Synthesis and Characterization of Tin Oxide: A Review

Download as pdf or txt
Download as pdf or txt
You are on page 1of 4

International Journal for Research in Applied Science & Engineering Technology (IJRASET)

ISSN: 2321-9653; IC Value: 45.98; SJ Impact Factor:6.887


Volume 5 Issue XI November 2017- Available at www.ijraset.com

Synthesis and Characterization of Tin Oxide: A


Review
S. Kannan 1, Dr. N.P. Subiramaniyam 2, M. Sathishkumar 3
1, 2, 3
Department of Electronics, Nehru Arts and Science college, Coimbatore -641 105, Tamilnadu, India.

Abstract: This review focuses on Tin oxide has been extensively investigated different synthesized method, Tin oxide nano
materials with different morphologies and spatial assemblies have been fabricated in the last few years in order to improve
their performances. This review describes the recent developments of different synthesized method for potential applications.
Tin oxide is a candidate for applications requiring high electrical conductivity and optical transparency, such as a gas
sensor material, oxidation catalyst, and transparent conductor, photo anode in dye-sensitized solar cells (DSSCs), due to
their higher optical transparency and wider electron mobility to compare other metal oxide semiconductors (MOS), the
chemical and physical structures of tin oxide to make suitable material for these applications.
Keywords- Transparent Conducting oxides, Tin oxide, Gas sensor, Oxidation catalyst, Photo anode, dye-sensitized solar
cells .

I. INTRODUCTION
Tin oxide is widely used transparent conductive oxide, because of good electrical conductivity and optical transparency and
also it is a promising material to use different applications such as photovoltaic’s, biosensors and flat-panels [1] Tin oxide has
exceedingly attracted more than one oxidation state due to its dual valency and more prefers to possess the oxidation states of
2+ or 4+, which greatly promotes the variation in the composition of surface oxygen [2] The mineral form of Tin oxide is called
‘cassiterite’ (Figure 1) and is the color less solid raw material in nature [3] Tin Oxide (SnO2) is a n-type semiconductor with
wide energy band gap (3.7 eV). The SnO2 has high optical transparency and low electrical resistance in the visible range of the
electromagnetic spectrum. These properties make tin oxide suitable for many applications [4-5].

II. LITERATURE SURVEY


A. Structure and properties of SnO2
Tin (VI) oxide or stannic oxide (not to be confused with stannous oxide with tin in the oxidation state of 2+ is an amphotheric
colorless solid. This inorganic compound shows high optical transparency and high reflectivity in the infrared region and the
material is characterized by its good chemical and thermal stability SnO2 has been considered for many applications Among
others, the material was evaluated as a catalyst, as a sensor, and as a raw material for transparent films, infra-red mirrors or
optoelectronic devices Also, the strongly oxidizing properties make the oxide an ideal tool for the elimination of pollutants from
water and many other sources [6-7].
The crystal structure type of SnO2 is similar to the rutile phase structure of TiO2 (dimensions of the unit cell: a = b = 0.47374
nm and c = 0.31864 nm, polar crystal with octahedral and space group no. 136 P42/mnm In one unit cell, the tin(IV) ion is
surrounded by 6 oxygen ions and every oxygen is bordered by 3 tin(IV) ions, resulting in a coordination structure [8-10] as
shown in Figure 1. The discovery of the photocatalytic properties of TiO2 also led to a range of proposals for photocatalytic
applications of related oxides. The high photosensitivity and thermo stability, as well as their low cost and toxicity made ZnO
and SnO2 valuable alternatives as photocatalysts [11-12]. The octahedral network is considered a prerequisite for high
photocatalytic activity because it increases the mobility of e−–h+ pairs and consequently affects the probability of their reaching
the reaction sites on the surface of the photo catalyst [13].Some of the physicochemical characteristics of SnO2 are summarized
in Table 1.

Figure 1 Tin Oxide

©IJRASET (UGC Approved Journal): All Rights are Reserved 2370


International Journal for Research in Applied Science & Engineering Technology (IJRASET)
ISSN: 2321-9653; IC Value: 45.98; SJ Impact Factor:6.887
Volume 5 Issue XI November 2017- Available at www.ijraset.com

Table 1 Properties of SnO2


Crystal structure Rutile structure
Lattice constant a = 0.47374 nm and c = 0.31864 nm
Molecular weight 150.69 g/mol
Density 6.90 g/mol
Melting point 1500–1630 ◦C
Boiling point 1800–1900 ◦C

Generally in semiconductors the lower energy band (conduction band, CB) is packed with electrons while the upper band
(valence band, VB) is free of electrons. The energy difference between these bands, also called the energy band gap (Ebg), is
responsible for the electronic properties of the material [14]. Together with the Fermi level (hypothetical energy level of
electrons), the band gap is an important parameter for describing the potential of a material to act as semiconductor [15].
Generally less energy is required to excite electrons if the energy band gap between CB and VB decreases .The electronic
properties of semiconductors is also, and to a much greater extent, determined by the presence of small amounts of impurities in
the lattice structure of the metal oxide. These impurities either create an excess of free holes (p-type semiconductor) or free
electrons (n-type semiconductor) [16]. The doping process changes the Fermi level by shifting the CB in the n-type or the VB in
the p-type semi-conductor, and thus narrows the Ebg. As a consequence, less energy is required to generate excited electrons
and photocatalytic activity can be observed upon irradiation of the catalyst with electromagnetic radiation in the visible range
The electrical conductivity of SnO2 can moreover be attributed to the presence of the inherent defects in the metal oxide [17-18].
Such defects contribute to a significant narrowing of the Ebg band, thus improving the properties of the material as a
semiconductor. In this respect, additional oxygen anions trigger the oxidation of Sn2+ to Sn4+ in order to maintain the overall
electrical neutrality [19-20].The large band gap energy of SnO2 of 3.6 eV, which corresponds to photo activation in the UV
range of the electromagnetic spectrum, makes this material, as well as ZnO and SnO2 , ideal photocatalysts for the degradation
of a variety of organic pollutants Modification of the metal oxides reduces the band gap energy and electro-magnetic radiation
with lower energy can be utilized for the activation of the catalyst. The band gaps of silicon and a variety of metal oxides are
shown in Table 2 In summary, SnO2 combines many positive properties, such as low electrical resistance, high electrical
conductivity and high optical transparency in the visible region of the electromagnetic range and the material has found many
useful applications [21-22].

Table 2 Band gap energy some semiconductors


Si 1.1
TiO2 (rutile) 3.0
SnO2 3.6
WO3 2.7
ZnS 3.7
ZnO 3.3
TiO2 (anatase) 3.2
SnO ∼2.5–3.0
CdS 2.4
ZnO 3.2

B. Synthesis and characterization of SnO2


The chemical vapour deposition method is proposed to prepare tin oxide using in atmospheric pressure. XRD studies indicate
synthesized SnO2 have a tetragonal structure and highly oriented along the (110) plane. Four-probe method and Hall voltage
measurement experiments give useful information regarding the electrical properties of films. The films indicated conductivity
in the range 108 to 169 W-1cm-1. [23] The synthesized Fluorine doped and pure SnO2 was prepared by electro deposition
method from aqueous solutions containing SnCl2, HCl and butyl rhodamine Blue dye was used as a structure directing complex
agent to control the growth of SnO2 during the experiment. The scanning electron microscopy (SEM) micrographs of the films
prepared in the absence of rhodamine Blue revealed irregularly connected nanoparticles randomly stacked in large domain. On
the other hand, it can be seen that many smaller particles produce a larger porous particle with an average diameter of 50 nm for

©IJRASET (UGC Approved Journal): All Rights are Reserved 2371


International Journal for Research in Applied Science & Engineering Technology (IJRASET)
ISSN: 2321-9653; IC Value: 45.98; SJ Impact Factor:6.887
Volume 5 Issue XI November 2017- Available at www.ijraset.com

the addition of 100 μM and 20 nm for 150 μM . The XRD data show that the film is SnO2 with tetragonal rutile structure. The
average grain size about 24 nm, which was determined using the Scherrer equation. The films were deposited on copper
substrate by one step electro deposition without the pre treatment of electrolytes. An effect of deposition potential on the
morphological properties was investigated using scanning electron microscopy [24-26] Pulsed laser deposition method as
reported by Dolbec and Phillips et al [27-28 ]. The alumina and quartz substrates are use to synthesis SnO2 with using of pure
polycrystalline SnO2 phase, SnO2 films with a thickness between1000-2000 Å were successfully deposited on glass substrate.
They point out that the films grown using Sn target exhibit a relatively high transmittance of 80% in the visible region. Fan and
Reid report was discussed XRD patterns of pulsed laser deposited SnO2 films at different stages of post deposition annealing
and it is conclude at intermediate temperatures was influenced that the formation of the litharge of SnO and orthorhombic phase
of SnO2 are clearly visible. The effects of oxygen partial pressure percentage in the range of 1% to 10% on the magnetron
sputtered tin oxide films have been studied by Leng et al [29]. The results indicate that introduce of oxygen would suppress the
deposition process and the growth of films. They found when oxygen pressure was increase, resistivity of the film also reduces
with its indicated in electrical measurement. In pure argon atmosphere SnO2 films with resistivity was found 232 Wcm.Stedile
et al [30] report was found magnetron sputtered SnO2 films were submitted to thermal annealing and exposed to butane gas, its
highly disordered. The SnO2 films are modified under thermal processing and gas exposure, changing the oxygen vacancy
concentration as could be observed in their experiment. They conclude that these behaviors should affect the steady state
response of tin oxide sensors. Electrical measurements have been investigated on sputtered SnO2 films at various anneal
temperatures. The variation of the Hall mobility and conductivity with the annealing temperature could be attributed to increase
in the grain size and to reduce in the oxygen vacancies of the SnO2 thin films after heat treatment process. Czapla et al [31-32]
prepared SnO2 films using reactive sputtering technique. The obtained results reflect that the excess tin atoms locate in
interstitial positions of the tetrahedral crystal. The influence of substrate temperature on the properties of SnO2 films deposited
by ultrasonic spray pyrolysis method was reported by Achour et al [33]. The average crystallite sizes and band gap energies
were increased from 6.52 to 29.8 nm, and 4.03-4.133 eV, respectively with increasing substrate temperature from 400 to 500 °C.
The warming applications SnO2high transmittance in the infrared region like 800 nm, as use to make good material. Jahnavi et
al [34] was reported about thermal evaporation of Tin oxide thin films . They observe that band gap energy increases with an
increasing annealing temperature for SnO2 films. UV-visible transmission spectra of these films indicated that high
transmittance of 99% in the visible region. From Shadia [35] report Thermally evaporated SnO2 films has 100-600 nm of
thickness were successfully deposited onto glass substrate and XRD pattern reveals that these films are amorphous. It was
observed from the SEM micrograph study that the surface of the film is smooth, uniform and well covered with the material.
EDAX indicated that these films are deficient in oxygen and SnO2 films were prepared by chemical bath deposition method at
55 °C using tin chloride pentahydrate in aqueous medium. High quality SnO2 films with transmittance more than 80% in the
visible region are observed [36]. Annealed films are orthorhombic, highly stoichiometric, strongly adhesive and transparent
with band gap about 4.4 eV. Chemical bath deposited tin oxide films were prepared on glass substrate with stannous chloride
and urea as the precursor and buffer in aqueous medium. The peaks respond to the (110), (101) and (211) planes of rutile
structure could be observed in XRD pattern. The influence of stannous chloride concentration and weight ratio of urea/water on
the properties of The increasing of SnCl2 concentration and the reducing weight ratio of urea/water is observed to improve the
crystalline of the SnO2 films. Chemical bath deposited SnO2 films have been prepared onto soda lime glass substrate in the
presence of tin chloride and methanol solution as reported by Yusuf et al [37]. The Scherer formula was used to calculate the
grain size. It is interesting to note that the average grain size was observed to be 29.6 nm, which increased to 30.04 nm after
annealing in air at 400 °C. In the transmission spectra, optical transmittance was about 80 % in the visible range. chemical bath
deposition method [38-40].The chemical bath contains tin chloride, hydrogen peroxide, deionized water, triethanolamine and
ethylene diaminetetraacetic acid solution. Deposition was carried out about pH 7 and at 110 °C. The average crystalline size was
about 18 nm. SEM studies reveal that the grains are well defined, spherical and of almost similar size (16 nm). Finally, the
Fourier transform infrared spectroscopy (FTIR) spectrum displays the strong presence of SnO2 .

III CONCLUSIONS
In this review, we have covered synthesis and characterization of Tin oxide (SnO2) has been successfully prepared by using
various deposition methods. The morphology, structure, composition and optical properties have been investigated by using
different tools during the experiment. The obtained results reflect that the various deposition conditions have great influence on
the properties of SnO2 thin films.

REFERENCES
[1] M.Z.H. Khan, Cogent Engineering, 3 ,11, 70097, 2016
[2] Batzill, M., Diebold, U., Prog. Surf. Sci. 79, 47–154 , 2005

©IJRASET (UGC Approved Journal): All Rights are Reserved 2372


International Journal for Research in Applied Science & Engineering Technology (IJRASET)
ISSN: 2321-9653; IC Value: 45.98; SJ Impact Factor:6.887
Volume 5 Issue XI November 2017- Available at www.ijraset.com

[3] Greenwood, N.N., Earnshaw, A., 1984. Angew. Chem. Int. Ed. 97, 719–720, 1984
[4] J.C. Manifacier, M. De Murcia, J.P. Fillard, E. Vicario. (1977). Thin Solid Films. 41, 127-144,1977
[5] H.L. Hartnagel, Semiconducting Transparent Thin Films, 1a ed. Institute of Physics Publishing, Philadelphia, 1995.
[6] Bouras, K., Rehspringer, J. Mater. Chem. C 2, 8235–8243, 2014
[7] Anandan, K., Rajendran, V, Superlattices Microstruct. 85, 185–197,2015
[8] Dou, M., Persson, C., J. Appl. Phys. 113, 083703, 2013
[9] Yu, H., Wang, S., Xiao, C., Cryst. Eng. Commun. 17, 4316–4324, 2013
[10] Entradas, T., Cabrita, J., Dalui, Mater. Chem. Phys. 147,563–571, 2014
[11] Chaisitsak, S, Sensors 11, 7127–7140, 2011
[12] Rakibuddin, M., Ananthakrishnan, R., New J. Chem. 40,3385–3394, 2016
[13] Abdel-Messih, M.F., Ahmed, M.A., J. Photochem. Photobiol. A: Chem. 260, 1–8.2013.
[14] Linsebigler, A.L., Lu, G., J Chem.Rev. 95, 735–758.1995
[15] Van Eldik, R., Hubbard, C.D, Advances in InorganicChemistry. Academic Press,2009
[16] Kim, D.-H., Lee, G.-W., Kim, Y.-C., Solid State Commun. 152, 1711–1714, 2012
[17] Mete, E., Uner, D., Gülseren, O., Ellialtıo˘glu, S, Phys. Rev. B 79, 125418, 2009
[18] Zhang, Y.C., Du, Z.N., Li, K.W., Zhang, ACS Appl.Mater. Interfaces 3, 1528–1537, 2011
[19] Zulfiqar, Yang, Y., Wang, J., J. Mater. Sci. Mater. Electron. 27, 12119–12127, 2016
[20] Sanal, K.C., Jayaraj, M.K., Mater. Sci. Eng. B 178, 816–821, 2013
[21] Kruefu, V., Ninsonti, H., Wetchakun, N., Eng. J. 16, 91–100, 2012
[22] Mistry, B.V., Avasthi, D.K., Joshi, U.S., Appl. Phys. A 122,1024, 2016
[23] P. Saikia, A. Borthakur, P.K. Saikia, Indian J. Phys., 85, 551-558. 2011
[24] J. Yang, X. Li, S.L. Bai, R.X. Luo, A.F. Zhang,Thin Solid Films, 529, 6241-6245, 2011
[25] A.Y. El-etre, S.M. Reda, Appl. Surf. Sci., 256, 6601-6606. 2010
[26] X. Chen, J. Liang, Z. Zhou, Mater. Res. Bull., 45, 2006-2011, 2010
[27] R. Dolbec, K.M.A. El, A.M. Serventi,Thin Solid Films, 419, 230-236, 2002
[28] H.M. Phillips, Y. Li, Z. Bi, B. Zhang, Appl. Phys. A, 63, 347-351, 1996
[29] H. Fan, S.A. Reid, Chem.Mater.,15, 564-567. 2013
[30] D. Leng, L. Wu, H. Jiang, Y. Zhao, Int. J. Photoenergy, 70, 28-35, 2012,
[31] F.C. Stedile, B.A.S.D. Barros, Thin Solid Films, 170, 285-291, 1989
[32] M.D. Giulio, D. Manno, G. Micocci, Sol. Energy Mater. Sol. Cells, 31, 235-242, 1993
[33] A. Czapla, E. Kusior, M. Bucko, Thin Solid Films, 182, 15-22, 1989
[34] R. Achour, B. Atmane, Super lattices Microstruct., 86, 403-411, 2015
[35] V.S. Jahnavi, S.K. Tripathy, Indian J. Res. Pharm. Biotechnol., 78-82, 2014
[36] J.I. Shadia, Int. J. Mater. Chem., 2, 173-177, 2012
[37] H. Khallaf, C. Chen, L. Chang, Appl. Surf. Sci., 258, 6069-6074, 2012
[38] A. Rifai, M. Iqbal, N. Tapran, AIP Conf. Proc., 2011
[39] G.T. Yusuf, A.M. Raimi, T.O. Familusi, J Am. Phys. Soc., 2013,
[40] S. Suresh, P. Jiban, Soft NanoscienceLett. 5, 55-64, 2015

©IJRASET (UGC Approved Journal): All Rights are Reserved 2373

You might also like