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Photonic crystals in biology

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Poster Session, Tuesday, June 15<br />

Theme A1 - B702<br />

Prepar<strong>in</strong>g ZnO:Mn Nanoparticles: A Comparison Between Sol Gel and Gel Combustion Method<br />

Majid Ebrahimizadeh Abrishami, 1 Seyed Mohammad Hosse<strong>in</strong>i 1 , Ebrahim Attaran Kakhki 1 and Mahdi Ghasemifard 1<br />

1 Matterials and Electroceramics Lab., Department of Physics, Ferdowsi University, Mashhad, Iran<br />

Abstract— We prepared ZnO:Mn nanoparticles us<strong>in</strong>g two different routes which are sol gel and gel combustion. TEM images<br />

showed that the size of nanoparticles, prepared us<strong>in</strong>g gel combustion method, were 40% smaller than the other. The effect of<br />

synthesis process on structural and optical properties was <strong>in</strong>vestigated by XRD analysis and UV absorbance spectra.<br />

Z<strong>in</strong>c oxide (ZnO) holds a great position <strong>in</strong> fabricat<strong>in</strong>g the<br />

electronic devices due to remarkable electrical and optical<br />

properties such as piezoelectricity, controllable conductivity,<br />

large band gap energy (3.3eV), transparency <strong>in</strong> the visible<br />

range and etc [1,2]. Furthermore, ZnO is considered for<br />

sp<strong>in</strong>tronics applications with magnetic ions (Co, Ni, V, Fe and<br />

Mn) dop<strong>in</strong>g. In this direction, Mn doped ZnO has became a<br />

reasonable choice for Diluted Magnetic Semiconductors<br />

(DMS). Even, ferromagnetic state was reported below and<br />

above room temperature [3]. However, <strong>in</strong> recent years,<br />

synthesis of nanopowders of ZnO, MnO and dop<strong>in</strong>g ZnO with<br />

transition metals by different routes such as wet chemical<br />

methods like sol-gel [4], co-precipitation [5], and combustion<br />

[6] <strong>in</strong> nanotechnology is custom <strong>in</strong> worldwide.<br />

In this work, Zn 1-x Mn x O (x = 0.00, 0.06 and 0.10)<br />

nanoparticles were synthesized us<strong>in</strong>g two different wet<br />

chemical methods which are sol gel and gel combustion. The<br />

start<strong>in</strong>g materials were comprised of z<strong>in</strong>c and Mn acetates,<br />

diethanolam<strong>in</strong>e and acetic acid. Process of prepar<strong>in</strong>g cations<br />

solution with no particulates and precipitates, stable sol and<br />

clear gel <strong>in</strong> both methods were similar. In the sol gel method,<br />

the acceptable gel was fired directly on hot plate and<br />

calc<strong>in</strong>ated at 400C. But, we synthesized the ZnO:Mn<br />

nanopowders with add<strong>in</strong>g nitric acid as a fuel, <strong>in</strong> gel<br />

combustion method.<br />

TEM images presented that the ZnO:Mn nanoparticles,<br />

prepared us<strong>in</strong>g gel combustion method, were smaller <strong>in</strong> size.<br />

As shown <strong>in</strong> Figure, the acceptable homogeneity <strong>in</strong> size<br />

distribution and spherical shapes of particles were clearly<br />

observed <strong>in</strong> samples prepared us<strong>in</strong>g two different routes.<br />

Next, we <strong>in</strong>vestigated the structural properties of<br />

nanopowders us<strong>in</strong>g X-ray diffractometer. XRD patterns<br />

showed that all the samples were crystallized <strong>in</strong> s<strong>in</strong>gle phase<br />

wurtzite structure and no impurity phases were explored. In<br />

other words, the Mn solubility was clearly <strong>in</strong>creased.<br />

Furthermore, the Full Width at Half Maximum (FWHM) of<br />

XRD reflection peaks were more broadened <strong>in</strong> samples<br />

prepared us<strong>in</strong>g gel combustion method. In addition, XRD<br />

analysis confirmed that the growth <strong>in</strong> Mn concentration<br />

resulted <strong>in</strong> <strong>in</strong>creas<strong>in</strong>g lattice parameters <strong>in</strong> samples<br />

synthesized us<strong>in</strong>g both techniques.<br />

Also, we consider the optical properties us<strong>in</strong>g UV<br />

diffractometer. UV absorbance spectra of all nanopowders<br />

have only one characteristic peak which is gradually shifted to<br />

lower wavelengths with <strong>in</strong>creas<strong>in</strong>g Mn content. This peak<br />

illustrates the optical absorbance edge. In this case, we<br />

determ<strong>in</strong>ed the optical band gaps E g of samples us<strong>in</strong>g Morales<br />

approach [7]. This <strong>in</strong>vestigation showed the decreas<strong>in</strong>g E g<br />

with <strong>in</strong>creas<strong>in</strong>g Mn content. However, the values for E g ,<br />

extracted from UV absorbance spectra of nanoparticles<br />

prepared us<strong>in</strong>g gel combustion method, were more severely<br />

decreased with <strong>in</strong>creas<strong>in</strong>g Mn content.<br />

Table. The variation <strong>in</strong> structural and optical properties of ZnO:Mn<br />

nanopowders due to Mn dop<strong>in</strong>g and synthesis process.<br />

Sol gel<br />

Gel Combustion<br />

Mn content (x) 0.00 0.06 0.10 0.00 0.06 0.10<br />

latt. const. a (Å) 3.247 3.248 3.249 3.246 3.247 3.248<br />

latt. const. c (Å) 5.198 5.201 5.202 5.196 5.199 5.201<br />

absorb. edge (nm) 379.9 382.9 385.9 370.0 395.0 410.0<br />

E g (eV) 3.22 3.14 3.12 3.22 3.10 3.02<br />

Figure: TEM images of ZnO nanoparticles prepared us<strong>in</strong>g (a) sol gel<br />

method. (b) gel combustion method.<br />

In summary, we showed that different routes to prepare<br />

nanoparticles have effect on structural and optical properties.<br />

Our results open a new w<strong>in</strong>dow to control the synthesis<br />

process, size of particles, lattice constant changes and band<br />

gap energy variations and etc.<br />

*Correspond<strong>in</strong>g author: ebrahimizadeh@ymail.com<br />

[1]M. Ohtaki, K. Araki and K. Yamamoto, J. Elect. Mater. 38, 1234<br />

(2009).<br />

[2]S. S. Kwon, W. K. Hong, G. Jo, J. Maeng, T. W. Kim, S. Song and<br />

T. Lee, Adv. Mater. 20, 4557 (2008).<br />

[3]M. Ebrahimizadeh Abrishami, S. M. Hosse<strong>in</strong>i, E. Attaran Kakhki<br />

and A. Kompany, Mod. Phys. Lett. B, <strong>in</strong> press (2010).<br />

[4]Q. Xu, S. Zhou and H. Schmidt, J. Allo. and Comp.,<br />

doi:10.1016/j.jallcom.2009.08.033.<br />

[5] R. S. Yadav, A. C. Pandey, S. S. Sanjaya, Chalcogenide Lett. 6,<br />

233 (2009).<br />

[6]N. Riahi-Noori, R. Sarraf-Mamoory, P. Alizadeh and A.<br />

Mehdikhani , J. Ceram. Process. Res. 9, 246 (2009).<br />

[7]A. E. Morales, E. S. Mora and U. Pal, Revista Mexicana de<br />

F´isicas, 53, 18 (2007).<br />

6th Nanoscience and Nanotechnology Conference, zmir, 2010 288

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