Biochar-Supported BiOx for Effective Electrosynthesis of Formic Acid from Carbon Dioxide Reduction

The electrochemical reduction of carbon dioxide (CO2) to value-added chemicals and fuels has attracted worldwide interest for its potential to address various contemporary global issues such as CO2-related climate change, the earth’s carbon deficit and the energy crisis. In the development of this technology, many efforts have been focused on the design of inexpensive, eco-friendly and effective catalysts. In this work, a bismuth (Bi)-based material was simply synthesized via a scalable method and fully characterized by physical, chemical and electrochemical techniques. The catalyst material consisted of Bi/Bi2O3 nanoparticles and a biochar prevenient from the pyrolysis of brewed coffee waste. It was observed that the surface of the biochar was thoroughly decorated with nanoparticles. Due to its uniform surface, the biochar–BiOx electrode demonstrated good selectivity for CO2 reduction, showing a faradaic efficiency of more than 90% for CO and HCOOH formation in a wide potential range. Particularly, the selectivity for HCOOH reached more than 80% from −0.9 V to −1.3 V vs the reversible hydrogen electrode and peaks at 87%. Besides the selectivity, the production rate of HCOOH also achieved significant values with a maximum of 59.6 mg cm−2 h−1, implying a good application potential for biochar–BiOx material in the conversion of CO2 to HCOOH.


Introduction
Carbon dioxide (CO 2 ) is a well-known greenhouse gas, and its accumulation in the atmosphere can trap infrared radiation, thereby disturbing the energy balance on the earth's surface. In the last decade, CO 2 emissions and atmospheric CO 2 concentrations have become the most important topics in politics and scientific debate because unprecedented wildfires and superstorms have made global warming impossible to ignore. Using CO 2 as feedstock to produce value-added chemicals and fuels is considered to be a promising approach for reducing atmospheric CO 2 and consequently mitigating climate change. Many technologies have been exploited for CO 2 valorization, including thermocatalysis, photocatalysis, electrocatalysis and bio-synthesis [1][2][3]. Among these methods, the electrochemical conversion of CO 2 is closest to commercialization with start-ups and well-established companies such as Carbon Recycling International, Mitsui Chemicals, Dioxide Materials, Carbon Electrocatalytic Recycling Toronto and Opus-12 [4]. Electrochemical conversion presents several advantages: (1) possible use of green electrolytes and electricity without contributing to new CO 2 emissions [5]; (2) Tunable products and production rates by using different catalysts and test conditions [6]; and (3) development Bismuth(III) nitrate pentahydrate (Bi(NO 3 ) 3 ·5H 2 O, 99%), Potassium bicarbonate (KHCO 3 , 99.7%), Nafion ® 117 solution (5 wt.%) and isopropanol were purchased from Sigma-Aldrich (Merck). All chemicals were used as received.

Synthesis
The coffee waste was collected from Bar Katia (Turin, Italy) supplied by Vergnano. First, the coffee waste was dried at 105 • C for 72 h to eliminate any moisture. Then, 100 g of the dried waste was pyrolyzed using a tubular furnace (Carbolite TZF 12/65/550) under a nitrogen flow (40 mL min −1 ). The heating rate was 15 • min −1 until a temperature of 800 • C was reached. The sample was kept at 800 • C for 30 min and cooled down to room temperature. The obtained biochar was collected.
The Bi(NO 3 ) 3 ·5H 2 O was used as precursor salt and used biochar as support. In a typical synthesis procedure, 3.5 g of Bi(NO 3  solution became clear. Then 1.0 g of pyrolyzed biochar was added slowly and continuously into the solution with constant stirring for more than 30 min. To achieve homogeneity in the composite solution, the mixture was sonicated for 20 min (amplitude 40%, Sonic Vibracel sonicator). The composite mixture was then heated in a furnace at 150 • C for 2 h to completely evaporate the water content. The obtained solid composite material was then calcinated at 400 • C in a N 2 atmosphere for 2 h. After calcination, the sample was allowed to cool naturally inside the furnace. The final free flowing catalyst was then ready for the fabrication of the electrodes.

Physical and Chemical Characterizations
The morphology and elemental composition of the composite powder was investigated by field-emission scanning electron microscopy (FE-SEM, ZEISS-MERLIN) equipped with high-resolution energy-dispersive (ENERGY 450) X-ray spectroscopy (EDS, OXFORD INCA). For FESEM-EDS analysis, the composite sample was coated with a 5 nm thin layer of platinum to avoid the charging effect.
The crystalline phases of the catalysts were examined by X-ray diffraction (XRD). Measurements were performed using a PANalytical X'Pert Pro instrument (Cu-Kα radiation, 40 kV and 30 mA) equipped with an X'Celerator detector.
Operando TGA-IR was made on a Thermogravimetric Analyzer (TGA) NETZSCH TG209 F1Libra instrument coupling line to a Fourier transform infrared (FTIR) Bruker Tensor II spectrophotometer equipped with DTGS detector and a Bruker heated gas chamber analysis accessory. Approximately 3 mg of sample in alumina pans were heated from 30 to 900 • C, using a heating ramp of 20 • C min −1 , under air (flow rate = 20 mL min −1 ). Nitrogen flow was used as protection gas (flow rate = 20 mL min −1 ). The FTIR analysis was collected in the absorbance mode in the 650-4400 cm −1 range. The gas development kinetics were followed at the adsorption maximum for different molecules: CO, 2179 cm −1 [38]; CO 2, 2349 cm −1 [39]; and H 2 O, 3735 cm −1 [40].

Preparation of the Electrodes
Electrodes were made by preparing a slurry containing 3.45 mg of the synthesized catalyst, 30 µL of a Nafion ® 117 solution, and 90 µL of isopropanol through sonication for 30 min. The obtained suspension coated a carbon paper (GDL; SIGRACET 28BC, SGL Technologies) by the drop-casting method. The solvents were evaporated overnight at room temperature. The catalyst mass loading was about 2.3 mg cm −2 .

Electrochemical Characterizations for the CO 2 RR and Product Analysis
Cyclic voltammetry (CV) was performed in a three-electrode cell at room temperature with a CHI760D electrochemical workstation. The working electrode was a catalyst-coated carbon paper with a geometric area of 0.1 cm 2 . A Pt wire was used as the counter electrode and an Ag/AgCl (3 M NaCl) was used as the reference. To study the electrocatalytic performance of the electrode, CV measurements were performed from +0.2 V to −1.3 V vs. the reversible hydrogen electrode (RHE) at a scan rate of 10 mV s −1 in N 2 -and CO 2saturated 2.0 M KHCO 3 aqueous solution. Hereafter, the potentials refer to the RHE unless otherwise specified. CO 2 electrolysis was carried out in controlled potential mode by applying chronoamperometric (CA) technique with a potentiostat(CHI760D). The potential was corrected by compensating the ohmic potential drop, of which 85% by the iR-compensation method of the instrument and 15% by manual shifting after calculation.
The CO 2 RR performance of the bare biochar and biochar-BiO x electrodes was compared in a two-compartment, three-electrode batch cell as shown in Scheme 1a. A proton exchange membrane (Nafion™ Membrane N117, Ion Power) was used as the separator for the anodic and cathodic sides. The reference electrode was a mini Ag/AgCl (1 mm, leak-free LF-1) inserted into the catholyte. A Pt foil (3.3 × 3.3 cm 2 ) was used as the anode and inserted into the anolyte. The working electrode was carbon paper coated with the synthesized catalyst (geometric area: 1.5 cm 2 ). The electrolyte was 0.1 M KHCO 3 aqueous solution (pH 6.8). During the CA tests, a constant CO 2 flow of 15 mL min −1 was purged through both sides in order to supply CO 2 at the cathode and to maintain a constant pH at the anode.
Then, CA tests were conducted at the biochar-BiO x electrode in a customized threecompartment, three-electrode semi-flow cell, as shown in Scheme 1b. In the flow cell configuration, the cathodic side was composed of two compartments, one with the catholyte flow and the other with the CO 2 gas flow. During the CA tests, both the catholyte and anolyte were 25 mL of 2.0 M KHCO 3 aqueous solution (pH 8.3) and were circuited at 2 mL min −1 The CO 2 gas was purged through the anolyte at a constant flow rate of 5 mL min −1 in order to maintain a constant pH. A CO 2 flow of 25 mL min −1 was maintained at the gas compartment of the cathodic side to supply the CO 2 reactant and bring out the products. leak-free LF-1) inserted into the catholyte. A Pt foil (3.3 × 3.3 cm 2 ) was used as the anode and inserted into the anolyte. The working electrode was carbon paper coated with the synthesized catalyst (geometric area: 1.5 cm 2 ). The electrolyte was 0.1 M KHCO3 aqueous solution (pH 6.8). During the CA tests, a constant CO2 flow of 15 mL min −1 was purged through both sides in order to supply CO2 at the cathode and to maintain a constant pH at the anode. Then, CA tests were conducted at the biochar-BiOx electrode in a customized threecompartment, three-electrode semi-flow cell, as shown in Scheme 1b. In the flow cell configuration, the cathodic side was composed of two compartments, one with the catholyte flow and the other with the CO2 gas flow. During the CA tests, both the catholyte and anolyte were 25 mL of 2.0 M KHCO3 aqueous solution (pH 8.3) and were circuited at 2 mL min −1 The CO2 gas was purged through the anolyte at a constant flow rate of 5 mL min −1 in order to maintain a constant pH. A CO2 flow of 25 mL min −1 was maintained at the gas compartment of the cathodic side to supply the CO2 reactant and bring out the products. During the CO2 electrolysis, the gaseous products were analyzed on-line with a micro gas chromatograph (µGC, Fusion ® , INFICON). The µGC was equipped with two channels: one, a Rt-Molsieve 5A column (10 m) and the other, a Rt-Q-Bond column (8 m). A microthermal conductivity detector (micro-TCD) was used for both channels. At the end of each test, the catholyte was collected and analyzed by a high-performance liquid chromatograph (Thermo Scientific Ultimate3000 HPLC) to determine the liquid products. The HPLC was equipped with a UV-Vis detector (210 nm) and a ReproGel (300 × 8 mm 2 ) column. A solution of 9.0 mM H2SO4 at a flow rate of 1.0 mL min −1 was used as the mobile phase.
Faradaic efficiency (FE) was the key parameter for determining the selectivity toward a specific product. The FE for a product can be calculated by dividing the charge consumed to produce a determined amount of this product by the total charge passed through the cathode as in Equation (1), where Q is the total charge consumed at the cathode (coulombs, C); n is the mole of electrons required to obtain 1 mole of this product (n = 2 for CO, HCOOH and H2 production); N is the mole of an identified product (mol); and F is the Faraday constant (96,485 C mol −1 ).
The partial current density for HCOOH formation jHCOOH can be obtained using Equation (2), * where jtotal is the total geometric current density at the cathode, and FEHCOOH is the faradaic efficiency for HCOOH production. During the CO 2 electrolysis, the gaseous products were analyzed on-line with a micro gas chromatograph (µGC, Fusion ® , INFICON). The µGC was equipped with two channels: one, a Rt-Molsieve 5A column (10 m) and the other, a Rt-Q-Bond column (8 m). A microthermal conductivity detector (micro-TCD) was used for both channels. At the end of each test, the catholyte was collected and analyzed by a high-performance liquid chromatograph (Thermo Scientific Ultimate3000 HPLC) to determine the liquid products. The HPLC was equipped with a UV-Vis detector (210 nm) and a ReproGel (300 × 8 mm 2 ) column. A solution of 9.0 mM H 2 SO 4 at a flow rate of 1.0 mL min −1 was used as the mobile phase.
Faradaic efficiency (FE) was the key parameter for determining the selectivity toward a specific product. The FE for a product can be calculated by dividing the charge consumed to produce a determined amount of this product by the total charge passed through the cathode as in Equation (1), where Q is the total charge consumed at the cathode (coulombs, C); n is the mole of electrons required to obtain 1 mole of this product (n = 2 for CO, HCOOH and H 2 production); N is the mole of an identified product (mol); and F is the Faraday constant (96,485 C mol −1 ). The partial current density for HCOOH formation j HCOOH can be obtained using Equation (2), where j total is the total geometric current density at the cathode, and FE HCOOH is the faradaic efficiency for HCOOH production. The production rate of HCOOH (mg h −1 cm −2 ) can be calculated by applying Equation (3), where F is the Faraday constant (96,485 C mol −1 ); t is the seconds in one hour (3600); j HCOOH is the partial current density for HCOOH formation (mA cm −2 ); and M is the molar mass of HCOOH (g mol −1 ).

Physical and Chemical Characterizations of the Synthesized Catalysts
FESEM-EDS analysis was performed on the biochar-BiO x composite sample. Figure 1a shows the porous nature of the biochar with a pore size distribution of 100 to 1000 nm. Biochar wall thickness and length ranged from few nanometers to a micrometer. This microporous structure of biochar provided plenty of surface on which to decorate BiO x nanoparticles (Figure 1b). The uniform layer of the granular-sized BiO x nanoparticles on the biochar surface was observed. It is likely that all available biochar surface was completely covered by the BiO x nanoparticles layer (Figure 1c). It confirmed that the goal of achieving uniform decoration over a biochar surface was satisfactory. The diameter of granular BiO x nanoparticles was in nano-scale varying from 10 to 50 nm (Figure 1d), which gave them the added advantage of providing a highly catalytic surface.
The production rate of HCOOH (mg h −1 cm −2 ) can be calculated by applying Equation where F is the Faraday constant (96,485 C mol −1 ); t is the seconds in one hour (3600); jHCOOH is the partial current density for HCOOH formation (mA cm −2 ); and M is the molar mass of HCOOH (g mol −1 ).

Physical and Chemical Characterizations of the Synthesized Catalysts
FESEM-EDS analysis was performed on the biochar-BiOx composite sample. Figure  1a shows the porous nature of the biochar with a pore size distribution of 100 to 1000 nm. Biochar wall thickness and length ranged from few nanometers to a micrometer. This microporous structure of biochar provided plenty of surface on which to decorate BiOx nanoparticles ( Figure 1b). The uniform layer of the granular-sized BiOx nanoparticles on the biochar surface was observed. It is likely that all available biochar surface was completely covered by the BiOx nanoparticles layer (Figure 1c). It confirmed that the goal of achieving uniform decoration over a biochar surface was satisfactory. The diameter of granular BiOx nanoparticles was in nano-scale varying from 10 to 50 nm (Figure 1d), which gave them the added advantage of providing a highly catalytic surface. A quantitative elemental analysis of biochar-BiOx composite was performed by EDS ( Figure 2). Elemental mapping and scanning was performed on the targeted surface of the A quantitative elemental analysis of biochar-BiO x composite was performed by EDS ( Figure 2). Elemental mapping and scanning was performed on the targeted surface of the composite (Figure 2a). The mapping of the surface confirmed the presence of three elements, bismuth (Bi) in green, carbon (C) in red, and oxygen (O) in blue (Figure 2b-e). The mapping also confirmed the uniform distribution of the BiO x layer over the carbon surface. To quantify the elemental compositions, EDS surface scanning was performed  (Figure 2a). The mapping of the surface confirmed the presence of three elements, bismuth (Bi) in green, carbon (C) in red, and oxygen (O) in blue (Figure 2b-e). The mapping also confirmed the uniform distribution of the BiOx layer over the carbon surface. To quantify the elemental compositions, EDS surface scanning was performed (Figure 2f). Bismuth showed the maximum amount of 65.6 wt.% in the composite, followed by oxygen (8.9 wt.%) and carbon (25.4 wt.%).     Figure 4a) shows a slight weight loss of 0.3% below 100 °C, which was related to the desorption of some physisorbed gases. Then, a weight increase of ~2.5% associated with the oxidation of the bismuth was detected until 315 °C. This was followed by thermal degradation of the biochar-BiOx sample, which occurred completely below 400 °C. The maximum degradation of the biochar-BiOx sample was observed at 349 °C, and the IR spectrum acquired at this temperature is shown in Figure 4b. The gases developed were mainly CO2 (2359 cm −1 ) and water (3750 and 1543 cm −1 ), being obtained by the degradation of the biochar and the release of some OH surface groups from BiOx, respectively. CO (2180 cm −1 ) was also observed but in a small amount (Figure 4b inset). The residue of the biochar-BiOx degradation at 900 °C was 89.6%, which was related to the Bi2O3 derived from BiOx in air at high temperature [41,42] and the residue of biochar. Figure 4c shows the TGA of the bare biochar and 12.6% of residue was found. Table 1 listed the calculated weight percentage of BiOx in the composite sample and compared it with the nominal one. The calculated value was higher than the nominal percentage, probably due to the loss of a part of the biochar during the decoration of BiOx.   Figure 4a) shows a slight weight loss of 0.3% below 100 • C, which was related to the desorption of some physisorbed gases. Then, a weight increase of~2.5% associated with the oxidation of the bismuth was detected until 315 • C. This was followed by thermal degradation of the biochar-BiO x sample, which occurred completely below 400 • C. The maximum degradation of the biochar-BiO x sample was observed at 349 • C, and the IR spectrum acquired at this temperature is shown in Figure 4b. The gases developed were mainly CO 2 (2359 cm −1 ) and water (3750 and 1543 cm −1 ), being obtained by the degradation of the biochar and the release of some OH surface groups from BiO x , respectively. CO (2180 cm −1 ) was also observed but in a small amount (Figure 4b inset). The residue of the biochar-BiO x degradation at 900 • C was 89.6%, which was related to the Bi 2 O 3 derived from BiO x in air at high temperature [41,42] and the residue of biochar. Figure 4c shows the TGA of the bare biochar and 12.6% of residue was found. Table 1 listed the calculated weight percentage of BiO x in the composite sample and compared it with the nominal one. The calculated value was higher than the nominal percentage, probably due to the loss of a part of the biochar during the decoration of BiO x .

Electrochemical Properties of the Biochar-BiO x Electrode toward the CO 2 RR
In order to study the electrocatalytic performance of the biochar-BiO x electrode toward the CO 2 RR, CV was carried out in a N 2 -purged or CO 2 -saturated 2.0 M KHCO 3 aqueous solution. N 2 or CO 2 gas was bubbled through the electrolyte for 30 min before the measurements and the same gas flux was maintained during the measurements. Only the HER occurred in the N 2 atmosphere at negative potentials, while both the HER and CO 2 RR happened in the CO 2 atmosphere. Hence, it is widely believed that the comparison of the geometric current densities in N 2 and CO 2 electrolytes could be suggestive for electrode selectivity between the HER and CO 2 RR [11,43,44]. An electrode that generates a higher geometric current density in the CO 2 electrolyte than in the N 2 one is usually more selective for the CO 2 RR with respect to the HER at the corresponding potential. As shown Crystals 2021, 11, 363 9 of 13 in Figure 5, the current density in the CO 2 electrolyte was significantly higher than that in the N 2 one at potentials more negative than -0.7 V. This outcome indicated that the biochar-BiO x electrode could have high activity and good selectivity for the CO 2 RR at negative potentials (<−0.7 V). ous solution. N2 or CO2 gas was bubbled through the electrolyte for 30 min before the measurements and the same gas flux was maintained during the measurements. Only the HER occurred in the N2 atmosphere at negative potentials, while both the HER and CO2RR happened in the CO2 atmosphere. Hence, it is widely believed that the comparison of the geometric current densities in N2 and CO2 electrolytes could be suggestive for electrode selectivity between the HER and CO2RR [11,43,44]. An electrode that generates a higher geometric current density in the CO2 electrolyte than in the N2 one is usually more selective for the CO2RR with respect to the HER at the corresponding potential. As shown in Figure 5, the current density in the CO2 electrolyte was significantly higher than that in the N2 one at potentials more negative than -0.7 V. This outcome indicated that the biochar-BiOx electrode could have high activity and good selectivity for the CO2RR at negative potentials (<−0.7 V). To verify the performance of the biochar-Bi2O3 electrode, CA tests were firstly carried out in 0.1 M KHCO3 electrolyte at different potentials in a customized three-electrode, two-compartment batch cell. An electrode composed of bare biochar was also tested for comparison. As shown in Figure 6a, the biochar showed no selectivity toward the CO2RR, since the faradaic efficiency for the H2 formation was almost 100%. In contrast, the biochar-Bi2O3 electrode showed significant selectivity for the CO and HCOOH formation, especially at higher overpotentials ( Figure 6b). However, the current density for HCOOH formation was rather low, probably due to the high resistance of the diluted buffer electrolyte. To verify the performance of the biochar-Bi 2 O 3 electrode, CA tests were firstly carried out in 0.1 M KHCO 3 electrolyte at different potentials in a customized three-electrode, two-compartment batch cell. An electrode composed of bare biochar was also tested for comparison. As shown in Figure 6a, the biochar showed no selectivity toward the CO 2 RR, since the faradaic efficiency for the H 2 formation was almost 100%. In contrast, the biochar-Bi 2 O 3 electrode showed significant selectivity for the CO and HCOOH formation, especially at higher overpotentials ( Figure 6b). However, the current density for HCOOH formation was rather low, probably due to the high resistance of the diluted buffer electrolyte. Hence, CA tests were further performed on the biochar-Bi2O3 electrode in a customized flow cell at potentials ranging from −0.6 V to −1.3 V in more concentrated electrolyte (2.0 M KHCO3). The i-t curves at different potentials are shown in Figure 7a. The current density increased as the overpotential increased, which is in agreement with the CV result in the same electrolyte. The major products and their FE values are shown in Figure 7b. H2 was the main product at −0.6 V and its production dramatically reduced at −0.7 V. As the electrode was polarized at more negative potentials, H2 became a minor product and HCOOH became the predominant product, while the FECO remained less than 6% in all the investigated potential range. The selectivity for the CO2RR significantly outcompeted that for the HER at potentials more negatively than −0.7 V, which is consistent with the CV result. It is worth noting that the FE for CO and HCOOH production occupied more than 90% from −1.0 V to −1.3 V. As the main product, HCOOH reached good FE values (>80%) in a wide potential range from −0.9 V to −1.3 V, with a maximum of 87% at −1.1 V.  Figure 7a. The current density increased as the overpotential increased, which is in agreement with the CV result in the same electrolyte. The major products and their FE values are shown in Figure 7b. H 2 was the main product at −0.6 V and its production dramatically reduced at −0.7 V. As the electrode was polarized at more negative potentials, H 2 became a minor product and HCOOH became the predominant product, while the FE CO remained less than 6% in all the investigated potential range. The selectivity for the CO 2 RR significantly outcompeted that for the HER at potentials more negatively than −0.7 V, which is consistent with the CV result. It is worth noting that the FE for CO and HCOOH production occupied more than 90% from −1.0 V to −1.3 V. As the main product, HCOOH reached good FE values (>80%) in a wide potential range from −0.9 V to −1.3 V, with a maximum of 87% at −1.1 V. The partial current density for HCOOH formation as a function of potential is displayed in Figure 7c. The HCOOH production rate became significant at −0.8 V, which was 5.5 mg cm −2 h −1 . It increased progressively with enhancing the driving force and ended with 59.6 mg cm −2 h −1 at −1.3 V (Figure 7d). The biochar-BiOx electrode also showed good stability during a 5-h test at a current density of 77.5 mA cm −2 (Figure 7e). Concisely, the biochar-Bi2O3 electrode showed good performance for the CO2RR to HCOOH for both selectivity and production rate, which was in line with the best results reported on the HCOOH-selective materials as listed in Table 2.  The partial current density for HCOOH formation as a function of potential is displayed in Figure 7c. The HCOOH production rate became significant at −0.8 V, which was 5.5 mg cm −2 h −1 . It increased progressively with enhancing the driving force and ended with 59.6 mg cm −2 h −1 at −1.3 V (Figure 7d). The biochar-BiOx electrode also showed good stability during a 5-h test at a current density of 77.5 mA cm −2 (Figure 7e). Concisely, the biochar-Bi 2 O 3 electrode showed good performance for the CO 2 RR to HCOOH for both selectivity and production rate, which was in line with the best results reported on the HCOOH-selective materials as listed in Table 2.

Conclusions
A new material composed of BiO x and biochar was synthesized through an easy and scalable route. The Bi species were metallic Bi and Bi 2 O 3 , which comprised about 87.1 wt.% of the composite. The BiO x particles were on the nanoscale and uniformly decorated on the surface of the biochar. By careful electrochemical characterizations and product analyses, the biochar-BiO x material is demonstrated to be a promising candidate for converting CO 2 to HCOOH, showing a maximum faradaic efficiency of 87% and the highest current density of 70 mA cm −2 for HCOOH production. In addition to its low price and eco-friendly nature, this proposed BiO x -biochar catalyst could be produced on a mass scale via the simple route and be used in the electrosynthesis of HCOOH from CO 2 on an industrial scale. Funding: This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors.
Institutional Review Board Statement: Not applicable.

Informed Consent Statement: Not applicable.
Data Availability Statement: Data is contained within the article.