3.1. Characterization of CZTS-ultrathin film
Figure 2a indicates that the thicknesses of CZTS-ultrathin films deposited by ablating the target with 2400, 4800, 9600 and 12000 laser pulses and then thicknesses of deposited thin films have been measured to be 61 nm, 112 nm, 242 nm, and 313 nm, respectively. It has been determined that the thicknesses of CZTS-ultrathin films have been increased as the laser pulse numbers increase [46, 47]. CZTS-ultrathin films in polycrystalline tetragonal structre, which have been crystallised in (112), (200) and (220) crystal planes appeared at 2θ = 28o, 33o and 47o angles [45, 48] (JCPDS Card No: 01-075-4122), respectively. In the lowest thickness, CZTS-ultrathin film (61 nm) has the poorest crystal structure. As laser pulse number applied for ablation is increased, the amount of ablated and then deposited material are increased. Therefore, the thickness of thin film increases, so in this case, atoms of CZTS strucrue have reached on the substrate that fill the appropriate vacancies in crystal plane and make an ideal nucleation, thereby the crystal structure is improved. Thus, it was observed that some increase in the thickness of thin film causes an improvement in the crystal structure of thin film to increase the main (112) peak density [49]. Therefore, CZTS-ultrathin film (313 nm) for the case of the highest thickness presents the most advanced crystal structure.
The Scherrer Equation (Eq. (1)) is used to calculate the main crystal size of CZTS-ultrathin films:
$$S=0.94\lambda /\beta {Cos}\theta \text{ }\left(1\right)$$
S is the crystalline size, λ is X-Ray wavelength, θ is Bragg diffraction angle, β is the full width at half-maximum of diffraction peak. The main crystalline sizes of ultrathin CZTS films of 61 nm, 112 nm, 242 nm and 313 nm in thicknesses have been calculated to be 7.34 nm, 10.71 nm, 17.79 nm, and 22.25 nm, respectively. It can be indicated that as thin film thickness increases, the crystal size developes [41].
Figure 3a shows that the absorption capacity of CZTS-ultrathin films expands from UV region to Vis region. So, as some increases in film thickness causes particle formation in thin films to produce enlarged particles in size and denser film. Thus, the absorptivity of thin films increases with augmenting thickness.
The Tauc law stated in Eq. (2) is used to calculate the band gap of CZTS-ultrathin films:
$$\alpha h\nu = A(h\nu -{E}_{g}{)}^{1/2}\text{ }(2)$$
A is a constant, hv is photon energy, \({E}_{g}\) is band gap. \({E}_{g}\) is determined by a straight line on photon energy \(\left(h\nu \right)\) in Tauc-plot presented in Fig. 3b. \({E}_{g}\) values of CZTS (61 nm), CZTS (112 nm), CZTS (242 nm) and CZTS (313 nm) ultrathin films were obtained to be 1.95 eV, 1.90 eV, 1.50 eV and 1.45 eV, respectively. Some increase in particle size with augmenting thickness reduces the transmission of light, and thus higher photon absorption of CZTS-ultrathin films causes some decreases in the band gap value [45]. Among ultrathin films, it has been determined that CZTS (242 nm) ultrathin film has an ideal band gap value of 1.5 eV [41].
AFM images in Fig. 4a and 4b show the morphological structures of CZTS (61nm) and CZTS (313 nm) ultrathin films of the lowest and highest thicknesses, respectively. Since the deposition of CZTS material is in the lowest amount as the material is ablated by the lowest laser pulse number, few atoms reach on the substrate. The lower number of atoms were deposited on top of each other and side by side that limiting particle coalescing and thus, particles with smaller size were formed. CZTS (61nm) ultrathin film produced by ablation performance of 2400 laser pulses consists of small-sized particles as seen in Fig. 4a. On the contrary, with the augment of the laser pulse-numbers, the particles deposited in high density that combine with each other and cause particle growth as seen in Fig. 4b. SEM image in Fig. 5a also confirms the morphology of CZTS (61nm) ultrathin film, which is composed of particles in low density and small sizes. When the laser pulse number is increased from 2400 to 12000, the number of atoms deposited on the substrate also increases. This situation leads to an enlarged the particle size and increased the particle density [46, 47], as indicated in AFM and SEM images of CZTS (313 nm) ultrathin film in Fig. 4b and 5c, respectively.
The tables given as an inset of EDX spectra in Figs. 5b and 5d give the atomic weight ratios of the elements that form CZTS (61 nm) and CZTS (313 nm) ultrathin films, respectively. CZTS (61 nm) ultrathin film of low thickness contains low amount of Copper (Cu) and Sulfur (S), and high rate of Tin (Sn) and Zinc (Zn) elements. VCu (Copper vacancy) - ZnCu (Zn replace Cu vacancy) acceptor defects and SnCu (Sn replace Cu vancancy) - VS (Sulfur vacancy) donor defects may occur in CZTS (61 nm) ultrathin film [50]. With an augment in thickness of CZTS-ultrathin film, Cu and S amounts increased while Sn and Zn rations decreased. Thus, CZTS (313 nm) ultrathin film components tended to provide stoichiometric transfer. However, even in the latter case, CZTS (313nm) ultrathin films were observed to be somewhat Cu-poor, Zn and Sn-rich [41].
3.2. Photocatalytic properties of CZTS thin films
Photocatalysis is one of the most important methods used in the solution of many problems, especially in the removal/reduction of environmental pollution in waste water [51, 52]. Organic dyes compose an important part of industrial pollutants. These dyes doesnt only cause environmental pollution, but also negatively affects the health of living things [53]. In this study, ultrathin CZTS films produced by PLD method were used to remove MB dye, which is one of the organic pollutants. Taking into account our team's previous research as well as works reported in literature, the pH effect was the first investigated parameter in photocatalysis studies [54]. One of the reasons for photocatalysis studies have been carried out at different pH values is that pH is one of parameters that significantly affect the efficiency and kinetics of photo-oxidation processes. In this way, separation of the e– h+ pairs in thin films from the photocatalyst surface can be facilitated [55]. Another reason is the sensitivity of the components used in photocatalysis to different pH values. An example of this situation is changes in the activity of MB, which is a cationic dye, at different pH values [56]. Therefore, the photocatalyst effect of pH on the photocatalytic activity of CZTS films has been examined first time in literature and the results obtained is given in Fig. 6a. Ultrathin film CZTS (242 nm) with the best photocatalytic efficiency was used to examine pH effects. As seen from Fig. 6a, the photocatalytic efficiency has been increased significantly by some increase in pH. In the photocatalysis application at pH = 4, only 40.1% of MB was removed in 540 min, while this value was measured as 77.2% for pH = 7 at the same time. However, at pH = 10, CZTS film has exhibited an impressive degradation efficiency, removing 96.1% of MB dye within 240 min. Some increase in photocatalytic activity as a function of pH change that can probably be associated with a modification of charges on the surface and some increase in surface adsorption. In addition, due to the basic environment, electrostatic interaction occurs between the negative surface of the photocatalyst and MB cations, so higher dye degradation is expected [57].
In Fig. 6b, there was systematically studied that the percentage of degradation values occurring due to the initial concentration of MB in the presence of ultrathin CZTS films coated in different thicknesses (61, 112, 242, and 313 nm) by PLD method. In these tests, firstly, the photocatalyst and dye solution were kept in the dark for 30 min to ensure the adsorption-desorption equation, and it was observed that there was no significant change in MB concentration as a result of the measurement. This indicates that the dye adsorption of thin films is negligible. In addition, it was investigated whether only MB dye has exhibited degradation under visible light without using photocatalysis or not, and it was determined that only 4.2% of MB dye degraded during 240 min. The photocatalysis studies have been carried out in the presence of CZTS film photocatalyst in different thicknesses, it has been determined that the efficiency of photocatalysis increases as a function of thin film thickness up to a certain thickness value, and it has started to decrease with further increase in the thickness value. In other words, it was observed that as thickness of CZTS photocatalyst increases from 61 nm to 242 nm, the photocatalytic activity of the photocatalyst increases, and, in oppositely, decreases beyond 242 nm thickness value such as 313 nm. This variation in photocatalytic activity is in agreement with what reported in literature [58, 59]. Some increases in the photocatalytic activity of CZTS with increasing thickness; (i) some increament in surface area due to some increament in surface roughness and pore size, and thus the ability of the photocatalyst to interact with more light and dye, and (ii) some decrease in the band gap of the thin film with some increase in thickness, resulting in more e−-h+ can be explained by the formation of the pair. However, when thickness is further increased, the photocatalytic activity decreases with some increase in recombination that tak place in the system at high thicknesses, in addition to the difficulty of interaction of the thin film with the dye solution and light, and the difficulty of photon absorption [60, 61]. Among all the photocatalysts, the photocatalyst with a thin film catalisor of CZTS in thickness of 242 nm has exhibited the highest photocatalytic performance by showing the success of removing 96.1% of MB in 240 min.
The photocatalytic activities of ultrathin CZTS films produced in different thicknesses by PLD method were compared using the Langmuir-Hinshelwood first-order kinetic model (ln (Ct/C0) = kt) in Fig. 6(c). In the graph, linear gradients of CZTS films in different thickness values show that the degradation is in accordance with the first-order kinetic model. The reaction rate constant of MB dye degradation was calculated to be only 0.0962 h-1 by providing all photocatalysis conditions (pH = 10) without using any catalyst. When CZTS (242 nm) thin film photocatalyst with the highest photocatalytic activity was used, the rate constant value was 0.816 h-1. The rate constant values exhibited by thin-film photocatalysts with 61, 112 and 313 nm thickness, which were calculated to be 0.438, 0.607 and 0.484 h-1, respectively.
In Fig. 6d, there has been given that the real degradation graph of the photocatalyst with the highest photocatalytic efficiency (CZTS (242 nm)) among ultrathin CZTS film photocatalysts produced in different thicknesse. As seen in Fig. 6d, it has been observed that the characteristic peak of MB formed at ~ 664 nm, gradually and almost linearly decreases over time and completely disappears at the end of process as it has been exposed to visible light. The disappearance of this peak over time that indicates to us that the degradation of the dye by thin film photocatalyst and visible light that is its conversion to carbon dioxide (CO2) and water (H2O). For a better understanding of this situation, the reaction mechanism is given as an inset of Fig. 6d.
Scavengers were used to determine which radicals in CZTS film photocatalysts play an active role in the degradation of organic dyes. These chemicals are IPA, EDTA-2Na and BQ are used to detect, h+ and radicals, respectively. The dye degradation values obtained in the photocatalysis experiments performed in the presence and absence of IPA, EDTA-2Na and BQ scavengers that have been given in Fig. 7. Also, during the time until the end of 240 minutes, the total dye degradation scavengers are given as an inset of Fig. 7. While 96.1% degradation was observed when no scavenger was used, this value remained constant at 58% in the presence of BQ scavenger. The significant decrease in dye degradation in the presence of BQ shows that radicals have a very important role in photocatalysis studies in the case of usage of CZTS photocatalysts. In the presence of IPA as a scavenger, the rate of degradation was found to be higher (80%) than in the presence of BQ. This means that ’s is partially effective in the degradation. Finally, in the presence of EDTA-2Na, a result (92%) has been obtained very close to the photocatalysis efficiency obtained without using any scavenger. This result means that h+’s has the least effect on the degradation mechanism compared to other radicals.
Based on the above discussion, a representative schematic illustration is given to show through which process and how organic dyes can be removed under visible light in the presence of ultrathin CZTS film photocatalyst (Fig. 8). For a briefly explanation, the photochemical process over CZTS film photocatalysts is that photons with an energy equal to or higher than the band gap of CZTS semiconductor are absorbed by CZTS film, and thus the generation of photo-induced e− - h+ pairs can be obtained. However, these pairs either lose energy and recombine, or they reach the photocatalyst surface and participate in reduction-oxidation reactions. The related equation is given by Eq. 3 below. The resulting holes, oxidize water molecules and allow the formation of hydroxyl () radicals, as shown in Eq. 4. At the same time, electrons reduce oxygen molecules attached to the surface of the photocatalyst to superoxide anions () (Eq. 5). These radicals provide the formation of hydroperoxyl radicals (\(H{O}_{2}\)) together with H2O as shown in Eq. 6. As a result, these, \(H{O}_{2}\) and radicals play an important role in the conversion of organic pollutants into (CO2) and (H2O) (Eq. 7) [62].