)₂ and 2AgOH. On heating at 110°C the product obtained was pure ZnO-doped Ag₂O like (Zn–O–Ag) in the precursor. Through the solvothermal process, the precursor reduced by acetone gradually and Zn–O–Ag bond formation between Ag-doped ZnO nanocomposite materials, which has been explained as

2.2. Characterization of Ag:ZnO Nanocomposite Material

Several techniques were used to characterize Ag:ZnO nanocomposite material like UV-Visible spectroscopy, XRD and FT-IR. The crystalline nature of nanocomposite was characterized by XRD, using PANalytical Xpert-Pro diffractometer equipped with Cu Kα₁ radiation (). Morphology of the sample was studied by using SEM (Model FEG-Nova 600 Nano SEM). The UV-Vis spectra were recorded with multimode microplate reader (Synergy HT) in the wavelength range between 300 and 800 nm. An FT-IR spectrum was recorded using Perkin-Elmer instrument (model spectrum RX₁). Further Ag:ZnO nanocomposite material was characterized by using various techniques like DLS and TEM.

3. Results and Discussion

This work reports that the synthesis of Ag-doped ZnO nanocomposite material through chemical coprecipitation method overpoweringly achieves the synthesis through pulse mode dispersion by ultrasonication. In this study, it was clearly observed that the catalyst ammonia plays a primary role in forming the shape of a particle during the synthesis process. Moreover, the shape of the nanocomposite changed to rod from spheres when it was doped with silver ions, and it was an interesting morphology observed through TEM analysis. Most of the reports were about silver and gold nanocomposite [39, 40], but only a few data were available for doping of wide band semiconductor like ZnO with silver ions. The comprehensive structural studies are not available, and the methods of preparation of doped NPs are still evolving [41, 42]. In the synthesis method, pH also plays an important role in the formation of diverse morphology [43].

3.1. X-Ray Diffraction Study

The average crystallite size can be determined through Full Width at Half Maximum (FWHM) of X-ray diffraction peak by using Debye-Scherer’s equation as where is grain size (nm), is wavelength of the XRD used, is FWHM, and is Bragg’s angle. X-ray diffractogram was analyzed to obtain information about various crystalline aspects of Ag:ZnO nanocomposite material. The X-ray diffraction patterns of Ag:ZnO nanocomposite material are wurtzite hexagonal phase [44] and were shown in Figure 1 which indicates the well-indexed XRD peaks corresponding to the planes (100), (002), and (101), JCPDS no. 89-1397. The peak (103) indicates the presence of silver (Ag), and no other impurities were observed (the standard file of JCPDS no. 89-3722). These results indicate that the products consisted of pure phases. Furthermore, the diffraction peaks were more intensive and narrower, implying a good crystalline nature of Ag:ZnO nanocomposite products. The size range of Ag:ZnO nanocomposite material was from 26 nm to 136 nm in diameter according to Debye-Scherer’s equation.

3.2. Fourier Transform Infrared Spectroscopy Study

Synthesized Ag:ZnO nanocomposite material was analysed by FT-IR in the range from 400 to 4000 cm⁻¹ at room temperature (Figure 2). The FT-IR spectrum of the Ag:ZnO nanocomposite material contains several bands with remarkable features. The bands between 400 and 750 cm⁻¹ correlated to metal oxide bond (ZnO) [45–47]. Bands around 900–1500 cm⁻¹ are due to the oxygen stretching and bending frequency [48, 49]. The spectral band at 463.01 cm⁻¹ and band at 723.96 cm⁻¹ clearly show the presence of ZnO and Ag ions approximately equal to those reported in the literature [50]. On doping, stronger and wider absorption were bands observed in the region ~723.96 cm⁻¹ due to the organic capping of silver [51]. Bands at 1394.82 cm⁻¹ and 1507.07 cm⁻¹ correspond to C=O and O–H bending vibrations, respectively. The presence of weak band near 1604.07 cm⁻¹ is assigned to H–O–H bending may due to the adsorption of moisture. Bands at 3465.60 cm⁻¹ indicate the presence of OH group. It is evident from the FTIR data that the Zn–O vibrational mode was more prominently observed, and this clearly concludes a strong doping between Ag and ZnO nanocomposite materials [52].

3.3. UV-Visible Absorption Study

The UV-Vis absorption spectra (Figure 3) of Ag:ZnO nanocomposite material were recorded at room temperature. The synthesized nanocomposites were dispersed in ethanol with the concentration of 0.1% water, and the solution was used to record UV-Vis spectra at wavelength range between 300 and 600 nm. The spectra reveal a characteristic absorption peak of Ag:ZnO nanocomposite material at 360 nm [53, 54]. The absorbance increases in the higher wavelength side indicating the role of nano Ag particles in ZnO. More numbers of Ag are dispersed into ZnO, and these metallic particles rest on the surface of ZnO nanocomposite making the surface area increased and showing plasmonic resonance peak in the UV-Vis spectra. This is an important method in which Ag:ZnO composite nanorod has been shown and elevated by UV absorption. This high absorbance of the Ag:ZnO composite nanorods has an important implication for various industrial applications.

3.4. DLS Study

Malvern particle size analyzer (Model, Micro-P) was used to measure the size of synthesized Ag:ZnO nanocomposite materials. The average size obtained by the DLS distribution plot was around 60 to 300 nm, in this 163 nm particles were more (Figure 4). The dimension of Ag-doped zinc oxide averages in the form of an equivalent sphere and hence does not give the distribution in the range of lengths or widths of the nanorods. The average sizes from DLS result that the particle also coincide with SEM and TEM results [55].

3.5. SEM and TEM Analyses of the Ag:ZnO Nanocomposite Materials

The SEM uses a focused beam of higher energy electrons to generate a variety of signals at the surface of solid specimens. The signals that derive from electron sample interactions reveal information about the sample including external morphology. When samples were viewed under SEM, the truncated nanorod morphology with irregular size was observed, which was randomly orientated. The diameter and length of the Ag-doped zinc oxide nanorod were found, approximately 54 to 226 nm diameters and from 601 to 1420 nm length with one-dimension were segregated (Figures 5(a) and 5(b)).

(a)

(b)

TEM characterization was carried out in diffraction and imaging modes by using FEI-TECNAI G2-20 working at 200 KV. Images of Ag:ZnO NPs shown in Figures 6(a) and 6(b) are monodisperse, and the selected area diffraction (SAED) pattern apparently showed clear truncated nanorod structure of the nanocomposite. From the TEM micrograph, the diameter of Ag-doped zinc oxide was found to be approximately 48 to 126 nm and the length was 232 to 1255 nm with one-dimension of nanorod. The doping of silver with zinc oxide nanocomposite material changes spherical ZnO to rod shape Ag:ZnO particles. The entire particle sizes results obtained were almost the same in XRD, DLS, SEM, and TEM when comparing with one another. Finally, The shape and size of the Ag:ZnO nanocomposite was confirmed by the comprehensible techniques such as SEM and TEM.

(a)

(b)

4. Conclusions

From the above presented experimental results and discussion, it is clear that the synthesis through ultrasonication method gives the following conclusions.(a)Chemical Coprecipitation is an easy and simple method that played an efficient task in the synthesis of Ag:ZnO nanocomposite material when compared with other methods.(b)In pulse mode synthesis, precursor and reducing agent are main reasons for the morphological changes during synthesis.(c)Addition of Ag⁺ ions during dispersion (Pulse mode) through ultrasonication increases high crystalline nature and change in morphology. (d)Ag⁺ ion rests upon the surface of the zinc oxide at some stage to form truncated nanorod morphology.(e)Temperature, time, and alteration of initial and final pH also play prominent role in forming different size and morphological evolution of Ag-doped zinc oxide nanocomposite (Ag:ZnO).

Finally, it was concluded that the several unique features of synthesized Ag:ZnO were observed with the deserved special comments. The generality and simplicity for the synthesis of Ag-doped ZnO nanocomposite material are involved in trouble-free steps. Several researchers have recently reported the chemical coprecipitation synthesis of nanocomposite, nanowires, and nanorods [56–59]. However, our chemical coprecipitation method allows the synthesis of nanorods in easy way where the dispersion method by ultrasonicator plays novelty in the formation of nanorod Ag:ZnO.

Acknowledgments

The authors owe sincere thanks to UGC and UGC-RFSMS for providing financial support and MoE&F for providing instrumentation facility. The authors thank Dr. N. P. Lalla UGC-DAE CSR Indore for TEM measurement that is highly appreciable and commendable. Sincere thanks are to Department of Chemistry and Physics, Bharathidasan University, Tiruchirappalli, for their valuable suggestions and comments.

Supplementary Materials

The Synthesis of Silver-doped Zinc oxide (Ag:ZnO) Nanocomposite material was achieved using a simple chemical co-precipitation method. In which 0.2 M zinc chloride and 0.001 M silver nitrate co-precipitated with 25% ammonia solution by pulse mode dispersion using ultrasonicator. The obtained slivery white precipitate dried overnight at 110ºC in hot air oven and collected the powder. The resulted Ag:ZnO nanocomposite was structurally and optically characterized using various techniques. The X-ray Diffraction (XRD) pattern clearly showed the presence of crystalline Ag:ZnO particles. Further, UV-Vis spectrophotometer and Fourier Transform Infrared Spectroscopy (FT-IR) results showed the presence of Ag:ZnO nanocomposite at specific wavelengths. The Scanning Electron Microscopy (SEM) and Transmission electron Microscopy (TEM) analysis conforms that the synthesized Ag:ZnO Nanocomposite material was truncated nanorod in shape and has 48 to 226 nm size in diameter.

Supplementary Figure

References

Y. K. Mishra, V. S. K. Chakravadhanula, V. Hrkac et al., “Crystal growth behaviour in Au-ZnO nanocomposite under different annealing environments and photoswitchability,” Journal of Applied Physics, vol. 112, Article ID 064308, 2012.
View at: Google Scholar
K. Nomura, H. Ohta, K. Ueda, T. Kamiya, M. Hirano, and H. Hosono, “Thin-film transistor fabricated in single-crystalline transparent oxide semiconductor,” Science, vol. 300, no. 5623, pp. 1269–1272, 2003.
View at: Publisher Site | Google Scholar
S. Y. Lee, E. S. Shim, H. S. Kang, S. S. Pang, and J. S. Kang, “Fabrication of ZnO thin film diode using laser annealing,” Thin Solid Films, vol. 473, no. 1, pp. 31–34, 2005.
View at: Publisher Site | Google Scholar
R. Könenkamp, R. C. Word, and C. Schlegel, “Vertical nanowire light-emitting diode,” Applied Physics Letters, vol. 85, no. 24, pp. 6004–6006, 2004.
View at: Publisher Site | Google Scholar
Z. L. Wang, X. Y. Kong, Y. Ding et al., “Semiconducting and piezoelectric oxide nanostructures induced by polar surfaces,” Advanced Functional Materials, vol. 14, no. 10, pp. 943–956, 2004.
View at: Publisher Site | Google Scholar
Y. Ushio, M. Miyayama, and H. Yanagida, “Effects of interface states on gas-sensing properties of a CuO/ZnO thin-film heterojunction,” Sensors and Actuators B, vol. 17, no. 3, pp. 221–226, 1994.
View at: Google Scholar
H. Harima, “Raman studies on spintronics materials based on wide bandgap semiconductors,” Journal of Physics Condensed Matter, vol. 16, no. 48, pp. S5653–S5660, 2004.
View at: Publisher Site | Google Scholar
S. J. Pearton, W. H. Heo, M. Ivill, D. P. Norton, and T. Steiner, “Dilute magnetic semiconducting oxides,” Semiconductor Science and Technology, vol. 19, no. 10, pp. R59–R74, 2004.
View at: Publisher Site | Google Scholar
L. Wang and M. Muhammed, “Synthesis of zinc oxide nanoparticles with controlled morphology,” Journal of Materials Chemistry, vol. 9, no. 11, pp. 2871–2878, 1999.
View at: Publisher Site | Google Scholar
J. E. Rodríguez-Paéz, A. C. Caballero, M. Villegas, C. Moure, P. Durán, and J. F. Fernández, “Controlled precipitation methods: formation mechanism of ZnO nanoparticles,” Journal of the European Ceramic Society, vol. 21, no. 7, pp. 925–930, 2001.
View at: Publisher Site | Google Scholar
V. Khrenov, M. Klapper, M. Koch, and K. Müllen, “Surface functionalized ZnO particles designed for the use in transparent nanocomposites,” Macromolecular Chemistry and Physics, vol. 206, no. 1, pp. 95–101, 2005.
View at: Publisher Site | Google Scholar
I. A. Toutorski, T. E. Tkachenko, B. V. Pokidko, N. I. Maliavski, and V. I. Sidorov, “Mechanical properties and structure of zinc-containing latex-silicate composites,” Journal of Sol-Gel Science and Technology, vol. 26, no. 1–3, pp. 505–509, 2003.
View at: Publisher Site | Google Scholar
M. Purica, E. Budianu, E. Rusu, M. Danila, and R. Gavrila, “Optical and structural investigation of ZnO thin films prepared by chemical vapor deposition (CVD),” Thin Solid Films, vol. 403-404, pp. 485–488, 2002.
View at: Publisher Site | Google Scholar
N. Audebrand, J.-P. Auffrédic, and D. Louër, “X-ray diffraction study of the early stages of the growth of nanoscale zinc oxide crystallites obtained from thermal decomposition of four precursors. General concepts on precursor dependent micro structural properties,” Chemistry of Materials, vol. 10, no. 9, pp. 2450–2461, 1998.
View at: Google Scholar
Y. Yang, H. Chen, B. Zhao, and X. Bao, “Size control of ZnO nanoparticles via thermal decomposition of zinc acetate coated on organic additives,” Journal of Crystal Growth, vol. 263, no. 1–4, pp. 447–453, 2004.
View at: Publisher Site | Google Scholar
D. Polsongkram, P. Chamninok, S. Pukird et al., “Effect of synthesis conditions on the growth of ZnO nanorods via hydrothermal method,” Physica B, vol. 403, no. 19-20, pp. 3713–3717, 2008.
View at: Publisher Site | Google Scholar
C.-H. Lu and C.-H. Yeh, “Influence of hydrothermal conditions on the morphology and particle size of zinc oxide powder,” Ceramics International, vol. 26, no. 4, pp. 351–357, 2000.
View at: Publisher Site | Google Scholar
Y. Zhu and Y. Zhou, “Preparation of pure ZnO nanoparticles by a simple solid-state reaction method,” Applied Physics A, vol. 92, no. 2, pp. 275–278, 2008.
View at: Publisher Site | Google Scholar
T. Tani, L. Mädler, and S. E. Pratsinis, “Homogeneous ZnO nanoparticles by flame spray pyrolysis,” Journal of Nanoparticle Research, vol. 4, no. 4, pp. 337–343, 2002.
View at: Publisher Site | Google Scholar
S. Jebril, H. Kuhlmann, S. Müller et al., “Epitactically interpenetrated high quality ZnO nanostructured junctions on microchips grown by the vapor-liquid-solid method,” Crystal Growth and Design, vol. 10, no. 7, pp. 2842–2846, 2010.
View at: Publisher Site | Google Scholar
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.
View at: Google Scholar
B. P. Lim, J. Wang, S. C. Ng, C. H. Chew, and L. M. Gan, “A bicontinuous microemulsion route to zinc oxide powder,” Ceramics International, vol. 24, no. 3, pp. 205–209, 1998.
View at: Google Scholar
M. Inoguchi, K. Suzuki, K. Kageyama, H. Takagi, and Y. Sakabe, “Monodispersed and well-crystallized zinc oxide nanoparticles fabricated by microemulsion method,” Journal of the American Ceramic Society, vol. 91, no. 12, pp. 3850–3855, 2008.
View at: Publisher Site | Google Scholar
S. Hingorani, V. Pillai, P. Kumar, M. S. Multani, and D. O. Shah, “Microemulsion mediated synthesis of zinc-oxide nanoparticles for varistor studies,” Materials Research Bulletin, vol. 28, no. 12, pp. 1303–1310, 1993.
View at: Google Scholar
S. Hingorani, D. O. Shah, and M. S. Multani, “Effect of process variables on the grain growth and microstructure of ZnO-Bi₂O₃ varistors and their nanosize ZnO precursors,” Journal of Materials Research, vol. 10, no. 2, pp. 461–467, 1995.
View at: Google Scholar
X. D. Gao, X. M. Li, and W. D. Yu, “Structural and morphological evolution of ZnO cluster film prepared by the ultrasonic irradiation assisted solution route,” Thin Solid Films, vol. 484, no. 1-2, pp. 160–164, 2005.
View at: Publisher Site | Google Scholar
K.-K. Kim, H.-S. Kim, D.-K. Hwang, J.-H. Lim, and S.-J. Park, “Realization of p-type ZnO thin films via phosphorus doping and thermal activation of the dopant,” Applied Physics Letters, vol. 83, no. 1, pp. 63–65, 2003.
View at: Publisher Site | Google Scholar
K. Y. Gao, T. Seyller, L. Ley et al., “Al₂O₃ prepared by atomic layer deposition as gate dielectric on 6H-SiC(0001),” Applied Physics Letters, vol. 83, no. 9, pp. 1830–1832, 2003.
View at: Publisher Site | Google Scholar
D. C. Look, G. M. Renlund, R. H. Burgener II, and J. R. Sizelove, “As-doped p-type ZnO produced by an evaporation/sputtering process,” Applied Physics Letters, vol. 85, no. 22, article 3, pp. 5269–5271, 2004.
View at: Publisher Site | Google Scholar
Y. J. Zeng, Z. Z. Ye, W. Z. Xu et al., “Dopant source choice for formation of p -type ZnO: Li acceptor,” Applied Physics Letters, vol. 88, no. 6, Article ID 062107, 2006.
View at: Publisher Site | Google Scholar
S. Limpijumnong, S. B. Zhang, S.-H. Wei, and C. H. Park, “Doping by large-size-mismatched impurities: the microscopic origin of arsenicor antimony-doped p-type zinc oxide,” Physical Review Letters, vol. 92, no. 15, Article ID 155504, 2004.
View at: Publisher Site | Google Scholar
X. Pan, Z. Ye, J. Li et al., “Fabrication of Sb-doped p-type ZnO thin films by pulsed laser deposition,” Applied Surface Science, vol. 253, no. 11, pp. 5067–5069, 2007.
View at: Publisher Site | Google Scholar
F. X. Xiu, Z. Yang, L. J. Mandalapu, D. T. Zhao, J. L. Liu, and W. P. Beyermann, “High-mobility Sb-doped p-type ZnO by molecular-beam epitaxy,” Applied Physics Letters, vol. 87, no. 15, Article ID 152101, 3 pages, 2005.
View at: Publisher Site | Google Scholar
F. X. Xiu, Z. Yang, L. J. Mandalapu, D. T. Zhao, and J. L. Liu, “Photoluminescence study of Sb-doped p -type ZnO films by molecular-beam epitaxy,” Applied Physics Letters, vol. 87, no. 25, Article ID 252102, 3 pages, 2005.
View at: Publisher Site | Google Scholar
R. Chauhan, A. Kumar, and R. P. Chaudhary, “Synthesis and characterization of silver doped ZnO nanoparticles,” Archives of Applied Science Research, vol. 2, no. 5, pp. 378–385, 2010.
View at: Google Scholar
O. Lupan, L. Chow, L. K. Ono et al., “Synthesis and characterization of ag- or sb-doped zno nanorods by a facile hydrothermal route,” Journal of Physical Chemistry C, vol. 114, no. 29, pp. 12401–12408, 2010.
View at: Publisher Site | Google Scholar
C. X. Mei, J. Yong, G. X. Yong, and Z. X. Wei, “Ag-doped ZnO nanorods synthesized by two-step method,” Chinese Physics B, vol. 11, no. 21, Article ID 116801, 2012.
View at: Google Scholar
M. Mahanti and D. Basak, “Ag-ZnO nanorods having enhanced emission and photocurrent properties,” AIP Conference Proceedings, vol. 1447, pp. 713–714, 2011.
View at: Google Scholar
Y. Zhang and J. Mu, “One-pot synthesis, photoluminescence, and photocatalysis of Ag/ZnO composites,” Journal of Colloid and Interface Science, vol. 309, no. 2, pp. 478–484, 2007.
View at: Publisher Site | Google Scholar
V. G. Pol, A. Gedanken, and J. Calderon-Moreno, “Deposition of gold nanoparticles on silica spheres: a sonochemical approach,” Chemistry of Materials, vol. 15, no. 5, pp. 1111–1118, 2003.
View at: Publisher Site | Google Scholar
K. Singh, S. Kumar, N. K. Verma, and H. S. Bhatti, “Photoluminescence properties of Eu³⁺-doped Cd_1−x Zn_x S quantum dots,” Journal of Nanoparticle Research, vol. 11, no. 4, pp. 1017–1021, 2009.
View at: Publisher Site | Google Scholar
Z. Li, Y. Ding, Y. Xiong, Q. Yang, and Y. Xie, “Room-temperature surface-erosion route to ZnO nanorod arrays and urchin-like assemblies,” Chemistry, vol. 10, no. 22, pp. 5823–5828, 2004.
View at: Publisher Site | Google Scholar
U. Pal and P. Santiago, “Controlling the morphology of ZnO nanostructures in a low-temperature hydrothermal process,” Journal of Physical Chemistry B, vol. 109, no. 32, pp. 15317–15321, 2005.
View at: Publisher Site | Google Scholar
Y. Zheng, C. Chen, Y. Zhan et al., “Photocatalytic activity of Ag/ZnO heterostructure nanocatalyst: correlation between structure and property,” Journal of Physical Chemistry C, vol. 112, no. 29, pp. 10773–10777, 2008.
View at: Publisher Site | Google Scholar
Y. J. Kwon, K. H. Kim, C. S. Lim, and K. B. Shim, “Characterization of ZnO nanopowders synthesized by the polymerized complex method via an organochemical route,” Journal of Ceramic Processing Research, vol. 3, no. 3, pp. 146–149, 2002.
View at: Google Scholar
R. F. Silva and M. E. D. Zaniquelli, “Morphology of nanometric size particulate aluminium-doped zinc oxide films,” Colloids and Surfaces A, vol. 198–200, pp. 551–558, 2002.
View at: Publisher Site | Google Scholar
H. Li, J. Wang, H. Liu et al., “Sol-Gel preparation of transparent zinc oxide films with highly preferential crystal orientation,” Vacuum, vol. 77, no. 1, pp. 57–62, 2004.
View at: Publisher Site | Google Scholar
S. Kurien, S. Sebastian, J. Mathew, and K. C. George, “Structural and electrical properties of nano-sized magnesium aluminate,” Indian Journal of Pure and Applied Physics, vol. 42, no. 12, pp. 926–933, 2004.
View at: Google Scholar
B. S. R. Devi, R. Raveendran, and A. V. Vaidyan, “Synthesis and characterization of Mn²⁺-doped ZnS nanoparticles,” Pramana, vol. 68, no. 4, pp. 679–687, 2007.
View at: Publisher Site | Google Scholar
S. Suwanboon, “Structural and optical properties of nanocrystalline ZnO powder from sol-gel method,” ScienceAsia, vol. 34, no. 1, pp. 31–34, 2008.
View at: Publisher Site | Google Scholar
A. H. Shah, E. Manikandan, M. Basheer Ahmed, and V. Ganesan, “Enhanced bioactivity of Ag/ZnO nanorods-A comparative antibacterial Study,” Journal of Nanomedicine & Nanotechnology, vol. 4, no. 3, pp. 2–6, 2013.
View at: Google Scholar
D. Sahu, B. S. Acharya, and A. K. Panda, “Role of Ag ions on the structural evolution of nano ZnO clusters synthesized through ultrasonication and their optical properties,” Ultrasonics Sonochemistry, vol. 18, no. 2, pp. 601–607, 2011.
View at: Publisher Site | Google Scholar
H. Karami and E. Fakoori, “Synthesis and characterization of ZnO nanorods based on a new gel pyrolysis method,” Journal of Nanomaterials, vol. 2011, Article ID 628203, 11 pages, 2011.
View at: Publisher Site | Google Scholar
Y. Ni, X. Cao, G. Wu, G. Hu, Z. Yang, and X. Wei, “Preparation, characterization and property study of zinc oxide nanoparticles via a simple solution-combusting method,” Nanotechnology, vol. 18, no. 15, Article ID 155603, 2007.
View at: Publisher Site | Google Scholar
E. A. Meulenkamp, “Synthesis and growth of ZnO nanoparticles,” Journal of Physical Chemistry B, vol. 102, no. 29, pp. 5566–5572, 1998.
View at: Google Scholar
Y. W. Koh, M. Lin, C. K. Tan, Y. L. Foo, and K. P. Loh, “Self-assembly and selected area growth of zinc oxide nanorods on any surface promoted by an aluminum precoat,” Journal of Physical Chemistry B, vol. 108, no. 31, pp. 11419–11425, 2004.
View at: Publisher Site | Google Scholar
H. Zhang, D. Yang, Y. Ji, X. Ma, J. Xu, and D. Que, “Low temperature synthesis of flowerlike zno nanostructures by cetyltrimethylammonium bromide-assisted hydrothermal process,” Journal of Physical Chemistry B, vol. 108, no. 13, pp. 3955–3958, 2004.
View at: Google Scholar
S. López-Cuenca, L. A. Pérez Carrillo, M. Rabelero Velasco et al., “High-yield synthesis of zinc oxide nanoparticles from bicontinuous microemulsions,” Journal of Nanomaterials, vol. 2011, Article ID 431382, 6 pages, 2011.
View at: Publisher Site | Google Scholar
K. Nejati, Z. Rezvani, and R. Pakizevand, “Synthesis of ZnO nanoparticles and investigation of the ionic template effect on their size and shape,” International Nano Letters, vol. 1, no. 2, pp. 75–81, 2011.
View at: Google Scholar

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Copyright © 2013 T. Siva Vijayakumar 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.

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