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Structural, Morphological and Thermoelectric Studies of SnTe-Te Nanocomposite Satyendra Singh a) , Surasree Sadhukhan, Prakash Behera and R. Venkatesh Low Temperature Laboratory, UGC-DAE Consortium for Scientific Research, University Campus, Khandwa Road, Indore 452 001, M.P, India a) Corresponding author: [email protected] Abstract. SnTe-Te nanocomposites have been synthesized by Microwave assisted solvothermal process to study the structural, morphological and thermoelectric properties. The X-ray diffraction studies reveals a cubic FCC nature of the SnTe sample along with hexagonal structure of Te. Morphological studies from FESEM measurements indicates that the two-dimensional sheets of SnTe sample (~370 nm) coexist along with the Te nanorods of length ~1.4 µm and diameter~145 nm. Interestingly, the thermoelectric properties of nanocomposites with p-type carriers show S=56µV/K at room temperature which is 36% higher than that of the pure SnTe nanoparticle as reported in literature. Enhanced thermoelectric power in SnTe-Te nanocomposites can be attributed to the presence of Te nanorods which are acting as the phonon scattering centre. These SnTe-Te nanocomposites synthesized through scalable microwave synthesis with enhanced thermoelectric power and linear temperature dependence can open up a new gateway as potential materials for high temperature thermoelectric applications. 1. INTRODUCTION Tin telluride is (IV-VI) group compound which is fascinating the research attention of the researchers due to its promising thermoelectric properties from several decades. But now a days, this material is renowned for their novel topological properties. Tin telluride (SnTe) is a n-type [1] and p-type [2] narrow band gap semiconductor with direct band gap 0.18e.V. Normally, tin telluride forms p-type extrinsic semiconductor due to tin vacancies and it is a low temperature superconductor [3]. Theoretical studies state that the n- type tin telluride thermoelectric performance may be particularly good [4]. Tin telluride is a thermoelectric material at high temperature as well as

Title Goes Here - NCPCM · Web viewTopological properties are exhibited in nanomaterials due to the enhancement of surface to bulk contribution. Topological Insulators have odd number

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Title Goes Here

Structural, Morphological and Thermoelectric Studies of SnTe-Te Nanocomposite

Satyendra Singha), Surasree Sadhukhan, Prakash Behera and R. Venkatesh

Low Temperature Laboratory, UGC-DAE Consortium for Scientific Research,

University Campus, Khandwa Road, Indore 452 001, M.P, India

a)Corresponding author: [email protected]

Abstract. SnTe-Te nanocomposites have been synthesized by Microwave assisted solvothermal process to study the structural, morphological and thermoelectric properties. The X-ray diffraction studies reveals a cubic FCC nature of the SnTe sample along with hexagonal structure of Te. Morphological studies from FESEM measurements indicates that the two-dimensional sheets of SnTe sample (~370 nm) coexist along with the Te nanorods of length ~1.4 µm and diameter~145 nm. Interestingly, the thermoelectric properties of nanocomposites with p-type carriers show S=56µV/K at room temperature which is 36% higher than that of the pure SnTe nanoparticle as reported in literature. Enhanced thermoelectric power in SnTe-Te nanocomposites can be attributed to the presence of Te nanorods which are acting as the phonon scattering centre. These SnTe-Te nanocomposites synthesized through scalable microwave synthesis with enhanced thermoelectric power and linear temperature dependence can open up a new gateway as potential materials for high temperature thermoelectric applications.

1. INTRODUCTION

Tin telluride is (IV-VI) group compound which is fascinating the research attention of the researchers due to its promising thermoelectric properties from several decades. But now a days, this material is renowned for their novel topological properties. Tin telluride (SnTe) is a n-type [1] and p-type [2] narrow band gap semiconductor with direct band gap 0.18e.V. Normally, tin telluride forms p-type extrinsic semiconductor due to tin vacancies and it is a low temperature superconductor [3]. Theoretical studies state that the n-type tin telluride thermoelectric performance may be particularly good [4]. Tin telluride is a thermoelectric material at high temperature as well as topological material at low temperature. SnTe is a novel topological material which is the counter part of the topological insulator. Topological materials are those which have conducting surface states but interior part (bulk) of these materials are insulating due to presence of internal magnetic field. In topological insulator time reversal symmetry plays a crucial role but in SnTe topological crystalline insulator surface states are protected by mirror symmetry instead of time reversal symmetry [5]. Nanomaterials are responsible for high thermoelectric performance due to low lattice thermal conductivity [6]. Topological properties are exhibited in nanomaterials due to the enhancement of surface to bulk contribution. Topological Insulators have odd number of Dirac cones on the surface states while TCI`s have even number of Dirac cones on the surface states due to which TCI`s have high tunability properties [7]. Nanocomposite materials are known for their high thermoelectric performance due to reduction in the lattice thermal conductivity by scattering of phonons.

2. SAMPLE PREPARATION AND CHARACTERIZATION2.1 Microwave Assisted Synthesis of SnTe-Te Nano Composites

A microwave-assisted solvothermal synthesis technique was used for the preparation of SnTe-Te nanocomposites. Microwave synthesis technique provides fast, scalable, uniform heating, easy handling and sufficient amount of materials with higher reproducibility. Temperature can be controlled more precisely in this process as conditions required. In this synthesize technique, we followed a procedure similar to R. Metha et al; [8] for the preparation of sample by this microwave-assisted solvothermal synthesis procedure. For the synthesis of SnTe-Te nanocomposite materials; SnCl2.2H2O (451.6 mg), Te powder (382.7 mg), 5 ml TOP, 14 ml Pentane-di-ol and 3 mL TGA have been taken as precursor materials. The dissolved solution of SnCl2.2H2O, Pentane-di-ol (PD), TGA, Tellurium Powder and Tri-octyl phosphine (TOP) were mixed, microwave heated for 3 minutes and left up to room temperature for cooling around 1hr. The obtained black precipitate was centrifuged and washed 3 times with ethyl alcohol and acetone respectively.

2.2 Characterization

The structural measurements were investigated by XRD (Bruker D8 Advance X-ray diffractometer system with Cu Kα radiation source). There is presence of tellurium peaks in the xrd measurements matched with the JCPDS card No: 00-036-1452 as well as SnTe JCPDS card No: 03-065-7162, followed the microwave synthesis technique. From the observed pattern of xrd, the composite material shows the hexagonal Te phase along with SnTe cubic phase. All the diffraction peaks are indexed to the FCC cubic SnTe (with space group Fm-3m) and Te (with space group P3121) as shown in Fig 1(a). The Te peaks and SnTe peaks are shown by blue and red colour respectively in Fig 1(a). The crystallite size of SnTe and Te in prepared nanocomposite is estimated to be ~54 nm and ~75 nm corresponding to the main peak as determined by Debye Scherrer formula (τ=Kλ/βcosθ). Where τ is the crystallite size, K is a constant taken to be 1, λ is the wavelength of Cu K alpha X-ray (1.54Å), β is the full width at half maximum (FWHM) obtained from the main peak and θ is the diffraction angle. The EDS compositional analysis was carried out using “Bruker made XFlash X130”. The EDS spectrum is taken over the single Tellurium nanorods present in the SnTe-Te nano composite as shown in inset of Fig 1(b) which confirms the presence of Te nanorods along with the SnTe nanoparticles. This is in correspondence with the structural analysis.

b

a

Figure 1. (a) XRD plot of SnTe nanomaterials along with Te peaks. Red colour peaks indicate the SnTe peaks while blue colour indicate Te peaks. (b) shows the eds spectrum of nanocomposites of SnTe-Te and inset shows the FESEM image of the composite sample.

2.3 Morphology Studies

Morphological studies of SnTe nanomaterials were studied with the instrument FEI made “NOVA NANO SEM 450”. The morphology obtained from FESEM images imply that the SnTe nanoparticle are coexisting with the Tellurium nanorods as shown in Fig 2a), 2b) and 2c). The cross-sectional edge to edge length of the SnTe is found to be ~370nm. The length of the Tellurium nanorods were found to be ~1.4 µm with diameter~145 nm with the analysis of Image J software.

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Figure 2. FESEM images of SnTe-Te nanocomposites a), b) and c) from lower to higher magnification respectively prepared with microwave assisted solvothermal technique.

2.4 Thermoelectric Properties of the Composite Material of SnTe-Te

The thermopower measurement has been performed in homemade Thermoelectric power measurement setup by “DC Differential Sandwich method”. The thermopower of composite (SnTe-Te) has been shown in Fig 3 as the function of temperature which indicates the p-type nature of the composite. Temperature dependence of S is fitted with linear fit which shows the metallic nature like behavior and the absence of hump confirms the single band conduction. The linear increase in S with T shows that this SnTe-Te nanocomposite is favourable for high temperature thermoelectric applications. Magnitude of room temperature thermoelectric power of our nanocomposite sample is compared with the reported SnTe values from literature is as shown in Fig3.

Figure 3. Graph shows the thermopower of SnTe-Te composite as the function of temperature with linear fitting. The dots indicate the room temperature comparison with SnTe.

3.Result and Discussion

Structural and morphological properties confirm the presence of SnTe-Te nanocomposites. These nano structuring with enhanced surface to volume ratio by fast, facile and scalable microwave synthesis technique is beneficial in probing the topological properties of SnTe system. Nano structuring of SnTe materials are responsible for the potential applications in thermoelectric materials which is used in many energy sources. In fact, both SnTe and Te are good P-type thermoelectric materials which have good thermoelectric performance. The thermopower of our composite material is also in line with previous reported literature on this composite [9]. The Seebeck coefficient for SnTe material addressed by Dongyang Wang et al; and E. Z. Xu et al; is 21.5µV/K and 41 µV/K at room temperature respectively. The room temperature thermopower of composite (SnTe-Te) has been obtained ~56 µV/K which is higher than the thermoelectric power value reported for SnTe material. The drop in the lattice thermal conductivity due to the phonon scattering on the interfaces of (SnTe-Te) is reported to play the key role for high thermoelectric performance in composites made of bulk materials [9]. As the thermal conductivity of nanocomposites would be further lower than the bulk materials. A combined thermal conductivity measurement, thermopower measurement and electrical conductivity measurements at high temperature can prove that these nanocomposites are promising for high temperature thermoelectric application.

Conclusion

The nanomaterials of TCI`s SnTe have been synthesized successfully by Microwave-assisted solvothermal synthesis procedure. A nano composite of SnTe and Te have been obtained during the synthesis of SnTe nanomaterials in presence of excess heat. To control the morphology of the SnTe nanomaterials, TGA is used as the shape directing and reducing agent. The synthesized SnTe-Te nanocomposites by this fast, facile and scalable microwave are advantageous for the point of thermoelectric applications and enhanced surface property of the sample for the topological point of view. High value of thermopower in composite materials concludes that composites are useful for thermoelectric performance due to low lattice thermal conductivity.

Acknowledgments

Authors thank Director and Centre Director of UGC-DAE CSR, Indore for their support. The authors would like to express their gratitude to Dr. Mukul Gupta and Dr. D.M.Phase for XRD and FESEM measurements respectively. LT labmates are acknowledged for their precious help.

References

Xin Chen et al; Sci Rep 3, 3168 (2013)

Gangjian Tan et al; J. Am. Chem. Soc., 136, 7006−7017 (2014)

R. A. HEIN and P. H. E. MEIJER Phys. Rev. 179, 497 (1969)

David J. Singh Funct. Mater. Lett. 03 (4): 223–226 (2010) 

Y. Tanaka et al; Nat. Phys. 8(11) 800-803 (2012)

Shan Li et al; J. Mater. Chem. A, 6, 11686-11693 (2018)

Wang et al; Chin. Phys. B, 25(11), 117313 (2016)

R. J. Mehta et al; Nano Lett. 12.9 4523-4529 (2012)

Bin Yang et al; Intermetallics 112 106499 (2019)

Dongyang Wang et al; J. Alloys Compd S0925-8388 33474-1 (2018)

E. Z. Xu et al; Nanoscale, 7, 2869-2876 (2015)

Bin Yang et al; J. Mater. Sci. Mater. Electron 29:18949–18956 (2018)

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