Effect of Temperature and Capping Agents on Structural and Optical Properties of Tin Sulphide Nanocrystals

Oluwalana, Abimbola E.; Ajibade, Peter A.

doi:https://doi.org/10.1155/2019/8235816

Journal of Nanotechnology

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Abstract Introduction Experimental Results and Discussion Conclusion Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 8235816 | https://doi.org/10.1155/2019/8235816

Effect of Temperature and Capping Agents on Structural and Optical Properties of Tin Sulphide Nanocrystals

Abimbola E. Oluwalana¹and Peter A. Ajibade¹

Academic Editor: Eduard Llobet

Received18 Aug 2018

Revised01 Nov 2018

Accepted05 Nov 2018

Published02 Jan 2019

Abstract

SnS nanocrystals were synthesized using bis(phenylpiperazine dithiocarbamate)tin(II) in oleic acid (OA) and octadecylamine (ODA) at three different temperatures (150, 190, and 230°C). XRD diffraction pattern confirms that OASnS and ODASnS nanoparticles are in the orthorhombic phase and the type of capping agent used affects the crystallinity. Transmission electron microscopy (TEM) images shows spherically shaped nanocrystals for oleic acid capped SnS (OASnS) while octadecylamine (ODASnS) are cubic. Monodispersed SnS of size range 10.67–17.74 nm was obtained at 150°C for OASnS while the biggest-sized nanocrystals were obtained at 230°C for ODASnS. Temperature and capping agents tuned the crystallite sizes and shapes of the as-prepared nanocrystals. Electron dispersive X-ray spectroscopy indicates the formation of tin sulphide with the presence of Sn and S peaks in the nanocrystals. Flowery and agglomerated spherical-like morphology were observed for ODASnS and OASnS nanocrystals, respectively, using a SEM (scanning electron microscope). Direct electronic band gaps of the synthesized SnS nanocrystals are 1.71–1.95 eV and 1.93–2.81 eV for OASnS and ODASnS nanocrystals, respectively.

1. Introduction

Tin is one of the relatively abundant metals having mild toxicity in comparison with other elements such as lead, mercury, and cadmium. Its rich structural chemistry is partly due to the +2 oxidation state which enable it to form compounds with different coordination geometries ranging from 2 to 9 [1–3]. SnS is a IV–VI semiconductor like PbS, PbSe, GeS, and SnS among others that exhibit size-dependent, luminescent, electrical, and optical properties [4–7]. Tin sulphide exists in three main forms: SnS, SnS₂, and SnS₃, with SnS having a band gap of 1.4 eV which is relatively close to that of silicon (1.1 eV) [8]. Tin sulphide exists as a orthorhombic crystal like distorted NaCl structure in which the Sn anion is surrounded by six S atoms separated by Van der Waals forces [2]. SnS nanoparticles have unique properties suitable for a wide range of nanoscale electronics, photodetectors, sensing devices, infrared detectors, storage of energy, and fabrication of photovoltaics [9–20]. SnS possesses photoconducting, photocatalytic, and Pieter effects making them useful in thermoelectric cooling, thermoelectric power generation, and near-infrared photoelectronics [16, 21–25].

Synthetic routes such as hydrothermal [26], solvothermal [27], hot injection [28], aqueous solution [29], pyrolysis [30], colloidal route [31], single-source approach [32, 33], precipitation [34], microwave [35], electrodeposition [36], and so on have been utilized for the synthesis of SnS nanoparticles. The single-source precursor has proven to be a more effective route that forms nanoparticles of high qualities with well-defined size and shape. The use of solvothermal decomposition of single-source precursors as capping agents at low temperatures resulted in high-quality SnS nanocrystals [37]. SnS usually form anisotropic nanostructure with various morphologies such as spherical or close to spherical [38], tetrahedral [39], nanocubes [40], triangular shape [41], nanorods [42], nanoflowers [43, 44], nanowires [36], nanoplatelets [45],and nanosheets [46]. Koktysh et al. [47] synthesized oleylamine-capped SnS nanoparticles from bis(diethyldithiocarbamato)tin(II) with particle size in the range of 5–10 nm. It has been established that the control of nanoparticles morphology, size, and shape is influenced by the molecular precursor, the capping agents, and the reaction temperature [32, 48] which inherently affects the surface energy [49]. We report the effects of the capping agents and thermolysis temperature on the structural and optical properties of the as-prepared SnS nanoparticles from bis(phenylpiperazine dithiocarbamato)tin(II).

2. Experimental

2.1. Materials and Physical Measurements

N-phenyl piperazine, carbon disulphide, sodium hydroxide, tin(II) chloride dihydrate, trioctylphosphine, oleic acid, and octadecylamine of analytical grade were purchased from Sigma-Aldrich and used without further purifications. The FTIR of the ligand, complex and nanocrystals spectra were recorded using an Agilent technologies Cary 630 FTIR spectrometer in the frequency range of 4000–650 cm⁻¹. ¹H and ¹³C-NMR of ligand and complex were recorded on an 400 MHz Bruker Avance III NMR spectrometer with tetramethylsilane serving as internal standard. Absorption spectra were obtained using an Agilent technologies Cary 100 UV-Vis spectrophotometer in the wavelength range of 200–800 nm. Photoluminescence emission was obtained using a PerkinElmer LS 45 fluorescence spectrometer. Melting point calculated using stuart SMP3 version 5.0. Transmission electron microscope (TEM) images of the nanocrystals were determined using a JEOL JEM-1400 transmission electron microscope with an accelerating voltage of 120 kV. The powder X-ray diffraction analysis was done using a Bruker D8 advanced diffractometer (Billerica, MA, USA). The morphology and compositions of tin sulphide nanocrystals were analysed using a Zeiss Evols 15 scanning electron microscope equipped with energy dispersive X-ray spectroscopy.

2.2. Synthesis of N-Phenyl Piperazine Dithiocarbamate Sn(II) Complex

Bis(phenylpiperazine dithiocarbamato)tin(II) was synthesized using modified literature procedures [33]. Briefly, 1.2 g (0.03 mol) of sodium hydroxide was dissolved in distilled water and allowed to cool in ice to which N-phenyl piperazine (4.58 mL, 0.03 mol) was added followed by cold carbon disulphide and allowed to stir in ice bath for 4 h. The product obtained (PhPipdtc) was filtered and washed using diethyl ether and allowed to dry. The dried sodium N-phenyl piperazine dithiocarbamate (PhPipdtc) was then dissolved in 50 mL of methanol, and 0.015 mol of tin(II) chloride dihydrate dissolved in 25 mL of methanol was added dropwise to the dithiocarbamate methanolic solution and stirred at room temperature for 3 hours (Scheme 1). The resulting precipitate was washed with water then followed by diethyl ether. The complex [Sn(PhPipdtc)₂] obtained was orange in colour. Yield: 83.99%, 1.9897 g; melting point: 212.4–214.9°C. PhPipdtc: anal. cal. for C₁₁H₁₃N₂NaS₂·H₂O: C, 44.58; H, 5.78; N, 9.45; found: C, 44.22; H, 5.65; N, 9.16. ESIMS (m/z): 237 [M-Na]^-, selected IR bands (cm⁻¹): 1006 (CS₂), 1462 (N-CS₂). ¹H-NMR: (D₂O) δ 3.23 (t, 4H–CH₂), 4.50 (t, 4H–CH₂), 7.07–7.41 (m, 5H-C₆H₅); ¹³C-NMR: (D₂O) δ 49.70–50.45 (C₄N₂), 117.98–150.33 (C₆H₅), 209.0 (CS₂). [Sn(PhPipdtc)₂]: anal. cal. for C₂₂H₂₈N₄NaS₄Sn: C, 44.38; H, 4.74; N, 9.41; found: C, 44.54; H, 5.01; N, 9.09. ESIMS (m/z): 618 [M-Na]⁺, selected IR bands (cm⁻¹): 915 (CS₂), 1489 (N-CS₂). ¹H-NMR: (DMSO) δ 3.18 (t, 4H–CH₂), 3.31 (t, 4H–CH₂), 6.88–7.27 (m, 5H-C₆H₅); ¹³C-NMR: (DMSO) δ 43.70–47.2 (C₄N₂), 116.4–150.94 (C₆H₅), 204.3 (CS₂).

2.3. Synthesis of SnS Nanocrystals

0.2 g of Sn(II) phenyl piperazine dithiocarbamate complex was dispersed in 1 mL trioctylphosphine (TOP). The resulting solution was injected into hot 4 g of octadecylamine in a three-necked round bottom flask at 150, 190, and 230°C. There was a reduction in temperature of about 12–25°C, after which it was allowed to stabilize at the desired temperature and then stirred for 1 hour. The reaction was left to cool to 70°C followed by the addition of cold methanol. The flocculate was then centrifuged at 3500 rpm for 30 minutes, and the supernatant was decanted and washed severally. The nanocrystals were dispersed in hexane for further analysis. The same procedure was repeated using 6 mL of oleic acid. The resulting nanocrystals prepared from octadecylamine were labelled ODASn1 (150°C), ODASn2 (190°C), and ODASn3 (230°C). Those prepared from oleic acid were labelled OASnS1 (150°C), OASnS2 (190°C), and OASnS3 (230°C).

3. Results and Discussion

3.1. Spectroscopic Studies of PhPipdtc and [Sn(PhPipdtc)₂]

The phenyl-piperazine dithiocarbamate (Phpipdtc) electronic spectrum exhibited three absorption bands attributed to π⟶π of υ|N−C=S| at 252 nm, π⟶π of υ|C−S=S| at 277 nm, and n⟶π of the sulphur atoms at 337 nm [50]. On complexation, the absorption band of υ|C=N| chromophore was observed at 265 nm due to the thioureide group intramolecular transition in the Sn(II) dithiocarbamate complex [51]. The υ|N−CS₂| band observed at 1462 cm⁻¹ in the ligand spectrum shifted to 1489 cm⁻¹ in the complex due to the delocalization of the electron from the nitrogen attached to the thioureide moiety confirming the coordination of tin(II) ion to the ligand [52]. The ν|C−S| symmetrical vibrational band peak observed in the ligand at 994 cm⁻¹ as two peaks shifted to 915 cm⁻¹ as a single peak on coordination to tin(II) ion. It has been established that a single band around 1000 ± 70 cm⁻¹ in metal dithiocarbamate complexes is attributed to bidentate coordination of the dithiocarbamate moiety while the splitting of the band in this region indicates the monodentate coordination mode [53]. The ¹H-NMR spectrum of PhPipdtc showed the methylene proton of piperazine signals at 3.23 ppm and 4.50 ppm as triplet. The downfield resonance at 4.50 ppm is because of the thioureide nitrogen while the phenyl proton resonated at a higher frequency of 7.07–7.41 ppm. On complexation, phenyl protons shifted to 6.88–7.27 ppm, while the methylene protons resonated at 3.18 and 3.31 ppm. The desheilding effect is due to delocalization of thioureide nitrogen towards the sulphur atoms which increases electronegativity of the surrounding protons [54]. The ¹³C-NMR spectrum shows the piperazine carbon resonating at 49.70–50.45 ppm, and the phenyl carbons resonating at 117.98–150.33 ppm with the thioureide carbon resonating at 209.0 ppm. On complexation, the piperazine carbon shifted upfield to 43.7–47.2 ppm, while the phenyl carbons have a desheilding resonance at 116.4–150.94 ppm. The thioureide carbon shifted to 204.3 ppm because of the coordination of tin(II) ion to the thioureide sulphur.

3.2. Structural Studies of SnS Nanocrystals

3.2.1. X-Ray Diffraction of SnS Nanocrystals

The XRD patterns of oleic acid capped tin sulphide nanoparticles (Figure 1(a)) show four well-defined peaks at 30.90°, 34.73°, 39.37°, and 60.36° corresponding to (111), (101), (131), and (201) planes of orthorhombic crystal structure of SnS. The preferred orientation along the (111) plane was observed correlating with the standard values of JCPD card no 39–0354 [55]. The relatively smaller broad diffraction peaks suggest smaller particle sizes. Sharp intense peaks in the XRD patterns of ODASnS (Figure 1(b)) at 22.37°, 24.78°, 25.45°, 27.54°, 33.65°, 41.90°, and 47.27° correspond to (110), (110), (120), (120), (111), (311), and (002) of SnS which is similar to Pullabholla and Maliba [56] observation using HDA (hexadecylamine) as a capping agent. The sharp and narrow peaks of (120) and (101) with high intensity show that the nanoparticles are purely SnS which is also of orthorhombic phase. The difference in the XRD pattern is due to the different capping agents used.

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3.2.2. Transmission Electron Microscopic Analysis of SnS Nanocrystals

TEM images of SnS nanocrystals showed spherical and cubic shapes as presented in Figure 2. The as-synthesized SnS nanocrystals show diverse size and shape by varying the temperature and capping agents. OASnS nanocrystals has monodispersed spherical shape with different sizes at various temperatures such as 10.67–28.74 nm, 12.82–17.10 nm, and 35.25–75.10 nm, respectively, for 150, 190, and 230°C showing that temperature influences the sizes of the nanocrystals obtained. ODASnS nanocrystals are spherical shaped of size range 22.00–28.32 nm at 150°C, which changed to agglomerated nanocrystals cubes at 190°C with particle size in the range of 28.15–33.36 nm. At 230°C, there was increase in size to 67.04–80.15 nm while maintaining the cubic shape. Agglomeration was observed to increase as the temperature increases this could be due to surface attraction of the nanocrystals. OA and ODA capped SnS nanocrystals followed the trend of increase in size with increase in temperature. The capping agents used showed various degrees of sizes. Oleic acid gave smaller size SnS nanocrystals of monodispersed spherical shape, while octadecylamine has bigger agglomerated nanocrystals with cube-like shape.

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3.2.3. SEM Analysis and EDX Spectra of SnS Nanocrystals

The influence of capping agents and reaction temperature on the SnS nanoparticle morphology was investigated using SEM as shown in Figure 3. OASnS nanocrystals had spherical aggregates. The morphologies of ODASnS were different from those of OASnS as they showed flaky-like morphology [57]. The SEM images show diversity in morphology due to different capping agents used in the preparation of tin sulphide. Temperature has no effect on the morphology of OASnS and ODASnS. Carbon and oxygen signals were observed in the EDX (electron dispersive X-ray) spectra (Figure 4) of SnS nanocrystals; this is because of the capping agents used and the carbon tape. The presence of Sn and S peaks is an indication that SnS nanocrystals were formed. OA-capped SnS showed elemental composition of 53% to 47% of Sn and S at all temperatures, and ODASnS nanocrystals composition was 52% to 48%. The presence of excess sulphur is an indication of dangling sulphur bonds. In all the SnS nanocrystals of various capping agents, the composition of Sn is slightly more than S, while a change in temperature has no effect on the composition of SnS nanocrystals showing its stability [58].

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3.4. Optical Studies of SnS Nanocrystals

Quantum confinement makes semiconductors’ nanoscale band gap deviate from their bulk band gap, and this is caused by photogenerated electron-hole pairs [40, 59]. To obtain the band gap of the synthesized SnS nanocrystals, the absorption spectra data were measured in the wavelength range of 300–800 nm at room temperature. Tauc’s analysis was used for conversion by utilizing the near-edge absorption equation (αhv)ⁿ = A(hv − Eg), where α is the wavelength-dependent absorption coefficient, A is a constant, hv is the photon energy, and Eg is the band gap. The transition process was denoted as “n” which can be 1/2 for indirect allowed transitions, 1/3 for indirect forbidden transition, 2/3 for direct forbidden transition, and 2 for direct allowed transition. In this study, the direct allowed transition was used as a good fit of extrapolation was obtained by plotting (αhv)² against hv and extrapolating the x-axis value [33, 60]. The band gap is in the range of 1.71–1.95 eV for OASnS and 1.93–2.81 eV for ODASnS nanocrystals (Figure 5) which is higher than 1.4 eV of bulk SnS [61] exhibiting blue shift of the band gap. SnS band gap for direct allowed transitions of 1.0–1.7 eV has been reported [62–64]. Increase in the band gap of the SnS nanoparticle could be attributed to combination of strain, particle size confinement, and defects and disorder of grain boundaries [33, 65]. The capping agents and temperature influence the band gap; the highest band gap energy (2.81 eV) was obtained at 230°C for ODASnS nanoparticle. The UV-Vis absorption spectra presented in Figure 5 show the nanocrystals having absorption at 337 nm for OASnS1 and 345 nm for ODASnS1 while those of the remaining nanocrystals occurred at 348 nm. Wavelength band shows quantum confinement effect as lower wavelength implies smaller diameter and vice versa [59, 66]. The photoluminescence spectra of SnS nanocrystals were recorded at room temperature at an excitation wavelength of 350 nm (Figures 6–7); strong and broad emission peaks maximum was obtained at 408–431 nm for ODASnS while OASnS has a sharp emission band [51, 67].

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3.5. FTIR Studies of SnS Nanocrytals

The FTIR spectra of OASnS and ODASnS nanocrystals were compared with their respective capping agents for the confirmation of their coating (Figure 8). NH₂ bending modes were observed at 927–966 and 1058–1070 cm⁻¹ in ODASnS nanocrystals which were present at 964 cm⁻¹ in the capping agents alongside the N-H wagging mode at 793 cm⁻¹ which is absent in the nanocrystal spectra. This can be attributed to the inhibition of the wagging mode due to its attachment to the surface of SnS as reported in literature [68–70]. C-N bending vibrations were observed at 1468 cm⁻¹, and the combination of NH₂ scissor and bending vibration at 1668 cm⁻¹ in the capping agents and their nanocrystals. The difference observed is that the nanocrystals has less intensity compared to the capping agents, and a shift of 20–60 cm⁻¹ was observed for the NH₂ scissors and bending vibrations. The N-H asymmetric peak observed at 3329 cm⁻¹ is weak in the nanocrystals confirming interaction between the amine and the SnS surface [71]. C-H vibrations were found at 2851–2919 cm⁻¹ which is common to (CH₂)_n chains more than 3. Carbonyl vibration, deformed vibration, and rocking vibration of CH₂ were observed, respectively, at 1710, 1465, and 722 cm⁻ in OASnS nanocrystals apart from the carbonyl bond which disappeared and a new band at 1599–1606 cm⁻¹ appeared which is the asymmetric mode of carboxylate metal salt [68, 72, 73].

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4. Conclusion

In conclusion, we report the synthesis and use of bis(phenylpiperazine dithiocarbamate)tin(II) complex as a single molecular precursor to prepare oleic acid and octadecylamine capped at 150, 190, and 230°C. The crystallinity of the synthesized tin sulphide nanoparticles was affected by the capping agents used though the same orthorhombic phase was observed with the XRD pattern. Monodispersed spherical-shaped SnS nanoparticles were obtained in OASnS, while ODASnS nanocrystals gave aggregated cubic nanocrystals. At 150°C, small-sized nanocrystals in the range of 10–28 nm were favoured in all the capping agents, while at 230°C, bigger size in the range of 35–80 nm was obtained. The morphology was influenced by the capping agents used as flower-like, and spherical-like morphologies were obtained for ODASnS and OASnS nanocrystals. Band gap measurements were in the range of 1.71–1.95 and 1.93–2.81 eV for OASnS and ODASnS, respectively; the highest band gap is affected by particle size confinement. Temperature and capping agents were found to influence the size and shape of the nanocrystals. SnS FTIR showed that they were coated with the capping agents.

Data Availability

The data used to support the findings of this study are available from the authors upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Authors’ Contributions

AE Oluwalana carried out the experimental in the laboratory of PA Ajibade and under his guidance.

Acknowledgments

The authors acknowledge the award of research grant by the National Research Foundation and Sasol, South Africa.

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Copyright © 2019 Abimbola E. Oluwalana and Peter A. Ajibade. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Journal of Nanotechnology

Effect of Temperature and Capping Agents on Structural and Optical Properties of Tin Sulphide Nanocrystals

Abstract

1. Introduction

2. Experimental

2.1. Materials and Physical Measurements

2.2. Synthesis of N-Phenyl Piperazine Dithiocarbamate Sn(II) Complex

2.3. Synthesis of SnS Nanocrystals

3. Results and Discussion

3.1. Spectroscopic Studies of PhPipdtc and [Sn(PhPipdtc)2]

3.2. Structural Studies of SnS Nanocrystals

3.2.1. X-Ray Diffraction of SnS Nanocrystals

3.2.2. Transmission Electron Microscopic Analysis of SnS Nanocrystals

3.2.3. SEM Analysis and EDX Spectra of SnS Nanocrystals

3.4. Optical Studies of SnS Nanocrystals

3.5. FTIR Studies of SnS Nanocrytals

4. Conclusion

Data Availability

Conflicts of Interest

Authors’ Contributions

Acknowledgments

References

Copyright

3.1. Spectroscopic Studies of PhPipdtc and [Sn(PhPipdtc)₂]