Table of Contents Author Guidelines Submit a Manuscript
Journal of Nanomaterials
Volume 2011, Article ID 850930, 7 pages
Research Article

ZnO Nanowire Formation by Two-Step Deposition Method Using Energy-Controlled Hollow-Type Magnetron RF Plasma

Department of Electrical Engineering, Graduate School of Engineering, Tohoku University, Miyagi, Sendai 980-8579, Japan

Received 14 June 2011; Accepted 16 September 2011

Academic Editor: Renzhi Ma

Copyright © 2011 Hideki Ono and Satoru Iizuka. 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 nanowire was produced in RF (radio frequency) discharge plasma. We employed here a two-step deposition technique. In the 1st step, zinc atoms were sputtered from a zinc target to create zinc nuclei on a substrate before the growth of ZnO nanostructure. Here, we used pure argon plasma for physical sputtering. In the 2nd step, we employed an oxygen discharge mixed with argon, where oxygen radicals reacted with zinc nuclei to form ZnO nanostructures. Experimental parameters such as gas flow ratio and target bias voltage were controlled in O2/Ar plasma. Properties of the depositions were analysed by SEM and Raman spectroscopy. We found that many folded and bundled nanowires formed in the 2nd step. The diameter of wires was typically 10–100 nm. We also discussed a growth mechanism of ZnO nanowires.

1. Introduction

ZnO is an oxide semiconductor with a wide band gap of 3.37 eV at room temperature and has a large exciton binding energy of 60 meV in comparison with GaN [13]. Therefore, ZnO was expected to develop a light emitting device, especially for a blue-light emission diode, instead of GaN.

ZnO nanostructures such as nanowires and nanorods are expected to make nanophotonic devices [4]. ZnO nanowires and nanorods have been believed to grow via vapour-liquid-solid (VLS) process [5, 6]. However, several other techniques for the growth have been reported. For example, molecular beam epitaxy (MBE) and pulsed-laser deposition (PLD) are generally employed for the growth processes of ZnO thin layers. These techniques take an advantage for the formation of high-quality ZnO crystals. Metal organic chemical vapour deposition (MOCVD) process is also one of the remarkable processes nowadays [7, 8].

Here, the growth process of ZnO by a plasma processing was studied. This is superior to the other processes for low-temperature and large-area deposition. Moreover, when we control the energy of plasma, we would make ZnO thin films or ZnO nanoparticle, selectively. However, very few studies referred to the energy-controlled plasma.

In this study, we investigated how zinc, sputtered from a zinc target, reacted with oxygen in O2/Ar plasma when discharge parameters such as gas pressure, gas flow ratio, and target bias voltage were changed. We employed a two-step deposition technique for the formation of ZnO nanostructures. In the 1st step, zinc atoms were sputtered from a zinc target to create zinc nuclei for the base of ZnO nanostructure growth. Here, we used pure argon plasma for physical sputtering. In the 2nd step, we employed an oxygen discharge with argon, where oxygen radical reacted with zinc nuclei on a substrate to form ZnO nanosuructures. Dependence on the deposition time was investigated in O2/Ar plasma.

2. Experimental Setup

Experimental apparatus [9, 10] is schematically shown in Figure 1. Plasma was generated by a hollow-type magnetron (HTM) RF plasma source at frequency of 13.56 MHz [11, 12]. The HTM consists of powered electrode made of stainless cylinder of 4.8 cm in diameter and 5.5 cm height, which is covered by a grounded stainless steel cylinder of 5.2 cm diameter and 6.0 cm height. Furthermore, two magnet rings are wound around outside of a grounded cylinder with spacing of 2 cm to confine the plasma and to prevent the electrode from sputtering by deep self-bias voltage.

Figure 1: Experimental apparatus.

A zinc target was set on a bottom plate. Target DC bias voltage controlled the Zn sputtering. We can change gas pressure ratio O2/Ar and target DC voltage . In this experiment a grid used for the electron temperature control was removed. Plasma parameters were measured by a Langmuir probe. Wavelength of optical emission from the plasma was measured by a spectroscope (OES). Substrate was fixed at 2.5 cm above the top of the electrode. Deposition of ZnO on the substrate was estimated by scanning electron microscope (SEM) and Raman spectroscope.

3. Experimental Results

3.1. Growth of ZnO Nanowires

Blue-light emission from Zn neutrals produced in the plasma was found to be one of the most important factors for a deposition of ZnO nanowires. Typical spectrum of the optical emission is shown in Figure 2. The spectrum can be characterized by a strong blue emission line of zinc neutral around 460 nm. However, the blue-light emission diminished drastically when O2 gas was slightly mixed with Ar. This phenomenon markedly influenced ZnO deposition. In case of weak blue-light emission, we could not detect materials consisting of ZnO nanowires on the substrate.

Figure 2: Typical optical emission spectrum.

In case of simultaneous processing with Zn sputtering and its oxidization by using a mixed gas of O2 and Ar, we clearly observed a formation of nanowires. After turning on the plasma with blue-light emission, the substrate was inserted into the plasma for the deposition of ZnO. Deposition period was varied in a range 10–600 sec. Typical SEM image of the materials deposited under strong blue-light emission is shown in Figure 3. We found many folded nanowires bundled on the substrate. The diameter of wires was of the order of 100 nm. From Raman spectroscopy, we found that these wires consisted of ZnO.

Figure 3: Typical SEM image of nanowires.

Almost all nanowires were bent and twisted complicatedly as shown in Figure 3. The structure was in principle one dimensional, but the shape was complicated, which might be preferably available for an increment of effective surface area of ZnO materials. Total surface area could be much larger than that of flat and smooth ZnO surface. However, from a viewpoint of practical application in industries, it would be better for these nanowires to grow straight in one direction on the substrate. One-dimensionally grown nanowires will make it easy to produce an electronic device like PN junction for blue-light emission. Therefore, we intended to investigate the mechanism by which nanowires were bundled on the substrate. In order to clarify the growth process the deposition period was varied under various conditions.

3.2. Dependence on Deposition Time

We tried first to examine initial growth process of ZnO nanowires. From a comparison with Raman spectrum, we confirmed that Zn stacked up first on the substrate to form thin Zn layer, then oxygen reacted with zinc to construct nanowires. Thickness of Zn layer was an important factor for ZnO nanowire growth. If Zn layer was too thin, for example, we could not obtain nanowires. Even when oxygen reacted with Zn, the reaction could not result in construction of nanowires. So, next we tried to find out a dependence of the growth of ZnO nanowires on the thickness of Zn layer deposited initially.

Therefore, for this reason, we separated processing procedures, that is, Zn deposition process and its oxidization process. So, the deposition period for Zn layer formation was separated from the period for oxygen reaction. We can control reaction time of oxygen, independently. Then, we would find a mechanism of the growth of ZnO nanowires.

In the experiments we fixed RF power at 100 W and substrate temperature at 150°C. In the deposition period of Zn layer (1st period) Ar gas pressure was fixed at 10 Pa. No oxygen gas was fed in, and the target bias voltage was fixed at –200 V for zinc sputtering. In the oxygen reaction period (2nd period), however, Ar gas pressure was fixed at 9.5 Pa under fixed O2 gas pressure at 0.5 Pa. No target bias voltage was applied in this case. The 1st period was varied in a range of 5–600 sec, and the 2nd period was varied in a range of 0–600 sec.

When the deposition period of Zn is short ( = 60 s), thin film including only Zn was generated on the substrate, instead of ZnO nanowires. Figure 4(a) shows a typical SEM image taken from the top of the substrate after deposition period of = 60 s. From a detailed observation, we confirmed that the layer consisted of many small-size zinc particles. The size was 50–100 nm, and the particles were distributed almost randomly on the surface.

Figure 4: SEM images with deposition time as a parameter in case of = 60 s: = (a) 0 s, (b) 60 s, (c) 300 s, and (d) 600 s.

In the 2nd period we introduced oxygen to oxidize the surface of Zn particles and oxygen reaction period was varied. Then, thin layer including ZnO was generated on the top of Zn particles, as shown in Figures 4(b) and 4(c), where we found many small pillows. After oxidization period of 600 s, that is, = 600 s, many pillars changed their shape to something like hexagon pillars, as shown in Figure 4(d). These pillars grew in time and were distributed on the surface of the substrate. These pillars seem to grow from the bottom of the deposited Zn particles. The hexagonal structure indicates that these were consisting of ZnO crystal [13]. Increasing oxidization period the shape of hexagon structure gradually disappeared, and more smooth structure came out, eventually. The size was also gradually decreased by the effect of Ar sputtering. We could not observe nanowire formation in this case.

We have checked similar oxidization in case of = 300 s. Figure 5 shows SEM images for the case of = 300 s. As shown in Figure 5(a), we clearly found many pillars after the deposition of Zn layer. The pillars grew in length and in diameter, and the cross-section of the top turned to a hexagonal structure as shown in Figure 5(b). However, then, the shape was gradually changed and more smaller hexagon pillars were generated as shown in Figure 5(c). The size was decreased to about 50–100 nm and the shape was changed to something like a pillar again. Then, finally, further oxidization caused an evolution of thin nanowires, growing from the dwindled hexagon pillars, as shown by the arrow in Figure 5(d). We find clearly characteristic structures of ZnO nanowires, though the hexagon pillars shrink simultaneously by the effect of oxidization and Ar sputtering. The condition for the growth of nanowires seemed to correspond to a production of smaller size structure like shrunken hexagon pillows.

Figure 5: SEM images with deposition time as a parameter in case of = 300 s: = (a) 0 s, (b) 30 s, (c) 60 s, and (d) 90 s. The nanowire is pointed by arrow in (d).

Since no additional Zn was supplied from the plasma, the growth of nanowires came to an end finally. Therefore, the diameter of wires remained thin compared with that in Figure 3. After further oxidization such nanowires were almost completely removed by Ar sputtering and only homogeneous thin film of ZnO was left instead of the nanowires.

Figure 6 shows cross sectional view of deposited layers in case of = 300 s. The growth of nanowires was found in Figures 6(c) and 6(d). In case of initial growth, most of the wires looked straight as one-dimensional needles, as shown in Figure 6(c). However, the direction of the growth was quite random because of an irregularity of the background zinc layers. With increasing the length, the wires had a tendency to bend, as shown by the arrow in Figure 6(d). This might be due to a stoichiometric unbalance between Zn and O. Therefore, the crystallization was not enough in this growth phase.

Figure 6: SEM images of cross-section with deposition time as a parameter in case of = 300 s: = (a) 0 s, (b) 30 s, (c) 60 s, and (d) 90 s. The nanowire is pointed by arrow in (d).

4. Discussion

Formation process of ZnO nanowires was studied by using two-step deposition technique. The growth processes were schematically shown in Figure 7. In the 1st step, only Zn layers were deposited as shown in Figure 7(a). The shape of Zn layer was something like particulates and pillars. In the 2nd period, though no additional zinc was supplied on the substrate, growth of ZnO nanowires took place. This means that oxygen could be taken into Zn layer to provide oxidization layer near the surface.

Figure 7: Growth model of ZnO nanowires in case of Figure 5. (a) Irregular surface of Zn layer with particulate and pillar-like structures is formed in the 1st step. (b) Particulate and pillar-like structures are changed to hexagonal pillars, growing with time, by oxidization in the 2nd step. (c) Then, the hexagonal pillars start shrinking by Ar ion sputtering, which triggers a start of ZnO nanowire growth. (d) ZnO nanowires grow and bend in the presence of Ar ion bombardment. (e) The nanowire growth stops and decays with time by the ion sputtering, and finally smooth surface of ZnO layer comes out.

The shape of deposited zinc surface was changed to hexagonal pillar, which had grown in time, as shown in Figure 7(b). In this case the pillars might consist of crystallized ZnO. The shape of this structure was straight with no bending component. We could not observe nanowires at this moment. The beginning time of nanowire growth seemed to be related with the initial size of hexagonal pillars. Though ZnO pillars grew first, they finally shrunk due to Ar sputtering. So, the size of pillars diminished in time (Figure 7(c)). The start point of nanowire growth was related with this timing. As the size was reduced, the growth of ZnO nanowires started as shown in Figures 7(c) and 7(d). However, after further oxidization, the nanowire growth stopped and decayed in time. Finally, such nanowires were almost completely removed by Ar sputtering and smooth surface of ZnO layer came out (Figure 7(e)).

As another important mechanism, it should be pointed out that a supply of Zn took place from the bottom of nanowires. Ar ions impinging on the substrate could heat Zn surface to provide a liquid-solid state, in which Zn atoms could move and react with oxygen to form the structure of ZnO. Therefore, the growth point of ZnO should be the bottom end of nanowires as shown in Figure 8. Zn pillar of small size, formed initially on Zn thin film, was oxidized from its surface. Therefore, ZnO crystallization started first at the tip of the pillar. Since Zn could be supplied from the Zn layer to the region of excess oxygen, the crystallized part of ZnO extended upward as a form of nanowire, being accompanied with diffusion of Zn from the Zn layer. Finally, the growth of ZnO nanowire would be completed because of a limit of Zn diffusion. Initial zinc layer played as a kind of catalysis, which promoted not only the growth of ZnO hexagonal pillars but also the growth of ZnO nanowires. Two-step growth technique is quite important for investigating and controlling the growth of ZnO nanostructures.

Figure 8: Growth model of ZnO nanowires, corresponding to the phase (c) in Figure 7. Zn pillar of small size, formed initially on Zn thin film, is oxidized from its surface. Crystallization of ZnO occurs first at the tip of the pillar, and excess oxygen extracts Zn from the Zn layer. Then, ZnO nanowire extends upward, being accompanied with the Zn supply from the Zn layer. Finally, the growth of ZnO nanowire is completed because of a limit of Zn diffusion from the Zn layer.

In case of one-step growth by using a mixed gas of O2 and Ar, typical spectrum of Raman shifts revealed that the intensity of ZnO signal clearly increased with deposition time. However, before and even during the growth of ZnO, we always observed another peak at 540 cm−1, which always appeared in case of zinc deposition. This indicated that supply of Zn atom on the substrate dominated the supply of oxygen for ZnO production. In other words, the amount of oxygen radicals O* might be lacked relatively. For this reason, nanowires contained not only ZnO component but also metallic Zn. The reason why the wires were bending would come from an irregularity in one-dimensional growth of ZnO crystal because of excess Zn supply during the growth.

5. Conclusions

Here, we employed a two-step deposition method for the formation of ZnO nanostructures. We separated the zinc deposition from its oxidization process, that is, the deposition period for Zn layer formation was separated from the period for oxygen reaction. This method makes it possible to control the time of oxygen reaction.

By separating the period of ZnO nanowire formation from the period of Zn layer formation, we found ZnO nanowires grown in the 2nd step in O2/Ar RF plasma. We found also that the size of Zn pillars formed in the 1st step was crucial for the nucleation and growth of ZnO nanowires in the 2nd step. A formation model of ZnO nanowires was proposed. We also observed a formation of thin homogeneous ZnO film, as a result of further oxidization, accompanied with Ar sputtering. The method proposed here would be useful for understanding the growth mechanism of ZnO nanostructures.


The work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan.


  1. K. Hüemmer, “Interband magnetoreflection of ZnO,” Physica Status Solidi B, vol. 56, no. 1, pp. 249–260, 1973. View at Google Scholar · View at Scopus
  2. A. Ohtomo, K. Tamura, M. Kawasaki et al., “Room-temperature stimulated emission of excitons in ZnO/(Mg, Zn)O superlattices,” Applied Physics Letters, vol. 77, no. 14, Article ID 2204, 3 pages, 2000. View at Google Scholar
  3. 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. View at Google Scholar
  4. F. Patolsky, G. Zheng, and C. M. Lieber, “Nanowire sensors for medicine and the life sciences,” Nanomedicine, vol. 1, no. 1, pp. 51–65, 2006. View at Publisher · View at Google Scholar
  5. R. S. Wagner and W. C. Ellis, “Vapor-liquid-solid mechanism of single crystal growth,” Applied Physics Letters, vol. 4, no. 5, pp. 89–90, 1964. View at Publisher · View at Google Scholar
  6. A. M. Morales and C. M. Lieber, “A laser ablation method for the synthesis of crystalline semiconductor nanowires,” Science, vol. 279, no. 5348, pp. 208–211, 1998. View at Publisher · View at Google Scholar
  7. X. Liu, X. Wu, H. Cao, and R. P. H. Chang, “Growth mechanism and properties of ZnO nanorods synthesized by plasma-enhanced chemical vapor deposition,” Journal of Applied Physics, vol. 95, no. 6, pp. 3141–3147, 2004. View at Publisher · View at Google Scholar
  8. S. Choopun, H. Tabata, and T. Kawai, “Self-assembly ZnO nanorods by pulsed laser deposition under argon atmosphere,” Journal of Crystal Growth, vol. 274, no. 1-2, pp. 167–172, 2005. View at Publisher · View at Google Scholar · View at Scopus
  9. H. Ono and S. Iizuka, “Growth of ZnO nanowires in hollow-type magnetron O2/Ar RF plasma,” Thin Solid Films, vol. 518, no. 3, pp. 1016–1019, 2009. View at Publisher · View at Google Scholar · View at Scopus
  10. K. Kumeta, H. Ono, and S. Iizuka, “Formation of ZnO nanostructures in energy-controlled hollow-type magnetron RF plasma,” Thin Solid Films, vol. 518, no. 13, pp. 3522–3525, 2010. View at Publisher · View at Google Scholar
  11. J. Emi, K. Kato, T. Abe, and S. Iizuka, “Formation of nanoparticles by control of electron temperature in hollow-typed magnetron radio frequency CH4/H2 plasma,” Japanese Journal of Applied Physics, vol. 45, no. 10, pp. 8071–8074, 2006. View at Publisher · View at Google Scholar
  12. J. Emi and S. Iizuka, “Characteristics of carbon-related materials deposited in electron-energy controlled CH4/H2 RF discharge plasmas,” Diamond and Related Materials, vol. 20, no. 4, pp. 568–572, 2011. View at Publisher · View at Google Scholar
  13. K. Prabakar and H. Kim, “Growth control of ZnO nanorod density by sol-gel method,” Thin Solid Films, vol. 518, no. 24, pp. e136–e138, 2010. View at Publisher · View at Google Scholar · View at Scopus