INTRODUCTION
With the rapid growth of industrialization, a significant amount of waste continues to be discharged into the environment. Despite clean water’s value to society, these ongoing waste management systems appear to compromise water quality for everyday use. When dye contaminants from the cloth, food, leather, and paper industries, among others, are improperly disposed of, they pollute the atmosphere. The only way to deal with these dye contaminants is to establish safe disposal mechanisms and methodologies that will enable them to coexist with the ecosystem while maintaining a green environment. Photocatalysis is one technique used based on its eco-compatibility, energy sustainability, and partial or total decomposition of the dye contaminants [1]. Photocatalysis is among the most promising environmental remediation approaches, and a tremendous amount of research work has been reported on several metal oxide-based nanomaterials [2]. TiO2 semiconductor has unique properties and has been applied in diverse applications due to its chemical stability, low cost, mechanical robustness, strong oxidizing ability and efficient photocatalytic activity [3-6]. TiO2 exists in nature under ambient temperature in three interconvertible polymorphs (brookite, rutile, anatase) [7, 8], and their properties are based on the type of polymorph. Besides, TiO2 is an intrinsic N-type semiconductor due to oxygen vacancies generated during the heat treatment, mainly when anatase composition is higher than that of other phases [9]. The anatase phase is the primary product in experimental synthesis, with a minor amount of either the brookite phase or rutile phase being formed. However, rutile is most thermodynamically stable among the metastable anatase and brookite phases [10].
To prepare TiO2 with the desired properties, different methods have been employed, such as hydrothermal [11], sol-gel [12], electrochemical [13], chemical vapor deposition [14], and hydrolytic precipitation [15, 16]. Amongst these methods, the sol-gel has been recognized as the most appropriate and straightforward chemical technique based on its versatility, low processing temperature, low-cost, stability, and high homogeneity [17]. Sol-gel involves the hydrolysis and condensation of the titanium alkoxides in aqueous media to produce different morphologies such as aerogels, wires, tubes, quantum dots, sheets, rods, and nanoparticles. In the presence of water, alkoxides are hydrolyzed and then polymerized to form a 3D oxide network as represented in Eq. (1) and (2) [18]. 

           (1)
         
Condensation incudes; dehydration (i) and dealcoholation (ii)

                                                                          (i)    
         (ii)

The overall equation

                                      (2)

where R is alkyl group, M- Ti, Si etc. Water molecules in the overall equation (2) always bear a positive partial charge [19]. Thus, oxolation and Olation can proceed simultaneously during nucleation and growth, leading to TiO2.nH2O (amorphous hydrous oxide), where the number (n) of water molecules depends on experimental conditions. However, even with the study of synthesized TiO2 nanoparticles (NPs), no clear and comprehensive understanding of the synthesis parameters that affect the structure, morphology, optical, and photocatalytic properties. The experimental procedure determines the precipitation of TiO2 to form either anatase or rutile [20]. When deoxolation (O = Ti-OH2 → HO – Ti-Ti-OH) does not occur during nucleation, Olation leads to a linear growth along with one of the two equivalent directions in the equatorial plan of [TiO2O2(OH)4(OH2)4]o dimers. Then, Oxolation between the resulting TiO(OH)2(OH)2 linear chains after an internal proton transfer leads to corner-sharing octahedral chains (Ti3O bridges) characteristics of the rutile structure. The formation of rutile may then be associated with the metastability of apical Ti=O bonds within monomers or dimers. If deoxolation occurs before Olation, condensation can continue along apical direction leading to skewed chains typical of the anatase structure. Controlling the stage of deoxolation before Olation can be obtained by adjusting the pH, which is one of the parameters that affect the final products of TiO2.
 Different structures and morphologies of titanium dioxide have been synthesized using different methods and pH values. For instance, Santhi et al. [20] synthesized nanorods at pH 7 and 9 while pure anatase phase was prepared by Anajafi et al. [21]  at pH ranging from 8-12 using the hydrothermal method. Synthesis of mesoporous TiO2 by Mutuma et al. [16] using a modified sol-gel method obtained a mixture of anatase-rutile phase at a pH of 2 and 9. Rod-like morphology was exhibited at pH 7 with a length ranging from 300–350 nm and a diameter of 70–100 nm, while at pH 9, the morphology changed from rod to nanoplatelet. Ismagilov et al. [22] deliberated the effect of nanoscale TiO2 on cell responses by synthesizing four modifications of the TiO2 (amorphous, anatase, brookite, and rutile) by varying the nature of precursor, pH, temperature, and addition of a complexing agent. The effect of pH (acid solution) on the structural, morphological, and optical properties of TiO2 rutile nanorods was investigated by Selman et al. [23] for optoelectronic nanodevice applications. Moreover, the outcome observed at different pH is also determined by the solvents used. According to Sridevi et al., anatase-brookite phases were obtained at pH 6, 8, and 10, when 2- propanol solvent was used [24, 25].
The above research works show that pH plays a crucial role in the formation of TiO2 NPs. Herein we report a reproducible one-step sol-gel method to synthesize TiO2 nanoparticles. The reactions were carried out at acidic, neutral, and alkali pH (4, 6, 7, 8, and 10) to investigate the effect of pH on the nano-structural and opto-electronic properties of the samples. The effect of how varied pH on the optical properties can affect the photocatalytic activity of  TiO2 NPs has not been widely explored. A comparison on photocatalytic activity was performed on the synthesized samples by degradation of methylene blue dye solution. 

MATERIALS AND METHODS 
Tetra isopropyl orthotitanate (C12H28O4Ti) purity >98% purchased from Sigma Aldrich was used as titanium precursor, ethanol absolute (C2H6O), purity (>99.9%) as a solvent medium, ethanolamine as a stabilizer, and Deionized water to enhance the hydrolysis process. In contrast, ammonium hydroxide and hydrochloric acid were used for pH adjustment. All reagents were as received from the manufacturer.

TiO2 synthesis procedure
TiO2 sols were prepared by hydrolysis and condensation of Tetra isopropyl orthotitanate (TIP). 5 mL of TIP was dissolved in 20 mL of ethanol of spectroscopic grade with continuous stirring at room temperature, which was termed solution A.  Ethanol was a preferred solvent since it has a lower dielectric constant (80) than water (24.3).  Further, five different solutions were made with pH values varied as 4, 6, 7, 8, and 10 using ammonium hydroxide (18.1 M) and hydrochloric acid (12.1 M) and termed as solution B. Thereafter, solutions A and B were mixed under vigorous stirring using a Teflon-coated stirrer bar. After stirring the resultant solution for 30 min, 5 mL of ethanolamine was added dropwise, followed by a few drops of water to enhance the hydrolysis process , the sol was allowed to stir until the gel was formed. Following this procedure, the local precipitation effect was avoided. The gel was dried at 100 °C in a hot oven for 2 h to evaporate the residual solvents and water. Subsequently, the dried samples were annealed at 450 °C for 2 h in the air to crystallize the TiO2 NPs [9]. The obtained products were crushed to a fine powder after cooling at ambient temperature, ready to be subjected for further characterization. The sol-gel method was adopted because it can synthesize a well-crystallized TiO2 with anatase phase at very low temperature since TiO2 formation is a water-driven process that occurs even at room temperature.

 Characterizations
 X-ray diffraction
The samples’ structural analysis was done using Bruker AXS Discover diffractometer with CuKα (0.15406 nm) monochromatic radiation. The machine was set to scan at 40 mA and 40 kV in its reflective mode based on the Bragg–Brentano geometry conventional for powder samples. The powder samples were loaded on a Silicon low background sample holder and carefully placed on the XRD machine sample stage.  The samples were scanned in the range of 20◦ ≤ 2θ ≤ 70◦ at a 2◦/min scanning speed with a 0.02◦ fixed step size in 2θ. The crystalline phase’s identity was justified based on the joint committee powder diffraction standard (JCPDS) from the International Centre for diffraction database. The average crystallite size (D) was estimated in comparison using the Scherrer equation (3) and Williamson-Hall (4) [20], the strain (4), dislocation density (δ) (5), Lattice parameters (tetragonal a = b, c) (6) below.
                                                                                     (3)
                                                                 (4) 
                                                                         (5)

                                                                                             (6)

where ‘λ’ is the wavelength of Cukα radiation (1.54Å), ‘β’ is the profile broadening, i.e., full width at half maxima (FWHM), in radians, while ‘θ’ is the Braggs’ angle and where dhkl is the spacing between the planes corresponding to h, k, l, miller indices calculated using Bragg’s law.

Morphology/elemental studies
The surface morphologies and particle sizes of the synthesized samples were obtained using A Zeiss supro-field emission gun scanning electron microscope (SEM) and A JEOL 200CX high-resolution transmission electron microscopy (HRTEM, at an acceleration voltage of 200kV). 

 UV–VIS–DRS spectroscopy
The UV–VIS spectra of all samples were recorded by the Perkin Elmer Lambda 950 UV–Vis–NIR spectrophotometer fitted with Carry 100 software. The measurements were done with a wavelength ranging from 250 to 800 nm equipped with an IRS 240 integrating sphere attachment. The spectra were recorded against the BaSO4 reference. 

Photoluminescence properties (PL)
The room temperature PL was done by the Cary Eclipse fluorescence spectrophotometer equipped with a 150 W xenon lamp as the excitation source and a grating to select a suitable wavelength for excitation. The grating slits were set at 10 nm for the excitation and 10 nm for the emission, while photomultiplier voltage was maintained at 500 mV. Each sample was loaded into a circular holder and excited with 315 nm radiation from the pulsed xenon lamp. The emission spectra were scanned in the range of wavelengths from 380 nm to 700 nm.

FTIR spectroscopic studies
To determine the nature and types of groups and their bonding, FTIR spectroscopy was characterized in the potassium bromide (KBr) phase using a Thermo-Scientific Nicolet FTIR Spectrometer attached to an automatic data acquisition center.  Before measurement, KBr was dried at 80◦C overnight. Transparent Pellets were made using a pellet press from finely grounded 0.001g of sample mixed with 0.2 g of KBr. A pure KBr pellet was also prepared in the same method and used as a reference spectrum. The measurement of the transmittance spectra was in the range 4000 cm−1 to 400 cm−1.

Photocatalytic evaluation. 
This study was performed using the Shimadzu-1700 UV-vis spectrophotometer to acquire MB absorption spectra from 200 to 800 nm. The experiments of the adsorption and photocatalytic performance of TiO2 were performed using a 300 W xenon lamp for150 min, and the temperature of the solution was maintained at 25oC throughout the experiment. 0.3g of the nanopowders were added to the 250 mL of methylene blue solution (12 ppm). The solution was magnetically stirred to ensure homogeneity. Before the light irradiation, the reaction system was stirred for 30 min in darkness to ensure the adsorption-desorption equilibrium. The suspension was irradiated under the UV light as a function of the irradiation time under constant stirring. Samples were taken at an interval of 15 min and centrifuged under 4000rpm for 2 min before measurements. Irradiation of MB without the photocatalyst was carried as the control for the experiment.

RESULTS AND DISCUSSION
Structural analysis
Fig. 1. (a) shows the XRD patterns of TiO2 NPs samples prepared at various pH conditions. The peaks obtained at 2(theta) values 24.25o, 37.7o, 47.8o, 52.8o, 54.5o, 62.5o, 69.4o, 75.2o corresponds to (1 0 1), (0 0 4), (2 0 0), (1 0 5), (2 1 1), (2 0 4), (1 1 6), (2 2 0) crystal planes of the anatase TiO2 phase (JCPDS card no.86-1157). The crystal structure of TiO2 (anatase) is tetragonal with space group l41/amd with lattice parameters a = b = 3.7845 Å and c = 9.5143 Å. The prominent peak for all the prepared samples was observed at around 24.25o, corresponding to the (101) plane. 4 wt% amount of rutile phase was observed at pH 7, with a peak at 26.8o corresponding to (110) crystal planes (JCPDS # (86-0147). Rutile has a tetragonal structure with a space group of P42/mnm and lattice parameter of a = b = 4.59330 Å and c = 2.95920 Å. The anatase to rutile transformation at neutral pH might have occurred during the titanium precursor hydrolysis, such that deoxolation (O=Ti-OH2) HO-Ti-Ti-OH conversion) did not happen. In this case, Olation can cause linear growth in the equatorial direction of the dimer [Ti2O2(OH)4(OH2)4] o. This was followed by Oxolation between TiO (OH)2(OH)2 linear chains that lead to octahedral chains with corner-sharing, which is the characteristic of the rutile phase. The samples’ peaks were strong and sharp evident to the samples’ crystalline nature, while the intensities were found to vary non-uniformly according to Fig.1(b). The results in table 1, obtained by Scherrer equation and Williamson-Hall (W-H), suggested that the obtained crystallite size has an optimum pH value at neutral. In comparison, the average crystallite size values obtained by the Scherrer equation and W-H analysis showed considerable variation because the W-H plot considers the strain’s effect. The crystalline sizes recorded for W-H were between 25 and 98 nm and agreed with Scherrer’s equation, ranging between 16 and 40 nm crystallite size. The result from both methods indicated that the TiO2 crystal structure is more crystallized at pH 7. According to table 1, the crystal sizes obtained at pH 6 and 8 suggested that weak acids and bases suppress crystal growth [24]. The strain caused in powders because of crystal imperfection and distortion in table 1 shows that the samples were experiencing expansive (positive) strain, while others had a compressive (negative) strain.
The crystallographic defects or irregularities formed during crystal formation give rise to dislocations. The dislocation density (δ), tabulated in Table 1, is inversely proportional to the crystallite size of TiO2 calculated from Scherrer’s equation.  The dislocation density decreased toward the neutral pH, which indicated that weak acids and alkali improve the crystallinity nature of the TiO2 NPs. Lattice parameters  (tetragonal a=b, c) [25, 26] were found to increase slightly, as displayed in Table 1, with increased synthesis pH and are somewhat lower than the lattice parameters from the reference file.

Morphology and composition analysis
SEM/EDS analysis
The morphology, crystallinity, and elemental composition of the synthesized samples were shown in Fig. 2. As observed in Fig. 2 (a-c), the images have nearly spherical spongy-like shapes, agglomerated nanoparticles and seem to be porous. When the pH was varied, the average particle sizes were around 25 nm and were larger than the crystallite sizes determined by Scherrer’s equation, meaning that the particles observed in the SEM images are aggregated. There was no noticeable change in shape when the pH was increased.  The sample prepared at pH 10 has the smallest grains, as seen in Fig.2(c), and Fig. 2(b) had larger grains that seemed to be uniformly distributed with good dispersion compared to (a) and (c). According to numerous studies, the variety of TiO2 surface charges are pH-dependent. TiO2 in sols possess an electric charge because of the absorption of H+ or OH- in aqueous suspension  [18]. The surface charge of TiO2 can be determined by chemisorption of (iii) and (iv) : 
For H+
    for pH ˂ 3.5                    (iii)
For OH-

   for pH ˃ 3.5                      (iv)

The strong repulsive charge among particles in acidic and alkaline media reduces the likelihood of particle coalescence and allows for the formation of more stable sols. Growth of the grain sizes and morphology was probably controlled by the nucleation and growth methodology of TiO2 NPs, which is identified with the pH in the TiO2 integrated arrangement [27]. Studies by Su et al. [28] have indicated that the isoelectric of TiO2 powder varies between the pH range 5-7. Based on this range, on account that samples 2(a) and (c) synthesized at pH of 4 and 10 are far from the scope of isoelectric factor, much fewer aggregates and smaller TiO2 particles are formed. Our maximum particle size was at a pH of 7, which coincides with the isoelectric range of TiO2. It is found that the morphology markedly depends on the synthesis pH.
The EDS results in Fig. 2 (d), (e), and (f) show that the synthesized samples are TiO2 nanoparticles as confirmed by the presence of prominent peaks of Ti and O. These results confirm the XRD measurements on the absence of impurity element on the samples. The carbon traces observed are from carbon tape used during the characterization. The elements’ stoichiometric ratio was clearly understood by converting the weight to the compound’s atomic percent. However, when pH was increased, there was a slight change in the synthesized samples’ chemical composition ratios. This change determines the variations observed in the morphology. Although the samples are slightly Ti-rich and O-poor, they are near the expected stoichiometric ratio of 1:2 of TiO2 nanoparticles. This oxygen deficiency could lead to the defect-related blue emission in the PL analysis.

TEM/HRTEM analysis
The morphology, size, and structure of the prepared material were further illustrated using TEM, HRTEM, and SAED. The TEM images demonstrate that the synthesized samples are composed of nanosized, spherical-like particles confirming the SEM results. The image in Fig. 3(b) seems to have larger grain sizes than those in (a) and (c). The TEM images have an average particle size of ≈29 ± 5 nm. Further insight on the synthesized samples was gained by HRTEM measurements in Fig. 3(d) and (e). Fig. 3 (d) demonstrated a clear dispersion of the nanoparticles in the range of 24.5-31.0 nm. Besides, some agglomerations could be seen on the surface. 
Fig. 3(e) shows that the lattice fringes and the nanoparticle’s lattice planes can be assigned from a distance. It shows that the fringes have a distinct spacing of 0.35 nm corresponding to the crystalline (101) plane of the anatase phase, which has the highest intensity in the XRD plot [29].  Fig. 2 (f) shows the SAED patterns of anatase TiO2 at pH 7. It shows the apparent ring diffraction patterns with concentric circles of small spots indicating the material’s polycrystalline nature and revealed the diffraction spots for TiO2 anatase. The diffraction rings are indexed as (101), (004), and (200) planes confirming the formation of the tetragonal anatase phase, which is per the XRD results.

Optical and luminescence analysis
 UV-vis spectroscopy analysis
Fig. 4(a) shows the UV–vis diffuse reflectance (R) spectra of all the samples. The Kubelka Munk re-emission F(R) [30] in Eq. (7) is proportional to the absorption co-efficient after eliminating the scattering effect was used to estimate the bandgap of the samples.
                                                                                 (7) 

F(R) versus wavelength plot for the TiO2 nanoparticles was given in an inset of Fig. 4(a). It displayed a sharp absorption band around 400 nm, which was assigned to the optical bandgap due to electron transition from the valence to conduction band subtracting the exciton formation energy. A blueshift of the absorption edge is observed with an increase in pH values, indicating an increase in bandgap. The sample at pH 7 displayed the highest reflectance over the alternative samples due to its large crystal size and the induced oxygen vacancy (defect sites) [29]. A linear fit graph of (F(R) hv)2 vs hv was plot to obtain the bandgap of the synthesized NPs, as shown in Fig.4(b). Where hv is the photon energy for each sample. The energy bandgap, Eg, was determined by extrapolating the linear section of the curve to the x-axis. At the x-intercept,  [31]. It was evident from the plot an inset of Fig.4(b) that the bandgap values of the TiO2 nanoparticles increased with an increase in pH. The rise in bandgap might be due to a decrease in crystallite size that determines the quantum size effect, which causes the blue shift of the absorption edge in the diffuse reflectance [32, 33].  The bandgaps (range from 2.76 - 3.10 eV) are significantly less than the intrinsic bandgap of the bulk TiO2 as given in the introduction (3.20 eV - anatase), signifying that the possible defect effects and exciton formation, play an essential role in the absorption.

Photoluminescence (PL) analysis
Photoluminescence (PL) emission spectra have been widely used to investigate the efficiency of charge carrier trapping, migration and to understand the state of electron-hole pairs in semiconductors. All Samples excited at a wavelength of 315 nm were shown in Fig:5 (a). Fig. 5(b) shows the PL intensities plot against the synthesis pH for the TiO2 nanoparticles. The sample at neutral pH had the lowest PL intensity, ascribed to a high rate of non-radiative recombination and reduced number free charge carriers that can take part in pollutant degradation, hence decreasing the photocatalytic activity. All samples showed a broad emission band, which was deconvoluted using a Gaussian fit in Fig. 5c. From the deconvolution, four emission peaks were observed. The first emission peak located at 420 nm was attributed to a Self-trapped exciton localized on TiO6 octahedra, which can be created by the direct recombination of a trapped electron in the lattice site with a hole or by the indirect recombination assisted by an oxygen vacancy [34]. The emission Peaks 450 and 466 nm were attributed to shallow traps close to the conduction band edge, while the emission peak at 514 nm was ascribed to the deep trap state. The primary defects in TiO2 are oxygen vacancies, which lead to the creation of Ti3+ centers. The electrons located on the oxygen vacancy state affect the electronic structure of TiO2 by forming the donor level below the conduction band as shown in Fig:5(d) [34]. The defects are mainly located on the nanostructures’ surface and could form a series of energy levels within the bandgap of TiO2 by trapping electrons from the valence band. 

FTIR analysis
FTIR technique allows the identification of the functional groups and chemicals present in the synthesized samples. Fig. 6 shows the FTIR spectra of the TiO2 Synthesized by the sol-gel method, obtained in the range of 4000-400 cm-1. The broad absorption band centered 3420 cm−1 was assigned to hydroxyl groups’ intermolecular interaction for water molecules with TiO2 surface [35]. The peak observed at 1618 cm−1 was characteristic of -OH of water’s bending vibration mode associated with surface adsorbed water [36]. The band noticed at 1387 cm−1 was assigned to the  -CH2, C-H, and -CH3 stretching vibrations [37, 38]. Broadband with shoulder centered at 849 cm−1 was assigned to the presence O-Ti-O stretching band, which is the characteristic peak of TiO2 [39]. The sharpening of the metal oxide’s distinct peaks shows that the crystalline nature of TiO2 increases with an increase in pH.

Photocatalysis
The samples’ photocatalytic activity was investigated by the degradation of methylene blue (MB) dye under artificial UV light irradiation. Photocatalytic degradation is a complex process that involves at least interactive nanoparticles/semiconductors, water, and light [40]. The proposed photocatalytic process occurs when TiO2 NPs are irradiated with electromagnetic radiation with energy equal to or greater than its bandgap. The absorption measurements were carried out to determine the degradation with respect to time. The absorption spectra’ peak area is a direct measurement of the molecule concentration. Thus, its decrease with UV-irradiation time is a measure of the photocatalytic decomposition of the molecules. The degradation efficiency (%D) was obtained in relation to Beer-Lambert law according to Fig.7(a), which states that the concentration is directly proportional to the absorbance using Eq: (7) as follows; 

                                                    (8)

is the absorbance at time t = 0, and the is the absorbance at time (min) [41]. The MB photo-discoloration ratio was also calculated based on (Eq: 9) Langmuir-Hinshelwood model [42].  The model is established so that the only molecules degraded are those adsorbed by the catalyst, MB spinoffs are not measured, and the adsorbed molecules control the reaction rate. 
Langmuir-Hinshelwood model can be stated as follows:

                                                          (9)

where r is the rate of degradation, C is the target pollutant concentration, t is the time (min), k is the rate constant of photodegradation reaction, and K is the absorption coefficient. When C is low, which is always the case for dyes (KC ˂˂1), the reaction rate can be simplified to a pseudo-first-order kinetic model (Eq:10) with respect to the target dye concentration. K is estimated as the slope of the linear regression    Versus t.

                                                                                                                (10)
A high photocatalytic degradation rate corresponds to high photocatalytic activity. It shows that the degradation of MB strongly depends on the synthesis pH of TiO2. The synthesis solution’s initial pH determines the charge on the surface of TiO2, and the adsorption of the pollutant on the catalyst surface is affected by these charges. Fig. 7 (a) shows MB’s degradation efficiency for various pH values with respect to time. It was observed that %D was 60%, 39%,38%, 82%, and 71% for pH 4, 6, 7, 8 and 10 respectively. The degradation efficiency elevated with increasing initial pH in the range 4–8. Fig. 7 (b) displays a similar relationship as 7 (a). The data shows a good linear correlation, and the slopes calculated from the linear regression fit provided us with the value of the photocatalytic degradation reaction constants for each sample. It can be seen that the k constant improved from 0.026 min-1 at pH 4 to 0.048 min-1 at pH 8. The high k constant acquired at high pH 8 might be because the high pH favors OH’s formation through oxidation of OH- by photo holes [43]. 

CONCLUSION
The TiO2 NPs were prepared with varied synthesis pH by the sol-gel method. XRD confirmed that pH has a significant impact on the crystallinity and crystal size of TiO2. The morphology of the different samples was not affected by pH, apart from the particle size. UV spectra showed that the bandgap of the synthesized TiO2 NPs increased with an increase in pH value. It was observed that large crystal size leads to small surface area and therefore gives lower PL intensities. pH 8 was observed to have the highest degradation of 82% and decolorization rate of 0.0048/min after 120 min irradiation time. Therefore, longer electron-hole pair life would make the charge carriers contribute to the anatase phase’s surface reaction. A lower electron-hole recombination rate is more desirable because increasing surface area adsorption of the reactants over the photocatalyst would increase the light absorption.

ACKNOWLEDGEMENTS 
The authors wish to thank Dr. Bridget Mutuma for continued advice received during the work.

CONFLICT OF INTEREST
The authors declare that there are no conflicts of interest regarding the publication of this manuscript.