Ultrasensitive Electrochemical Detection of Butylated Hydroxy Anisole via Metalloporphyrin Covalent Organic Frameworks Possessing Variable Catalytic Active Sites

Three novel two-dimensional metalloporphyrin COFs (MPor−COF−366, M = Fe, Mn, Cu) were fabricated by changing the metal atoms in the center of the porphyrin framework. The physicochemical characteristics of MPor−COF−366 (M = Fe, Mn, Cu) composites were fully analyzed by diverse electron microscopy and spectroscopy. Under optimal conditions, experiments on determining butylated hydroxy anisole (BHA) at FePor−COF−366/GCE were conducted using differential pulse voltammetry (DPV). It is noted that the FePor−COF−366/GCE sensor showed excellent electrocatalytic performance in the electrochemical detection of BHA, compared with MnPor−COF−366/GCE and CuPor−COF−366/GCE. A linear relationship was obtained for 0.04–1000 μM concentration of BHA, with a low detection limit of 0.015 μM. Additionally, the designed sensor was successfully employed to detect BHA in practical samples, expanding the development of COF-based composites in electrochemical applications.


Introduction
As a synthetic phenolic antioxidant, butylated hydroxy anisole (BHA) is frequently employed in food packaging, biofuels, and pharmaceutical formulations [1]. It has the effect of preventing or delaying the oxidative deterioration of food, thereby improving food stability and prolonging the shelf life of food [2,3]. If the content of BHA exceeds the specified level, it can cause serious health problems in humans, including nutrient loss and even toxic effects [4,5]. Hence, the negative impacts of BHA on human health restrict its application in food goods, and a quick, sensitive, and accurate method to quantify BHA is required.
Several techniques have been developed for determining BHA, including micellar electrokinetic capillary chromatography, gas chromatography, high-performance liquid chromatography, and spectrophotometry [6][7][8][9][10]. However, these methods often encounter difficulties associated with cumbersome or time-consuming procedures. Electrochemical technology has been utilized for the quantitative analysis of BHA owing to its advantages of simple operation, high sensitivity, and rapid response [11][12][13][14]. However, developing advanced materials to achieve high electrochemical performance remains a major research goal.
Covalent organic frameworks (COFs) are formed by powerful covalent links between light elements with a reticular network of molecular building blocks, and exhibit an exceptionally high surface area and high stability, displaying a wide range of applications [15][16][17][18]. Porphyrins are widely used as building blocks for the assembly of covalent organic frameworks because of their high stability, easy chelation with metal ions, and ease of modification [19]. Several porphyrin-based COFs (Por-COFs) have been constructed for use in electro chemiluminescence, heterogeneous catalysis, and photooxidization reactivity [20][21][22].
In addition, metalloporphyrin COFs (MPor-COFs) possess a unique N-C framework, which offers a novel platform for the preparation of self-supporting M-N-C sites with intrinsic metal coordination for use as porous electrocatalysts [23]. However, to our knowledge, the usage of MPor-COFs as electrode materials to improve electrochemical performance has rarely been investigated.
Por−COF−366 (20.0 mg) and FeSO 4 ·7H 2 O (25 mg, 0.1 mM) were dissolved in a mixture of 12 mL dichloromethane and methanol. The mixture was stirred continuously for 24 h. After centrifugation, the composites were washed with CH 2 Cl 2 and were dried under vacuum at 60 • C for 12 h to obtain the product FePor−COF−366. After replacing the metal salts with MnCl 2 ·6H 2 O and CuCl 2 ·6H 2 O, MnPor−COF−366 and CuPor−COF−366 were obtained by the same synthesis process.

Preparation of Samples
Rapeseed, corn, and peanut oils were bought at a nearby grocery. Then, 1.0 g of the material was dissolved in 10 mL of ethanol. The product was centrifuged after being oscillated for 10 min. The supernatant was collected, and filtered through a Millipore nylon filter with a 0.22 µm pore size. A 1.0 mL aliquot of the final product was put into 9.0 mL of pH 4.0 PBS for further analysis.

Characterizations
The morphology of the composites was examined using transmission electron microscopy (TEM, Tecnai 12, 120 KV, Amsterdam, Netherlands) and scanning electron microscopy (SEM, S-4800II, Tokyo, Japan). A Cary 610/670 infrared microspectrometer (Varian, Palo Alto, Santa Clara, CA, USA) was employed to obtain the FTIR spectra. Utilizing a D8 Advance X-ray diffractometer (Bruker Co., Karlsruhe, Germany), the X-ray diffraction (XRD) patterns were gathered from 1.5 • to 80 • at ambient temperature. XPS testing was carried out using an ESCALAB 250Xi XPS spectrometer from Thermo Scientific, Massachusetts, USA with an aluminum Kα X-ray source.

Electrochemical Analysis
A CHI852C electrochemical analyzer (Shanghai Chenhua Co., Shanghai, China) was applied for all electrochemical tests. A standard three-electrode system was employed to perform cyclic voltammetry (CV) and differential pulse voltammetry (DPV).

Characterizations of Synthesized Composites
The morphologies of Por−COF−366 and MPor−COF−366 composites were characterized using SEM and TEM measurements. In Figure 1A, it is shown that Por−COF−366 is a generally spherical nanomaterial with a size of 180 nm on average. After coordination with metal ions, the surfaces of MPor−COF−366 composites became rough, but the morphology did not change significantly. Rapeseed, corn, and peanut oils were bought at a nearby grocery. Then, 1.0 g of the material was dissolved in 10 mL of ethanol. The product was centrifuged after being oscillated for 10 min. The supernatant was collected, and filtered through a Millipore nylon filter with a 0.22 μm pore size. A 1.0 mL aliquot of the final product was put into 9.0 mL of pH 4.0 PBS for further analysis.

Characterizations
The morphology of the composites was examined using transmission electron microscopy (TEM, Tecnai 12, 120 KV, Amsterdam, Netherlands) and scanning electron microscopy (SEM, S-4800II, Tokyo, Japan). A Cary 610/670 infrared microspectrometer (Varian, Palo Alto, USA) was employed to obtain the FTIR spectra. Utilizing a D8 Advance Xray diffractometer (Bruker Co., Karlsruhe, Germany), the X-ray diffraction (XRD) patterns were gathered from 1.5° to 80° at ambient temperature. XPS testing was carried out using an ESCALAB 250Xi XPS spectrometer from Thermo Scientific, Massachusetts, USA with an aluminum Kα X-ray source

Electrochemical Analysis
A CHI852C electrochemical analyzer (Shanghai Chenhua Co., Shanghai, China) was applied for all electrochemical tests. A standard three-electrode system was employed to perform cyclic voltammetry (CV) and differential pulse voltammetry (DPV).

Characterizations of Synthesized Composites
The morphologies of Por−COF−366 and MPor−COF−366 composites were characterized using SEM and TEM measurements. In Figure 1A, it is shown that Por−COF−366 is a generally spherical nanomaterial with a size of 180 nm on average. After coordination with metal ions, the surfaces of MPor−COF−366 composites became rough, but the morphology did not change significantly. To further confirm the structure and crystallinity of the produced Por−COF−366 and MPor−COF−366, spectral PXRD analysis was performed. As displayed in Figure 2A, the obvious characteristic diffraction peak at 2θ = 3.5° was attributed to the (100) plane. Other To further confirm the structure and crystallinity of the produced Por−COF−366 and MPor−COF−366, spectral PXRD analysis was performed. As displayed in Figure 2A, the obvious characteristic diffraction peak at 2θ = 3.5 • was attributed to the (100) plane. Other weaker peaks appeared at 2θ = 6.1 • and 7.9 • , corresponding to the (110) and (200) planes, respectively, which were consistent with the reported data [25]. In addition, Por−COF−366 and MPor−COF−366 composites exhibited sharp pyrrole ring vibration at 797 cm −1 , and the characteristic stretching vibrations of C=N at 1623 cm −1 were seen in FTIR spectrum  Figure 2B). There were also absorbance peaks at 1691 cm −1 and 3325 cm −1 , which were attributed, respectively, to the residual C=O and stretching N-H vibration of residual -NH 2 groups [26]. weaker peaks appeared at 2θ = 6.1° and 7.9°, corresponding to the (110) and (200) planes, respectively, which were consistent with the reported data [25]. In addition, Por−COF−366 and MPor−COF−366 composites exhibited sharp pyrrole ring vibration at 797 cm −1 , and the characteristic stretching vibrations of C=N at 1623 cm −1 were seen in FTIR spectrum ( Figure 2B). There were also absorbance peaks at 1691 cm −1 and 3325 cm −1 , which were attributed, respectively, to the residual C=O and stretching N-H vibration of residual -NH2 groups [26]. Furthermore, Figure 3 shows the XPS measurements to evaluate the chemical state of the as-synthesized Por−COF−366 and MPor−COF−366 composites. The survey spectrum is shown in Figure 3A, revealing that the composites were composed of Fe, Mn, Cu, N, O, and C species. Figure 3B shows the spectrum of Fe 2p. The FePor−COF−366 was successfully synthesized, as evidenced by the four main peaks at 711.4, 715.9, 724.5, and 728.5 eV, which were consistent with the Fe 2+ 2p3/2, Fe 3+ 2p3/2, Fe 2+ 2p1/2, and Fe 3+ 2p1/2, respectively [27,28]. Additionally, Mn 2p in the XPS spectra shown in Figure 3C contained peaks at around 642.3 and 654.6 eV that were attributed to Mn 2p2/3 and Mn 2p1/2, respectively. Manganese ions were found to exist as Mn 4+ with spin-orbital splitting of 12.3 eV [29]. Another peak at 646.7 eV was assigned to Mn 3+ , indicating that the process may have created Mn in a lower oxidation state [30]. Additionally, as depicted in Figure 3D, the typical peaks at 954.2 and 934.4 eV corresponded to Cu 2p1/2 and Cu 2p3/2, respectively [31]. Typical peaks of the Cu(II) state were observed as two satellite peaks at about 963.12 and 943.46 eV [32]. These findings agreed with those of the XRD and FTIR analyses. Furthermore, Figure 3 shows the XPS measurements to evaluate the chemical state of the as-synthesized Por−COF−366 and MPor−COF−366 composites. The survey spectrum is shown in Figure 3A, revealing that the composites were composed of Fe, Mn, Cu, N, O, and C species. Figure 3B shows the spectrum of Fe 2p. The FePor−COF−366 was successfully synthesized, as evidenced by the four main peaks at 711.4, 715.9, 724.5, and 728.5 eV, which were consistent with the Fe 2+ 2p 3/2 , Fe 3+ 2p 3/2 , Fe 2+ 2p 1/2 , and Fe 3+ 2p 1/2 , respectively [27,28]. Additionally, Mn 2p in the XPS spectra shown in Figure 3C contained peaks at around 642.3 and 654.6 eV that were attributed to Mn 2p 2/3 and Mn 2p 1/2 , respectively. Manganese ions were found to exist as Mn 4+ with spin-orbital splitting of 12.3 eV [29]. Another peak at 646.7 eV was assigned to Mn 3+ , indicating that the process may have created Mn in a lower oxidation state [30]. Additionally, as depicted in Figure 3D, the typical peaks at 954.2 and 934.4 eV corresponded to Cu 2p 1/2 and Cu 2p 3/2 , respectively [31]. Typical peaks of the Cu(II) state were observed as two satellite peaks at about 963.12 and 943.46 eV [32]. These findings agreed with those of the XRD and FTIR analyses.

Electrochemical Properties
The changes between the electrode interface and the solution were investigated using electrochemical impedance spectroscopy (EIS) in 5.0 mM [Fe(CN) 6 ] 3−/4− electrolyte [33]. The characteristic EIS plots of the different electrodes are shown, and an equivalent circuit (Randles model) is provided in the inset of Figure 4A. The Randles equivalent electrical circuit model consists of the electrode surface resistance (Rs), the element of interfacial electron transfer resistance (Rct), Warburg impedance (Zw), and the constant phase angle element (CPE). In the Nyquist impedance plot, a straight line at low frequencies was associated with a diffusion-limited process, and a small semicircle at high frequencies was associated with an electron-transfer-limited process. The semicircle is equal to the value of Rct, and the GCE revealed the largest Rct value (166.5 Ω).

Electrochemical Properties
The changes between the electrode interface and the solution were investigated using electrochemical impedance spectroscopy (EIS) in 5.0 mM [Fe(CN)6] 3−/4− electrolyte [33]. The characteristic EIS plots of the different electrodes are shown, and an equivalent circuit (Randles model) is provided in the inset of Figure 4A. The Randles equivalent electrical circuit model consists of the electrode surface resistance (Rs), the element of interfacial electron transfer resistance (Rct), Warburg impedance (Zw), and the constant phase angle element (CPE). In the Nyquist impedance plot, a straight line at low frequencies was associated with a diffusion-limited process, and a small semicircle at high frequencies was associated with an electron-transfer-limited process. The semicircle is equal to the value of Rct, and the GCE revealed the largest Rct value (166.   The electrochemical behaviours of GCE, Por−COF−366/GCE, and MPor−COF−366/GCE were investigated through CV. As exhibited in Figure 4B, the redox peaks in the modified electrodes were well-defined and the electrochemical activity was significantly improved compared with the weak redox peaks on GCE. The anodic peaks located at 0.106 and 0.247 V belonged to butylated hydroquinone and BHA, respectively. The cathodic peak at 0.014 was assigned to tert-butylquinone (TBQ). Compared with Cu-Por−COF−366/GCE and MnPor−COF−366/GCE, a narrowed redox peak potential separation (ΔEp) and enhanced peak current value were observed after modification with  The electrochemical behaviours of GCE, Por−COF−366/GCE, and MPor−COF−366/ GCE were investigated through CV. As exhibited in Figure 4B, the redox peaks in the modified electrodes were well-defined and the electrochemical activity was significantly improved compared with the weak redox peaks on GCE. The anodic peaks located at 0.106 and 0.247 V belonged to butylated hydroquinone and BHA, respectively. The cathodic peak at 0.014 was assigned to tert-butylquinone (TBQ). Compared with CuPor−COF−366/GCE and MnPor−COF−366/GCE, a narrowed redox peak potential separation (∆E p ) and enhanced peak current value were observed after modification with FePor−COF−366/GCE. The ∆E p value in a cyclic voltammogram is one of the important factors for estimating the electron charge-transfer rate at the electrode-electrolyte interface. Generally, the ∆E p value is inversely proportional to the charge-transfer rate constant. Here, the . This phenomenon may be due to the fact that atomically dispersed Fe in the porphyrin macrocycle was coordinated as the catalytically active centre, which was fully exposed to the interaction with BHA, providing a greater specific surface area, increasing the quantity of open active sites, and improving the speed of electron transfer in the composite. Figure 5A depicts the results of investigation into the effect of pH values on the DPV response of BHA, for FePor−COF−366/GCE over a potential range of 0.1 to 0.8 V at various pH ranges from 2.0 to 6.0. With the increase of solution pH, the oxidation peak current of BHA showed first an increasing trend and then a decrease. The maximum current of BHA was reached at pH 4.0. At pH values between 4.0 and 6.0, a decrease was observed in the oxidation peak current value. Hence, PBS with pH value of 4.0 was selected for the analysis that followed. Furthermore, as the electrolyte pH increased, the anodic peak potential (E pa ) of BHA oxidation exhibited markedly negative movement, showing that protons were implicated in the electro-oxidation of BHA. The linear formula for the relationship between pH and the oxidation peak potential of BHA is: E pa (V) = −0.0572 pH + 0.6832 (R 2 = 0.9949). The peak potential and pH are related by: Substituting the equivalency of the slope values of the E p versus pH plot resulted in an m/n ratio of 1, showing that the process involved an equal number of protons and electrons [34].

Optimization of the Experimental Parameters
CV experiments at various scan speeds were carried out to investigate the electrochemical redox reaction kinetics of BHA on FePor−COF−366/GCE surfaces. Figure 5B indicates how the peak current grew progressively as the scan rate increased between 25 and 350 mV s −1 . The anodic and cathodic peak currents and the square root of the scan rates were linearly related, and followed the equations: I pa (µA) = −0.3314 + 0.3415 ν 1/2 , (R 2 = 0.9986); I pc (µA) = −0.1525 − 0.0737 ν 1/2 , (R 2 = 0.9834) (Inset a in Figure 5B). Diffusion was therefore primarily in charge of controlling the redox reaction process. The reduction peak potential (E pc ) shifted in a more negative direction as the scan rate increased, while the oxidation peak potential (E pa ) steadily moved in a more positive direction. The peak potentials and lnν can be represented by the linear equations: E pa (V) = 0.4346 + 0.0163 lnν, (R 2 = 0.9967); E pc (V) = 0.0812 − 0.0216 lnν, (R 2 = 0.9833) (Inset b in Figure 5B). The Laviron equation states: The linear slopes of E pa and E pc relative to lnν are RT/αnF and RT/((1 − α)nF), respectively. n can be calculated as 2.1. Because the oxidation of BHA is a two-electron transfer process, two electrons and two protons are included in the redox reaction [35]. The reaction mechanism is shown in Figure 6.
containing 50 μM BHA at different scan rates, the insets are (a) the linear relationship between currents and sweep-speed square root, and (b) the linear relationship between redox peak potentials (Ep) and lnν.
Substituting the equivalency of the slope values of the Ep versus pH plot resulted in an m/n ratio of 1, showing that the process involved an equal number of protons and electrons [34].
CV experiments at various scan speeds were carried out to investigate the electrochemical redox reaction kinetics of BHA on FePor−COF−366/GCE surfaces. Figure 5B indicates how the peak current grew progressively as the scan rate increased between 25 and 350 mV s −1 . The anodic and cathodic peak currents and the square root of the scan rates were linearly related, and followed the equations: Ipa (μA) = −0.3314 + 0.3415 1/2 , (R 2 = 0.9986); Ipc (μA) = −0.1525 − 0.0737 1/2 , (R 2 = 0.9834) (Inset a in Figure 5B). Diffusion was therefore primarily in charge of controlling the redox reaction process. The reduction peak potential (Epc) shifted in a more negative direction as the scan rate increased, while the oxidation peak potential (Epa) steadily moved in a more positive direction. The peak potentials and ln can be represented by the linear equations: Epa (V) = 0.4346 + 0.0163 ln , (R 2 = 0.9967); Epc (V) = 0.0812 − 0.0216 ln , (R 2 = 0.9833) (Inset b in Figure 5B). The Laviron equation states: The linear slopes of Epa and Epc relative to lnν are RT/αnF and RT/((1 − α)nF), respectively. n can be calculated as 2.1. Because the oxidation of BHA is a two-electron transfer process, two electrons and two protons are included in the redox reaction [35]. The reaction mechanism is shown in Figure 6.  Furthermore, the accumulation step can be considered an effective method for improving the assay sensitivity. As shown in Figure 7A, the influence of accumulated potential on the peak current of BHA was tested from −0.3 to 0.2 V. The peak current reached its maximum value at −0.1 V, indicating that −0.1 V was favourable for the detection of BHA. As indicated in Figure 7B, considering the accumulation time, the peak current rose and reached its highest value at 60 s. As the amount of time increased, saturation of the BHA molecules occurred on the modified electrode. Therefore, 60 s was selected for subsequent studies.
Biosensors 2022, 12, 975 8 Furthermore, the accumulation step can be considered an effective method for proving the assay sensitivity. As shown in Figure 7A, the influence of accumulated po tial on the peak current of BHA was tested from −0.3 to 0.2 V. The peak current reac its maximum value at −0.1 V, indicating that −0.1 V was favourable for the detectio BHA. As indicated in Figure 7B, considering the accumulation time, the peak current and reached its highest value at 60 s. As the amount of time increased, saturation of BHA molecules occurred on the modified electrode. Therefore, 60 s was selected for sequent studies.

Analytical Performance
DPV was applied under optimal conditions to study the relationship between p current and BHA concentration ( Figure 8A). According to the linear regressions i trated in Figure 8B, the peak currents of BHA were proportional to its concentrations tween 0.04-100 and 100-1000 μM, with the linear regressions: Ipa (µ A) = 0.3415 C − 0. (C: 0.04-100 μM, R 2 = 0.998) and Ipa (µ A) = 0.1525 C − 0.0737 (C: 100-1000 μM, R 2 = 0.9 The two linear regions in Figure 8B can be explained as follows: when the concentra

Analytical Performance
DPV was applied under optimal conditions to study the relationship between peak current and BHA concentration ( Figure 8A). According to the linear regressions illustrated in Figure 8B, the peak currents of BHA were proportional to its concentrations between 0.04-100 and 100-1000 µM, with the linear regressions: I pa (µA) = 0.3415 C − 0.3314 (C: 0.04-100 µM, R 2 = 0.998) and I pa (µA) = 0.1525 C − 0.0737 (C: 100-1000 µM, R 2 = 0.997). The two linear regions in Figure 8B can be explained as follows: when the concentration of BHA was low, BHA was deposited on the electrode surface; at this time, the electrochemical oxidation process was mainly controlled by the adsorption process, and BHA molecules on the electrode surface were rapidly transformed. With the increase of BHA concentration, more BHA molecules were deposited on the surface of the modified electrode, and the mass transfer resistance increased, leading to the decrease of sensitivity. The detection limit was calculated as 0.015 µM, using a signal-to-noise ratio of 3 (S/N).

Analytical Performance
DPV was applied under optimal conditions to study the relationship between peak current and BHA concentration ( Figure 8A). According to the linear regressions illustrated in Figure 8B, the peak currents of BHA were proportional to its concentrations between 0.04-100 and 100-1000 μM, with the linear regressions: Ipa (µ A) = 0.3415 C − 0.3314 (C: 0.04-100 μM, R 2 = 0.998) and Ipa (µ A) = 0.1525 C − 0.0737 (C: 100-1000 μM, R 2 = 0.997). The two linear regions in Figure 8B can be explained as follows: when the concentration of BHA was low, BHA was deposited on the electrode surface; at this time, the electrochemical oxidation process was mainly controlled by the adsorption process, and BHA molecules on the electrode surface were rapidly transformed. With the increase of BHA concentration, more BHA molecules were deposited on the surface of the modified electrode, and the mass transfer resistance increased, leading to the decrease of sensitivity. The detection limit was calculated as 0.015 μM, using a signal-to-noise ratio of 3 (S/N). According to the data in Table 1, comparing the performance of FePor−COF−366/GCE with other BHA sensors, FePor−COF−366/GCE had the lowest detection limit and the widest linear region. Several factors could account for its high analytical performance: (1) The metal porphyrins exist in a monomolecular state through the connection of metal ions, so that the metal ions are separated from each other and avoid aggregation, thereby increasing the catalytic active site and improving the catalytic activity; (2) the rigid and conjugated structure of Por-COFs at the molecular level endows them with inherent porous properties, enabling them to adsorb more BHA molecules; (3) Por-COFs have abundant π electron conjugated macrocycles, which can enhance affinity for BHA by π-π stacking and hydrogen bonding.

Interference, Stability, and BHA Detection
A number of potential coexisting substances were evaluated by DPV in 50 µM BHA, to examine the selectivity of the sensor. These experiments showed that many inorganic ions, including Zn 2+ , Mn 2+ , Mg 2+ , Cl − , and SO 4 2− , did not obstruct the measurement of BHA. Furthermore, the BHA measurement was unaffected by ascorbic acid, glucose, and L-cysteine concentrations that were 20-fold greater. Butylated hydroxytoluene (BHT) is another phenolic antioxidant which shares the same hydroxyl group as BHA and can be oxidized close to the potential of BHA. It was found that BHT had no impact on the detection of BHA, even at a 20-fold concentration. Together, these findings demonstrate the great selectivity of the electrochemical sensor for BHA detection. Storage stability was assessed by storing a batch of freshly manufactured electrodes in a refrigerator at 4 • C and taking measurements every three days. After a lengthy storage period of 21 days, it was discovered that approximately 91.2% of the initial value was maintained. The outcomes amply demonstrated the sensor's ideal stability. Moreover, there was no evident decrease of current response observed after 35 cycles, and 95% of its original value was maintained. Three parallel measurements were taken for each sample, using the standard addition method, to assess the usefulness of the constructed electrochemical sensor. Table 2 showed that the recoveries ranged from 98.4 to 102.2%, and the RSD values ranged from 1.5% to 3.4%, indicating that the electrochemical sensor was capable of detecting the presence of BHA in actual samples.

Conclusions
In conclusion, the pre-designed Por-COFs were successfully used as metallization modification matrixes, and the metal atoms were regulated in the form of coordinated metal-N4 as special functional modulators. The resulting FePor-COFs demonstrated distinctly higher electrocatalytic response for BHA in terms of wide linear range, low detection limit, high sensitivity, superior selectivity, and good reproducibility. This study not only describes an attractive and efficient catalyst electrode for BHA determination, but also opens a new avenue for the design and development of two-dimensional porphyrin COFs as sensors for electrochemical detection of small molecules.
Author Contributions: Conceptualization, methodology, data curation and writing-original draft, H.C.; methodology, data curation, X.S.; methodology, data curation, X.Z.; writing-review and editing, S.U.K.; funding acquisition, Y.W. All authors have read and agreed to the published version of the manuscript.