The International Journal of Engineering And Science (IJES) ||Volume|| 1 ||Issue|| 1 ||Pages|| 22-29 ||2012|| ISSN: 2319 1813

3 ISBN: 2319 1805

Evaluation Of Microstructural Paramaters Of The Synthesised Teo2 Nanocrystals Using Xrd Principles
A.Sinthiya
Depart ment of Physics, St. Josephs College(Autonomous), Trichy -620 002, Tamil Nadu, Ind ia .

----------------------------------------------------------Abstract----------------------------------------------------------------The synthesised -TeO2 nanocrystalshave been indexed in orthorhombic system with lattice energy 81.21 eV. Strain is caused by the presence of dislocations. This has possibility to have dislocations in nanoscale has little significance. The X-ray peak profile study provides peak broadening and asymmet ric peak shapes and to understand the micro structural parameters for crystallite size and strain. Present work deals with systematic application of Hall-Williamson method for crystallite size estimation, and the modified Williamson -Hall p lot and the modified Warren-Averbach methods yielded physically well justified data for particle size and dislocation densities. The reflections {020}{151} and {002} have the same peak breadth and reflections while {120}{101}{200} and {122} have more or less same peak breadth. The successful application of the new procedures have indicated that even in nanocrystalline particles dislocations are present.

Keyword: Lattice energy, M icro structural parameters, Crystal size and strain, Nanocrystalline Date of Submission: 07, November, 2012 I. Introduction

particles dislocations. ----------------------------------------------------------------------------------------------------------------------------------------

Date of Publication: 10, November 2012

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The microstructure of nanomaterials and its relation to macroscopic properties is essential for the development and application of nanomaterials. The structure of TeO 2 -based glasses, are promising materials for use in optical fibre o r in non-linear optical devices [1]. X-ray diffract ion is a pro mising tool for structural analysis of solid or amo rphous materials and approaches such as use of Sherrer equation, integral breadth analysis, single-line approximat ion, Hall-Williamson method, etc., have been developed for estimation of crystallite size. Nu merous experiments have shown that the strain broadening caused by dislocations can be well described by a special logarith mic series expansion of the Fourier coefficients of Bragg reflect ion peak profiles. X-ray diffraction peak pro file analysis is used for the characterization of microstructure either in the bulk or in loose powder materials, which is a nondestructive method yielding a series of interesting microstructural parameters[4].Present work deals with systematic application of Hall-Williamson method for the estimation of crystallite size and the strain [2] of the synthesised -TeO2 nanocrystals. Also incorporation of the classical methods of Williamson Hall and Warren Averbach and the modified Williamson Hall a nd modified Warren Averbach methods, for the analysis of particle size and dislocation densities as suggested by Ungar[3] have been attempted for -TeO2 .

II.

Experimental

Grey color Telluriu m metal was mixed in lime water (10ml) and 16 drops of nitric acid was added to it, and after a day, yellow co lor mineral telluriu m d io xide was obtained at room temperature. After 20 days grown crystals were filtered and dried at roo m temperature. Lime water helps to spread the ions evenly. III. Results And Discussion 2.1 Powder XRD pattern The powder sample subjected to X-ray diffracto meter within 2 range of 20-60 at a scan speed of 7 per minute using a Cu target and Cu-K radiation of 0.15406 nm wavelength at a powder rating of 40kV, 40mA using Brukker D8 diffracto meter. The XRD pattern (Fig. 1a) has been indexed in Table 1 falls in the orthorhombic system whose unit cell parameters are tabulated in Table 2.

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Evaluation Of Microstructural Paramaters Of The Synthesised -Teo2 Nanocrystals

A bar diagram is drawn between I/I max and , which is shown in Figure- 1b, suggests that for the plane {020} the density of atom is high compared to other planes and the least in the plane {15 1}. The density of atoms present in one plane is calculated fro m the fo rmula = , where d is the spacing between each plane, N the number of atoms in the unit cell and V the volu me of the atom[6]. 2.2Cohesi ve energ y of i onic crystal -TeO2 Cohesive energy of an ionic crystal can be determined used even if the crystal structure is not known with the help of Kapustinskii equation [15]. Kapustinskii noted an emp irical increase in the value of Madeling constant, A, as the coordination number of the ions in the molecular formu la of the compound. Any deviation in the rule is compensated by a consequent change in the value of Re (the sum of the ionic radii for the cation and anion) and the reduced Madelung constant proposed by Kapustinskii (A div ided by the number of ions in the formula) to calculate the lattice energy of an ionic crystal to a good approximat ion, no matter what its geometry may be.Kapustinskii collected the reduced Madeulang constant [15], the length conversion factor , and the energy conversion factor into a simple form o f lattice energy equation U. U={ 287.2 v/( + )}*{1-(0.345/( + ))} kcal/ mo l --- (1) whereZc, Za are the charge on cation and anion, + the ionic radii, and v the number of ions in the molecule. This is calculated to be 81.21eV for -TeO2 . 2.3 Methods of profile anal ysis For the case that the strain is caused by dislocations, Wilkens computed the mean square strain, assuming that the dislocations are restricted rando mly and distributed [7][8][9],

<

>=

ln {

--- (2)

where the b is the length of burger vector, the dislocation density, R e the outer cut-off radius and C is the contrast factor of the dislocations.The contrast factor depends on the relative orientation of line -burgers- and diffraction vector as well as the elastic constants of the material. Because of the actual dislocation distribution in a sample, it is necessary to average over the screw dislocations, different slip systems and orientation of the slip system with respect to the diffraction vector, denoting the average contrast factor by C. Ungar and Tichy [10], showed that for cubic or hexagonal crystals, if the burgers vector distribution is completely random, the dependence of C on the hkl can be exp licit ly calculated.The intensity of the profile is given by the convolution of size and strain broadening. Thus in Fourier space, it is possible to separate the contributions via the well knownWarren-Averbachequation . ln A L = ln + ln --- (3)

Here A L are the Fourier coefficient computed fro m the profile, and are the coefficients associated with size broadening and strain broadening respectively. The strain broadening coefficients are computed using the relation = exp (-2 2 L2 g 2 < >) --- (4) > is the mean square strain. It depends on the

where L is the Fourier length, g is the diffraction vector and < diffraction order and vanishes for g 2 =0.

Inserting Eq.(4 & 5) in Eq.(3) g ives the modified WarrenAverbach equation [11].

ln A L = ln + L2 b 2 C ln ( ) --- (5) If the strain is caused by dislocations, then the modified Warren -Averbach analysis suggest that ln AL must be plotted against g 2 C instead of g 2 . The successful application of this scheme to TeO2 result a smooth curve is shown in Fig 2.

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Evaluation Of Microstructural Paramaters Of The Synthesised -Teo2 Nanocrystals

2.4 Crystallite size estimation According to the Scherrer equation [14], the broadening due to small crystallite size may be expressed as = k / t cos . --- (6) where is the broadening, solely due to small crystallite size, k a constant whose value depends on particle shape and usually taken as 1.0, t the crystallite size in nanometers, the Braggs angle and the wave length of incident X-ray beam in n m. It is found for the synthesized TeO2 nanostructured material the calculated crystallite size is 170.627 n m for K=1 and crystallite size is 153.565n m for K= 0.9. The Hall-Williamson method is a more accurate method than Scherrer equation for crystallite s ize estimation of powder samples in view of the ability of the former approach to measure pure breadth of the diffraction peaks i.e., that solely due to smaller crystallite size [2] The total peak broadening is given by cos = + sin ---(7) where is the strain distribution. Fig. 3 shows a plot of Brcos versus sin with the linear fit yields the slope = 0.58065 for the target, with the wavelength of the incident X-ray beam used in 0.154 n m. Fo llo wing this, the evaluated crystallite size calculated fro m the intercept is 53.18n m for K=1 and t =47.865n m for K = 0.9.The peak breadths of the {020}{101}{120}{200}{002}{122} and {151} reflections, scaled in terms of cos, where and are the Bragg angle and half of the FWHM, respectively are shown in Figure 4 with average contrast factors according to modified Williamson Hall p lot resulting a slope 0.06487, obtained from the linear fit. The reflections {020}{151} and {002} have the same peak breadth and the reflections {120}{101}{200} and {122} have more or less same peak breadth. This conforms that the peak profiles has peak broadening and asymmetric peak shapes. 2.5 Grain size and dislocation densities Irrespective of diffract ion order, for size broadening and dependence on strain broadening, Williamson and Hall suggested that the FWHM of diffract ion peak profiles can be written as the sum of the two broadening effects [12]. It is expressed as K = 0.9/D + KD --- (8) D where K is the strain contribution to peak broadening and D is the average grain size or particle size. Here K= 2 sin/, K = 2 cos /,( , , and are the diffraction angle, half of the FWHM of the diffract ion peak and the wavelength of X-rays, respectively) and g = K at the exact Bragg position. In the conventional Williamson Hall p lot, it is assumed that KD is either a linear or quadratic function of K [12]. It is exp ressed as K = 0.9/D + (Ab 2 /2) (KC) + (A'b 2 /2) Q (K2 C) --- (9)

where A and A' are the parameters determined by the effective outer cutoff radius of dislocations, b the burger vector of dislocations, C the contrast factor, the dislocation density and Q correlation factor. Eq. (9) shows that if dislocations are the source of strain in a crystal the proper scaling factor of the breadths (or FWHM) of the peak profiles is (KC) instead of merely K. The FWHM according to conventional Williamson- Hall p lot is shown in Fig 5. The unsymmetric FWHM fo llo w an apparently unsystematic behaviour as a funct ion of diffraction vector K (or g). Plotting the same data of FWHM according to the modified Williamson -Hall p lot , a smooth curve is obtained as expected from Eq.(2) and it is shown in Fig.6The average contrast factors corresponding to the most common type of edge and screw dislocations in f.c.c and b.c.c crystals were evaluated as a function of the elastic constants of crystals in a wide range of the elastic anisotropy, A i [ where A i = 2C44 /(C11 C12 ) and Cij are the elastic constants] in the range of 7.2405. C or q = a{1-exp (-A i /b)} + c A i + d --- (10) where the parameters a,b,c and d are fitted to the calculation. The C factors were averaged by assuming that all slip systems permitted in given crystal are equally populated , and that edge and the screw dislocations are present with equal probability. The contrast factors were calculated using the following elastic constants for TeO2 C11 = 29.6 GPa, C12 = 21.7 GPa and C44 = 28.6 [13].The average C factor used in the present evaluation is listed in Table 3. The insertion at K = 0 of the curve in Fig. 6 fitted by the standard least square method provides a particle size to be D =12.6275 n m. 2.6 Scatter matri x To account the grain size of the sample the study on the peak profile is important. The peak profiles of the observed reflections of the specimen, in the form of scatter matrix are shown in Figure 7. It is the topographical view to study the relation between the intensities and their corresponding K. It is observed that

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Evaluation Of Microstructural Paramaters Of The Synthesised -Teo2 Nanocrystals

except {151} reflection all other reflections are confined, the correspond ing intensities are normalized to and centered around the maxima of the profiles. The FWHM of {101} and {120} reflections are identical within the experimental error. Similarly the FWHM of {020} and {151} reflections are identical.

IV.

Conclusions

Though every method has its advantages and disadvantages, yet they are independent to determine set of quantities/parameters. It is always useful to make use of all possibilities of evaluation thereby enhancing the accuracy of the results as well as identifying better procedure. The system has been indexed analytically with reference to[13], in orthorhombic system yields lattice energy as 81.21 eV. For the plane {020} the density of atom is high compared to other planes with the least in{151}. Strain is caused by the presence of dislocations. This has possibility to have dislocations in nanoscale has little significance.The perfect applicability of modified Williamson-Hall plot indicates that in the nanocrystalline -TeO2 , strain is caused by the presence of dislocations. This has to be considered as a clear answer to the question raised in the debate about the possibility to have dislocations in nanoscale.Fro m the conventional Williamson Hall plot the calculated = 0.58065 fro m the slope is very close to the both theoretical value and the cf.[13]. Thus in the sequence of length scales, it is established that grain size is less than crystallite size. The crystallite size is certainly the smallest length scale in microstructure, which is not directly related to dislocation densities or distances between dislocation. Table 4 summarises the calculated grain size and crystallite size of -TeO2 .Fro m the conventional Williamson Hall p lot, the reflections {020}{151} and {002} have the same peak breadth and the reflec tions while {120}{101}{200} and {122} have more or less same peak breadth. The peak profile has peak broadening and asymmetric peak shapes and this value provides the micro structural parameters for crystallite size and strain.Fro m the modified Warren-Averbach analysis, including the contrast factor we got the smooth curve and thus it conforms that the strain is caused by dislocations.

V.

Acknowledgements

We are thankful to Sastra university, Tanjore, Tamil Nadu, India for the Powder XRD data collection , and to our Institution for providing the opportunity to carry out the work. List of symbols Gamma -TeO2 Meta stable form of Telluriu m Dio xide eV Electron volt ml milli liter XRD X-ray diffraction Cu Copper target K Radiat ion line due to energetic K-electrons nm Nano meter kV Kilo volt mAM illi A mpere Teta d Inter planar distance Angstrom Un it I Intensity Imax Maximu m intensity Density of atoms in one plane g/cm1 Grams per centimeter inverse Density of the unit cell

N Nu mber of ato ms in unit cell hkl miller indices ln Lograthemic expansion eq. Equation FWHM Full width half maximu m f.c.c Face centered cubic crystals b.c.c Base centered cubic crystals GPa Giga Pascal Eta

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Evaluation Of Microstructural Paramaters Of The Synthesised -Teo2 Nanocrystals Reference

[1]. Vogel .E.M.; Weber .M.J.;Krol.D.M .;Phys. Chem. Glasses, 1991, 32,pp 231. [2]. Rehani et al., Crystallite size estimation by XRD principles, Indian J. Pure&Appl.Phys., Feb2006 , 44,pp 157-161. [3]. T.Ungar, Strain broadening caus ed by dislocations, Copyright (C) JCPDS - International center for diffraction data 1997. [4]. Michael B. Kerber et al., Rev.Adv.Mater.Sci. 2005, 10,pp 427-433. [5]. T.Ungar, Material Science and Engineering ,2001 , A309-310,pp 14-22. [6]. M.A.Wahab,Solid State Physics, Second edition (2010), Narosa publishing House, New Delhi, pp 36. [7]. M.Wilkens et al.,Phys.Stat.Sol.,1970, A2, pp 359. [8]. M.Wilkens, In: Fundamental Aspects of Dislocation theory, Vol II, ed. By J.A Simmons,R. de lt and R.Bu llough [Nat. Bu r. Stand. (US) Spec. Publ. No. 317, Washington D.C., 1970], pp. 1195. [9]. M.Wilkens et al.,Phys. Stat.Sol. , 1987, A 104, ppK1. [10]. T.Ungarand G. Tichy et al., Phys.Stat.Sol.,1999, (a) 171,pp 425. [11]. T.Ungar and A.Borbely et al., Appl. Phys. Lett..1996, 69,pp3173. [12]. G.K. W illiamson and W.H. Hall, Acta metal. 1953, 1, pp 22. [13]. J.C. Champarnaud-Mesjard ,J.of Physical and chemistry of solids, 2000, 61, pp 1499-1507. [14]. Scherrer P, Math Phys K,1981, 1 , pp 98. [15]. M.A.Wahab,Solid State Physics, Second edition, Narosa publishing House, New Delhi, 2010;pp 66

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