## Introduction

Recently, isolated and purified natural products have gained considerable attention in the synthesis and cap of metallic nanoparticles. These natural product-induced metallic nanoparticles (NPIMNPs) have been widely used in the biological, environmental, electrochemical, and catalytic fields1,2,3,4,5,6,7,8. Albeit plant extracts are considered as general sources for the green synthesis of metallic nanoparticles9, the extracts compositions and concentrations of substances are highly variable, affected by the method of extraction, harvesting season and geographical parameters. As an alternative, the pure natural products with a well–defined concentration of reactant can synthesize reproducible metallic nanoparticles, and the purification of nanoparticles is more facile10,11.

Furthermore, physicochemical and biological characteristics of natural products can improve the biological, electrochemical, and catalytic properties of NPIMNPs. In this regard, natural products e.g., phenolic compounds, alkaloids, terpenoids, amino acids, flavonoids, glutathiones, quinones antioxidants, polysaccharides, organic acids, and coumarins have been used12. The synthesis of nanoparticles by these natural products is a clean, non-toxic, and environmental-friendly13. Compared to their counterparts, synthesized by other methods, NPIMNPs possess improved bioactivities and catalytic characteristics12.

Among metallic nanoparticles, silver nanoparticles have been widely studied for catalytic activities. AgNPs can demonstrate light absorption and significant visible light catalytic activity due to its narrow bandgap energy to the many colorant/textile combinations under visible or sunlight illumination4,14. The high absorption property of Ag-based NPs in the visible light region, together with preventing the recombination of electron and hole pairs within the photocatalytic process, drew enormous attention in the application of silver nanoparticles for the catalytic field. This aspect of AgNPs makes them an excellent choice for multiple roles in the industrial area14. Furthermore, AgNPs have been demonstrated to be good and impressible catalysts for non-enzymatic electrochemical detection of H2O215,16,17,18,19,20. A large number of nanostructures decorated with chemically-stabilized AgNPs have been synthesized and used for this porpose21.

Current techniques for the synthesis of AgNPs, including photochemical methods, chemical reduction, electron irradiation, gamma irradiation, and laser ablation22, are expensive and require high temperature and pressure. Besides, they need toxic and hazardous chemicals like dimethylhydrazine, hydrazine and sodium borohydride and produce toxic organic byproducts that are responsible for various biological risks23.

In addition to the synthesis limitations, the stabilization of AgNPs on the electrode surface hampered its application in the field of electrochemistry. In most of the cases, investigators used nonconductive polymers such as Nafion and chitosan as a binder24,25,26. Composites formed with nonconductive binders suffer from their low conductivity, which effects on the electrochemical response of nanocomposite-modified electrode, especially in traces analysis27,28. It is expected that the nonconductive materials can decrease the electrochemical performance of the nanomaterials. Therefore, the as-prepared binder-free electrode materials as stable catalysts with high conductivity and active surface area are highly demanded.

To address these unmet technical needs, in the present study, isoimperatorin was applied as a bio-reducing agent; photocatalytic and electrochemical activates of Iso-AgNPs were evaluated. Isoimperatorin is a furanocoumarin isolated from edible Apiaceous plants such as Angelica dahurica29 and Prangos ferulacea30. It showed anti-inflammatory, anti-Alzheimer, analgesic, spasmolytic31,32, potential cancer prevention33, antibacterial and anti-cancer effects34,35,36,37. There are no reports on photo- or electrochemical-catalytic activities of isoimperatorin. However, there are some reports on electro-catalytic activities of other coumarins as chemo-sensors for the detection of fluoride ions, hydrogen sulfide (H2S), mercury (Hg2+) ions, hypochlorite, and cyanide anions in aqueous solution38,39,40,41,42.

Although the different flavonoids, e.g. hesperidin, naringin, diosmin, quercetin diphosphate, and quercetin pentaphosphate, resveratrol and fisetin have been applied for the synthesis of AgNPs, and catalytic activity of synthesized NPs have been investigated43,44, to our best of knowledge, there is no report on the synthesis of silver nanoparticles using isoimperatorin and evaluation of their catalytic properties. Therefore, in this work, we synthesized and characterized Iso-AgNPs using UV–visible spectrophotometer, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) with energy dispersive X-Ray (EDX) detector X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM). The electrocatalytic activity of Iso-AgNPs toward H2O2 reduction and their photocatalytic performance against three toxic mutagenic dye pollutants consist of New-fuchsine (NF), Methylene Blue (MB) and Erythrosine B (ER), and 4-chlorophenol (4-CP) as a non-dye pollutant were evaluated.

## Results and Discussion

### Physical and chemical characterization of Iso-AgNPs

The reduction of the Ag+ to AgNPs using isoimperatorin was approved by a color change from pale pink to dark brown after two h exposure; the absorption of Iso-AgNPs was shown in Fig. 1. The formation of dark brown color in the reaction mixture, indicating the excitation of Surface Plasmon Resonance (SPR) of Iso-AgNPs is a sign for the synthesis of AgNPs45,46. Iso-AgNPs showed a clear and single SPR band with λmax (maximum absorption) at 439 nm (Fig. 1A).

Iso-AgNPs had a face-centered cubic crystalline nature according to the XRD pattern (Fig. 1B). Four reflection peaks were detected in the 2θ range of 20–80°; peaks at 38.1, 44, 64.3, and 77.3° are allocated to the (111), (200), (220), and (311) planes for Iso-AgNPs respectively. The extra picks presented in the spectrum can belong to isoimperatorin47.

The possible changes in the structure of isoimperatorin after synthesis of AgNPs were evaluated by FTIR. The FTIR spectra of pure isoimpratorin and synthesized AgNPs are shown in Fig. 2A. Comparing to the isoimperatorin spectrum, some functional groups were disappeared, and new peaks appeared in the FTIR spectrum of Iso-AgNPs. The FTIR spectrum of isoimperatorin indicated the characteristic peak at 1724 cm−1 related to stretching vibrations of carbonyl bands from ester group, and the peak at 1249 and 1091 cm−1 corresponding to -C-O- of ester group, but the Iso-AgNPs spectrum showed the peak at 1705 cm−1 related to stretching vibrations of carbonyl bands from carboxylic acid group, and the peak at 1095 cm−1 attributed to C-O- stretching vibration of carboxylic acid group. Also, the broad peak of the OH group at 3444 cm−1 was appeared affirming the presence of the carboxylic acid group. Due to the presence of Ag+ ions in the stereochemical medium, carboxylate anion is formed, and then carboxylate anion becomes carboxylic acid by the catalytic effect of nitric acid (the byproduct of carboxylate anion). The possible reaction of AgNO3 with isoimperatorin is illustrated in Fig. 3. For further characterization of Iso-AgNPs, Raman spectroscopy data has been provided. In Fig. 2B, the Raman spectrum of isoimperatorin, is compared with the spectra of Iso-AgNPs. Characteristic peaks (1685, 1613, 1577, 1551, 1441, 1377, 1253, 1198, 1132, 964, 501, 471, and 379 cm−1) from Iso-AgNPs were attributed to isoimperatorin10,48,. The result indicates that the isoimperatorin is mainly involved in the fabrication of silver nanoparticles. Based on the proposed mechanism for the reaction of AgNO3 with isoimperatorin (Fig. 3), the C=O function related to the ester group converts to the carboxylic acid group; therefore, C=O stretching in the Raman spectrum of pure isoimperatorin (1735 cm−1) was abolished. These results confirm FTIR results.

The SEM analysis showed well defined uniformly spherical Iso-AgNPs without any agglomeration and their small size (Fig. 4A). EDX analysis confirmed the presence of elemental silver in the sample (Fig. 4B). The sharp peak at 3.030 keV represented the existence of elemental silver.

The morphology and particle size of Iso-AgNPs were evaluated by TEM image (Fig. 5A); nanoparticles were spherical in shapes. The spherical nanostructure had a diameter range of 79–200 nm. The presence of large particles can be related to slow reaction speed49,50. Isoimperatorin solubility in water is low, and using a high concentration of it in the aqueous medium is impossible. Therefore, the rate of nucleation was low, and crystals had enough time for growth.

Figure 5B shows the HRTEM image of the Iso-AgNPs. In inset Fig. 5B, the interplanar distance of 2.21°A can be observed. The crystallinity of Iso-AgNPs was observed by selected area emission diffraction (SAED), which recorded by directing the electron beam perpendicular to NPs. The characteristic fringe array can be indexed as (111), (200), (220) and (311) of the pure face-centered cubic (fcc) lattice structure commonly found for Ag crystal (Fig. 5C). The formation of fcc structured Iso-AgNPs was also confirmed using the XRD patterns.

### Photo-catalytic performance of Iso-AgNPs

The photocatalytic activity of Iso-AgNPs was analyzed by photo-degradation of NF, MB, ER dyes as a model. As shown in Fig. 6, the degradation of tree dyes under sunlight irradiation initially identified by the color change into light color and then colorless after 60 min for MB, ER, and NF dyes. The UV–vis absorption spectra indicated the decreased peaks for three studied dyes at different time intervals. Initially, the sharp decline occurred for absorption peaks at 548 nm for NF (Fig. 6A), 665 nm for MB (Fig. 6B), and 526 for ER (Fig. 6C) at 15 min under sunlight irradiation. It was continued with the increase of the exposure time. The degradation rates of MB, ER, and NF dyes were 96.5%, 92%, and 96.0%, respectively, at 60 min (Fig. 7A).

In order to examine the reusability and durability of as prepared Iso-AgNPs photocatalyst, a recycling study of Iso-AgNPs was carried out with a stock solution of NF (as a dye molecule model for this section) under identical conditions. Hence, the stability of the Iso-AgNPs was tested for successive four recycling runs. As shown in Fig. 7B, the reusability of the Iso-AgNPs photocatalyst was demonstrated up to a fourth cycle run with a low decrease in photo-degradation efficiency, i.e., 96% to about 88% in the first to fourth cycle runs. The results presented in Fig. 7B demonstrate that the Iso-AgNPs possess robust and excellent cycle stability.

### Possible photo-catalytic mechanism of Iso-AgNPs

$${\rm{I}}{\rm{s}}{\rm{o}}-{\rm{A}}{\rm{g}}{\rm{N}}{\rm{P}}{\rm{s}}+{\rm{s}}{\rm{u}}{\rm{n}}{\rm{l}}{\rm{i}}{\rm{g}}{\rm{h}}{\rm{t}}\to {\rm{I}}{\rm{s}}{\rm{o}}-{\rm{A}}{\rm{g}}{\rm{N}}{\rm{P}}{\rm{s}}({{\rm{e}}}_{{\rm{C}}{\rm{B}}}^{-}+{{\rm{h}}}_{{\rm{V}}{\rm{B}}}^{+})$$
(1)
$${\rm{D}}{\rm{y}}{\rm{e}}+{\rm{s}}{\rm{u}}{\rm{n}}{\rm{l}}{\rm{i}}{\rm{g}}{\rm{h}}{\rm{t}}\to {{\rm{D}}{\rm{y}}{\rm{e}}}^{\ast }$$
(2)
$${{\rm{Dye}}}^{\ast }+{\rm{Iso}}-{\rm{AgNPs}}\to {\rm{Dye}}{\cdot }^{+}+{\rm{Iso}}-{\rm{AgNPs}}({{\rm{e}}}_{{\rm{CB}}}^{-})$$
(3)
$$({{\rm{O}}}_{2})+{\rm{Iso}}-{\rm{AgNPs}}({{\rm{e}}}_{{\rm{CB}}}^{-})\to {\rm{Iso}}-{\rm{AgNPs}}+({{\rm{O}}}_{2}{\cdot }^{-})$$
(4)
$$({{\rm{O}}}_{2}{\cdot }^{-})+{{\rm{H}}}^{+}\to {{\rm{HO}}}_{2}\cdot$$
(5)
$$2{{\rm{HO}}}_{2}\cdot \to {{\rm{O}}}_{2}+{{\rm{H}}}_{2}{{\rm{O}}}_{2}$$
(6)
$${{\rm{H}}}_{2}{{\rm{O}}}_{2}+({{\rm{O}}}_{2}{\cdot }^{-})\to {{\rm{HO}}}^{-}+{\rm{HO}}\cdot +{{\rm{O}}}_{2}$$
(7)
$${{\rm{e}}}^{-}+{{\rm{H}}}_{2}{{\rm{O}}}_{2}\to {\rm{HO}}\cdot +{{\rm{HO}}}^{-}$$
(8)
$$({{\rm{H}}}_{2}{\rm{O}})+{\rm{Iso}}-{\rm{AgNPs}}({{\rm{h}}}_{{\rm{VB}}}^{+})\to {\rm{Iso}}-{\rm{AgNPs}}+({\rm{HO}}\cdot )+({{\rm{H}}}^{+})$$
(9)
$$({{\rm{HO}}}^{-})+{\rm{Iso}}-{\rm{AgNPs}}({{\rm{h}}}_{{\rm{VB}}}^{+})\to {\rm{Iso}}-{\rm{AgNPs}}+({\rm{HO}}\cdot )$$
(10)
$$\begin{array}{c}{\rm{Dye}}+{\rm{Iso}}-{\rm{AgNPs}}({{\rm{O}}}_{2}{\cdot }^{-},{\rm{HO}}\cdot ,{{\rm{h}}}_{{\rm{VB}}}^{+}\,{\rm{or}}\,\cdot {\rm{OOH}})\to \to \to {{\rm{H}}}_{2}{\rm{O}}\\ \,+{{\rm{CO}}}_{2}+{\rm{byproducts}}+{\rm{Free}}\,{\rm{Iso}}-{\rm{AgNPs}}\,{\rm{for}}\,{\rm{reuse}}\end{array}$$
(11)

For approving that the fading of dye is photo-degradation, not a dye sensitization, carcinogenic 4-chlorophenol (4-CP) as a colorless organic pollutant was selected as a target to measure the photocatalytic activity. The evolution of UV-vis spectra of carcinogenic 4-CP under natural sunlight in the presence of the Iso-AgNPs is presented in Fig. 9A; the intensities of peaks at 225 nm and 280 nm characteristic of 4-CP, was decreased in a function of difference irradiation times. Although many aspects regarding the detailed degradation mechanisms of the 4-CP remain unidentified and open to further scrutiny, some primary degradation pathway includes a series of hydroxylation, dehydrogenation, dechlorination and aromatic ring cleavage steps56,57,58,59. According to the literature, decomposition of 4-CP to H2O and CO2 molecules as the final products often is a complex process occurring through three primary intermediates: benzoquinone (BQ), hydroquinone (HQ), and 4-chlorocatechol (4-CC)60,61. The characteristic absorption peaks of these compounds emerge as intermediates at similar wavelengths as those of 4-CP, i.e. at 246 nm for BQ, 221 nm and 290 nm for HQ, 221 and 284 nm for 4-CC62. As can be seen, a gradual decrease of both absorption peaks of 4-CP during photocatalytic procedure may be an indication of decomposition of 4-CP. On the other hand, the lack of the absorption peak characteristic of BQ intermediates at 246 nm in the spectra observed in Fig. 9A suggests that reaction pathway in the presence of Iso-AgNPs is via 4-CC intermediate62.

As shown in Fig. 9A, prior to the photocatalytic tests, the adsorption of 4-CP was evaluated. However, the dark physical adsorption of the 4-CP after 60 min onto the nano-photocatalysts was negligible (point line, Fig. 9A) while in photocatalytic process, the decrease of the absorption band of 4-CP was quick. This notable decrease indicated that the removal was also mainly originated from the photocatalytic degradation, not from physical adsorption.

To well understand the presence and role of active species in the photocatalytic degradation route of the organic compounds, the scavenger quenching experiments for 4-CP photo-degradation was selected and carried out at 40 ppm 4-CP concentration for 60 min. Various scavengers used in the present study were ammonium oxalate as an H+ scavenger, methanol as an HO• scavenger, and in deoxygenated solutions to conquer the formation of O2• by oxygen reduction.

As indicated in Fig. 9B, by addition of oxalate, a slight inhibitory effect was found where around 66% of 4-CP was degraded under natural sunlight. Conversely, deoxygenation of the 4-CP solution significantly decreased the 4-CP molecule photocatalytic degradation rate, where only 34% of 4-CP is removed. Similarly, the existence of methanol leads to an impressive decrease in 4-CP degradation, where about 48% of 4-CP is degraded under natural sunlight. This suggests that the superoxide radicals and then hydroxyl radicals play an important role and acts as main reactive species in the pollutant photo-decomposition. The 4-CP decomposition efficiency was 95.0% without using any scavenger.

### Electrochemical properties of Iso-AgNPs

The electrocatalytic activity of the Iso-AgNPs as a binder‐free catalyst for H2O2 reduction was investigated by recording cyclic voltammograms in presence of the H2O2. Figure 10A shows the electrochemical reduction of 1.0 mM H2O2 at Iso-AgNPs/GCE (Glassy Carbon Electrode) in N2-saturated 0.1 M PBS (pH 7.4) at the scan rate of 100 mV/s. As can be seen, at the unmodified GCE, there is no obvious current for the reduction of H2O2. However, the presence of Iso-AgNPs on the electrode surface had a great improvement on the electrocatalytic reduction of H2O2, which indicated that the Iso-AgNPs facilitate the electron transfer and increased active surface area. Furthermore, the binder-free Iso-AgNPs can further improve electrochemical performance and electron kinetics of H2O2 reduction. In the following, to investigate the sensitivity of Iso-AgNPs on the reduction of H2O2, the cyclic voltammograms were obtained at a different concentration of H2O2 in N2-saturated 0.1 M PBS (pH 7.4), (Fig. 10B). As expected, the peak current increased with the increasing concentration of H2O2, indicating the catalytic activity of Iso-AgNPs to the reduction of H2O2. Also, the sensing stability of binder‐free Iso-AgNPs was examined by successive cyclic voltammograms in the presence of H2O2. As shown in Fig. 10C, after 9 cycles, the reduction peak currents only varied ~6%, indicating that Iso-AgNPs has good stability on the electrode surface for electrochemical reduction of H2O2. Therefore, the as-prepared Iso-AgNPs could be used as an electrocatalyst without any binder and shows the acceptable stability on the electrode surface.

Differential pulse voltammetry (DPV) was used for the analytical performance of the electrochemical sensor based on Iso-AgNPs toward the reduction of H2O2. Figure 11 shows the DPV response of Iso-AgNPs/GCE obtained at different H2O2 concentration in N2-saturated 0.1 M PBS (pH 7.4). As expected, the response of Iso-AgNPs/GCE corresponding to the H2O2 increased with increasing the concentration of H2O2. The calibration curves of the H2O2 sensor showed that there was a linear relationship between the electrochemical responses and H2O2 concentrations from 0.1 µM to 4 mM. Based on the calibration curves in Fig. 11D,E, the plot of electrochemical responses vs. H2O2 concentration formed a line that had an equation of I (μA) = 0.0762 CH2O2 (μM) + 0.715. Furthermore, the limit of detection (LOD) was estimated as 0.036 μM from the calibration plot with a signal-to-noise ratio of 3. The results of the proposed electrochemical sensor based on Iso-AgNPs are comparable with other modified electrode for H2O2 sensing and are displayed in Table 163,64,65,66,67,68,69,70,71,72. However, our electrochemical sensor is characterized by a binder‐free, simple design and easy preparation in contrast with other sensors previously described.

## Conclusion

Isoimperatorin, isolated from Prangos ferulacea roots, was used successfully to synthesize silver nanoparticles as a simple and cost-effective, precise and eco-friendly methodology. Preparation of Iso-AgNPs was confirmed by UV–Vis spectroscopy and characterization was conducted using XRD, FTIR, SEM, EDX, Raman spectroscopy, TEM and HRTEM. The Iso-AgNPs reveal photo-catalytic performance under sunlight irradiation and can be used for the improvement of the environment through the purification of water. Also, Iso-AgNPs shows the excellent electrocatalytic activity toward H2O2 as an appropriate option in many biological systems without extra binder and conductive additives. Altogether, the synthesized nanoparticles demonstrate a broad range of catalytic applications.

## Materials and Methods

### Materials

Silver nitrate salt (AgNO3), MB, NF, EB, 4-CP, ammonium oxalate, methanol, heptane, ethyl acetate, and silica gel were bought from Merck, Germany. Deuterochloroform (CDCl3) was supplied from Sigma–Aldrich, USA. Other reagents, solid materials, Silica gel used in gravity column chromatography and solvents were bought from Merck (Germany).

## Experimental

### Apparatus

A Young Lin apparatus equipped with PDA detector (YL 9160) and a binary pump (YL 9111 S) together with VERTISEP (Reversed-phase, RP18 250 × 30 mm) and Eurospher II (Normal phase, Si 250 × 20 mm) columns with flow rate of 10 mL/min have been used for high-performance liquid chromatography (HPLC) analysis.

The NMR spectrum of Isoimperatorin was recorded on a BRUCKER (500 MHz) instrument, using CDCl3 as a solvent. MS analysis was performed on an AGILENT 6410 Triple Quadrupole mass spectrometer (AGILENT Technologies, Palo Alto, CA, USA)73 coupled with an AGILENT Mass Hunter Workstation B.01.03. TLC plates (Silica gel 60 GF254 precoated plates, Merck) were analyzed by UV observation at 254 and 366 nm, and by spraying with cerium sulfate/ molybdate74.

The synthesis of Iso-AgNPs was confirmed by UV–vis spectrometer (SHIMADZU, Lambda UV mini-1240 instrument) in the absorption wavelength range of 200 to 700 nm. The FTIR of isoimperatorin and Iso-AgNPs was performed by IR-Prestige-21 (SHIMADZU Spectrometer, Kyoto, Japan); KBr Pellets of samples were used to measure transmittance percentage. The spectrum was recorded at a resolution of 4 cm−1. The XRD spectrum of the dried nanoparticles was recorded by APD 2000-Italian Structures X-ray generator; to carry out XRD, the samples were coated on the XRD grid, and a voltage of 40 kV with a current of 30 mA using Cu K−1 radiation was applied. The SEM and EDX (FESEM-TSCAN, Czech), were performed for the analysis of surface topographies and chemical composition of Iso-AgNPs. Raman spectroscopy was performed by NICOLET-910, USA. The morphological analysis of NPs was evaluated by TEM microscopy (ZEISS – EM10C, Germany) and HRTEM microscopy (FEI – TEC9G20, USA) at an accelerating voltage of 100 kV and 200 kV, respectively. The aqueous suspension of Iso-AgNPs was loaded on the carbon-coated copper grid. After evaporation of solvent at room temperature for one-hour, clear microscopic views were observed in the different range of magnifications. The light intensity in the place of the sample was gotten from Kermanshah weather bureau. Electrochemical studies were conducted with an AUTOLAB PGSTAT101 potentiostat/galvanostat (ECO CHEMIE, Netherlands) with standard three-electrode system, using GCE or a modified GCE as working electrode, a platinum wire as a counter electrode and Ag/AgCl/KCl as a reference electrode.

### Isolation of isoimperatorin

Isoimperatorin was isolated from Prangos ferulacea roots as described previously75. In brief, a MeOH-soluble (in −20 °C) part of acetone extract of roots was fractionated using heptane ethyl acetate (7:3) as the eluant and silica gel as the stationary phase. The final purification was performed by normal phase preparative HPLC.

Isoimperatorin; EI-MS m/z 270 [M]+, 255 [M-CH3], 227 [M-(CH3)2CH] +.H1NMR (CDCl3, 500 MHz): 8.19 d (1 H, J: 9.6, H-4), 7.62 d (1 H, J: 2.3, H-2′), 7.19 s (1 H, H-8), 6.99 d (1 H, J: 2.3, H-3′), 6.30 d (1 H, J: 9.6, H-3), 5.75 t (1 H, J: 6.8, H-2′′), 4.95 d (2 H, J: 6.8, H-1′′), 1.84 s (3 H, CH3–5′′), 1.73 s (3 H, CH3–6′′).

### Synthesis of AgNPs with isoimperatorin

The isoimperatorin solution (2 mmol/L) was obtained by dissolving isoimperatorin in 2 mL ethanol. Then, the ethanol solution was added dropwise to 6 mL deionized water and incubated for 10 min at room temperature. Then, the isoimperatorin solution was quickly added to 12 mL aqueous solution of AgNO3 (1 mmol/L). Finally, the reaction was placed under sunlight (The light intensity was 25.5 MJ/m2) to change the color from pale yellow to reddish-brown which indicates the formation of Iso-AgNPs.

### Photocatalytic properties of Iso-AgNPs

Using the four kinds of hazardous pollutant involve three dyes model (MB, NF, and ER) and carcinogenic 4-CP as a non-dye pollutant, the photocatalytic activity of Iso-AgNPs was demonstrated under sunlight irradiation by a slightly modified method of Roy et al.76. Primarily, the dye and non-dye solutions were prepared at a concentration of 10 mg/L and 40 mg/L in DI water respectively. Afterward, 5 mg of Iso-AgNPs was added to 25 mL of each dye solution (at first, powder of Iso-AgNPs was sonicated in 5 mL DI water for 15 min and then added to 20 mL pollutant solution). These colloidal suspensions were then placed under natural sunlight irradiation with constant stirring. The average temperature of the ambiance during the test was around 14 °C (geographical coordinates: 34.3277°N and 47.0778°E) and the light intensity was 7.7 MJ/m2 for MB, NF, and ER. In the case of 4-CP, the average temperature was around 21 °C and the light intensity was 9.9 MJ/m2. At regular intervals time (every 15 min for dye model and every 10 min for 4-CP), 2 mL suspension was taken from the colloidal mixture and centrifuged at 5,000 rpm for15 min to obtain clean supernatant of the tested pollutant. Finally, the absorbance maxima of dye models at different time intervals (0, 15, 30, 45, 60 min) was monitored using UV–visible spectrophotometer at a different wavelength from 200 to 800 nm for evaluation of dye degradation. The absorbance maxima of 4-CP were monitored at 0, 10, 20, 30, 40, 50 and 60 min time intervals.