Selective Growth of Vertical-aligned ZnO Nanorod Arrays on Si Substrate by Catalyst-free Thermal Evaporation
© to the authors 2008
Received: 3 July 2008
Accepted: 5 August 2008
Published: 21 August 2008
By thermal evaporation of pure ZnO powders, high-density vertical-aligned ZnO nanorod arrays with diameter ranged in 80–250 nm were successfully synthesized on Si substrates covered with ZnO seed layers. It was revealed that the morphology, orientation, crystal, and optical quality of the ZnO nanorod arrays highly depend on the crystal quality of ZnO seed layers, which was confirmed by the characterizations of field-emission scanning electron microscopy, X-ray diffraction, transmission electron microscopy, and photoluminescence measurements. For ZnO seed layer with wurtzite structure, the ZnO nanorods grew exactly normal to the substrate with perfect wurtzite structure, strong near-band-edge emission, and neglectable deep-level emission. The nanorods synthesized on the polycrystalline ZnO seed layer presented random orientation, wide diameter, and weak deep-level emission. This article provides a C-free and Au-free method for large-scale synthesis of vertical-aligned ZnO nanorod arrays by controlling the crystal quality of the seed layer.
In the recent years, quasi-one-dimensional (1D) ZnO nanostructures such as nanopores,  nanowires,  nanobelts , and nanorods  have attracted great interest due to their unique electrical and photonic properties for potential applications in chemical sensors, optoelectronics, and field-effect transistors. Thanks to the high surface-volume ratio, controllability of the nucleation position, and superior ultraviolet lasing and photoluminescence (PL) property of ZnO nanorods or nanoarrays [5–7], the realization of vertically well-aligned 1D ZnO nanorods is very important for its application in nanoscale light-emitting diodes (LEDs), nanosensors, and field emitters [8–11]. In order to fabricate ZnO nanorods, various methods including thermal evaporation [12–15], chemical vapor deposition , metal organic chemical vapor deposition (MOCVD) [17, 18], and solution-based methods have been used . Among the numerous researches on the synthesis and properties of ZnO nanorods, uniform ZnO nanorod arrays have been successfully prepared on sapphire substrates by Au-catalyzed vapor–liquid–solid (VLS) growth with or without the use of GaN template [5, 20]. However, Au impurities will be unavoidably left on the tip of the nanorods after the growth , which is detrimental to device performance. In addition, the insulating and expensive sapphire substrate is also disadvantageous for the integration of nanorod arrays with the current primary stream of the Si-based device technology. At the same time, using ZnO film as seed layer, vertical-aligned ZnO nanorods have been grown on silicon substrate by thermal evaporation of ZnO–C powder mixture [13–15]. Since the type of such nanorods growth is dominated by the carbothermal reduction of ZnO–C powder mixture , the introduction of C atoms will possibly bring adverse effect on nanorods application in device integration. Furthermore, this type of nanorods growth usually needs a relatively high ramp rate of furnace temperature (e.g., 25 °C/min) to obtain a high Zn saturation pressure , and even much higher ramp rate (e.g., 75 °C/min) has to be satisfied in order to increase the spacing between the nanorods . It is well known that there is a big difference in the thermal expansion coefficients as well as the big lattice mismatch between Si (2.56 × 10−6 K−1) and ZnO (4.75 × 10−6 K−1) , such high ramp rate is not good for the relaxation of the thermal strain in the underlying ZnO film, which can accelerate the generation of structure defects or even cracks , and then greatly affects the properties of the upper nanorods. Therefore, new techniques are required in order to obtain vertical-aligned ZnO nanorods on Si substrate. On the other hand, although ZnO seed layer is very important for the nucleation and growth of ZnO nanorods or nanoarrays [19, 24–26], there is very little literature about the influence of ZnO seed layer quality on the orientation, morphology, crystal, and optical quality of the upper ZnO nanorods grown by thermal evaporation method.
In this article, a catalyst and carbon-free evaporation method was demonstrated to synthesize high-density well-aligned ZnO nanorod arrays on Si(100) substrates pre-deposited by ZnO seed layers with different crystal quality and morphology. A low rate was adopted during the ramping and cooling of the furnace considering the large difference in the thermal expansion coefficient of Si and ZnO. It was found that the nanorod arrays grown on the ZnO films with better crystal quality have vertical orientation as well as better optical and crystal quality. This method not only provides a very easy way for the large-scale synthesis of nanorod arrays on semiconductor substrates, but also avoids the introduction of the impurities caused by metal catalysts or carbon.
Two ZnO film templates (a and b) were prepared by RF sputtering and pulsed laser deposition (PLD) on Si(100) substrates for the deposition of ZnO nanorod arrays, respectively. High-purity ZnO powder (4 N) was put into an alumina crucible placed at the center of an alumina tube furnace (Φ6.0 × 100 cm). The ZnO/Si(100) substrates were placed at 24 cm away from the evaporation source in the alumina tube. After being purged by high-purity Ar for 30 min, the furnace temperature was raised to 800 °C with a rate of 10 °C/min under a constant Ar flow of 60 sccm. After the furnace was maintained at 800 °C for 30 min, it was heated to 1,400 °C within 120 min and maintained at 1,400 °C for the evaporation of ZnO onto prior ZnO/Si template for 90 min, during which the pressure was kept within 0.025–0.03 MPa. Then the furnace was cooled down with a rate of 5 °C/min. The substrates were taken out the furnace after it was cooled down to room temperature, and a white wax-like layer can be clearly seen deposited onto the substrates.
The morphology and crystal quality of the ZnO nanorod arrays and the pre-deposited ZnO films were investigated by field-emission scanning electron microscopy (FE-SEM, JEOL JSM-6700F) and X-ray diffraction (XRD, Brukers D8) measurements. Further microstructure information was studied by a high-resolution transmission electron microscopy (HRTEM, Tecnai G20). The optical property of the the ZnO nanorod arrays was examined by PL measurements executed at room temperature using He–Cd laser (325 nm) as excitation source.
Results and Discussion
Based on the above property of the seed layers and nanorod samples, a possible growth mechanism for ZnO nanorods was proposed. It has long been held that ZnO nanorods always nucleate from the concave tip near the grain boundary between two ZnO film grains , the high-density small grains shown in Fig. 4a and b naturally provide numerous nucleation sites for ZnO growth. For the seed layer with good wurtzite structure, ZnO will adopt the same epitaxial relationship as the seed layer. At the same time, the lateral growth of ZnO is greatly limited while the growth along  direction dominates the whole growth process considering the different growth rate of various growth facets which followed in the order of . Therefore, well vertical-aligned ZnO nanorods will be obtained on the ZnO template prepared by PLD. As for the template with poor crystal quality, though the preferential growth direction is along  ZnO azimuth, the orientation of the nanorods will be very disordered relative to the substrate at the initial stage because of the randomly distributed grains in the ZnO seed layer. With growth time increasing, adjacent nanorods tend to coalesce into a wider nanorod with larger diameter once these thinner nanorods meet each other at side faces. Thus, though there is no obvious difference between the grain sizes of the two types of the seed layer, the diameter of the nanorods growing on them varies to a great degree. Therefore, the orientation and the diameter of the nanorods are highly dependent on the crystal quality of the underlying ZnO seed layer.
In conclusion, vertically well-aligned 1D ZnO nanorod arrays with high quality have been achieved without any catalyst or C on the ZnO seed layers prepared by PLD. The dependence of the orientation, morphology, crystal quality, and optical quality of the nanorod arrays on the quality of the seed layer is systematically studied by FE-SEM, XRD, HRTEM, and PL analysis. It is found that for the ZnO seed layer with good crystal quality, the nanorods grow exactly along ZnO  direction with perfect wurtzite structure, small diameter (150 nm), and high optical quality. While for the ZnO seed layer with poor crystal quality, the nanorods grow in random directions with weak deep-level emission and wider diameter (about 1.5 μm). This article not only provides an easy and clean way to fabricate large-scale well-aligned ZnO nanorods, but also sheds light on controlling the orientation, diameter, and quality of ZnO nanorods by increasing the crystal quality of ZnO seed layer.
This work is supported in part by the National Nature Science Foundation of China (No.50772032), MOST of China (No.2007CB936202), Research Fund for the Doctoral Program of China Education Ministry (20060512004), Natural Science Foundation Creative Team Project of Hubei Province (2007ABC005).
- Ding GQ, Shen WZ, Zheng MJ, Fan DH: Appl. Phys. Lett.. 2006, 88: 103106. 10.1063/1.2182025View ArticleGoogle Scholar
- Huang MH, Mao S, Feick H, Yan H, Wu Y, Kind H, et al.: Science. 2001, 292: 1897. COI number [1:CAS:528:DC%2BD3MXksVaqsb0%3D] COI number [1:CAS:528:DC%2BD3MXksVaqsb0%3D] 10.1126/science.1060367View ArticleGoogle Scholar
- Pan ZW, Dai ZR, Wang ZL: Science. 2001, 291: 1947. COI number [1:CAS:528:DC%2BD3MXhvVSnu7s%3D] COI number [1:CAS:528:DC%2BD3MXhvVSnu7s%3D] 10.1126/science.1058120View ArticleGoogle Scholar
- Li JY, Chen XL, Li H, He M, Qiao ZY: J. Cryst. Growth. 2001, 233: 5. COI number [1:CAS:528:DC%2BD3MXmtFansb4%3D] COI number [1:CAS:528:DC%2BD3MXmtFansb4%3D] 10.1016/S0022-0248(01)01509-3View ArticleGoogle Scholar
- Liu DF, Xiang YJ, Liao Q, Zhang JP, Wu XC, Zhang ZX, et al.: Nanotechnology. 2007, 18: 405303. 10.1088/0957-4484/18/40/405303View ArticleGoogle Scholar
- Han XH, Wang GZ, Wang QT, Cao L, Liu RB, Zou BS, et al.: Appl. Phys. Lett.. 2005, 86: 223106. 10.1063/1.1941477View ArticleGoogle Scholar
- Li C, Fang GJ, Su FH, Li GH, Wu XG, Zhao XZ: Nanotechnology. 2006, 17: 3740. COI number [1:CAS:528:DC%2BD28XhtVSrsbzI] COI number [1:CAS:528:DC%2BD28XhtVSrsbzI] 10.1088/0957-4484/17/15/021View ArticleGoogle Scholar
- Yoon A, Hong W-K, Lee T: J. Nanosci. Nanotechnol.. 2007, 7: 4101. COI number [1:CAS:528:DC%2BD2sXhtlSht73F] COI number [1:CAS:528:DC%2BD2sXhtlSht73F] 10.1166/jnn.2007.011View ArticleGoogle Scholar
- Park WI, Yi G-C: Adv. Mater.. 2004, 16: 87. COI number [1:CAS:528:DC%2BD2cXhtVaiurY%3D] COI number [1:CAS:528:DC%2BD2cXhtVaiurY%3D] 10.1002/adma.200305729View ArticleGoogle Scholar
- Arnold MS, Avouris P, Pan ZW, Wang ZL, Phy J: Chem. Br.. 2003, 107: 659. COI number [1:CAS:528:DC%2BD38XpslOnu70%3D] COI number [1:CAS:528:DC%2BD38XpslOnu70%3D]View ArticleGoogle Scholar
- Li SY, Lin P, Lee CY, Tseng TY: J. Appl. Phys.. 2004, 95: 3711. COI number [1:CAS:528:DC%2BD2cXitlKrurc%3D] COI number [1:CAS:528:DC%2BD2cXitlKrurc%3D] 10.1063/1.1655685View ArticleGoogle Scholar
- Pradhan AK, Williams TM, Zhang K, Hunter D, Dadson JB, Lord K, et al.: J. Nanosci. Nanotechnol.. 2006, 6: 1985. COI number [1:CAS:528:DC%2BD28XosVegsbw%3D] COI number [1:CAS:528:DC%2BD28XosVegsbw%3D] 10.1166/jnn.2006.318View ArticleGoogle Scholar
- Li C, Fang GJ, Liu NS, Li J, Liao L, Su FH, et al.: J. Phys. Chem. C. 2007, 111: 12566. COI number [1:CAS:528:DC%2BD2sXos1Gnt7g%3D] COI number [1:CAS:528:DC%2BD2sXos1Gnt7g%3D] 10.1021/jp0737808View ArticleGoogle Scholar
- Jie JS, Wang GZ, Chen YM, Han XH, Wang QT, Xu B, et al.: Appl. Phys. Lett.. 2005, 86: 031909. 10.1063/1.1854737View ArticleGoogle Scholar
- Kumar RTR, McGlynn E, McLoughlin C, Chakrabarti S, Smith RC, Carey JD, et al.: Nanotechnology. 2007, 18: 215704. 10.1088/0957-4484/18/21/215704View ArticleGoogle Scholar
- Liu Y, Liu M: J. Nanosci. Nanotechnol.. 2007, 7: 4529. COI number [1:CAS:528:DC%2BD1cXhtFegtbk%3D] COI number [1:CAS:528:DC%2BD1cXhtFegtbk%3D] 10.1166/jnn.2007.874View ArticleGoogle Scholar
- Park SH, Han SW: J. Nanosci. Nanotechnol.. 2007, 7: 2909. COI number [1:CAS:528:DC%2BD2sXot1enuro%3D] COI number [1:CAS:528:DC%2BD2sXot1enuro%3D] 10.1166/jnn.2007.604View ArticleGoogle Scholar
- Cong GW, Wei HY, Zhang PF, Peng WQ, Wu JJ, Liu XL, et al.: Appl. Phys. Lett.. 2005, 87: 231903. 10.1063/1.2137308View ArticleGoogle Scholar
- Kim Y-J, Lee C-H, Joon Y, Yi G-C, Kim SS, Cheong H: Appl. Phys. Lett.. 2006, 89: 163128. 10.1063/1.2364162View ArticleGoogle Scholar
- Zhou H, Wissinger M, Fallert J, Hauschild R, Stelzl F, Klingshirn C, et al.: Appl. Phys. Lett.. 2007, 91: 181112. 10.1063/1.2805073View ArticleGoogle Scholar
- Kodambaka S, Tersoff J, Reuter MC, Ross FM: Science. 2007, 316: 729. COI number [1:CAS:528:DC%2BD2sXkvVWrsLg%3D] COI number [1:CAS:528:DC%2BD2sXkvVWrsLg%3D] 10.1126/science.1139105View ArticleGoogle Scholar
- 22. O. Madelung, Numerical Data and Functional Relationships in Science and Technology (Springer, Heidelberg, 1982)Google Scholar
- Chen YF, Jiang FY, Wang L, Zheng CD, Dai JN, Pu Y, et al.: J. Cryst. Growth. 2005, 275: 486. COI number [1:CAS:528:DC%2BD2MXitlCgsL0%3D] COI number [1:CAS:528:DC%2BD2MXitlCgsL0%3D] 10.1016/j.jcrysgro.2004.12.019View ArticleGoogle Scholar
- Ahsanulhaq Q, Kim J-H, Hahn Y-B: Nanotechnology. 2007, 18: 485307. 10.1088/0957-4484/18/48/485307View ArticleGoogle Scholar
- Ahsanulhaq Q, Umar A, Hahn YB: Nanotechnology. 2007, 18: 115603. 10.1088/0957-4484/18/11/115603View ArticleGoogle Scholar
- Tak Y, Park D, Yong K: J. Vac. Sci. Technol. B. 2006, 24: 2047. COI number [1:CAS:528:DC%2BD28XnvVajsL8%3D] COI number [1:CAS:528:DC%2BD28XnvVajsL8%3D] 10.1116/1.2216714View ArticleGoogle Scholar
- Özgür Ü, Alivov YI, Liu C, Teke A, Reshchikov MA, Doğan S, et al.: J. Appl. Phys.. 2005, 98: 041301. 10.1063/1.1992666View ArticleGoogle Scholar
- Wang RC, Liu CP, Huang JL, Chen S-J: Appl. Phys. Lett.. 2005, 86: 251104. 10.1063/1.1948522View ArticleGoogle Scholar
- Stikant V, Clarke DR: J. Appl. Phys.. 1998, 83: 5447. 10.1063/1.367375View ArticleGoogle Scholar
- Hu JQ, Bando Y: Appl. Phys. Lett.. 2003, 82: 1401. COI number [1:CAS:528:DC%2BD3sXhs1egurs%3D] COI number [1:CAS:528:DC%2BD3sXhs1egurs%3D] 10.1063/1.1558899View ArticleGoogle Scholar
- Li Y, Cheng GS, Zhang LD: J. Mater. Res.. 2000, 15: 2305. COI number [1:CAS:528:DC%2BD3cXot1GjtLY%3D] COI number [1:CAS:528:DC%2BD3cXot1GjtLY%3D] 10.1557/JMR.2000.0331View ArticleGoogle Scholar