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The International Journal Of Engineering And Science (IJES)
|| Volume || 4 || Issue || 8 || Pages || PP -01-04 || 2015 ||
ISSN (e): 2319 – 1813 ISSN (p): 2319 – 1805
www.theijes.com The IJES Page 1
Growth and Structural studies of Zn doped L-Threonine
single crystal
1
S.Antony Dominic Christopher , 2
Dr.N.Neelakanda Pillai
(1)
Senior Lecturer, Noorul Islam Polytechnic College, Punkarai, Thiruvithancode Post ,TamilNadu, India.
(2)
Associate Professor, Aringnar Anna College,Aralvaimozhi post, Tamilnadu, India.
----------------------------------------------------------ABSTRACT-----------------------------------------------------------
Non linear optical phenomenon in material plays a major role in the emerging photonics and opto
electro technologies. In the search of new and efficient NLO material in organic element (Zn) doped L-
Threonine organic crystal were grown in the present study. The grown crystals were characterized by measuring
the density by floatation technique. The structure of the crystals were studied by FTIR spectrum. The lattice
parameters of pure and doped crystals were calculated from SXRD and PXRD respectively. The lattice
parameters shows the crystal belong to orthorhombic system
---------------------------------------------------------------------------------------------------------------------------------------
Date of Submission: 29 July 2015 Date of Accepted: 10 August 2015
---------------------------------------------------------------------------------------------------------------------------------------
I. Introduction
Recently much attention has been paid non-linear optical (NLO) materials mainly because of their
interacting potential applications. The compound of this type can be used in LASER technology, optic
communication and optical switching. Also, the NLO plays an important role in the merging photonic and opto
electronic technologies. The NLO properties of large organic molecules and polymers have been the subject of
extensive theoretical and experimental investigations during the past two decades [1]. Organic materials possess
several advantages compared with the traditional inorganic NLO materials like ADP, KDP and KTP such as
large second harmonic conversion efficiency birefringence and dispersion of refractive index which are finding
increase in use in the development of new photonic devices [2]. However, their often inadequate transparency,
poor optical quality and lack of robustness, low laser damage threshold and inability to grow to large size have
impeded the use of single crystal organic materials in practical device applications. Hence recent research is
concentrated on semi-organic materials due to their large non- linearity, high resistance to laser induced damage,
low angular sensitivity and good mechanical hardness. L-Threonine is a pure organic material. Mixing of
inorganic material may change the quality of the organic crystals. So, In the present study the Zinc Sulphate has
been doped instead of mixing in the L-Threonine single crystal to overcome the disadvantage of organic NLO
materials. L-Threonine is an important amino acid, which shows higher SHG(Second Harmonic Generation)
efficiency than that of many other non linear amino acids. Also it is an important polar amino acid and its
dipole moment is nearly similar to water [3]. Several work has been done in L- Threonine single crystal [4-10].
In the present study Zinc Sulphate doped L- Threonine crystal was grown and characterized. The results were
discussed here.
II. Experimental Details
Commercially available AR grade L-Threonine, ZnS𝑂4 and doubly distilled water were used to prepare
the solution. Saturated solution of L-Threonine was prepared at 35℃ according to the solubility data available in
the literature [11]. Pure and ZnS doped L-Threonine single crystals were grown from aqueous solution by slow
evaporation technique for the various dopant concentration ratio viz.1:0.002, 1:0.004, 1:0.006, 1:0.008 and
1:0.01. In the present study, totally six crystals were grown. The density of all the grown crystals were
determined by flotation technique. Carbon tetra chloride of density 1.594 gm/cc and Bromoform of density
2.890gm/cc were used as lower and higher density liquids respectively. The concentration of zinc atom
incorporated into the doped crystals were confirmed by the EDAX spectrum. The FTIR spectrum were recorded
to find the functional groups present. Powder X-ray diffraction data were collected by using an automated X-ray
powder diffractometer with scintillation counter and monochromatic copper 𝐾∝ wavelength (𝜆 =1.5406 Å)
radiation. The reflections were indexed following the procedures of Lipson and Steeple [12].SXRD was also
taken for the pure L-Threonine crystal for comparison.
Growth and Structural studies of Zn doped…
www.theijes.com The IJES Page 2
III. Results and Discussion
The photograph of all the pure and doped crystals of L-Threonine are shown in figure 1. All the
crystals grown in the present study are transparent and good quality crystals. All the crystals grown in c-
direction, needle shaped crystals are about 20 mm were grown.
Fig 1: Photograph of Pure and doped L-Threonine crystals
The densities of all the grown crystals are provided in table 1. The density of pure L-Threonine
measured in the present study agreed with the value reported by 1.3079gm/cc [13]. The densities of doped
crystals are greater than the pure L-Threonine crystal. This shows the incorporation of dopant atoms into the
host lattice. EDAX spectrum shown in the Fig 2 also confirms the incorporation of Zn atoms into the host
lattice.
Table 1: Values of density of pure and doped L-Threonine crystals
System Density gm/cc
Pure L-Threonine 1.30
Doped L-Threonine
1:0.002 Zn
1:0.004 Zn
1:0.006 Zn
1:0.008 Zn
1:0.010 Zn
1.308
1.362
1.338
1.380
1.350
Fig 2: EDAX spectrum of doped L-Threonine 1:0.008Zn
The FTIR spectrum of pure L-Threonine crystal is shown in fig 3. FTIR spectrum were recorded for all
the grown crystals in the range 4000cm-1
to 400 cm-1 .
The broad band observed in the range 3169.15 and
2874.03 cm-1
are due to hydrogen vibration of ammonia group. The bend observed at 2048.47 cm-1
is assigned
to nitrate . The bend observed at 1627.97cm-1
is assigned to asymmetric bending of NH3 . The bend observed at
1481.38 cm-1
assigned to CH2 bend. The bend observed at 1456.30 cm-1
is assigned to CH3 bend. The bend
observed at 1417.73 cm-1
is assigned to symmetric structure of CO2 [14].The bend observed in the range
1346.36 and 1247.99 cm-1
are due to bending vibration of CH group. The peaks observed at 1184.33 and
1112.96 cm-1
is assigned to rocking of NH3 structure . The peak observed at 1039.67 cm-1
is assigned to C-N
stretching . The bend observed at 869.92 cm-1
is assigned C-C-N stretching. The peak observed at 769.62 cm-1
is
assigned to CO2 bending. The bend observed at 700.18 cm-1
is due to wagging of CO2structure. The bend
observed at 559.38cm-1
is assigned to rocking of CO2. The peak observed at 489.94 cm-1
is assigned to
torsional mode of NH3.The bends observed at 416.64 and 443.64cm-1
are assigned to C-H rock.
Growth and Structural studies of Zn doped…
www.theijes.com The IJES Page 3
Fig 3: FTIR spectrum of pure L- threonine crystal
Fig 4: PXRD of 1:0.002 Zn doped L-Threonine crystal
Single crystal X-ray diffraction studies of pure LThreonine single crystal was carried out using Bruker
Kappa Apex II. The crystallography data obtained from single crystal X-ray diffraction of pure L-Threonine
crystal is presented in table (2). From these data, it was observed that the crystal belongs to orthorhombic
system with lattice parameters a=5.140 Å, b= 7.738 Å and c=13.546 Å and a space group P212121. The values
obtained in the present study are closed agreement with the reported values[15].Analysis of powder X-ray
diffraction data assuming the crystal structure and lattice parameters values obtained from single crystal SXRD
taken in the present study, by the available methods [16].The PXRD pattern of 1:0.002 Zn doped L-Threonine
crystal is shown in Fig 4. The peaks were indexed for doped L-Threonine crystal. The lattice parameters, thus
calculated from the PXRD for doped crystals are also provided in table 2.From the table it is found that there is
a slight variation in the lattice parameters of Zn doped L-Threonine crystals. This shows that there is a distortion
in the lattice due to dopant addition
Table 2: Values of lattice parameters of pure and doped L-Threonine
System Lattice Parameters Volume
(Å)3
a (Å) B (Å) C (Å)
SXRD for
Pure L-
Threonine
5.140
[5.139]
7.738
[7.723]
13.546
[13.579]
538.769
[538.9]
[15]
PXRD for Doped L- Threonine
1:0.002Zn
1:0.004Zn
1:0.006Zn
1:0.008Zn
1:0.010Zn
5.042
4.914
4.918
4.815
4.941
7.784
7.785
7.760
7.880
7.748
13.680
13.414
14.113
13.316
13.556
536.928
513.151
538.626
506.910
518.977
IV. Conclusion
Crystals grown in the present study are orthorhombic in structure. The density of the doped crystals
vary slightly from that of pure crystal. The incorporation of dopant atom into the host lattice is confirmed by
EDAX spectrum.
Growth and Structural studies of Zn doped…
www.theijes.com The IJES Page 4
V. Acknowledgement
The authors are grateful to the authorities of Sophisticated Analytical Instruments Facility(SAIF,
Cochin)
References
[1] V.Crasta.V.Ravindrachary S.Lakshmi, S.N. Prasad. M.A.Shudar. J.S. Prasad J. Crystal Growth (2005) e329.
[2] L.I.Zlendeng.W.I.J>Biachang S.U.Gento. J Crystal Growth 178 (1997) 539.
[3] M.H.Jiang.Q.Fang.Organic and Semi Organic non linear optical material Adv.mamater II (1999) 1147-1151.
[4] J. Madhavan and S. Ezhilarasi . International journal of scientific of Engineering Research volume 5,issue 3, March 2014.
[5] D.Subashini etal. .Advances in applied science research, 2013 4(2):238-242.
[6] G. Ramesh Kumar etal. Volume issue 9. May 2008, pages 1405-1409.
[7] S.Kalainathan. International journal of chem. Tech Research vol4, No.4 PP 1478-1484.Oct- Dec 2012.
[8] Ramesh Kumar etal. Advances in Material Science And Engineering (2009) Article Id 704294.
[9] R.Umaheswaria. Indian journal of research volume 2 issue 11. Nov.2013.
[10] S.Masilamani etal.Arabian Journal of Chemistry (2014).
[11] C.Ramesh Kumar.S.Gokul Raj R.Mohan R.Jayavel.J. Crystal Growth 275 (2005) e1947
[12] H.Lipson, H.Steeple, Interpretation of X-ray Powder Diffraction Patterns, Macmillan, New York 1970.
[13] www.guide chem.com/dictionary/en/72-19-shtml
[14] Silva.B.L Freire.P.T.C., Melo.F.E.A, Guedes.I, Araujo Siva. M.A. Medes Filho.I, Moreno.A.J.D, Braz. J.phys 1998 vol
28,n1
[15] Rameshkumar.G, Gokkul Raj.S, Mohan.R, Jeyavel.R, J.crystal Growth, 2005, no1-2 pp.el 1947- e1951
[16] B.E.Warren, X-ray Diffraction, Addison Wesley, California, 1969.

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Growth and Structural studies of Zn doped L-Threonine single crystal

  • 1. The International Journal Of Engineering And Science (IJES) || Volume || 4 || Issue || 8 || Pages || PP -01-04 || 2015 || ISSN (e): 2319 – 1813 ISSN (p): 2319 – 1805 www.theijes.com The IJES Page 1 Growth and Structural studies of Zn doped L-Threonine single crystal 1 S.Antony Dominic Christopher , 2 Dr.N.Neelakanda Pillai (1) Senior Lecturer, Noorul Islam Polytechnic College, Punkarai, Thiruvithancode Post ,TamilNadu, India. (2) Associate Professor, Aringnar Anna College,Aralvaimozhi post, Tamilnadu, India. ----------------------------------------------------------ABSTRACT----------------------------------------------------------- Non linear optical phenomenon in material plays a major role in the emerging photonics and opto electro technologies. In the search of new and efficient NLO material in organic element (Zn) doped L- Threonine organic crystal were grown in the present study. The grown crystals were characterized by measuring the density by floatation technique. The structure of the crystals were studied by FTIR spectrum. The lattice parameters of pure and doped crystals were calculated from SXRD and PXRD respectively. The lattice parameters shows the crystal belong to orthorhombic system --------------------------------------------------------------------------------------------------------------------------------------- Date of Submission: 29 July 2015 Date of Accepted: 10 August 2015 --------------------------------------------------------------------------------------------------------------------------------------- I. Introduction Recently much attention has been paid non-linear optical (NLO) materials mainly because of their interacting potential applications. The compound of this type can be used in LASER technology, optic communication and optical switching. Also, the NLO plays an important role in the merging photonic and opto electronic technologies. The NLO properties of large organic molecules and polymers have been the subject of extensive theoretical and experimental investigations during the past two decades [1]. Organic materials possess several advantages compared with the traditional inorganic NLO materials like ADP, KDP and KTP such as large second harmonic conversion efficiency birefringence and dispersion of refractive index which are finding increase in use in the development of new photonic devices [2]. However, their often inadequate transparency, poor optical quality and lack of robustness, low laser damage threshold and inability to grow to large size have impeded the use of single crystal organic materials in practical device applications. Hence recent research is concentrated on semi-organic materials due to their large non- linearity, high resistance to laser induced damage, low angular sensitivity and good mechanical hardness. L-Threonine is a pure organic material. Mixing of inorganic material may change the quality of the organic crystals. So, In the present study the Zinc Sulphate has been doped instead of mixing in the L-Threonine single crystal to overcome the disadvantage of organic NLO materials. L-Threonine is an important amino acid, which shows higher SHG(Second Harmonic Generation) efficiency than that of many other non linear amino acids. Also it is an important polar amino acid and its dipole moment is nearly similar to water [3]. Several work has been done in L- Threonine single crystal [4-10]. In the present study Zinc Sulphate doped L- Threonine crystal was grown and characterized. The results were discussed here. II. Experimental Details Commercially available AR grade L-Threonine, ZnS𝑂4 and doubly distilled water were used to prepare the solution. Saturated solution of L-Threonine was prepared at 35℃ according to the solubility data available in the literature [11]. Pure and ZnS doped L-Threonine single crystals were grown from aqueous solution by slow evaporation technique for the various dopant concentration ratio viz.1:0.002, 1:0.004, 1:0.006, 1:0.008 and 1:0.01. In the present study, totally six crystals were grown. The density of all the grown crystals were determined by flotation technique. Carbon tetra chloride of density 1.594 gm/cc and Bromoform of density 2.890gm/cc were used as lower and higher density liquids respectively. The concentration of zinc atom incorporated into the doped crystals were confirmed by the EDAX spectrum. The FTIR spectrum were recorded to find the functional groups present. Powder X-ray diffraction data were collected by using an automated X-ray powder diffractometer with scintillation counter and monochromatic copper 𝐾∝ wavelength (𝜆 =1.5406 Å) radiation. The reflections were indexed following the procedures of Lipson and Steeple [12].SXRD was also taken for the pure L-Threonine crystal for comparison.
  • 2. Growth and Structural studies of Zn doped… www.theijes.com The IJES Page 2 III. Results and Discussion The photograph of all the pure and doped crystals of L-Threonine are shown in figure 1. All the crystals grown in the present study are transparent and good quality crystals. All the crystals grown in c- direction, needle shaped crystals are about 20 mm were grown. Fig 1: Photograph of Pure and doped L-Threonine crystals The densities of all the grown crystals are provided in table 1. The density of pure L-Threonine measured in the present study agreed with the value reported by 1.3079gm/cc [13]. The densities of doped crystals are greater than the pure L-Threonine crystal. This shows the incorporation of dopant atoms into the host lattice. EDAX spectrum shown in the Fig 2 also confirms the incorporation of Zn atoms into the host lattice. Table 1: Values of density of pure and doped L-Threonine crystals System Density gm/cc Pure L-Threonine 1.30 Doped L-Threonine 1:0.002 Zn 1:0.004 Zn 1:0.006 Zn 1:0.008 Zn 1:0.010 Zn 1.308 1.362 1.338 1.380 1.350 Fig 2: EDAX spectrum of doped L-Threonine 1:0.008Zn The FTIR spectrum of pure L-Threonine crystal is shown in fig 3. FTIR spectrum were recorded for all the grown crystals in the range 4000cm-1 to 400 cm-1 . The broad band observed in the range 3169.15 and 2874.03 cm-1 are due to hydrogen vibration of ammonia group. The bend observed at 2048.47 cm-1 is assigned to nitrate . The bend observed at 1627.97cm-1 is assigned to asymmetric bending of NH3 . The bend observed at 1481.38 cm-1 assigned to CH2 bend. The bend observed at 1456.30 cm-1 is assigned to CH3 bend. The bend observed at 1417.73 cm-1 is assigned to symmetric structure of CO2 [14].The bend observed in the range 1346.36 and 1247.99 cm-1 are due to bending vibration of CH group. The peaks observed at 1184.33 and 1112.96 cm-1 is assigned to rocking of NH3 structure . The peak observed at 1039.67 cm-1 is assigned to C-N stretching . The bend observed at 869.92 cm-1 is assigned C-C-N stretching. The peak observed at 769.62 cm-1 is assigned to CO2 bending. The bend observed at 700.18 cm-1 is due to wagging of CO2structure. The bend observed at 559.38cm-1 is assigned to rocking of CO2. The peak observed at 489.94 cm-1 is assigned to torsional mode of NH3.The bends observed at 416.64 and 443.64cm-1 are assigned to C-H rock.
  • 3. Growth and Structural studies of Zn doped… www.theijes.com The IJES Page 3 Fig 3: FTIR spectrum of pure L- threonine crystal Fig 4: PXRD of 1:0.002 Zn doped L-Threonine crystal Single crystal X-ray diffraction studies of pure LThreonine single crystal was carried out using Bruker Kappa Apex II. The crystallography data obtained from single crystal X-ray diffraction of pure L-Threonine crystal is presented in table (2). From these data, it was observed that the crystal belongs to orthorhombic system with lattice parameters a=5.140 Å, b= 7.738 Å and c=13.546 Å and a space group P212121. The values obtained in the present study are closed agreement with the reported values[15].Analysis of powder X-ray diffraction data assuming the crystal structure and lattice parameters values obtained from single crystal SXRD taken in the present study, by the available methods [16].The PXRD pattern of 1:0.002 Zn doped L-Threonine crystal is shown in Fig 4. The peaks were indexed for doped L-Threonine crystal. The lattice parameters, thus calculated from the PXRD for doped crystals are also provided in table 2.From the table it is found that there is a slight variation in the lattice parameters of Zn doped L-Threonine crystals. This shows that there is a distortion in the lattice due to dopant addition Table 2: Values of lattice parameters of pure and doped L-Threonine System Lattice Parameters Volume (Å)3 a (Å) B (Å) C (Å) SXRD for Pure L- Threonine 5.140 [5.139] 7.738 [7.723] 13.546 [13.579] 538.769 [538.9] [15] PXRD for Doped L- Threonine 1:0.002Zn 1:0.004Zn 1:0.006Zn 1:0.008Zn 1:0.010Zn 5.042 4.914 4.918 4.815 4.941 7.784 7.785 7.760 7.880 7.748 13.680 13.414 14.113 13.316 13.556 536.928 513.151 538.626 506.910 518.977 IV. Conclusion Crystals grown in the present study are orthorhombic in structure. The density of the doped crystals vary slightly from that of pure crystal. The incorporation of dopant atom into the host lattice is confirmed by EDAX spectrum.
  • 4. Growth and Structural studies of Zn doped… www.theijes.com The IJES Page 4 V. Acknowledgement The authors are grateful to the authorities of Sophisticated Analytical Instruments Facility(SAIF, Cochin) References [1] V.Crasta.V.Ravindrachary S.Lakshmi, S.N. Prasad. M.A.Shudar. J.S. Prasad J. Crystal Growth (2005) e329. [2] L.I.Zlendeng.W.I.J>Biachang S.U.Gento. J Crystal Growth 178 (1997) 539. [3] M.H.Jiang.Q.Fang.Organic and Semi Organic non linear optical material Adv.mamater II (1999) 1147-1151. [4] J. Madhavan and S. Ezhilarasi . International journal of scientific of Engineering Research volume 5,issue 3, March 2014. [5] D.Subashini etal. .Advances in applied science research, 2013 4(2):238-242. [6] G. Ramesh Kumar etal. Volume issue 9. May 2008, pages 1405-1409. [7] S.Kalainathan. International journal of chem. Tech Research vol4, No.4 PP 1478-1484.Oct- Dec 2012. [8] Ramesh Kumar etal. Advances in Material Science And Engineering (2009) Article Id 704294. [9] R.Umaheswaria. Indian journal of research volume 2 issue 11. Nov.2013. [10] S.Masilamani etal.Arabian Journal of Chemistry (2014). [11] C.Ramesh Kumar.S.Gokul Raj R.Mohan R.Jayavel.J. Crystal Growth 275 (2005) e1947 [12] H.Lipson, H.Steeple, Interpretation of X-ray Powder Diffraction Patterns, Macmillan, New York 1970. [13] www.guide chem.com/dictionary/en/72-19-shtml [14] Silva.B.L Freire.P.T.C., Melo.F.E.A, Guedes.I, Araujo Siva. M.A. Medes Filho.I, Moreno.A.J.D, Braz. J.phys 1998 vol 28,n1 [15] Rameshkumar.G, Gokkul Raj.S, Mohan.R, Jeyavel.R, J.crystal Growth, 2005, no1-2 pp.el 1947- e1951 [16] B.E.Warren, X-ray Diffraction, Addison Wesley, California, 1969.