Abstract
Photocatalytic dye degradation is one of the simple and convenient ways to eliminate effluents produced by paper, plastic, printing, and textile industries. ZnS is one of the most investigated catalysts on which different modifications are applied. Here, PVP-assisted zinc sulfide (ZnS) nanopowder is prepared hydrothermally. The photoluminescence spectra signify the generated intermediate state which is attributed to sulfur (S) vacancy as obtained from the theoretical analysis. This defect-induced ZnS has shown excellent Rhodamine B (RhB) dye degradation of 95% in 100 min with dye sensitization effect under UV irradiation. Under visible light, the degradation of RhB is only 50% in the presence of ZnS. The sensitization of RhB in the presence of UV light signifies the generation of visible light through the intermediate states caused by S vacancy. However, to eliminate the disadvantage of photocatalysis in highly concentrated wastewater management and expense of UV source, RhB is degraded by sonocatalysis, and 70% of dye is removed within 100 min in the presence of ZnS nanopowder. Therefore, the efficient catalytic dye degradations are achieved employing the minimum amount of ZnS powder.
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Introduction
Since the last decade, environmental pollution is keeping a potentially harmful impact on human life as well as wildlife (Gupta 2009). The textile and allied industries release environmentally harmful effluents which pollute water acutely (Sharma et al. 2012). It has an adverse effect not only on the human being but also on the animal planet. The organic dyes which are not biodegradable are one of the major residues (Rai et al. 2005). Hence, organic dye degradation is one of the important fields of research, nowadays. Different conventional methods for dye removals such as precipitation, liquid–liquid extraction, filtration, and precipitations are limited by their own constraints (Sharma et al. 2012; Miretzky and Cirelli 2009; Huang et al. 2015; Hameed et al. 2007). Heterogeneous photocatalytic dye degradation is one of the modern and convenient ways to eliminate the pollutants from aqueous and gaseous medium (Vieira et al. 2020; Zhang et al. 2021). In this field, the wide bandgap semiconductors have attracted the attention of the researcher due to its interesting optical properties (Ghosh et al. 2017). In this perspective, few oxide materials, such as TiO2 and ZnO, are conventional wide bandgap semiconductors since the discovery of photocatalytic dye degradation process (Lakshmi et al. 1995; Sakthivel et al. 2003). Usually, they get activated by the light having UV wavelength. There have been numerous reports on the designing of semiconductor catalysts which get excited under visible light by creating defect states, doping, and composite or hybrid formation (Wu et al. 2020a, 2018, 2020b).
Zinc sulfide is a well-known n-type II-VI wide bandgap semiconductor in the field of photocatalysis since it can generate electron–hole pairs under UV photoexcitation (Lee and Wu 2017). It is one of the most popular photocatalysts for its substantially negative potential for excited electrons, low toxicity, and rapid generation of charge carriers (Fang et al. 2015). Apart from this, the intrinsic material properties like defect states, crystalline phases, and exposed facets are important factors to analyze the contribution of the catalyst in dye degradation (Fang et al. 2015; Wang et al. 2015; Kong et al. 2011; Pei et al. 2013; Zhang et al. 2008a). These factors can enhance the photocatlytic activity by the light-harvesting process (Zhang et al. 2008b). In addition, it can produce new adsorption sites preventing recombination of electron–hole pairs. However, optimum level of defects is beneficial because excessive defects can cause high rate of recombination degrading the photocatalytic activity (Wang et al. 2012; Lv et al. 2013). In the photocatalytic dye degradation process, vacancy defect modifies the electronic structure creating a new energy level in the forbidden region, which influences the properties of photo-generated charge carriers. ZnS is extensively studied including its Zn and S vacancy which have high impact on photocatalysis. S vacancies can cause the decrement of bandgap, whereas Zn vacancy leads to enlargement of bandgap (Chen et al. 2010; McCloy et al. 2013). Gang Wang reported controlled sulfur vacancy in the ZnS sphere which influenced the photocatalytic H2 evolution under visible light (Wang et al. 2015). Hao et al. reported intrinsically Zn-deficient ZnS which had shown enhanced photocatalytic H2 evolution under visible light irradiation (Hao et al. 2018). Intrinsically created sulfur vacancy and wurtzite-sphalerite phase junction in ZnS instigated the visible light activated H2 evolution as reported by Zhibin Fang (Fang et al. 2015). Fran Kurnia introduced defects in the forbidden region of ZnS nanoparticles in a controlled manner by which visible light absorption was achieved (Kurnia et al. 2016). T. Mahvelati-Shamsabadi et al. produced defect-induced ZnS by ultrasonication, and it showed outstanding performance in dye degradation under UV and sunlight irradiation (Mahvelati-Shamsabadi and Goharshadi 2017). Jaewon Lee prepared S vacancy controlled, porous, and hollow nanoplates of ZnS which had improved the UV-assisted photocatalytic activity than commercial material (Lee et al. 2018).
In UV-assisted photocatalytic dye degradation process, UV source is the major limitation for practical implementation due to its high cost and harmful effect. Apart from this, photocatalysis itself has a drawback of light penetration through highly concentrated and non-transparent dye wastewater (Farhadi and Siadatnasab 2016). Therefore, there are requirements to welcome new and innovative technologies and catalysts for highly concentrated dye removal. In this perspective, semiconductor-assisted sonocatalytic dye degradation can eliminate the drawback of photocatalysis by its strong penetration capacity through any water medium (Min et al. 2012). The process is based on hotspot theory and sonoluminescence (Zhou et al. 2015; Khataee et al. 2018).
In this work, PVP-capped ZnS is synthesized hydrothermally. It contains sulfur vacancy intrinsically as obtained from PL spectra and theoretical analysis. Although such vacancy is not able to activate ZnS under visible light spectra, a different UV light-assisted photocatalytic RhB degradation is observed with low concentration of ZnS. Besides, there is a limitation in practical implementation of expensive and harmful UV sources of light. There are different ways to eliminate the UV photocatalysis. One process is to modify the catalyst, and another is to apply different catalytic processes. In addition, it is difficult to degrade highly concentrated wastewater by photocatalysis process. Here, simple sonocatalytic dye degradation is performed in presence of ZnS. It also exhibits impressive catalytic dye degradation within 100 min as a first time report.
Experimental
Synthesis
All the reagents are of analytical grade and used without further purification. In this synthesis, 4 mmol zinc acetate dihydrate (Zn(CH3COO)2,2H2O) and 6 mmol of thiourea are dissolved in 80 mL of ethylene glycol, and 0.320 g of polyvinyl pyrrolidone (PVP) is added into the solution. After stirring for 30 min, the final precursor solution is transferred into a 100 mL Teflon lined stainless steel autoclave. The system is put in a preheated oven at 180°C for 24 h. The precipitates are centrifuged with deionized water and ethanol alternately. Then, the last contains are dried in a vacuum oven.
Computational details
Our density functional theory-based first-principles calculations are carried out using CASTEP code (Segall et al. 2002) which implements a supercell approach to density functional theory. Generalized gradient approximation, namely the Perdew Burke Ernzerhof (PBE) functional (Perdew et al. 1996), is used to describe the exchange and correlation terms. Vanderbilt ultrasoft pseudo-potentials (Vanderbilt 1990) are used to represent the ion cores of zinc, cadmium, and sulfur atoms, and plane waves up to energy cut off 290 eV are considered in the calculations. Brillouin zone integrations are carried out within the Monkhorst–Pack scheme (Monkhorst and Pack 1976) using a k-point mesh having effective separation of 0.071/Å in all directions. For geometrical optimization, both the atoms and cell dimensions are allowed to fully relax using BFGS (Broyden-Fletcher-Goldfarb-Shanno) scheme (Pfrommer et al. 1997) until the total energy converged to less than 2 × 10−5 eV/atom, the maximum force converged to lower than 0.05 eV/Å, and the maximum displacement is 0.002 Å. All calculations are performed in spin unrestricted manner; however no spin polarization is observed in any of the considered models.
In the current work, a 2 × 2 × 2 supercell of ZnS (F-43 M, IT#: 216) containing 32 Zn and 32 S atoms is used. Optimized lattice parameters of all considered systems are listed below in Table 1.
Table 1 lists the optimized lattice parameters as obtained from DFT analysis.
Catalytic dye degradation
Photocatalytic activity of ZnS is studied under visible and UV light irradiation in the laboratory set up. UV light source is the tube of 40 W with maximum emission of 256.4 nm. The visible light source is mercury lamp with the specification of HPL-N 400 W/542 E40 HG 1SL PHILIPS with luminous flux of 22,000 lm. Sonocatalytic dye degradation is investigated using probe sonicator (frequency = 20 kHz advanced probe sonicator PKS-750F with 13mm titanium probe, maximum output power = 750 W, 15% of maximum output amplitude is used) as a source of ultrasound by which RhB dye is degraded within 100 min.
Typically, 10 mg of ZnS is mixed in 60 mL of 10−5 mol L−1 RhB solution and stirred in the dark for 1 h to reach the adsorption–desorption equilibrium. Then, the system is placed under ultrasonic probe/visible/UV irradiation. For every experimental process, 5 mL of reaction solution is taken as specimen at regular time intervals, and then, it is centrifuged and filtered to get rid of the existing catalyst sample. The absorbance spectra of the collected specimens are examined by UV–Vis absorption spectroscopy. The experimental vessel is double walled with a continuous flow of cold water within the walls to sustain uniform temperature.
Degradation efficiency
The degradation efficiency is analyzed by Ct/C0 vs. time plot, where C0 is the initial concentration of dye and Ct is the concentration of dye at time t in the process of degradation. It also gives a perception about the percentage degradation of RhB dye in the presence of catalyst under ultrasound/visible/UV irradiation with respect to initial concentration of RhB. The equation is presented in Eq. (1) (Samanta et al. 2018).
Pseudo-first-order model
To define the reaction rate of catalytic dye degradation, a pseudo-first-order model is applied. As per condition, if C0 is small enough, the reaction is called pseudo-first-order with a constant rate coefficient (Samanta et al. 2018):
where kapp is the apparent reaction coefficient.
Characterizations
The as-synthesized ZnS is characterized by X-ray diffraction (XRD Bruker, D8 Advance) operating at 40 kV and 40 mA in the 2Ɵ range of 20°–80° for assuring its phase. The structural analysis of the sample is done by a field emission scanning electron microscope (FESEM, Hitachi, S-4800) operated at an accelerating voltage of 5 kV. High-resolution transmission electron microscopy is also carried out to understand its morphology and crystallinity (HRTEM, JEOL-JEM) more accurately. The bandgap from reflectance spectra and quantification of removal efficiency have been estimated by UV–Vis spectroscopy (Shimadzu, UV-3600). Photoluminescence study is performed using Edinburgh FLS980 PL spectrometer.
Results and discussion
The solvothermally synthesized white powder is characterized by XRD in Fig. 1a. It shows the prime XRD peak positions at 28.8º, 47.86º, and 56.66º, which completely agree with the JCPDS card number 06–0566. Therefore, it confirms the formation of the zinc blende phase of ZnS with high purity. In addition, there is a visible broadening in XRD peaks which indicates the formation of small crystallites in the particles. The detailed study is discussed in our previous reports (Ghosh et al. 2017).
The FESEM image of ZnS presented in Fig. 1b defines the agglomerated ZnS nanoparticles with diameters 80 to 120 nm. Since PVP acts as a capping agent, the structure of ZnS is not exactly spherical in nature. Furthermore, the structural analysis of ZnS is carried out using TEM, and it is displayed in Fig. 2a. It is reassuring about the formation of ZnS nanoparticles with diameter around 100 nm. Although exact spherical structure is not observed, ZnS comprises almost equal sized nearly spherical particles throughout the distribution. To reassure the observation, the histogram has been presented in the inset of Fig. 2a on the basis of TEM image of ZnS. It exhibits that the diameter of ZnS nanoparticles lies between 75 to 120 nm with the maximum number of nanoparticles containing the diameter of 100 ± 10 nm. It is depicted from the histogram that the mean diameter of ZnS nanoparticle is 100 nm with the standard deviation of 11 nm.
To determine the exact Zn to S ratio in the solvothermally synthesized ZnS nanopowder, the EDS analysis is carried out and shown in Fig. 2b–e. It is observed from Fig. 2b that there is no impurity in ZnS in the focused region. It is evident from the spatial distribution of zinc and sulfur in Fig. 2c and d, respectively, that Zn and S are homogeneously spread throughout the region. Figure 2e confirms the actual stoichiometry of zinc and sulfur in ZnS in terms of atomic % which is almost 1:1 with an acceptable error bar.
To obtain the bandgap of ZnS, UV–Vis diffuse reflectance spectroscopy (DRS) is performed and shown in Fig. 3a. ZnS has high reflectivity of 80 to 95% in the visible region. There is a sharp fall of reflectance curve at 355 nm. The bandgap (Eg) is calculated to be 3.73 eV from Kubelka–Munk formula considering ZnS a direct bandgap semiconductor (Lee and Wu 2017). Thus, such wide bandgap semiconductors can be activated by UV light irradiation only. The RAMAN spectra of ZnS show highly fluorescent property in Fig. 3b. Hence, no characteristic peak shifting is obtained.
To verify the photoluminescence (PL) property of ZnS (cf. Figure 3c), it is excited at 467 nm of wavelength equivalent to approximate energy of 2.65 eV. The excitation results in a broad and strong green emission at 524 nm equivalent to around 2.36 eV which was already presented in our previous report (Ghosh et al. 2017). It is actually defining the luminescence in the green region of visible light wavelength as obtained from the chromaticity diagram. Therefore, since the exciting and emitting both energies are lower than the bandgap energy of 3.73 eV, the intermediate states situated in the forbidden region are responsible for the photoluminescence property. To analyze such phenomenon, a schematic has been represented in Fig. 4a. It illustrates that in the forbidden region, there are intermediate states near the conduction band edges. By excitation of 467 nm of light, the electron gets excited from valance band (VB) to the intermediate states situated at 2.65 eV from VB. Consecutively, by non-radiative intra-band transition, the electron positions at the intermediate state of 2.36 eV, and then, it transfers to the VB by radiative emission of 524 nm and recombines with the hole in VB. Thus, the electron transfer process can be proposed in PL. Generally, two types of emissions are observed during the room temperature PL in II-VI semiconducting materials. One is intrinsic near band edge emission for bandgap property, and another is extrinsic deep level emission due to the presence of defect or modification of electronic structure. Denzer et al. proposed that different lattice defects caused luminescence with broad spectrum in lower energy region compared to the bandgap energy (Denzler et al. 1998). Such defects include interstitials and vacancies of Zn and S in ZnS lattices. The vacancy and interstitial of Zn can act as localized acceptor and donor level, while the vacancy and interstitial of S can be treated as localized donor and acceptor states, respectively (Bhattacharjee and Lu 2006). Hence, it can be assumed that such interesting PL property is primarily due to the experimentally induced lattice defects in ZnS.
For the convenience of calculation, vacancy of Zn and S in ZnS has been taken under considered. To find out the source of intermediate states in the forbidden region, first-principles computations of density of states (DOS) are conducted for pure ZnS and defect-induced ZnS with sulfur and zinc vacancy. Figure 4b describes that pure ZnS and ZnS with Zn vacancy have almost similar TDOS (Total DOS) with the same position of conduction band minima and valence band maxima. Sulfur vacancy in ZnS causes generation of new states near conduction band edge. Therefore, from this theoretical point of view, it can be said that the intermediate defect states are induced due to the sulfur vacancy near the zinc atom in ZnS. To elucidate the exact contribution of the orbital, PDOS (projected density of states) is calculated for Zn near S vacancy of ZnS. It elaborates that 3s and 4p orbitals of Zn atom near sulfur vacancy have high impact in the formation of intermediate states, whereas d orbital has no participation in it (cf. Figure 4c).
To investigate the catalytic activity of synthesized ZnS nanopowder, the RhB organic dye is employed as pollutant in water, and 10 mg of ZnS is used as catalyst under different types of irradiations. At first, photocatalytic RhB dye degradation is performed under two different light illuminations: (1) visible range and (2) UV range light. Figure 5a shows the absorbance spectra of RhB in presence of ZnS under visible light irradiation. Here, after certain adsorption of RhB on the catalyst surface after 1 h of dark stirring, ZnS exhibits poor catalytic degradation even after 100 min of illumination. Besides, Fig. 5b explores the UV-illuminated photocatalysis and dye sensitization with efficient dye removal ability of ZnS. Here, the degrading absorbance spectra and disappearance of characteristic peak of RhB after 100 min give the information about complete dye degradation under UV irradiation. There is a visible blue shift of absorbance spectra which may indicate N-de-ethylation of RhB (Barras et al. 2012; Wu et al. 1998). Since UV light source is highly expensive and harmful, ultrasound-assisted dye degradation is conducted here in the presence of ZnS as sonocatalyst, and corresponding absorbance spectra of RhB under ultrasound-assisted catalysis is presented in Fig. 5c. As it is observed that the absorbance peak of RhB is not totally disappeared even after 100 min of ultrasound irradiation, thus this pathway of catalysis in the presence of ZnS can be termed as moderate. It is not as efficient as UV light-assisted catalysis but also not as poor as visible light-driven photocatalysis. Additionally, it is environment-friendly and also cuts the expense of UV source as well as eliminates the necessity of any external light source. Moreover, it is efficient in the removal of highly concentrated organic dyes.
To investigate the rate of reaction in dye degradation under different conditions, degradation profile of RhB (Ct/C0 vs. time) is plotted at different time intervals in Fig. 5d. It exhibits that ZnS achieves adsorption–desorption equilibrium after 1 h of dark stirring and at t = 0 in Fig. 5d indicates the degradation of RhB in dark due to adsorption on the surface of ZnS. Here, Ct and C0 are the concentration of dye at time t and t = 0, respectively. The highest rate of degradation is observed under UV light illumination in the presence of ZnS photocatalyst, and poor degradation of RhB is achieved under visible light keeping the rest conditions unchanged, whereas sonication gives moderate rate of reaction in the same scenario.
The degradation percentage of RhB with time is plotted in Fig. 6a under different sources of activation. It shows that almost 30% of RhB is degraded by the adsorption on the ZnS surface during dark stirring. Rest 70% of dye is removed by different catalytic activities of ZnS under different conditions. From the analysis, it can be understood that 95% of RhB is degraded under UV light irradiation in the presence of ZnS, whereas the degradation percentage is 50% under visible light and 70% under ultrasound sonication in the same environmental condition. It can be assumed that the photocatalytic activity of ZnS is almost static under visible light irradiation since the degradation is only 20% under illuminating conditions. It is even quite obvious due to the wide bandgap nature of ZnS. The impressive UV light activated photocatalysis can be attributed to the wide bandgap of ZnS (Lee and Wu 2017; Fang et al. 2011) and dye sensitization which is also very rare under such conditions. Sonocatalysis pursues a completely different phenomenon which is able to activate ZnS in degrading the RhB dye. To investigate the reaction kinetics rate of RhB in the presence of ZnS under UV light and sonication, pseudo-first-order model is analyzed in Fig. 6b and c, respectively. The degradation rate of RhB (k) is 2.43 × 10−2 min−1 under UV radiation which is higher than k = 7.91 × 10−3 min−1 under ultrasound in presence of ZnS as catalyst.
Mechanism
UV-irradiated photocatalytic RhB degradation is the most efficient among all the above-mentioned procedures in the presence of ZnS. It is quite common and vastly reported that ZnS is ideal as a UV catalyst due to its wide bandgap nature which is true in this case also. In addition, hypochromic shift in absorbance spectra of RhB is observed under UV illumination which is not common. From the absorbance curve, it can be said that the degradation is not pure photocatalytic degradation, but there is a contribution of dye sensitization. RhB is well-reported to be sensitized under visible light, but the phenomenon is quite different here. To explain such a process, a schematic is proposed in Fig. 7 for elaborating the mechanism of RhB degradation using ZnS as photocatalyst. Figure 7 exhibits that ZnS gets excited by a UV light source creating electron–hole pair. It is already discussed that ZnS contains intermediate states which can act as trap states for excited electrons. After that, the electrons present in intermediate states recombine with the holes in the VB emitting visible light in the green wavelength which may excite the RhB to perform the N-de-ethylation by its own (Barras et al. 2012). The electrons excited in RhB due to intrinsic activation from catalyst are injected to the conduction band of ZnS. Then, RhB starts to be degraded by different ethylation reactions which are triethylrhodamine, die-thylrhodamine, ethylrhodamine, and rhodamine with different λmax at 539 nm, 522 nm, 510 nm, and 498 nm, respectively (Barras et al. 2012; Wu et al. 1998; Akir et al. 2016). Thus, a visible shifting in absorbance spectra of RhB is observed even under UV illumination, and RhB gets mineralized. The excited electrons participate in a reaction with molecular oxygen by forming superoxide radicals which initiate the complete degradation of RhB. The generated holes produce hydroxyl ions reacting with water molecules and degrade the organic dye producing CO2 and water.
When the material ZnS is concerned, the sonocatalytic dye removal is new to it. By ultrasonic irradiation, RhB is degraded using ZnS as sonocatalyst. There is a mechanism in Fig. 8 by which dye degradation phenomenon has occurred (Farhadi and Siadatnasab 2016; Min et al. 2012; Zhou et al. 2015). Generally, acoustic cavitation bubbles are formed under ultrasound, and they tend to be bigger attaining a critical size. After that, they start to collapse, and a high pressure is generated within the bubbles. By focusing toward the center of the bubbles, a shockwave directs and creates high pressure (1000 atm) and temperature (5000 K) at the core (Farhadi and Siadatnasab 2016; Zhou et al. 2015). This is called a hotspot which participates in the pyrolysis of water forming hydroxyl ions. In addition, the temperature generated in hotspot produces plasma when it collapses. It causes emission of light covering a wide spectral region. This phenomenon is termed as sonoluminescence which excites the electron of ZnS from valence band to conduction band and generated intermediate states. After that, the excited electrons react with oxygen resulting in superoxide radical which produces OH radicals. Additionally, the generated holes cause the creation of .OH. These radicals participate in the dye degradation procedure and transform the organic pollutant into CO2 and water.
Conclusion
Hence, it can be concluded that sulfur vacant defect enriched zinc sulfide nanopowder is synthesized successfully via one-step solvothermal process. Though it is not an efficient photocatalyst in visible light due to its wide bandgap, it is a very efficient photocatalyst under UV light which is not only for its bandgap but also the generated intermediate states. It is proved that such defects are induced by sulfur vacancy in ZnS. These states participate in sensitization of RhB under UV illumination by generating visible range photoemission. As it is well-known that UV light is expensive and hazardous to human health, ultrasound-assisted catalysis is introduced using ZnS as a catalyst. Although the removal rate of toxicity is not as fast as UV, it is efficient enough in degradation of RhB. Above all, the experiments are conducted with very low concentration of samples such as 0.16 g/L. Therefore, it is advantageous to separate the catalyst from the water. In future, the sonocatalytic activity of ZnS can be improved by developing new composites.
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Acknowledgements
This manuscript was selected from the papers presented at the 6th edition of biennial International Conference on Nanoscience and Nanotechnology (ICONN-2021).
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This manuscript is part of the special issue of selected papers from the 6th edition of biennial International Conference on Nanoscience and Nanotechnology (ICONN-2021). One of us (SG) wishes to thank the Council for Scientific and Industrial Research (CSIR) (File no: 09/096(0926)/2018-EMR-I), the Government of India, for providing her a senior research fellowship through “CSIR-SRF”, while (MS) (DST/INSPIRE Fellowship/2017/IF170868) wishes to thank the Department of Science and Technology (DST), the Govt. of India for awarding her a DST-INSPIRE’ research fellowship. SS wishes to acknowledge and thank the Science and Engineering Research Board (SERB), a statutory body of Department of Science and Technology (DST), Government of India (File No. EEQ/2018/001127) for providing financial support. The authors wish to acknowledge the University Grants Commission (UGC), the Govt. of India for the support under the “University with Potential for Excellence (UPE-II)” scheme.
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Ghosh, S., Samanta, M., Sen, D. et al. Photocatalytic and sonocatalytic dye degradation by sulfur vacancy rich ZnS nanopowder. J Nanopart Res 23, 160 (2021). https://doi.org/10.1007/s11051-021-05283-5
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DOI: https://doi.org/10.1007/s11051-021-05283-5