Microbe-Assisted Synthesis and Luminescence Properties of Monodispersed Tb<sup>3+</sup>-Doped ZnS Nanocrystals

Liang, Zhanguo; Mu, Jun; Han, Lei; Yu, Hongquan

doi:https://doi.org/10.1155/2015/519303

Journal of Nanomaterials

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Research Article | Open Access

Volume 2015 | Article ID 519303 | https://doi.org/10.1155/2015/519303

Microbe-Assisted Synthesis and Luminescence Properties of Monodispersed Tb³⁺-Doped ZnS Nanocrystals

Zhanguo Liang,¹Jun Mu,^1,2Lei Han,¹and Hongquan Yu¹

Academic Editor: Songjun Zeng

Received29 Aug 2014

Accepted19 Oct 2014

Published28 Jan 2015

Abstract

Tb³⁺-doped zinc sulfide (ZnS:Tb³⁺) nanocrystals were synthesized by spray precipitation with sulfate-reducing bacterial (SRB) culture at room temperature. The morphology of the SRB and ZnS:Tb³⁺ nanocrystals was examined by scanning electron microscopy, and the ZnS:Tb³⁺ nanocrystals were characterized by X-ray diffractometry and photoluminescence (PL) spectroscopy. The PL mechanism of ZnS:Tb³⁺ nanocrystals was further analyzed, and the effects of Tb³⁺ ion concentration on the luminescence properties of ZnS:Tb³⁺ nanocrystals were studied. ZnS:Tb³⁺ nanocrystals showed a sphalerite phase, and the prepared ZnS:Tb³⁺ nanocrystals had high luminescence intensity under excitation at 369 nm. The main peak position of the absorption spectra positively blueshifted with increasing concentrations of Tb³⁺ dopant. Based on the strength of the peak of the excitation and emission spectra, we inferred that the optimum concentration of the Tb³⁺ dopant is 5 mol%. Four main emission peaks were obtained under excitation at 369 nm:489 nm (⁵D₄→⁷F₆), 545 nm (⁵D₄→⁷F₅), 594 nm (⁵D₄→⁷F₄), and 625 nm (⁵D₄→⁷F₃). Our findings suggest that nanocrystals have potential applications in photoelectronic devices and biomarkers.

1. Introduction

Zinc sulfide (ZnS) is one of the most important II–IV semiconductors with a band gap of approximately 3.6 eV [1] and is commercially used as a phosphor and thin film in electroluminescent devices. ZnS has been investigated over a period of 20 years as the host material of phosphor layers of electroluminescent devices and field emission displays. ZnS phosphor layers containing transition metal or rare earth metal elements as luminescent centers have been deposited using sputter deposition, thermal evaporation, and electron beam evaporation [2]. Rare-earth-doped wide-band-gap semiconductors have attracted considerable interest in recent years because of attempts to develop novel optoelectronic devices, which combine the unique luminescence features of rare earth ions [3–5]. Since Bhargava et al. first reported the remarkable optical properties of Mn-doped ZnS nanocrystals prepared by chemical process at room temperature in 1994 [6, 7], a large number of investigations on semiconductor nanocrystals have focused on the photoluminescence properties of Mn-doped ZnS nanocrystals [8–16], Cu-doped ZnS nanocrystals [9, 17], Sm-doped ZnS nanocrystals [18], Tb-doped ZnS nanocrystals [18–20], and Eu-doped ZnS nanocrystals [21–25] prepared by different techniques [26]. These papers, however, do not report on ZnS:Tb³⁺ nanocrystals synthesized by spray precipitation method in sulfate-reducing bacterial (SRB) culture at room temperature.

The synthesis process of ZnS:Tb³⁺ nanocrystals is a two-pronged process: one phase involves prepreparation of the sulfur source and capping agent by SRB and the other phase involves synthesis of ZnS:Tb³⁺ nanocrystals by spray precipitation. The first phase shows high efficiency in reducing hexavalent or tetravalent sulfur ions to divalent sulfur ions, which are then effectively fixed in the form of precipitates in the second phase. Thus, reduction of the content of organic pollutants and sulfur in wastewater and synthesis of luminescent nanomaterials under lower energy consumption may simultaneously be achieved. We have also developed a spray precipitation method based on the conventional precipitation method. ZnS:Tb³⁺ nanocrystals prepared by spray precipitation are smaller and more uniform than those prepared by direct precipitation. The defect of direct precipitation is that its resultant nanoparticles are either too large or highly uneven in size. The spray precipitation method avoids this defect of direct precipitation. Thus, the proposed method may be promoted for the treatment of wastewater with high sulfur contents and the preparation of nanoscale materials.

In this work, the morphology, phase structure, and luminescence properties of ZnS:Tb³⁺ nanocrystals prepared by spray precipitation with different Tb³⁺ doping concentrations were studied.

2. Experiments

2.1. Prepreparation of Sulfur Source and Capping Agent

The SRB was isolated from seawater samples obtained from Heishijiao in Dalian, China. The morphology of the SRB is shown in Figure 1. The scanning electron microscopy (SEM) image in this figure shows that the SRB are a type of short-rod bacteria. The basal culture broth contained 0.5 g L⁻¹ KH₂PO₄, 1.0 g L⁻¹ NH₄Cl, 1.0 g L⁻¹ Na₂SO₄, 2.0 g L⁻¹ MgSO₄·7H₂O, 5.0 g L⁻¹ 70% sodium lactate, 0.1 g L⁻¹ CaCl₂·2H₂O, 0.5 g L⁻¹ FeSO₄·7H₂O, 0.1 g L⁻¹ sodium thioglycolate, and 0.1 g L⁻¹ vitamin C (pH 7.2).

SRB cultivation was performed in sealed glass bottles (125 mL) at 28°C for 3 wk with 5% (v/v) inoculum amount. The in the system was gradually reduced to S²⁻ during cultivation, producing a variety of amino acids (see (1)).

Metabolic products of the bacteria were harvested from the fermentate by centrifugation for 6 min at 10,000 r/min. S²⁻ and a variety of amino acids in the metabolic products were, respectively, used as the sulfur source and the synthesis capping agent:

2.2. Synthesis

ZnS:Tb³⁺ nanocrystals were prepared by spray precipitation using S²⁻ and a variety of amino acids obtained from the metabolic products as the sulfur source and the synthesis capping agent, respectively (see (2)).

Zinc acetate and terbium chloride hexahydrate with different molar ratios were dissolved in 100 mL of deionized water (see Table 1). Subsequently, 100 mL of the homogeneous solution was sprayed as fog particles on the surface of metabolic products with S²⁻ and a variety of amino acids. This procedure successfully yielded monodispersed ZnS:Tb³⁺ nanoparticles with different molar ratios at room temperature. The products were then washed three times with deionized water and ethanol and dried in a thermostatic vacuum drier. We prepared a large number of ZnS:Tb³⁺ nanoparticles with particle sizes of 80 nm and then studied the luminescence properties of these particles.

2.3. Characterization

The nanocrystal size and morphology of the samples were observed by using a scanning electron microscope (SEM, JSM-6360LV, JEOL, Japan) and a transmission electron microscope (TEM, JOEL-2100F, JEOL, Japan). Crystal structures were characterized by an X-ray power diffractometer (XRD) using a Netherlands Empyrean diffractometer with CuKα₁ radiation ( nm). UV-Vis absorption spectra (absorption wavelength range and maximum absorption wavelength) were obtained by using a V-550 ultraviolet spectrophotometer (JASCO Corp.). Photoluminescence (PL) spectra were measured using a Hitachi F-4500 fluorescence spectrometer.

3. Results and Discussions

ZnS:Tb³⁺ nanocrystals were synthesized by the direct precipitation and spray precipitation methods with SRB culture (Figures 2(a), 2(b), 2(c), 2(d), 2(e), 2(f), and 2(g)). ZnS:Tb³⁺ nanocrystals synthesized by direct precipitation agglomerated and formed large particles, whereas ZnS:Tb³⁺ nanocrystals synthesized by spray precipitation formed homogeneous first agglomeration spherical particles approximately 80 nm in diameter. Only slight second agglomeration was observed among spray-precipitated nanocrystals. From the TEM image of ZnS:Tb³⁺ nanocrystals, we may know that the most initial nanocrystals were approximately 10 nm in diameter (shown in Figure 2(g)). Agglomeration is attributed to two phenomena: simultaneous formation of large crystal nuclei on the droplet surface and liquid contact surface and crystal nucleus for nanocrystal gradually grew up in almost the same environment during the synthetic process of ZnS:Tb³⁺ nanocrystals which have been synthesized by spray precipitation method, but the direct precipitation nucleation has less nucleus conditions and growth environment is different each time.

(a)

(b)

(c)

(d)

(e)

(f)

(g)

The luminescence properties of the ZnS:Tb³⁺ with different doping concentrations will vary with their shapes and sizes. But the sizes and shapes of the ZnS:Tb³⁺ nanocrystals shown in Figures 2(b), 2(c), 2(d), 2(e), and 2(f) were almost identical because the nanocrystals were synthesized by the same method. So, the luminescence properties of the ZnS:Tb³⁺ nanocrystals mainly depend on the doping concentration rather than on their shapes and sizes.

The XRD patterns of different ZnS:Tb³⁺ nanocrystals and undoped ZnS nanocrystals are shown in Figure 3. The patterns reveal that the nanocrystals exhibit a zinc blende crystal structure. The three diffraction peaks observed correspond to the (111), (220), and (311) planes of face-centered cubic crystalline ZnS (JCPDS number 77-2100). Considering the size effect, the XRD peaks broadened and their widths increased as the crystals became smaller. The average sizes of the ZnS:Tb³⁺ nanocrystals calculated from the Debye-Scherrer equation were determined to be approximately 10 nm. The TEM image of ZnS:Tb³⁺ nanocrystals is shown in Figure 2(g); here, the average size of the ZnS:Tb³⁺ nanocrystals is between 8 nm and 12 nm, which agrees well with our XRD estimation. Tb³⁺ doping appeared to destroy the crystalline nature of ZnS, as can be seen from changes in the graph of the (220) and (311) crystal planes. This destruction causes lattice distortions and produces a large number of lattice defects. In addition, the spectrum-verified doping concentrations have different optical properties.

The UV-Vis absorption spectra of different ZnS:Tb³⁺ and undoped ZnS nanocrystals are shown in Figure 4. The maximum absorption wavelength range of ZnS:Tb³⁺ and undoped ZnS nanocrystals was nearly 300–400 nm. The maximum absorption wavelength of ZnS:Tb³⁺ nanocrystals was shorter than that of undoped ZnS nanocrystals, and the absorption peak band of the crystals positively blueshifted with increasing concentrations of the Tb³⁺ dopant. We believe that doping with Tb³⁺ changes the crystal structure and band gap structure of semiconductor ZnS.

Figure 5 shows the excitation spectra of ZnS:Tb³⁺ nanocrystals with doping concentrations of 1%, 3%, 5%, 7%, and 9% at an emission wavelength of 545 nm. The two peaks at 369 and 377 nm are characteristic Tb³⁺ excitation peaks. The peak intensity of the ZnS:Tb³⁺ nanocrystals increased at doping concentrations of 1%, 3%, and 5% and decreased at doping concentrations of 5%, 7%, and 9%. Therefore, the peak intensity of ZnS:Tb³⁺ nanocrystals is strongest at 5% doping concentration because of lattice saturation. Red shifting of the excitation peak position of ZnS at 5% doping compared with those of crystals at 1%, 3%, 7%, and 9% doping may also be observed.

Figure 6 shows the emission spectra of ZnS:Tb³⁺ nanocrystals with doping concentrations of 1%, 3%, 5%, 7%, and 9% at an excitation wavelength of 369 nm. As all emission spectra were recorded under the same conditions, the relative intensities of peaks obtained are directly comparable. The PL spectral features of lower doping concentrations are nearly identical, although their PL intensities are weak. The PL spectral features of higher doping concentrations are nearly identical, although their PL intensities vary significantly. The PL intensities were strongest at 5% doping concentration. The PL peak at ~545 nm was strongest in the investigated range, which indicates that ZnS:Tb³⁺ nanocrystals have strong green light emission. The intense green emission of ZnS:Tb³⁺ nanocrystals by F4500 excitation (at 369 nm) is visible to the naked eye. The strongest emission peak corresponds to the ⁵D₄→⁷F₅ (at ~545 nm) transition of Tb³⁺ ions. Other PL peaks identified correspond to the following transitions: ⁵D₄→⁷F₆ (at ~489 nm), ⁵D₄→⁷F₄ (at ~594 nm), and ⁵D₄→⁷F₃ (at ~625 nm).

Our experimental results show that the increase in doping concentration has important effects on the structure and luminescence properties of the resultant nanocrystals. As shown in Figure 6, the luminescence intensity of 5 mol% ZnS:Tb³⁺ nanocrystals was stronger than that of any other ZnS sample under excitation at 369 nm. The holes and electrons in ZnS:Tb³⁺ nanocrystals recombined to form excitons on the ZnS host, and the exciton energy then transferred to the resonance levels of Tb³⁺ ions to achieve the characteristic emissions of Tb³⁺. This energy is most efficiently transferred in 5 mol% ZnS:Tb³⁺ nanocrystals because 5 mol% Tb³⁺ has an adequate amount of saturated interspace in the whole body-centered cubic ZnS crystalline lattice (Figure 6).

4. Conclusions

In summary, we have successfully synthesized monodispersed ZnS:Tb³⁺ nanocrystals with diameters of approximately 10 nm by spray precipitation with SRB culture at room temperature. The ZnS:Tb³⁺ nanocrystals exhibited a zinc blende crystal structure. The main peak position of the absorption spectra positively blueshifted with increasing concentration of Tb³⁺ dopant. The luminescence intensity of 5 mol% ZnS:Tb³⁺ nanocrystals was the strongest among all other ZnS products obtained. Four emission peaks located at 489 nm (⁵D₄→⁷F₆), 545 nm (⁵D₄→⁷F₅), 594 nm (⁵D₄→⁷F₄), and 625 nm (⁵D₄→⁷F₃) at 369 nm excitation were observed. Of these peaks, the emission peak intensity was strongest at 545 nm (⁵D₄→⁷F₅). Hence, the 5 mol% ZnS:Tb³⁺ nanocrystals can be used as green fluorescent materials. Nanocrystals have potential applications in photoelectronic devices and biomarkers. We believe that many types of Re ion-doped ZnS nanocrystals can be synthesized by the spray precipitation method.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work was supported by the Liaoning BaiQianWan Talents Program (2012921052) and Chinese National Programs for High Technology Research and Development (2011AA09070305).

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Copyright © 2015 Zhanguo Liang et al. 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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