Study of the Potential of La/Bi<sub>2</sub>S<sub>3</sub> Catalyst for Photodegradation of Acid Yellow 42 Dye under Visible Light

Fenelon, Ernso; Ni’am, Achmad Chusnun; Wang, Ya-Fen; You, Sheng-Jie

doi:https://doi.org/10.1155/2022/2990466

Journal of Nanomaterials

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Abstract Introduction Results and Discussion Conclusion Data Availability Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2022 | Article ID 2990466 | https://doi.org/10.1155/2022/2990466

Study of the Potential of La/Bi₂S₃ Catalyst for Photodegradation of Acid Yellow 42 Dye under Visible Light

Ernso Fenelon,¹Achmad Chusnun Ni’am,²Ya-Fen Wang,^3,4and Sheng-Jie You^3,4

Academic Editor: Osman Ahmed Zelekew

Received15 Jul 2022

Revised16 Sept 2022

Accepted22 Sept 2022

Published06 Oct 2022

Abstract

The new catalyst (La/Bi₂S₃) applies for the photodegradation of Acid Yellow 42 (AY42) dye under visible light in this study. The La/Bi₂S₃ material is the motivating catalyst due to the excellent ability of Lanthanum (La) to increase the adsorption capacity and electron-hole separation of Bi₂S₃ for enhancing the degradation of AY42. The characterization analysis of the prepared material confirms a successful synthesis using the hydrothermal method. The efficiency of photodegradation AY42 using La/Bi₂S₃ is higher than pure Bi₂S₃. La on Bi₂S₃ (doped at 3%), which is devised on adsorption (40.24%) and photodegradation (51.86%), has the best degradation efficiency (92.1%). The trapping experiment and the analysis of electron spin resonance (ESR) spectra explain that the hydroxyl radical is the most active species in this photocatalytic process due to the total degradation efficiency decreasing from 92.1% to 57.16% by the scavenger using isopropyl alcohol (IPA). The hole (h⁺) shows its importance in the photodegradation of AY42 by detecting that OH^- is the intermediate species. The new material (La/Bi₂S₃) also shows excellent photostability in the reusability test. Finally, the result confirms that La is a suitable doping metal for Bi₂S₃ and is interesting for practical application under visible light. The new catalyst (La/Bi₂S₃) applies for the photodegradation of Acid Yellow 42 (AY42) dye under visible light in this study. The La/Bi2S3 material is the motivating catalyst due to the excellent ability of Lanthanum (La) to increase the adsorption capacity and electron-hole separation of Bi₂S₃ for enhancing the degradation of AY42. The characterization analysis of the prepared material confirms a successful synthesis using the hydrothermal method. The photodegradation efficiency of AY42 using La/Bi₂S₃is higher than pure Bi₂S₃. The doping of 3% weight of La on Bi₂S₃ shows the optimum degradation efficiency of 92.1%, devised on adsorption (40.24%) and photodegradation (51.86%). The pure Bi₂S₃ (46.7%) contains 17.1% of adsorption and 29.6% of photodegradation. The trapping experiment and the analysis of electron spin resonance (ESR) spectra explain that the hydroxyl radical is the most active species in this photocatalytic process due to the total degradation efficiency decreasing from 92.1% to 57.16% by the scavenger using isopropyl alcohol (IPA). The hole (h⁺) shows its importance in the photodegradation of AY42 by detecting that OH^- is the intermediate species. The new material (La/Bi₂S₃) also shows excellent photostability in the reusability test. Finally, the result confirms that La is a suitable doping metal for Bi₂S₃ and is interesting for practical application under visible light.

1. Introduction

Dye degradation is among the most complicated tasks for textile processing plants. Hundreds of synthetic colors are employed in the industry, some carcinogenic [1]. Among these dyes, azo dyes are considered the most persistent and dangerous industrial pollutants due to their ability to contaminate natural water [2]. It is the most utilized dyes, accounting for more than 60% of all commercially available dyes [3, 4]. Among the azo dyes, Acid Yellow 42 (AY42) is a commercial dye mainly used for wool dyeing, silk, glue printing, polyamide fiber dyeing, leather shading, inks for printing, food colorants, hair dye, tattoo inks, cosmetics, textiles, and colors for drugs [5]. So far, only a few preliminary studies have been conducted about a treatment method for the degradation of this target pollutant (AY42). The mineralization degradation of AY42 demonstrated a high degradation by adsorption [6]. However, the calcination method is not environmentally friendly as it produces air pollution and consumes a lot of energy [7]. It uses turnip peroxidases and enzymes that require the 1-hydroxy benzotriazole (HOBT) to decolorize most of the acid dyes [8].

Importantly, photocatalysis exhibits a successful way of treating industrial effluent [9]. The photocatalyst is rapidly expanding and is significantly efficacious due to the number of benefits, including environmental protection and total elimination of pollution [10]. The photocatalytic process promotes the oxidation and removal of most organic compounds, potentially allowing the complete elimination of organic contaminants [11]. The types of semiconductor catalysts, such as TiO₂, WO₃, ZnO, SnO₂, CeO₂, Bi₂S₃, and BiVO₄ photocatalysts, are commonly used [12] but are limited by large bandgaps or fast recombination of electron-hole pairs. Recently, more attention has been received from visible light photocatalysts, specifically materials containing bismuth [13]. Bismuth-based photocatalysts are commonly studied as visible photocatalysts guided by light, such as Bi₂O₃, BiVO₄, Bi₂WO₆, Bi₂S₃, and Bi-ZnWO₄ [14, 15]. Amid the catalysts, Bi₂S₃ is among the most efficient semiconductors and draws broad attention to Schottky diode [16], solar cells [17], sensors [18], supercapacitor electrodes [19], and thermoelectric devices [20]. Bi₂S₃ has a narrow bandgap of 1.3 eV and an excellent absorption coefficient for photocatalytic activities under visible light [21]. The photocatalytic of Bi₂S₃ is restricted due to the quick recombination of photoinduced electron-hole pairs [22].

According to the above limitation, the new dopant material (Lanthanum) is used to improve the ability of Bi₂S₃ in photocatalytic activities in this study. Due to the excellent command of lanthanum (La), which enhances the capacity of the material, some preview studies mentioned that La has a synergistic effect and influence to capture photoinduced electrons [23, 24] that are used to enhance the redox, textural, and structural aspects of the material [25]. In addition, La enhances the catalyst’s ability and modifies the material’s structure to demonstrate a high light absorption spectrum and to increase the electron-hole separation ability [23, 26, 27]. In the present study, La/Bi₂S₃ composite was prepared by hydrothermal method, and the performance of La/Bi₂S₃ was evaluated by different kinds of experiments, such as photocatalytic degradation activities of AY42, the effect of dyes concentration, catalyst amount, recycle test, and trapping test. La inhibits the recombination of photogenerated electron-hole pairs of Bi₂S₃ and improves the photodegradation performance of the prepared material. Thus, the La/Bi₂S₃ composite shows a great perspective and contribution to increasing photocatalytic activity under visible light.

2. Experimental Section

2.1. Reagents and Materials

This experiment used various chemicals: Bismuth nitrate (Bi (NO₃)₃·5H₂O) (mass fraction 0.990) was extended in China, thiourea (CH4N2S, China, 99.9%), isopropyl alcohol (IPA, Merck, 99.99%), potassium iodide (PubChem CID: 4875), and Acid Yellow 42 (PubChem CID: 228665). Table S1 details the structure of AY42 dye and demonstrates its degradation ability by the photocatalytic process due to its high carbon content. The ultra-pure water system of PURELAB flex 3 is used as the source for deionized water.

2.2. Preparation of Bi₂S₃ and La/Bi₂S₃

The synthesis of Bi₂S₃ has followed the previous study [28]: 3.881 g of Bi(NO₃)₃.5H₂O diluted in 100 mL of double-distilled water (DDW) and 20 mL of DDW mixed with 0.90 g of thiourea for 20 min separately; then, the solution of thiourea was dropped into the solution of Bi(NO₃)₃.5H₂O and then mixed at 60 °C for 30 min. Finally, the yellow solution was mixed at room temperature for 60 min and inserted in an autoclave at 150 °C for 24 hours. Afterward, the solid was recovered, filtered, and washed four times using DDW and ethanol ratio 5 : 1 to remove all the impurities. The final Bi₂S₃ dried at 60 °C for 10 hours. Furthermore, Bi₂S₃ calcinated for 2 hours at 400 °C to evaporate all the water in the material’s pores.

La/Bi₂S₃ was synthesized by adding a different percentage of La weight % (1, 3, 5, and 7) using La(NO₃)₃.6H₂O as a precursor into the mixture solution of Bi₂S₃. After achieving room temperature, it was stirred for 60 min and finally mimicked the exact condition of the hydrothermal, washing, drying, and calcination process to acquire La/Bi₂S₃. Figure 1 shows the synthesis procedure to synthesize the La/Bi₂S₃.

2.3. Characterization Techniques

Scanning electron microscopy (SEM) was used to observe the surface morphology of the material. The X-ray diffraction (XRD) pattern was studied to analyze the phase composition and crystalline structure. FT/IR-4700 FTIR Spectrometer from JASCO was used to determine the function group and the bonding materials. The instrument JEM 1400 JEOL was used to measure transmission electron microscopy (TEM) and observe the catalyst’s morphology. The electron spin resonance (ESR) was analyzed using a 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) agent.

2.4. Photocatalytic Degradation Activities

The research on photodegradation of AY42 under visible light using La/Bi₂S₃ was studied at the different weight percentages of La/doped on Bi₂S₃ (1% La/Bi₂S₃, 3% La/Bi₂S₃, 5% La/Bi₂S₃, and 7% La/Bi₂S₃) and was tested using 0.02 g of catalysts in all experiments. For all experiments, a beaker glass was applied as a reactor, and 60 mL of AY42 solution was introduced at initial concentrations of 10 mg L⁻¹. The liquid solution was placed in the dark for 30 min for adsorption and desorption of the catalyst. Finally, the photocatalytic activity was irradiated under visible light for 75 min, and the dye was analyzed at the interval of 15 min. A light emitting diode (LED) lamp of 42 volts with 7000 lm, and the wavelength () ≥420 nm was applied for the visible light source, and a UV-vis spectrometer measured AY42 removal at 410 nm wavelengths. All the photocatalytic measurements were performed at room temperature and repeated twice to calculate the error bars in the result of the experiment. The photocatalytic degradation of AY42 () is obtained by , where is the initial optimum absorbance () of AY42 () of the UV-vis and is the outlet absorbance at any time. A trapping test was realized by adding different scavengers of 10^-3 M into the solution of AY42 content 0.02 g of the catalyst. Potassium dichromate (K₂Cr₂O₇), isopropyl alcohol (IPA), and potassium iodide (KI) were applied as effective scavengers to control the photogenerated electron, hydroxyl radical, and the hole, respectively. The recycle test was realized by reusing four times the same material by selecting the best sample to analyze the stability of the as-prepared material. The kinetics first-order was studied using to measure the degradation rate of the pollutant and calculated using the absorbance of AY42 at the initial C0 after getting the adsorption and desorption in the dark and also the final concentration of AY42 at time t (min).

The degradation capacities of AY42 under visible light over La/Bi₂S₃ material are observed by calculating in the following equation: is the degradation capacity of the catalyst. and (mg L^-1) are the initial and equilibrium concentrations of the AY42, respectively. (L) is the volume of the AY42, and (g) is the weight of the catalyst.

3. Results and Discussion

3.1. Analysis of XRD Pattern

The analysis of the XRD pattern of the Bi₂S₃ and La/Bi₂S₃ composites presented in Figure 2 exhibits the crystalline structure. The pure Bi₂S₃ showed various peaks at 22.41°, 23.69°, 24.9°, 25.8°, 28.65°, 30.39°, 31.86°, 39.88°, 45.7°, 46.67°, 50.98°, 52.82°, 59.10°, and 63.09° which can be related to the diffraction peaks at (220), (101) (130), (310), (211), (221), (410), (430), (440), (501), (160), (312), (640), and (152) planes of phase, indicating the orthorhombic Bi₂S₃ (JCPDS No. 170320) crystalline structure. The XRD analysis proved that the presence of La in Bi₂S₃ decreased the crystallite size of the catalyst. For further studies, the particle size was analyzed to confirm that the reduction of the crystallite size developed when La-doped the material. However, adding La increased the intensity of the (211) plane of Bi₂S₃ at the diffraction peak . It indicated the bias of orientations of these crystallographic planes [29]. The 211 facets were the most dominant in Bi₂S_3, suggesting the formation of microsphere particles [30]. This result shows that the excess amount of La could harm the photocatalytic activities of La/Bi₂S₃.

3.2. FTIR Analysis of Bi₂S₃ and La/Bi₂S₃

Figure 3 shows the FTIR analysis of Bi₂S₃ and La/Bi₂S₃. The vibration bands around 1076 cm⁻¹ and 1100 cm⁻¹ showed evidence of the apparition of Bi₂S₃ [28, 31] and ascribed to Bi-S bonds [21], respectively. The band around 1620 cm⁻¹ is related to the (O-H) bending vibrations of the molecularly adsorbed water [32]. The peak of about 2380 cm⁻¹ is responsible for the stretching vibrations of C–H [33]. The wavelength at 3400 cm⁻¹ due to the O-H vibration is related to the water inside the samples [21]. The bands at 1076-1100 cm^-1 became stronger as the amount of lanthanum in the composite increased. The modification of the bands’ vibration of the Bi₂S₃ might explain the presence of La in the composite, and the XRD analysis could also confirm it.

3.3. Morphology of Bi₂S₃ and La/Bi₂S₃ Composites

Figure 4 shows the results of the SEM image of Bi₂S₃ and the different composites of La/Bi₂S₃. The pure microspheres Bi₂S₃ (Figure 4(a)) showed a particle size reduction while increasing the amount of La in the composite. Due to the material’s particle size reduction, an excessive amount of La can be depicted on the surface of Bi₂S₃ in the images of 5% and 7% percent La/Bi₂S₃, respectively. The high percentage of La in the composite could present a negative effect by reducing the active species and providing the recombination electron hole of pure Bi₂S₃ photocatalyst.

(a)

(b)

(c)

(d)

(e)

Material processing and degradation reports of AY42 show that the particle size distribution of Bi₂S₃ and La/Bi₂S₃ grades was an essential metric. The particle sizes of Bi₂S₃ and La/Bi₂S₃ materials were analyzed using a Nano Zetasizer ZS by Malvern Panalytical. The average size of Bi₂S₃, 1% La/Bi₂S₃, 3% La/Bi₂S₃, 5% La/Bi₂S₃, and 7% La/Bi₂S₃ were 4.88, 3.22, 2.05, 1.08, and 1.63 μm, respectively. The particle size result confirms that the XRD pattern of Bi₂S₃ changes significantly with the presence of La due to the significant decrease of the particle size of pure Bi₂S₃ with the presence of La. The SEM images present that the addition of La-doped of Bi₂S₃ decreased the crystallites of the compound and might increase the active site of the material for better photocatalytic activities in the degradation of AY42 under visible light.

The elemental mapping analysis shown in Figure 5 was measured to support the SEM images to confirm the presence of all elements in as-prepared material. The blue color was represented by bismuth (Bi), yellow was the sulfur (S), and purple by the presence of La in the composites. The mixed colors indicated that all the elements (Bi, S, and La) were present in the map of the SEM image, which confirmed the synthesis of La/Bi₂S₃ composite by the hydrothermal method. In the analysis result of the composite, the impurity detected was lower. So the composite morphology confirmed the successful synthesis of La/Bi₂S₃ material for photocatalytic activity.

The TEM analysis was studied by pure Bi₂S₃ and 3% La/Bi₂S₃. TEM analysis for 3% La/Bi₂S₃ shows evidence that La modified the morphology of Bi₂S₃ and the smaller particle size is formed for the benefits of the photocatalytic performance of the material. As a result, La worked to reduce the particle size of pure Bi₂S₃. The morphology of the prepared samples of pure Bi₂S₃ (Figures 6(a) and 6(b)) appearing in one block finally changed by adding La to the material, as shown in Figures 6(c) and 6(d) to improve the surface of distribution for more sites of active species to achieve a better photocatalytic activity of the material, so the TEM images proved the presence of La in the Bi₂S₃ material.

(a)

(b)

(c)

(d)

3.4. Photodegradation of Acid Yellow 42 under Visible Light by La/Bi₂S₃

The photodegradation experiment in Figure 7(a) reports a different percentage weight of La-doped on Bi₂S₃. The degradation of the pollutant was performed in the dark and the light for a better understanding of the catalyst. The result also shows that the catalyst also adsorbs a part of the AY42 due to the pores on the surface of the catalyst afterward, the photodegradation in the presence of the visible light. The total performance of pure Bi₂S₃, 1% La/Bi₂S₃, 3% La/Bi₂S₃, 5% La/Bi₂S₃, and 7% La/Bi₂S₃ resulted into 46.7%, 63.4%, 92.1%, 77.7%, and 66.3%, respectively. In this study, we found that the photodegradation increased when the amount of La-doped on Bi₂S₃ was increased from 1% to 3%. The decreasing efficiency of AY42 was detected by increasing the percentage of La (>3%) doped on Bi₂S₃. Since the absorbing and scattering catalyst photon increased by an excess of La in the photocatalytic process [27], the degradation rates were calculated by applying the kinetic first order (Figure 7(b)). The kinetic study shows that the degradation rate of the outstanding samples (3% La/Bi₂S₃) was better than the pure Bi₂S_3. It is explained that the presence of La also enhanced the removal rate under visible light. The degradation capacity was calculated to evaluate the mass in milligram (mg) of AY42 dyes that a specific weight can degrade in gram (g) of La/Bi₂S₃ catalyst under visible light. The calculation analysis is shown in Figure 7(c) that the degradation capacity of Bi₂S₃, 1% La/Bi₂S₃, 3% La/Bi₂S₃, 5% La/Bi₂S₃, and 7% La/Bi₂S₃ was 14.01 mg g^-1, 19.02 mg g^-1, 27.63 mg g^-1, 23.31 mg g^-1, and 19.89 mg g^-1, respectively; the percentage of error bars of the photocatalytic degradation of AY42 was around ±2.3% to ±3%. The degradation capacity of AY42 over La/Bi₂S₃ was compared with some previous studies in Table 1.

(a)

(b)

(c)

(d)

The recycle test was studied to analyze the photocatalytic stability of La/Bi₂S₃. La/Bi₂S₃ 3% was selected as the focus sample; as we can denote in Figure 7(d), there is no difference from the first to the third that was recycled, and it slightly decreased with the difference value of 7% between the first and the fourth. This decrease results from the remaining pollutant on the catalyst’s surface during the adsorption process. Therefore, the material La/Bi₂S₃ proved to show reasonable stability over the degradation of AY42. Besides the performance of La/Bi₂S₃ catalyst, it was also very competitive compared to some previous studies in Table 1 using Bi₂S₃ as base catalyst under visible-light-induced photodegradation of organic pollutant in the wastewater, and mostly better than the previous studies. It is concluded that La is an excellent doping metal for Bi₂S₃ in photocatalytic activities and shows the first application of the photocatalyst in degrading AY42 dye under visible light.

3.5. Effect of AY42 Dye Concentration

Figure 8 shows the result of the experiment of the effect of AY42 dye concentration realized with 20 mg of 3% La/Bi₂S₃ of catalyst. The removal of the efficiencies of 10, 20, 30, 40, and 50 ppm were 92.1%, 79.4%, 61.3%, 44.7%, and 33.2%, respectively, and the error bars were found around ±1.8% to ±2.5%. The degradation efficiencies decreased by increasing the concentration of AY42. The decrease in removal effectiveness of degradation is caused by a lack of active sites with a small amount of catalyst, and a lack of light penetration depth combined with the catalyst at the bottom of the reactor for the pollutant’s photodegradation activities under visible light.

3.6. Effect of Catalyst Amount

Figure 9 shows the analysis of different catalyst amounts for the photocatalytic degradation removal of AY42 with high concentrations. In this experiment, 50 ppm of AY42 was selected with different catalyst amounts of 20, 40, 60, 80, and 100 mg with a degradation efficiency of 33.2%, 48.1%, 55.3%, 53.1%, and 49.5%, respectively. The result shows that the degradation efficiency increased by increasing the catalyst amount because of the active surface sites. However, the excess amount of catalyst reduced the degradation efficiency of AY42 due to the increase of the catalyst amount, which may decrease the light penetration and thus decrease the light scattering due to the blurry solution.

3.7. Mechanism of Degradation of AY42

In the mechanism process of the degradation of AY42, K₂Cr₂O₇, IPA, KI, and 3% La/Bi₂S₃ were used to scavenge the electron, hydroxyl radical, and hole, respectively, in the trapping test (Figure 10(a)). This study looked into the species that are responsible for degrading AY42. The result denoted that the La/Bi₂S₃ electron was coupled with oxygen to create superoxide, which reacted with AY42 to degrade it. Additionally, the role of the Lanthanum ion (La³⁺) was utilized to improve the photogenerated electron of Bi₂S₃ and to determine the quick recombination of electron-hole pairs for improved photodegradation of AY42. The trapping test shows that the degradation efficiency of the AY42 scavenger by K₂Cr₂O₇ was decreased from 92.1% to 77.41%, explaining that the electrons were not the most crucial key in the degradation process. In this scavenger, the degradation efficiency decreased from 92.1% to 57.16% in the scavenger by IPA. The material’s noticeable drop in photocatalytic activity after adding IPA is due to both radical •OH radicals created directly and radical •OH radicals formed via intermediary processes that were repressed [34], which is the principal active species in the photodegradation activity. The hole (h⁺) shows its importance in the degradation of AY42 and explains that OH^- was the intermediate oxidative species.

(a)

(b)

Furthermore, the ESR spectra of 3% La/Bi₂S₃ (Figure 10(b)) during 12 min under visible light also confirmed that the hydroxyl radicals were the main factor for the degradation of AY42. The DMPO-ESR analysis also demonstrated the detection of the signal when the light was turned on. However, there is almost no signal projected in the dark. This mechanism confirms that the photodegradation of AY42 by the superoxide (•O₂) and hydroxide (^-OH) under visible light was successfully applied.

The photodegradation mechanism of AY42 present in Figure 11 is as follows: Under visible light irradiation, the excited electrons move from the valence band (VB) to the conduction band (CB), and the holes (h⁺) stay in VB, as shown in Equation (2). Then, the electrons (e^-) reacted with oxygen to produce ^•O₂⁻ (Equation (3)). La was used to support the CB to avoid the recombination of the photogenerated e^- and h⁺ of the catalyst. Adding La species to Bi₂S₃ can significantly increase the formation of ^•O₂⁻ radicals and the efficient separation of photogenerated electron-hole pairs, resulting in improved photocatalytic AY42 elimination [35]. The H₂O continually reacted with O₂⁻ to produce ^•OH radicals in Equations (4)–((6)()). h⁺ combines with OH⁻ from Equations (4) and (6) for the formation of OH; the holes subsequently reacted with water (Equation (7))). The radicals (O₂⁻ and OH) were keys to the degradation of AY42, as shown in Equations (8) and (9) [36].

4. Conclusion

This present study proved the hydrothermal method’s successful synthesis of La/Bi2S3 material and confirmed by the EDS analysis. The XRD and the particle size analysis showed that the presence of La decreased the crystallites of the Bi₂S₃ material and the La/Bi₂S₃ is indicated as high photodegradation of AY42 dye under visible light. The optimum photocatalytic activities were detected at 3% La/Bi₂S₃, two times more than the pure Bi₂S₃. The trapping test and ESR spectra analysis proved that the hydroxyl radical was the most efficient active species in this photocatalytic process and the h⁺ showed its importance in the degradation of AY42 by detecting that OH^- as the intermediate species for the degradation of AY42. The 3% La/Bi₂S₃ could be considered a stable catalyst due to the low percentage of its removal efficiency after reusing this composite four times for the photocatalytic degradation of AY42. Finally, the whole experiment concluded that La greatly influenced a vital role in Bi₂S₃ by modifying the material’s structure for the optimization of degradation of AY42 under visible light.

Data Availability

In our manuscript, we provided supporting information as a word document, applied for Section 2.1.

Conflicts of Interest

The authors in this study declare no competing financial interests.

Acknowledgments

We want to present our gratitude to Chung Yuan Christian University. The financial source of this research was Chung Yuan Christian University (Project No: 109609432), which sponsors all the material characterization fees.

Supplementary Materials

Table S1. Presentation of C.I. Acid Yellow 42. (Supplementary Materials)

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Copyright © 2022 Ernso Fenelon 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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Journal of Nanomaterials

Study of the Potential of La/Bi2S3 Catalyst for Photodegradation of Acid Yellow 42 Dye under Visible Light

Abstract

1. Introduction

2. Experimental Section

2.1. Reagents and Materials

2.2. Preparation of Bi2S3 and La/Bi2S3

2.3. Characterization Techniques

2.4. Photocatalytic Degradation Activities

3. Results and Discussion

3.1. Analysis of XRD Pattern

3.2. FTIR Analysis of Bi2S3 and La/Bi2S3

3.3. Morphology of Bi2S3 and La/Bi2S3 Composites

3.4. Photodegradation of Acid Yellow 42 under Visible Light by La/Bi2S3

3.5. Effect of AY42 Dye Concentration

3.6. Effect of Catalyst Amount

3.7. Mechanism of Degradation of AY42

4. Conclusion

Data Availability

Conflicts of Interest

Acknowledgments

Supplementary Materials

References

Copyright

Study of the Potential of La/Bi₂S₃ Catalyst for Photodegradation of Acid Yellow 42 Dye under Visible Light

2.2. Preparation of Bi₂S₃ and La/Bi₂S₃

3.2. FTIR Analysis of Bi₂S₃ and La/Bi₂S₃

3.3. Morphology of Bi₂S₃ and La/Bi₂S₃ Composites

3.4. Photodegradation of Acid Yellow 42 under Visible Light by La/Bi₂S₃