<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">ANP</journal-id><journal-title-group><journal-title>Advances in Nanoparticles</journal-title></journal-title-group><issn pub-type="epub">2169-0510</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/anp.2013.21006</article-id><article-id pub-id-type="publisher-id">ANP-27887</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Chemistry&amp;Materials Science</subject><subject> Engineering</subject></subj-group></article-categories><title-group><article-title>
 
 
  Single Step Solid-Solid Reaction Scheme for the Synthesis of Cobalt Sulphide-Oxide Nanoparticles in Polymer Matrix
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>arendra</surname><given-names>Rumale</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sudhir</surname><given-names>Arbuj</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Govind</surname><given-names>Umarji</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Manish</surname><given-names>Shinde</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Uttamrao</surname><given-names>Mulik</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Anuj</surname><given-names>Pokle</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Dinesh</surname><given-names>Amalnerkar</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>ELANTAS Beck India Ltd., Pimpri, India</addr-line></aff><aff id="aff3"><addr-line>Icon Analytical Equipment Pvt. Ltd., Mumbai, India</addr-line></aff><aff id="aff2"><addr-line>Centre for Materials for Electronics Technology (C-MET), Panchawati, India</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>amalnerkar@cmet.gov.in(DA)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>22</day><month>02</month><year>2013</year></pub-date><volume>02</volume><issue>01</issue><fpage>28</fpage><lpage>31</lpage><history><date date-type="received"><day>December</day>	<month>14,</month>	<year>2012</year></date><date date-type="rev-recd"><day>January</day>	<month>15,</month>	<year>2013</year>	</date><date date-type="accepted"><day>January</day>	<month>25,</month>	<year>2013</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   At present, there is considerable interest in polymer-metal chalcogenides/oxides based nano-composites on account of their tunable optical, magnetic, electronic and catalytic properties. Here in, we report a simple single step approach for the in-situ synthesis of combined cobalt sulphide/cobalt oxide in polyphenylenesulphide (PPS) polymer matrix. We have illustrated the suitability of this methodology by reacting commonly available cobalt precursors with engineering thermoplastic, PPS. The cobalt precursor was homogeneously mixed with PPS in the molar ratios of 1:1, 1:5, 1:10, 1:15, respectively, followed by heating the mixtures obtained at the melting temperature of the polymer (285?C) for six hours. The resultant products were characterized by X-ray Diffractometry (XRD), Field-Emission Scanning Electron Microscopy (FESEM), High Resolution Transmission Electron Microscope (HRTEM), Diffuse Reflectance Spectroscopy (DRS) technique and Fourier Transformation Infra red Spectroscopy (FTIR). Formation of mixed phases viz., sulphide and oxide of cobalt within modified PPS matrix was confirmed by XRD. The resultant nanoparticles of cobalt sulphide and cobalt oxide embedded in the PPS matrix showed crooked and chunk morphology. The optical properties of the resultant nanocomposites indicate the shift in the absorption hump due to nanoscale size effect. 
 
</p></abstract><kwd-group><kwd>Polymers; Nanocomposites; Cobalt Sulphide/Oxide; Solid-Solid Reaction</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>In the recent times metal sulphides-oxides embedded in polymeric matrices have represented a new class of nanostructured materials. These materials combine the properties of the polymer as well as the metal and its corresponding sulphide-oxide and show entirely a different set of properties in comparison to the original materials. These materials coalesce various properties such as optical transparency, magnetism, luminescence, UV-visible absorption etc. leading to exclusive functional materials that can be easily explored for numerous applications in different technological fields [<xref ref-type="bibr" rid="scirp.27887-ref1">1</xref>]. The transition metal sulfide nanomaterials have been the focus of considerable interest due to their unique optical and electrical properties and their wide variety of potential applications in nanoscale devices such as electroluminescence and nonlinear optical devices [<xref ref-type="bibr" rid="scirp.27887-ref2">2</xref>]. Cobalt sulphide-oxides are one of the most complicated systems known due to their number of phases and chemical compositions. Few phases of cobalt sulphide and oxides reported are CoS, Co<sub>3</sub>S<sub>4</sub>, CoS<sub>2</sub>, Co<sub>9</sub>S<sub>8</sub>, CoO, Co<sub>3</sub>O<sub>4</sub> etc. Cobalt sulphide/ oxides are one of the important classes of material which have found direct applications in solar selective coatings, photo detectors, solar cells, biological labeling, Li-ion battery, and magnetic devices etc. [3,4]. These materials have gained immense importance in recent time due to their magnetic properties and their use for fabrication of dilute magnetic semiconductor materials. Till date numerous techniques have been used for the synthesis of nanoscale cobalt sulphide and oxide nano-particles separately such as anodized alumina films for growth of cobalt disulphide nanowires by application of two electrical fields [<xref ref-type="bibr" rid="scirp.27887-ref5">5</xref>], colloidal synthesis of hallow nano-cobaltsulphide spheres [<xref ref-type="bibr" rid="scirp.27887-ref6">6</xref>], hallow metal oxides and sulphides by laser ablation in liquid [<xref ref-type="bibr" rid="scirp.27887-ref7">7</xref>], hydrothermal technique [<xref ref-type="bibr" rid="scirp.27887-ref8">8</xref>], biomolecule-assisted hydrothermal process [<xref ref-type="bibr" rid="scirp.27887-ref9">9</xref>], cobalt sulfide in montmorillonite by solid-solid reaction [<xref ref-type="bibr" rid="scirp.27887-ref10">10</xref>], co-precipitation method for generation of cobalt oxide nanoparticles [11,12], chemical bath deposition of thin films [<xref ref-type="bibr" rid="scirp.27887-ref13">13</xref>], Co<sub>3</sub>O<sub>4</sub> nanowalls by direct heating of cobalt foil on hot plate etc. [<xref ref-type="bibr" rid="scirp.27887-ref14">14</xref>]. In addition to the above, number of methods have been reported for in-situ generation of well defined nanoparticles in polymeric matrices such as ring opening metathesis polymerization (ROMP) to synthesize cobalt diblock copolymer [<xref ref-type="bibr" rid="scirp.27887-ref15">15</xref>], atom transfer radical polymerization (ARTP), nitroxide mediated polymerization (NMP), reverse addition fragmentation chain polymerization (RAFT) etc. [<xref ref-type="bibr" rid="scirp.27887-ref16">16</xref>].</p><p>In this communication, we report one step approach for the synthesis of cobalt sulphide-oxide nanoparticles in thermally stable polymer matrix of polyphenylenesulphide (PPS) by simple polymer inorganic solid-solid reaction scheme. The polymer PPS has been intentionally chosen as it serves dual purpose-first it acts as a chalcogen source and second it acts as a stabilizing media. The advantage of synthesizing semiconductor nanoparticles in the polymer matrix is that it provides good stabilization action and controls the agglomeration of nano-particles formed within the polymer matrix.</p></sec><sec id="s2"><title>2. Experimental Details</title><p>The reactant cobalt nitrate was obtained from Merck and was used as received, the polymer polyphenylenesulphide (PPS) with number average molecular weight 10,000 having glass transition temperature (Tg) 88˚C with melting temperature of 285˚C was obtained from Sigma Aldrich. The material was synthesized by reacting the precursors in the molar ratio of 1:1, 1:5, 1:10, 1:15, respectively, for cobalt nitrate and PPS. The materials for each molar ratio were mixed using agate mortar and pastel and a few drops of acetone were added for proper wetting of the reactants. The admixtures thus formed were then heated at the melting temperature of the polymer i.e. 285˚C for six hours in a muffle furnace under normal atmospheric conditions. The phase identification of the resultant powder products was conducted using X-ray diffractometer (Brucker D5005), using CuKa radiation. Material in powdered form was used for such analysis. The particle size and the surface morphology of the samples were investigated by HRTEM with FEI Tecnai G2, at an acceleration voltage of 200 KV. The samples for HRTEM were prepared by dispersing fine powder of the resultant product in isopropyl alcohol. The dispersion was than coated on carbon coated grid for further analysis. The surface morphology was determined using FESEM, Hitachi, S-4800, the solid samples were used as such for determination. In order to prevent the charging effect associated with FESEM, the samples were placed on carbon tape and coated with thin Au film. The Infrared study was carried out using Fourier transformation Infrared spectrophotometer (FTIR-Perkin Elmer Spectrum 100). Approximately 500 mg of sample was mixed with dried KBr powder, the mixture was grinded and pellets were formed for further IR analysis. The UV-DRS spectra were recorded on UV 3600, Shimadzu UV-VISNIR spectrophotometer for solid powder samples.</p></sec><sec id="s3"><title>3. Results and Discussion</title><p><xref ref-type="fig" rid="fig1">Figure 1</xref> depicts the XRD pattern obtained for the resultant products. Prominent formation of Co<sub>3</sub>O<sub>4</sub> for the 1:1 and 1:5 ratio of ratio of cobalt nitrate to PPS is observed (Figures 1(a) and (b)). The diffraction peak at 2q value of 36.8, 44.8, 59.3 and 65.2 respectively corresponds to (311), (400) planes, (511) and (440) indicating the formation of cubic Co<sub>3</sub>O<sub>4</sub> (JCPDS No.42-1467). For samples corresponding to 1:10 and 1:15 precursor to PPS ratio, mixed phases of Co<sub>3</sub>S<sub>4</sub> and Co<sub>3</sub>O<sub>4</sub> were obtained with dominance of Co<sub>3</sub>O<sub>4</sub> phase. This substantiates that the sulphur moiety from the polymer has reacted with the cobalt precursor. The diffraction peak at 26.7, 31.4, 38.1, 55.1 correspond to cubic Co<sub>3</sub>S<sub>4</sub>, (JCPDS No. 47-1738) whereas the peak at 36.8 corresponds to Co<sub>3</sub>O<sub>4</sub>. The peak observed at 2q value of 20.5˚ in Figures 1(b)-(d) matches with PPS.</p><p>The images in <xref ref-type="fig" rid="fig2">Figure 2</xref> elucidate the FESEM images for the obtained nanocomposites for the various ratios of cobalt precursor to PPS polymer. Formation of irregular shape morphology having size in the range of 30 nm to 100 nm is observed for the 1:1 ratio (<xref ref-type="fig" rid="fig2">Figure 2</xref>(a)). Uniform distribution of the Co<sub>3</sub>S<sub>4</sub> and Co<sub>3</sub>O<sub>4</sub> is observed for the higher proportion of PPS (Figures 2(c) and (d)). The composition with 1:10 cobalt to polymer shows uniform distribution with the average particle size of 30 nm.</p><p>The HRTEM analysis is shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>. The formation of nanoparticles embedded in the PPS matrix is observed for the Co<sub>3</sub>O<sub>4</sub> prepared using 1:1 ratio. The average particle size for the resultant composition was found to be in between 5 to 10 nm. The SAED pattern shown as inset of <xref ref-type="fig" rid="fig3">Figure 3</xref>(a) indicates the formation of cubic Co<sub>3</sub>O<sub>4</sub>, which is also evident from the XRD analysis for the resultant nanocomposites. The interplanar</p><p>spacing of 0.24 and 0.28 corresponds to (311) and (220) planes, respectively, thereby indicating the formation of crystalline Co<sub>3</sub>O<sub>4</sub>. HRTEM analysis of nanocomposites prepared using 1:5 ratio also indicates formation nano sized Co<sub>3</sub>O<sub>4</sub> having size in the range of 5 to 10 nm. Slight agglomerations of nano particles are observed. The SAED pattern and the lattice spacing (Figures 3(b) and (b')) confirms the formation of cubic Co<sub>3</sub>O<sub>4</sub> and also supports the XRD analysis. For higher ratio (1:10 and 1:15) the formation of distorted rod like morphology was observed. The SAED pattern and lattice spacing indicates the formation of Co<sub>3</sub>S<sub>4</sub> (Figures 3(c), (c') and (d), (d')) with lattice spacing of 0.2855 matching well with (311) plane of Co<sub>3</sub>S<sub>4</sub>.</p><p>DRS spectra of prepared nanocomposites are depicted in <xref ref-type="fig" rid="fig4">Figure 4</xref>. PPS indicates the absorption edge at 390 nm. The band edge of the nanocomposites was located at 790 nm (1.5 eV), had a blue shift of approximately 288 nm with respect to the band gap of 1078 nm (1.15 eV) for bulk Co<sub>3</sub>S<sub>4</sub>. The hump centered at 750 nm corresponds to the band gaps of Co<sub>3</sub>O<sub>4</sub> and Co<sub>3</sub>S<sub>4</sub> which, interestingly, are almost in the same range [17,18].</p><p>The FTIR spectra obtained for neat PPS and the resultant nanocomposites are depicted in <xref ref-type="fig" rid="fig5">Figure 5</xref>. Characteristic bands of PPS are observed at 1471 cm<sup>−1</sup> due to stretching vibration of C=C in benzene and 818 cm<sup>−1</sup> due</p><p>to deformation vibration of =C-H in 1, 4 place of benzene, also numerous sharp bands at 1091 cm<sup>−1</sup>, 1008 cm<sup>−1</sup>, and 485 cm<sup>−1</sup> which may be attributed to the crystalline nature of PPS are observed in <xref ref-type="fig" rid="fig5">Figure 5</xref>(a). In the spectra for nanocomposites of various ratios (Figures 5(b)-(e)), the peaks at 624 cm<sup>−1</sup> are characteristics of metal oxide bands. A peculiar peak at 2030 cm<sup>−1</sup> is observed for the resultant nanocomposites.</p></sec><sec id="s4"><title>4. Conclusion</title><p>In summary, we have successfully synthesized cobalt sulphide/oxide nanoparticles in polymer matrix by facile solid-solid reaction technique. The formation of cubic structure Co<sub>3</sub>O<sub>4</sub> and Co<sub>3</sub>S<sub>4</sub> embedded in the PPS matrix was confirmed by XRD and HRTEM. This technique, being quite simple, can be used for preparation of nanocomposites for future generation smart materials. The polymer PPS being an engineering thermoplastic with inherent flame retardant characteristics can be molded as desired for advanced device fabrication.</p></sec><sec id="s5"><title>5. Acknowledgements</title><p>One of the authors (N. P. Rumale) sincerely acknowledges to the Managing Director of ELANTAS Beck India Ltd. Mr. Rajeev Bhide, the Managing Director of Icon Analytical Equipment Pvt. Ltd., Mr. Anand Rao, Dr. B. B. Kale, Scientist, Centre for Materials for Electronics Technology (C-MET) for their kind support in carrying out this work.</p></sec><sec id="s6"><title>REFERENCES</title></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.27887-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">L. F. Nicolais and G. Carotenuto, “Synthesis of Polymer-Embedded Metal, Semimetal, or Sulfide Clusters by Thermolysis of Mercaptide Molecules Dissolved in Polymers,” Recent Patents on Materials Sciences, Vol. 1, No. 1, 2008, pp. 1-11. doi:10.2174/1874464810801010001</mixed-citation></ref><ref id="scirp.27887-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">X. H. 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