morphology change of self-assembled zno 3d nanostructures with different ph

ELSEVI Contents lists available at ScienceDirect Materials Chemistry and Physics journal homepage: www.elsevier.com/locate/matchemphys Morphology change of self-assembled ZnO 3D

ELSEVI

Contents lists available at ScienceDirect

Materials Chemistry and Physics

journal homepage: www.elsevier.com/locate/matchemphys

Morphology change of self-assembled ZnO 3D nanostructures with different pH

in the simple hydrothermal process

Jae-Min Jang?, Sung-Dai Kim”, Hee-Man Choi?, Jin-Yeol Kim?, Woo-Gwang Jung?**

4 School of Advanced Materials Engineering, Kookmin University, 861-1 Jeongneung-dong Seongbuk-gu, Seoul 136-702, Republic of Korea

b Department of Quality Non-Destructive Testing, Seoul Sanggye Vocational School, 771-2 Sanggye-dong, Nowon-gu, Seoul 139-831, Republic of Korea

Article history:

Received 28 January 2008

Received in revised form 21 July 2008

Accepted 25 July 2008

PACS:

62.23.—c

Keywords:

Zinc oxide

Morphology

Self-assembly

Hydrothermal process

pH

Nanostructure

Self-assembled ZnO 3D nanostructures were fabricated on a Si substrate using a simple hydrothermal process with ammonia and zinc acetate dihydrate solutions at 95°C The changes in morphology and characteristics of the ZnO nanostructures were investigated over a range of pH (9.0-11.8) The texture

of the ZnO crystal was evaluated using the texture coefficient (TC) for the specific reflecting plane The results showed that pH is the main factor affecting the morphology of the ZnO nanostructure The ZnO nanostructures fabricated were single-crystalline with good crystal quality The PL spectra showed that the ZnO nanostructures fabricated at pH >10.0 had good optical properties with low defect content This demonstrates that the morphology of ZnO nanostructures fabricated using a simple hydrothermal process can be controlled by the pH of the solution

© 2008 Elsevier B.V All rights reserved

1 Introduction

A wide variety of nanostructures of compound semiconductors

such as nanowires, nanotubes and nanorods have been reported

for oxides [1], nitrides [2], sulphides [3] and arsenides [4] Among

them, zinc oxide (ZnO) is a very important II-VI semiconductor with

a direct band-gap of 3.37 eV and a large exciton binding energy of

60 meV [5] In addition, it has many interesting properties includ-

ing near-ultra violet (UV) emission, transparent conductivity, and

piezoelectricity ZnO nano-materials are expected to be applied

widely in the manufacture of electrical devices, including transpar-

ent conducting electrodes in solar cells, flat panel displays, surface

acoustic devices, UV lasers and chemical and biological sensors

[6-10]

Many deposition methods have been used to fabricate ZnO

nanostructures [11-15] In most methods, complicated facilities

are required to fabricate a variety of nanostructures A simple

technique not involving complicated equipment with intricate

reactions might be a solution for the easy and economic platform

in ZnO nanostructure processing Some progress has been made

in this field with a variety of ZnO nanostructures being reported

* Corresponding author Tel.: +82 2 910 4643; fax: +82 2 910 4320

E-mail address: wgjung@kookmin.ac.kr (W.-G Jung)

0254-0584/$ - see front matter © 2008 Elsevier B.V All rights reserved

doi:10.1016/j.matchemphys.2008.07.108

[16-19] However, in these reports, the synthesis was performed at temperatures over 100°C or using an autoclave or other activator

In this study, a simple hydrothermal synthesis was developed

to produce self-assembled ZnO three-dimensional (3D) nanostruc- tures, and the morphology of the ZnO 3D nanostructures fabricated

at different pH in the synthesis solution was examined carefully This method includes only the reactions in aqueous solution at temperatures below 100°C Single crystalline ZnO nanostructures were fabricated without any supplementary equipment, such as an autoclave This method has many advantages over other chemical growth methods, i.e low cost, easy processing in large area and low temperature processing

2 Experimental

A solution of 0.17 mol zinc acetate dihydrate (Zn(CH3COOH)2-2H20) in 1000 ml deionised water was stirred at room-temperature for 20 min The solution was then adjusted to the desired pH by adding an aqueous solution of NH4OH droplets into

a well-stirred aqueous zinc acetate solution The pH of the mixed aqueous solution was controlled in the range from 9.0 to 11.8 The final solution was heated to 95°C on

a hot-plate During heating, the solution was stirred continuously When the aque- ous solution reached 95°C, a (100) Si substrate was dipped into the final solution for 120 min This growth time was used to ensure sufficient thickness of the ZnO nanostructures through the preliminary experiments After keeping the substrate

in aqueous solution for the desired time, the sample was washed several times in deionised water and dried with blowing nitrogen (Nz) gas

The ZnO nanostructures obtained were characterized by field emission scan- ning electron microscopy (FE-SEM, JEOL, JSM-7401F) The structural properties

390 J.-M Jang et al / Materials Chemistry and Physics 113 (2009) 389-394

os

As

al ig

Ƒ lỊ] = § = 8 Ẽc

5 | i | , #2 i + 228s §

~

= CN L se „2u VỀ | “3` `6

4 1 1 1 4 1 ¿ 1 4 1 4

20 30 40 50 60 70 80

2 theta (deg.)

Fig 1 X-ray diffraction patterns of the ZnO 3D nanostructures synthesized at dif-

ferent pH: (a) pH 9.0; (b) pH 9.5, 10.0; (c) pH 10.5, 11.0; (d) pH 11.5

were examined by X-ray diffraction (XRD, Bruker, D8) with Cu Ka radiation

(A= 1.540598 A) and high resolution transmission electron microscopy (HR-TEM,

JEOL, JEM-2100F) The optical properties were studied using a photolumines-

cence mapper (PL, Accent, RPM2000) with a Nd-YAG laser at a wavelength of

266nm

3 Result and discussion

The ZnO 3D nanostructures with various morphologies were

synthesized at pH 9.0-11.8 and 95°C in a hydrothermal process

Fig 1 shows the XRD patterns of the ZnO nanostructures synthe-

sized in solutions at different pH The patterns from the ZnO 3D

nanostructures shown in Fig 1 are in accordance with the typi-

cal wurtzite hexagonal structure in the reference data (JCPDS No

36-1451) The full width at half maximum (FWHM) of the main

peaks showed that the synthesized ZnO nanostructures were highly

crystalline, even though they had been prepared at temperatures

below 100°C A small peak at 20 = 53° corresponding to the Si sub-

strate was also observed No other peaks related to impurities were

detected in the pattern within the detection limit of XRD The

intensity from samples at pH 10.5, 11.0 and 11.5 was much higher

than that from samples at pH 9.0, 9.5 and 10.0 Because the same

growth time had been used for each preparation, it is estimated

that the growth rate of ZnO nanostructure in the pH 9.0, 9.5 and

10.0 solutions was much lower than that in the pH 10.5, 11.0 and

11.5 solutions This suggests a higher intensity in the XRD patterns

of the ZnO nanostructures at pH 10.5, 11.0 and 11.5 than at pH 9.0,

9.5 and 10.0

The preferential orientation of the ZnO crystallites at different

pH of solution was compared by calculating the relative texture coefficient (TC) using the following equation [20]:

IhkD/Is(hkD)

where N ¡is the number of diffraction peaks, l{h kl) and Io(h k]) are the integrated intensities corresponding to the (hk1) reflection of the sample containing the textured and randomly oriented crys- tallites, respectively A sample with randomly oriented crystallites presents aTC (hk J) of 1, while a larger value indicates an abundance

of crystallites oriented to the (hk!) plane Table 1 shows the calcu- lated texture coefficients for wurtzite ZnO samples synthesized in this work It is obvious that the (004) and (1 10) peaks have high texture coefficients when the pH of the solution was <10.0 The TCs for the (004) peak were 3.67 and 3.54, respectively, which are the highest values among the peaks observed in each sample On the other hand, the TC for the (100), (002), (101) and (103) peaks were larger then 1 when the pH was >10.0 When the pH was 11.5, the (1 00) peak showed the highest TC ofall diffraction peaks It was also observed that the TC of the (100) and (101) peaks increased with increasing pH For the (0 0 2) plane, the TC value increased with increasing pH in the lower pH range, showing a maximum value

at pH 10.5-11.0, and decreased at pH 11.5 As shown in Fig 2, the morphology of the ZnO nanostructures synthesized from the pH

>10.0 solutions shows a hexagonal shape nanorod-bundle From these observations, it was estimated that the morphology of the ZnO nanostructures were determined by competition between the values of TC (100), TC (101) and TC (002)

Fig 2 shows the FE-SEM images of the self-assembled ZnO 3D nanostructures, which were synthesized in an aqueous solution

at various pH The shape of the ZnO 3D nanostructures showed different morphologies for each sample depending on the solu- tion pH As shown in Fig 2(a-c), a budding flower shape ZnO was obtained from the solution at pH 9.0 and 9.5, and a blossom shape was recognized for processing at pH 10.0 Table 2 summarizes the morphology of the ZnO 3D nanostructures fabricated at different

pH using a hydrothermal process It was recognized from the FE- SEM images that the ZnO nanostructures formed at low pH were smaller and shorter At pH 10.5, the high magnification image in Fig 2(d) shows flower-shaped structures consisting of hundreds

of sharp-tipped hexagonal ZnO nanorods The diameter of these individual nanorods ranged from 200 to 300nm with a length of 3-4 um All the nanorods appeared to have originated from a single center arranging then in a spherical shape exhibiting a flower-like

Table 1

The texture coefficients of the different planes for the ZnO nanostructures synthesized at various pH

3 Indicates the highest texture coefficient at each growth condition.

Fig 2 FE-SEM images of the ZnO 3D nanostructures synthesized at different pH: (a) pH 9.0; (b) pH 9.5; (c) pH 10.0; (d) pH 10.5; (e) pH 11.0; (f) pH 11.5; (g) pH 11.8; (h) high magnification image of pH 11.8

morphology A similar morphology was observed in the samples

processed at pH 11.0 However, each ZnO nanorod at pH 11.0 had a

larger diameter and length than at pH 10.5 In Fig 2(e), the diam-

eter and length of the ZnO nanorod synthesized at pH 11.0 was

300-400 nm and 6-7 xm, respectively A similar flower-like mor-

phology was reported by Zhang et al in which growth occurred at

higher temperatures [21] Fig 2(f) shows the two types of ZnO 3D

nanostructures obtained while processing at pH 11.5 One type has

a similar morphology to that observed at pH 11.0, and the other

is a bundle of hexagonal ZnO nanorods that coalesced with each other, as shown in the inset in Fig 2(f) The spherical morphology shown in Fig 2(g) was obtained at pH 11.8 The image of the ZnO 3D nanostructure shows the sphere to consist of many bundles of ZnO nanorods which are similar to the bundles in the samples obtained

at pH 11.0 The magnified image in Fig 2(g) shows the hexagonal shape in the cross section of the coalesced ZnO nanorods

392 J.-M Jang et al / Materials Chemistry and Physics 113 (2009) 389-394

Table 2

Summary of shape of the ZnO 3D nanostructures fabricated in solutions at different pH using a hydrothermal process

Budding flower

As shown in Fig 2, the shape and morphology of the ZnO nanos-

tructures depends on the solution pH This behavior may indicate

the mechanism for the formation of this different morphology In

the lower pH solution, the leaf-like ZnO changed to a needle-like

shape with increasing pH, e.g very slender ZnO nanorods were syn-

thesized in pH 10.5 The diameter of the ZnO nanorods increased

with increasing pH This was attributed to the growth rates of spe-

cific planes of the ZnO nanorods At pH 10.5 and 11.0, the growth

rate for the (002) plane was large, and the growth rates of the

(100) and (110) planes increased at higher pH, resulting in a

hexagonal-shaped ZnO nanorod This was previously mentioned

and confirmed in the discussion of the texture coefficient in Table 1

The results showed that the crystallization and morphology of

ZnO nanostructures depend on the initial pH of solution Fig 3

shows the mechanism of ZnO formation in solution at different pH

It can be seen that ZnO formation is originated from the dehydra-

tion of Zn(NH3 )42* However, at pH <10.0, zinc cations (Zn(NH3 )42*)

transform easily to the zinc hydroxide (Zn(OH)2) precursor There-

fore, ZnO nanostructures nucleate in a heterogeneous system On

the other hand, when the pH is >10.0 through the addition of more

ammonia, all the zinc hydroxide dissolves resulting in the forma-

tion of a clear solution This behavior was demonstrated by the

observation that the aqueous solution became frosty with the for-

mation of white precipitates when a small amount ammonia water

was added The solution then turned clear after the addition of more

ammonia Therefore, the addition of more ammonia to the aqueous

solution to adjust the pH to 11.5 and 11.8, reduced the growth rate

of ZnO nanostructures by the large amount of Zn(OH)42~ because

the solubility of NH3 in this solution was lower [21] This resulted

in denser nanorods with a flat hexagonal shape under these growth

conditions

Fig 4 shows low and high magnification TEM images of a ZnO

nanorod synthesized at pH 10.5 with the selected area electron

diffraction (SAED) pattern The SAED pattern in Fig 4(a) shows the

Controlled pH by NH,OH

NH, + H,O

(Zinc acetate) Zn(CH,COO), - H,O

+

Deionized water

many single crystals of ZnO, and the inset in Fig 4(b) indicates them

to be single crystals The HR-TEM image in Fig 4(c) shows the appar- ently well-resolved lattice fringes of the ZnO nanorod crystals The interplanar spacing was measured to be 0.52 nm, which is equal to the lattice constant in the reference (JCPDS No 36-1451) for ZnO The SAED pattern in Fig 4(d) shows visible bright spots correspond- ing to all the crystal planes of the ZnO phase This indicates that the ZnO nanorod is a single crystal growing preferentially along the c-axis [0001]

Fig 5 shows the room-temperature photoluminescence spec- tra The spectra show a strong UV peak at approximately 374nm (3.33 eV) and a broad yellow emission ranging from 500 to 700 nm The PL data were not collected at 526 nm because of the secondary peak of the Nd-YAG laser A relatively very weak PL intensity was observed for the samples grown in the solutions at pH 9.0 and 9.5.A similar tendency was observed in the intensity of XRD patterns, as illustrated in Fig 1 The highest intensity was observed in the ZnO flower-like sample at pH 10.5, in which the morphology was most sharp The PL spectra show no shift in the PL peak in these ZnO 3D nanostructures due to a quantum confinement effect, probably due

to the large diameter and size of the nanostructures The position

of UV emission in Fig 5 is in accordance with that in the PL spec- tra for the samples fabricated by other investigators using a similar method [17,18,21] A weak and broad yellow emission near 600 nm (2.07 eV) was observed in the PL spectrum In particular, a relatively high intensity of yellow emission was observed in the samples grown at pH 9.0 and 9.5 This yellow emission was attributed mainly

to the recombination of electrons in the oxygen vacancies (Vo*) with the photo-excited holes in the valance band [22] This is strong evidence indicating an in increased concentration of oxygen vacan- cies The sharp excitonic emission and weak deep-level emission peak suggest that the ZnO flower-like nanostructures fabricated in the solutions at pH >10.0 have a lower defect concentration and high optical quality Overall, the best optical property and crystal

CH;COO- +H,O + CH,COOH + OH’ (1) Zn2++4NH, -> Zn(NH,)2+ (2)

Zn?+ + 40H: > Zn(OH),2 @)

i (NH,),2* + 20H: + id i (NH,),2* + 20H > ZnO+4N ae)

Đa

or?

pH <10.0

vie %

>O< - ắc

oF

PH 10.5 PH11.00 pH11.5 pH11.8

0.4 1/nm

Fig 4 HR-TEM images of the ZnO 3D nanostructure synthesized at pH 10.5: (a) an electron beam perpendicular to the wide surface; (b) a low magnification image of an individual ZnO nanorod; (c) high magnification image; (d) SAED pattern of an individual nanorod

—s—pH 95

= c[ †| | —v—pH 10.5 —s—pH 11.5

at

ieee $ \ 2” position ($26 nm) area

= = \ |

-

-

£ fT

—_

Wavelength (nm)

Fig 5 Room-temperature photoluminescence spectra from the ZnO 3D nanostruc-

tures grown in solutions of different pH (Aex =266 nm)

quality of self-assembled ZnO 3D nanostructure were obtained at

pH 10.5

4 Summary

Self-assembled Zinc oxide (ZnO) 3D nanostructures were fabri-

cated on a(1 00) Si substrate at 95°C using a simple hydrothermal

process in ammonia and zinc acetate dihydrate solutions The changes in morphology and the characteristics of the ZnO nanos- tructures were investigated at pHs ranging from 9.0 to 11.8 The texture was evaluated by the texture coefficient of the spe- cific planes in the ZnO nanostructures The change in shape was attributed to the growth rates of the specific planes in the ZnO nanostructure It was found that the solution pH is the main factor affecting the morphology of the ZnO nanostructure XRD and SAED showed that the ZnO nanostructures were single-crystalline with good crystallinity The PL spectra showed that the ZnO nanostruc- tures fabricated at pH >10.0 have good optical properties with a low defect concentration Overall, the best optical property and crystal quality of self-assembled ZnO 3D nanostructure were obtained at

pH 10.5

Acknowledgments This study was supported by the ERC (Center for Materials and Processes of Self-Assembly) program of MOST/KOSEF (R11- 2005-048-00000-0) and the Research Program 2008 of Kookmin University in Korea

Appendix A Supplementary data Supplementary data associated with this article can be found,

in the online version, at doi:10.1016/j.matchemphys.2008.07.108

394 J.-M Jang et al / Materials Chemistry and Physics 113 (2009) 389-394

References

[1] M.H Huang, S Mao, H Feick, H.Q, Yan, YY Wu, H Kind, E Weber, R Russo, P.D

Yang, Science 292 (2001) 1897

[2] W.-G Jung, S.-H Jung, P Kung, M Razeghi, Nanotechnology 7 (2006) 54

[3] J.H Zhan, X.G Yang, D.W Wang, S.D Li, Y Xie, Y Xia, Y Qian, Adv Mater 12

(2000) 1348

[4] J Noborisaka, J Motohisa, T Fukui, Appl Phys Lett 86 (2005) 213102

[5] C Klingshirn, Phys Status Solidi B 71 (1975) 547

[6] P Zu, Z.K Tang, G.K Wong, M Kawasaki, A Ohtomo, H Koinuma, Y Segawa,

Solid State Commun 103 (1997) 459

[7] D.M Bangall, Y.G Chen, Z Zhu, T Yao, Appl Phys Lett 70 (1997) 2230

[8] Y.C Kong, D.P Yu, B Zhang, W Fang, S.Q, Feng, Appl Phys Lett 78 (2001) 407

[9] Y Li, G.W Meng, L.D Zhang, F Philip, Appl Phys Lett 76 (2000) 2011

[10] K Omichi, K Kaiya, N Takahashi, T Nakamura, S Okamoto, H Yamamoto, J

Mater Chem 11 (2001) 262

[11] J.-Y Park, Y.-S Yun, Y.-S Hong, Appl Phys Lett 87 (2005) 123108

[12] H.-M Cheng, H.-C Hsu, Y.-K Tseng, L.-J Lin, W.-F Hsieh, J Phys Chem B 109

(2005) 8749

[13| X.H Zhang, Y.C Liu, X.H Wang, S.J Chen, G.R Wang, J.Y Zhang, Y.M Lu, D.Z Shen, X.W Fan, J Phys.: Condens Matter 17 (2005) 3035

[14] D Banerjee, J.Y Lao, D.Z Wang, J.Y Huang, Z.F Rena, Appl Phys Lett 83 (2005)

2061

[15] T Minemoto, T Negami, S Nishiwaki, H Takakura, Y Hamakawa, Thin Solid Films 372 (2000) 173

[16] U Pal, P Santiago, J Phys Chem B 109 (2005) 15317

[17] X Xia, Z Ye, G Yuan, L Zhu, B Zhao, Appl Surf Sci 253 (2006) 909 [18] Z Fang, K Tang, G Shen, D Chen, R Kong, S Lei, Mater Lett 60 (2006) 2530 [19] Z.Z Ye, F Yang, Y.F Lu, MJ Zhi, H.P Tang, L.P Zhu, Solid State Commun 142

(2007) 425

[20] C.S Barrett, T.B Massalski, Structure of Metals, Pergamon Press, Oxford, Eng- land, 1980 (Chapter 9)

[21] J Zhang, L Sun, J Yim, H Su, S Liao, C Yan, Chem Mater 14 (2002) 4172 [22] Z.L Wang, J Phys Condens Matter 16 (2004) R829.