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Friday, March 29, 2019

Properties of Topological Insulating Material: Bi2Te3-PANI

Properties of Topological Insulating Material Bi2Te3-PANISynthesis, depiction and galvanizing properties of a complicated of Topological Insulating Material Bi2Te3-PANIR. R. Urkudea*, P. T. Patilb, S. B. Kondawarb, U. A. PalikundwaraaX-ray Research Laboratory, Department of Physics, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur 440033, IndiabPolymer Nanotech Laboratory, Department of Physics, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur 440033, IndiaAbstractIn the stupefy work, we carried out a systematic landing field of structure, UV-Vis Spectra and come conduction of stark(a) Bi2Te3, beautiful Polyaniline (PANI) and Bi2Te3 (5%)-PANI (95%) intricate. Bi2Te3 was synthesized by a order exchangeable to solvothermal method, whereas, sensitive PANI and Bi2Te3-PANI composite were synthesized by a chemical substance oxidative method. The materials were structur everyy characterised and the galvanizing properties were investigated in the temperature ran ge from mode temperature to 100C. The galvanizing conductivity of the Bi2Te3-PANI composite is downstairscoat to be higher(prenominal) than that of its pure constituents at all the temperatures. The enhancement in the surface conductivity may be repayable to the PANI founderd ordered molecular agreement of Bi2Te3 in the Bi2Te3-PANI composite, as confirmed from disintegrate x-ray diffraction, UVvis unearthly analysis. 2015 The Authors. Published by Elsevier Ltd.Peer-review under responsibility of the International congregation on Nanomaterials and Technologies (CNT 2014).Keywords Topological insulators Bismuth telluride thermoelectric material Polyaniline composites electrical conductivity.1. IntroductionTopological insulators (TIs) ar electronic materials that have a protrude band gap want an ordinary insulator but have protected conducting states on their bank or surface (Hasan and Kane, 2010). Most of the current researches be foc apply on the materials, like Bism uth telluride (Bi2Te3), Antimony telluride (Sb2Te3) and Bismuth selenide (Bi2Se3) due to the topological insulating properties exhibited by them. Bi2Te3 is hotshot of the best TI materials. It is a semiconducting compound with narrow bulk band gap of 0.2 eV. It is also a ethical material for thermoelectric applications (Das and Soundararajan, 1988). It has shown a drastic change in its thermoelectric properties when it is doped with Polyaniline (PANI) (Li et al., 2011). It has also given added advantages of polymers like inexpensiveness, intrinsically low thermal conductivity, flexibility and good processability etc. (Marjanovic et al., 2013).Various research workers have attempted to synthesize and characterize composites of Bi2Te3 with polyaniline (Zhao et al., 2002 Xu et al., 2005 Hostler et al., 2006 Chatterjee et al., 2009 Toshima et al., 2011). Very recently, mechanical blending method was employed by Li et al. (2011) for the synthesis of Bi2Te3PANI they found that the mig htiness factor of the composite is slight than both of the individual components. However, a report on the synthesis of a Bi2Te3 and PANI hybrid by physical mixing and solution mixing showed a higher power factor in the case of the physical potpourri (Toshima et al., 2011). Though there is a vast literature available on the TE properties of Bi2Te3-PANI composites, experimental reports on TI Properties of the composites are not available. establish on this background, in the present work, we carried out a systematic study of structure, UV-Vis Spectra and surface conductivity of Bi2Te3 (5%)-PANI (95%) composite, pure Bi2Te3 and pure PANI. Bi2Te3 was synthesized by a method similar to solvothermal method (Deng et al., 2002), whereas, pure PANI and Bi2Te3-PANI composite were synthesized by a chemical oxidative method (Stejskal and Gilbert, 2002). The materials were structurally characterized and the electrical properties were investigated in the temperature range from room temperature to 100C. The electrical conductivity of the Bi2Te3-PANI composite is found to be higher than that of its pure constituents at all the temperatures. The enhancement in the surface conductivity may be due to the construction of highly ordered grasp structures of PANI on Bi2Te3, as confirmed from pulverise x-ray diffraction (XRD), UVvis spectral analysis.2. Experimental details2.1 Materials usedBismuth chloride (BiCl3), Tellurium (Te) metal powder, chiliad hydroxide (KOH), Sodium borohydrate (NaBH4), N-N dimethylformamide (DMF), Hydrochloric acid (HCl), Aniline (C6H5NH2), Acetone (CH3)2.CO, Methanol (CH3OH) were purchased from Merck Chemicals. ammonium ion persulphate (NH4)2S2O8 was purchased from Hi-media. All the chemicals were of analytical reagent grade and are used without further purification, pull up aniline which was purified prior to use.2.2 Preparation of Bi2Te3A mixture of BiCl3 (10 mmol), Te powder (15 mmol), KOH (80 mmol) and NaBH4 (30 mmol) were put into a beaker of 100 ml capacity. The beaker was then filled with N-N dimethylformamide (DMF) up to 90 ml and was kept into a muffle furnace. Temperature of the furnace was maintained at 100-180C for 24 hours and was then slowly cooled to the room temperature. The product was filtered, wash with double distilled water and dried in vacuum oven at 80C for 12 hours.2.3 Preparation of pure PANI and Bi2Te3 PANI CompositePANI was synthesized by exploitation chemical oxidative method (Stejskal and Gilbert, 2002) 0.2 mol Aniline with 0.25 mol ammonium persulphate was oxidized in acidic aqueous medium. Aniline and Ammonium persulphate were dissolved, separately, in 50 ml solution of 1.0 mol HCl in double distilled water. twain the solutions were kept at room temperature for 1h and were mixed together in a beaker. Du large number the process, the colour of the solution changed from colour little to light blue and then to minatory green. The solution was briefly stirred and was left to polymerize for 24 h. The devolve of PANI was collected on a filter paper, washed with distilled water, then with 20 ml of 0.1M HCl and with Methanol. PANI (emeraldine salt) powder was dried in vacuum oven at 80C. A similar procedure was followed for the synthesis of Bi2Te3-PANI composite, but this time Bi2Te3 was introduced in aniline solution.3. Characterization3.1 Structural paintingThe samples were structurally characterized by XRD and UVvis spectral analyses. XRD measurements were performed using a Diffractometer (Rigaku Miniflex II x-ray Diffractometer) with Cu K radiation ( = 1.541838 A). The UVvis spectra of the prepared samples were recorded by a spectrophotometer (UV-1800 Shimatzu Spectrophotometer) using samples dissolved in dimethyl formamide in a quartz cuvette.3.2 galvanising characterizationAll the prepared samples were pressed at pressure less than 5 tonnes, at room temperature, to form the compacted pellets for measurement of the electrical conductivity. The measurements were carried out, in the temperature range 20-100 C, by standard four-probe method with constant current cite kept at 2 mA.4. Results and Discussions4.1 Powder X-ray diffractionFigure 1 shows the XRD purposes of Bi2Te3, pure PANI and Bi2Te3-PANI composite. All the notes of the pattern for Bi2Te3 can be indexed in trigonal structure (JCPDS No 015-0863) with unit cell parameters a = 4.358A b = 4.358A and c = 30.48A. Broad peaks at 22 and 25 for pure PANI are observed, which are due to the adopt unit of monomer. Compared with the pure PANI, only one peak is clearly observed at 25, the same position, in the XRD pattern of Bi2Te3-PANI composite. The observation of a single peak is related to the monodistribution of the periodicity of the repeat unit of the PANI and ordering of the molecular arrangement of the Bi2Te3 in the PANI matrix (Talwar et al., 2014). This suggests that PANI generate an ordered molecular arrangement of Bi2Te3 in the Bi2Te3-PANI composite.Figure 1 XRD patterns of unmingle d PANI, Pure Bi2Te3 and Bi2Te3-PANI composite4.2 UV-vis spectroscopyFigure 2 shows the UVvis spectra of the samples used to explore the electronic states of Bi2Te3, pure PANI and the Bi2Te3-PANI composite. A characteristic band centred at 697 nm, a shoulder at 478 nm, corresponding to a polaronic transition (polaron- *) and a band around at 389 nm, assigned to the * electron orbital transition are observed in Bi2Te3-PANI composite. In comparison with UVvis spectra of the pure PANI a band around 385 nm, assigned to the * electron orbital transition, shifts to prolonged wavelength at 389 nm in Bi2Te3-PANI composite. The polaronic transition (polaron- *) is absent in the pure PANI but is observed in Bi2Te3-PANI composite. These show an interaction between the quinoid ring of PANI and Bi2Te3 (Xia and Wang, 2003). This is a signature of an ordered molecular arrangement in Bi2Te3-PANI composite and it is the purely surface conducting state.Figure 2 UV-vis spectra of Pure PANI, Bi2Te3 an d Bi2Te3-PANI composite4.3 Electrical characterizationFigure 3 Variation of the electrical conductivity with temperature of Bi2Te3, PANI and Bi2Te3-PANI composite.The variations of electrical conductivity as a function of temperature of the prepared samples are shown in figure 3. The value of electrical conductivity for Bi2Te3 slightly decreases with the cast up in the temperature. However, both PANI and Bi2Te3-PANI composite show increase in the value of electrical conductivity with temperature. The electrical conductivity of the Bi2Te3-PANI composite is higher than that of its pure constituents everyplace a whole temperature range. The enhancement in the surface conductivity indicates the increase in protected states at the surface compared to that of the pure Bi2Te3. This may be due to the large surface provided to the Bi2Te3 by the PANI generated ordered molecular arrangement of Bi2Te3 in the Bi2Te3-PANI composite.5. ConclusionsIn conclusion, we carried out a systematic study of structure, UV-Vis Spectra and surface conductivity of Bi2Te3 (5%)-PANI (95%) composite, pure Bi2Te3 and pure PANI. Bi2Te3 was synthesized by a method similar to solvothermal method, whereas, pure PANI and Bi2Te3-PANI composite were synthesized by a chemical oxidative method. The materials were structurally characterized and the electrical properties were investigated in the temperature range from room temperature to 100C. The electrical conductivity of the Bi2Te3-PANI composite was found to be higher than that of its pure constituents at all the temperatures. The enhancement in the surface conductivity may be due to the PANI generated ordered molecular arrangement of Bi2Te3 in the Bi2Te3-PANI composite, as confirmed from powder x-ray diffraction (XRD), UVvis spectral analysis.AcknowledgementsIt is a pleasure to thank Dr. S. B. Kondawar for implemental discussions. This work was supported by the Department of Science and Technology (DST), India, under women scientist scheme-A (WO S-A), File No. SR/WOS-A/PM-1001/2014.ReferencesChatterjee K., Suresh A., Ganguly S., Kargupta K., Banerjee D., 2009. Bismuth nitrate doped polyaniline Characterization and properties for thermoelectric application. Mater. Charact. 60, 597601.Das Damodara V., Soundararajan N., 1988. Size and temperature effects on the thermoelectric power and electrical resistivity of bismuth telluride thin films, Phys. Rev. B 37, 4552-9.Deng Yuan, Xi-song Zhou, Guo-dan Wei, Jing Liu, Ce-Wen Nan, Shu-jing Zhao 2002. Solvothermal preparation and characterization of nanocrystalline Bi2Te3 powder with different morphology, J. of Phy. and chem. of Solids. 63, 2119-2121.Hasan, M., Z., Kane, C., L., 2010. Colloquium Topological insulators, Reviews of modern physics 82, 3045-23.Hostler S., R., Kaul P., Day K., Qu V., Cullen C., Abramson A., R., 2006. thermal and electrical characterization of nanocomposites for thermoelectric, IEEE ITHERM 07803295, 24, 14005.Li Y., Zhao Q., Wang Y., Bi K., 2011. Synthesis and characterization of Bi2Te3/Polyaniline composites, Mater. Sci. Semicond. Proc. 14, 219-222.Marjanovic, G., C., 2013. new-fangled advances in polyaniline composites with metals, metalloids and nonmetals, Synthetic Metals 170, 31-56Stejskal J., Gilbert R.., G., 2002. Polyaniline Preparation of a Conducting Polymer, Pure Appl. Chem. 74, 857-867.Talwar V., Singh O., Singh R., C., 2014. ZnO aided polyaniline nanofibers and its application as ammonia gas sensor, Sensors and Actuators B 191, 276-282.Toshima N., Imai M., Ichikawa S., 2011. Organicinorganic Nanohybrids as Novel Thermoelectric Materials Hybrids of Polyaniline and Bismuth (III) Telluride Nano elements, J. Electron. Mater. 40, 898902.Xia H., Wang Q., 2003. Preparation of Conductive Polyaniline/ Nanosilica particle composites through Ultrasonic Trradiation, J. Appl. Polym. Sci 87, 1811-7.Xu X., Chen L., Wang C., Yao Q., Feng C., J., 2005. Template synthesis of heterostructured polyaniline/Bi2Te3 nanowires, Solid carry Ch em. 178, 2163-6.Zhao X., B., Hu S., H., Zhao M., J., Zhu T., J., 2002. Thermoelectric properties of Bi0.5Sb1.5 Te3/Polyaniline hybrids prepared by Mechanical blending, Mater. Lett. 52, 1479.** Corresponding author. Tel. +91 9921491567 autotype +0-000-000-0000 .E-mail reference book emailprotected Corresponding author. Tel. +91 9890155077 fax +0-000-000-0000 .E-mail address emailprotectedS1Elsevier to update with volume and page numbers.

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