Facile Synthesis of Sustainable Biomass-Derived Porous Biochars as Promising Electrode Materials for High-Performance Supercapacitor Applications

Preparing sustainable and highly efficient biochars as electrodes remains a challenge for building green energy storage devices. In this study, efficient carbon electrodes for supercapacitors were prepared via a facile and sustainable single-step pyrolysis method using spruce bark as a biomass precursor. Herein, biochars activated by KOH and ZnCl2 are explored as templates to be applied to prepare electrodes for supercapacitors. The physical and chemical properties of biochars for application as supercapacitors electrodes were strongly affected by factors such as the nature of the activators and the meso/microporosity, which is a critical condition that affects the internal resistance and diffusive conditions for the charge accumulation process in a real supercapacitor. Results confirmed a lower internal resistance and higher phase angle for devices prepared with ZnCl2 in association with a higher mesoporosity degree and distribution of Zn residues into the matrix. The ZnCl2-activated biochar electrodes’ areal capacitance reached values of 342 mF cm−2 due to the interaction of electrical double-layer capacitance/pseudocapacitance mechanisms in a matrix that favors hydrophilic interactions and the permeation of electrolytes into the pores. The results obtained in this work strongly suggest that the spruce bark can be considered a high-efficiency precursor for biobased electrode preparation to be employed in SCs.


Introduction
The development of sustainable and efficient energy storage systems (ESS) attracts massive attention in the literature due to their wide range of applications, from portable electronic devices to hybrid electric vehicles [1][2][3]. Among different types of ESS, supercapacitors (SCs) have favorable properties of relatively high specific power density (10 to 100,000 W/kg), outstanding cycling stability (minimal change in the electrochemical response after a few thousands of reuses), low resistance, fast charge/discharge, and a wide range of applications [4,5]. There are two typical mechanisms for charge storage in supercapacitors: electric double-layer capacitance (EDLCs) and pseudocapacitance (PC) [3,4]. EDLCs make use of the diffusion and accumulation of double-layer charges formed by the adsorption of electrolyte ions on the electrode's surface (physisorption); thus, electrodes with very high specific surface area (SSA) and a high level of hydrophilicity are generally required to fabricate EDLCs [3,4]. Differently, pseudocapacitors store energy not only through the formation of an EDL but also through reversible redox reactions with the fast insertion of the electrolyte ions onto the surface layer of the electrode [3,4].
known that the structure of the original biomass severely restricts the final structure of the synthesized carbon material. However, there is a lack of understanding regarding the relationship between biomass properties, process conditions, the resulting biochar properties, and the electrochemical performance of the carbon electrodes in SCs applications.
Generally, softwood bark is a low-value residue in forest-industrial production chains. In this work, Norway spruce (Picea abies (Karst.) L.) bark was used as the main precursor for producing electrode biochar for SCs. The bark's constitution of cellulose, hemicellulose, and lignin [16], makes it a suitable precursor for biochar to be used as electrodes for SCs [2,3,14]. Herein, we describe the preparation of two different electrode types, made from KOHand ZnCl 2 -activated Norway spruce bark, respectively. These two electrodes were fully characterized by various physicochemical and electrochemical analyses, displaying high specific capacitance and good rate capability.
To the best of our knowledge, only one paper employed spruce bark as the main precursor for the preparation of biochar electrodes for SCs [11]. Besides, the effect of different chemical activation and responses that describe the structural and chemical properties of the biochar materials and their resulting electrode performance are fully evaluated. These two electrodes were fully characterized by various physiochemical and electrochemical analyses, displaying high specific capacitance and good rate capability.

Chemicals and Reagents
The Norway spruce bark was provided by a Holmen paper (Stockholm, Sweden) and pulp mill in North-Eastern Sweden. The spruce bark was dried and milled (Fritsch Pulverisette 14, Idar-Oberstein, Germany) at a screen size of 500 µm. The chemicals potassium hydroxide (KOH), polyvinylidene fluoride (PVDF), zinc chloride (ZnCl 2 ), and hydroxide chloride (HCl) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Dimethylformamide (DMF) was purchased from Dinamica (Gorizia, Italy), and the carbon black was purchased from Micromeritics (Norcross, GA, USA).

Preparation Process
The biochars were prepared as follows: first, 50.0 g of bark were mixed with KOH at a ratio of 1:1 (weight), and then mixed with 30 mL of distilled water in a melting pot until a homogeneous paste was obtained [21,22]. The same procedure was followed with the ZnCl 2 activation process. The mixtures were left for 2 h at ambient temperature, whereafter it was dried in a drying oven at 105 • C overnight. Pyrolysis was performed at 900 • C for 2 h under nitrogen flow, with an initial heating rate of 10 • C per min. After pyrolysis, the samples were milled and washed with 1.0 M and 6.0 HCl for KOH and ZnCl 2 biochars, respectively. Finally, a washing step with distilled water was performed several times until the pH value of the filtrate reached a neutral value [21,22].

Biochar Characterization
The SSA and porosity data of the biochars were evaluated via nitrogen adsorptiondesorption isotherms using a Tristar 3000 apparatus, Micrometrics Instrument Corp. The biochars were subjected to degasification at 180 • C for 3 h, and the SSA and pore size distribution were obtained using the Brunauer-Emmett-Teller (BET) method.
The morphology of biochars was evaluated from the scanning electron microscopy (SEM) technique, using a Zeiss-Gemini microscope, and images were made at 20 µm scales with 2.5k× of magnification.
XPS analysis of the biochars was collected using a Kratos Axis Ultra DLD electron spectrometer using a monochromated Al K α source operated at 150 W. An analyzer of 160 eV for acquiring survey spectra and 20 eV for individual photoelectron lines were used. The samples were gently hand-pressed using a clean Ni spatula into the powder sample holder. Due to the electrical conductive behavior of the carbonaceous material, no charge neutralization system was used. The binding energy (BE) scale was calibrated following Raman spectra were collected using a Bruker Bravo spectrometer (Bruker, Ettlingen, Germany) connected to a docking measuring station. Shortly, 0.5 g of each biochar powder was placed in 2.5 mL glass vials and scanned in the 300-3200 cm −1 spectral range at 4 cm −1 resolution for 256 scans. Min-Max normalization over the 1000-2000 cm −1 region and smoothing (9 points) was conducted using the built-in functions of the OPUS software (version 7, Bruker Optik GmbH, Ettlingen, Germany). No baseline correction was needed.
Fourier transform infrared spectroscopy (FTIR) was exploited to determine the functional groups of the biochars. The FTIR spectra were recorded over the wavenumber range of 4000-400 cm −1 , utilizing a Bruker IFS 66v/S instrument (Bruker Optics, Ettlingen, Germany) with an acquisition of 64 scans min −1 and resolution of 4 cm −1 .
The X-ray diffraction pattern was measured in a Rigaku Miniflex X-ray diffractometer (Rigaku Corporation, Tokyo, Japan) with CuKα (λ = 1.4518 Å), with operation parameters of 40 kV and a current of 15 mA in a continuous can from 5 • to 6 • with a step of 0.02 • , speed of 10 • /min.

Preparation of Powder and Assembly of Two-Electrode Supercapacitors
As a first step in the electrode preparation, a slurry containing biomass charcoal (KOH biochar, ZnCl 2 biochar), carbon black, and PVDF in a mass ratio of 0.70, 0.20, and 0.10, respectively, was created. Firstly, 10 mg of PVDF was added to 500 µL of DMF; then, the solution was stirred for 5 min at 85 • C to solubilize the polymer. After that, 70 mg of biomass charcoal and 20 mg of carbon black were added. The resulting solution was kept under stirring for 10 min at 85 • C. After that, 1 cm × 1 cm graphite electrodes were applied as support (current collector to be coated with slurry). The electrode was prepared by dropping 25 µL of the as-prepared slurry on the surface of the graphite paper. After evaporating the solvent, the coated graphite paper was placed on a hotplate at 70 • C for 5 min. This process was repeated until the surface of the graphite paper was completely covered. At the end of this process, two electrode types were obtained, one containing the KOH biochar and the other the ZnCl 2 biochar. The SC was assembled in a sandwich-type, where a filter paper separated the electrodes. Both electrodes and the separator were impregnated with a KOH 5 M solution. Pictures for the assembled device are shown in Figure 1a,b, in which it is possible to identify the electrodes, the separator, and the final disposition of the parts. The samples were gently hand-pressed using a clean Ni spatula into the powder sample holder. Due to the electrical conductive behavior of the carbonaceous material, no charge neutralization system was used. The binding energy (BE) scale was calibrated following the ASTM E2108 and ISO 15472 standards. Processing of the spectra was accomplished with the Kratos software. Raman spectra were collected using a Bruker Bravo spectrometer (Bruker, Ettlingen, Germany) connected to a docking measuring station. Shortly, 0.5 g of each biochar powder was placed in 2.5 mL glass vials and scanned in the 300-3200 cm −1 spectral range at 4 cm −1 resolution for 256 scans. Min-Max normalization over the 1000-2000 cm −1 region and smoothing (9 points) was conducted using the built-in functions of the OPUS software (version 7, Bruker Optik GmbH, Ettlingen, Germany). No baseline correction was needed.
Fourier transform infrared spectroscopy (FTIR) was exploited to determine the functional groups of the biochars. The FTIR spectra were recorded over the wavenumber range of 4000-400 cm −1 , utilizing a Bruker IFS 66v/S instrument (Bruker Optics, Ettlingen, Germany) with an acquisition of 64 scans min −1 and resolution of 4 cm −1 .
The X-ray diffraction pattern was measured in a Rigaku Miniflex X-ray diffractometer (Rigaku Corporation, Tokyo, Japan) with CuKα (λ = 1.4518 Å ), with operation parameters of 40 kV and a current of 15 mA in a continuous can from 5° to 6° with a step of 0.02°, speed of 10°/min.

Preparation of Powder and Assembly of Two-Electrode Supercapacitors
As a first step in the electrode preparation, a slurry containing biomass charcoal (KOH biochar, ZnCl2 biochar), carbon black, and PVDF in a mass ratio of 0.70, 0.20, and 0.10, respectively, was created. Firstly, 10 mg of PVDF was added to 500 µ L of DMF; then, the solution was stirred for 5 min at 85 °C to solubilize the polymer. After that, 70 mg of biomass charcoal and 20 mg of carbon black were added. The resulting solution was kept under stirring for 10 min at 85 °C. After that, 1 cm × 1 cm graphite electrodes were applied as support (current collector to be coated with slurry). The electrode was prepared by dropping 25 µ L of the as-prepared slurry on the surface of the graphite paper. After evaporating the solvent, the coated graphite paper was placed on a hotplate at 70 °C for 5 min. This process was repeated until the surface of the graphite paper was completely covered. At the end of this process, two electrode types were obtained, one containing the KOH biochar and the other the ZnCl2 biochar. The SC was assembled in a sandwich-type, where a filter paper separated the electrodes. Both electrodes and the separator were impregnated with a KOH 5 M solution. Pictures for the assembled device are shown in Figure  1a,b, in which it is possible to identify the electrodes, the separator, and the final disposition of the parts.

Textural Properties and Morphology of the Biochars
SSA and porosity of the biobased carbon materials are essential properties that strongly influence their performance as materials regardless of their applications [2,3]. Both chemical activation methods yielded biochars with N 2 adsorption/desorption isotherm curves close to type I as the nitrogen adsorption increased at low partial pressure ( Figure 2). This describes an adsorption process resulting in micropores filling. However, hysteresis was observed in both samples, which characterizes mesoporous materials [23,24]. Both materials contain micro and mesoporosity due to the high N 2 adsorption volume at low and high pressure [23,24]. To a large extent, the activation process influenced the amount of adsorbed N 2 , which also is reflected in the SSA values.

Textural Properties and Morphology of the Biochars
SSA and porosity of the biobased carbon materials are essential properties that strongly influence their performance as materials regardless of their applications [2,3]. Both chemical activation methods yielded biochars with N2 adsorption/desorption isotherm curves close to type I as the nitrogen adsorption increased at low partial pressure ( Figure 2). This describes an adsorption process resulting in micropores filling. However, hysteresis was observed in both samples, which characterizes mesoporous materials [23,24]. Both materials contain micro and mesoporosity due to the high N2 adsorption volume at low and high pressure [23,24]. To a large extent, the activation process influenced the amount of adsorbed N2, which also is reflected in the SSA values. KOH biochar adsorbed a much higher N2 volume and, as a consequence, exhibited a much higher SSA value (2209 m 2 g −1 ) (see Table 1). Since the pyrolysis conditions were the same for both biochars, the differences in their SSA values could be exclusively related to the chemical activation mechanisms based on KOH and ZnCl2. The reaction between KOH and biomass usually leads to a much more violent chemic during the thermal treatment, indicated by the lower yield (13.7% for KOH and 28.1% for ZnCl2). KOH activation consists of several steps during the pyrolysis process-based solidliquid reactions because potassium hydroxide is diluted in water. Above 700 °C, potassium metallic is formed and may enhance the porosity; the metallic ion K + may act as a catalyst for gasification reactions, which helps to form and develop pore structures [25,26]. Additionally, a K intercalation process can occur; K ions may go between graphene layers KOH biochar adsorbed a much higher N 2 volume and, as a consequence, exhibited a much higher SSA value (2209 m 2 g −1 ) (see Table 1). Since the pyrolysis conditions were the same for both biochars, the differences in their SSA values could be exclusively related to the chemical activation mechanisms based on KOH and ZnCl 2 . The reaction between KOH and biomass usually leads to a much more violent chemic during the thermal treatment, indicated by the lower yield (13.7% for KOH and 28.1% for ZnCl 2 ). KOH activation consists of several steps during the pyrolysis process-based solidliquid reactions because potassium hydroxide is diluted in water. Above 700 • C, potassium metallic is formed and may enhance the porosity; the metallic ion K + may act as a catalyst for gasification reactions, which helps to form and develop pore structures [25,26]. Additionally, a K intercalation process can occur; K ions may go between graphene layers of the biochar, widening its pore network and straining the structure, which potentializes the pore formation and reaches very high SSA values.
Activation with ZnCl 2 , which is a Lewis acid, is a potent dehydrating reagent as it catalyzes the decomposition of lignocellulosic compounds. This activation involves dehydration, depolymerization, and ring-opening [25][26][27][28]. ZnCl 2 is an efficient catalyst for C-O and C-C bonds scission. Moreover, during pyrolysis, ZnCl 2 starts to melt at 290 • C and may, if evenly mixed with the biomass, reach the biomass' interior. Increasing the pyrolysis temperature leads to thermal dehydration of the zinc oxide chloride hydrate that forms a gaseous phase of ZnCl 2 and a solid phase of zinc oxide. The gaseous phase of ZnCl 2 is diffused through the carbonaceous structure to develop the pore network [26,27].
Thus, it can be stated that the activation process using KOH produced biochar with more developed porosity. In addition, the contributions of micropores and mesopores reaction in the biochar structures were evaluated. The percentage of mesopores in KOH biochar was 22.6% and in ZnCl 2 -BBC was 46%, while the share of micropores was 77.4% in KOH biochar and 54% in ZnCl 2 biochar.
In ESS applications, an adequate combination of micro/mesopores distribution and electrolyte ions type and size is highly required because the electrolyte ions can be efficiently transported in small-sized pores, reaching high charge storage capability at low current density [2,3,29]. Miao et al. [30] reported that a large number of micropores (size between 1 and 2 nm) could facilitate the charge separation (due to the available sites for charge accumulation), which affects the overall energy density of the device.
SEM analysis was performed to examine the effect of the chemical activation on the surface morphology of the biochars. Figure  the pore formation and reaches very high SSA values.
Activation with ZnCl2, which is a Lewis acid, is a potent dehydrating reagent as it catalyzes the decomposition of lignocellulosic compounds. This activation involves dehydration, depolymerization, and ring-opening [25][26][27][28]. ZnCl2 is an efficient catalyst for C-O and C-C bonds scission. Moreover, during pyrolysis, ZnCl2 starts to melt at 290 °C and may, if evenly mixed with the biomass, reach the biomass' interior. Increasing the pyrolysis temperature leads to thermal dehydration of the zinc oxide chloride hydrate that forms a gaseous phase of ZnCl2 and a solid phase of zinc oxide. The gaseous phase of ZnCl2 is diffused through the carbonaceous structure to develop the pore network [26,27].
Thus, it can be stated that the activation process using KOH produced biochar with more developed porosity. In addition, the contributions of micropores and mesopores reaction in the biochar structures were evaluated. The percentage of mesopores in KOH biochar was 22.6% and in ZnCl2-BBC was 46%, while the share of micropores was 77.4% in KOH biochar and 54% in ZnCl2 biochar.
In ESS applications, an adequate combination of micro/mesopores distribution and electrolyte ions type and size is highly required because the electrolyte ions can be efficiently transported in small-sized pores, reaching high charge storage capability at low current density [2,3,29]. Miao et al. [30] reported that a large number of micropores (size between 1 and 2 nm) could facilitate the charge separation (due to the available sites for charge accumulation), which affects the overall energy density of the device.
SEM analysis was performed to examine the effect of the chemical activation on the surface morphology of the biochars. Figure 3 display the surface morphology of the two biochars. The images show that KOH activation results in a sponge-like structure ( Figure  3a) full of roughness and irregular structure and tons of small holes. On the other hand, the sample made with ZnCl2 ( Figure 3b) shows a much denser structure, with more elongated cavities and holes of different sizes and shapes. Thus, by the SEM analysis (and to corroborate the BET analysis), it is possible to infer that the choice of activation method strongly affected the surface characteristics of the biochars. Moreover, both materials have a significant presence of macropores and ultramacropores; vital because they serve as vectors to the electrolyte passage until it attains smaller pores (in the interior of the biochars). In terms of relevance for supercapacitorbased applications, it provides the possibility to provide electrolyte permeation along with the porous structure for the following step of charge accumulation into the cavities (more accessible channels).

Chemical and Functional Characterization of the Biochars
The chemical state and the main composition of the elements in the biochars were evaluated via the XPS technique [16,25,31], which gives detailed and valuable information Thus, by the SEM analysis (and to corroborate the BET analysis), it is possible to infer that the choice of activation method strongly affected the surface characteristics of the biochars. Moreover, both materials have a significant presence of macropores and ultramacropores; vital because they serve as vectors to the electrolyte passage until it attains smaller pores (in the interior of the biochars). In terms of relevance for supercapacitor-based applications, it provides the possibility to provide electrolyte permeation along with the porous structure for the following step of charge accumulation into the cavities (more accessible channels).

Chemical and Functional Characterization of the Biochars
The chemical state and the main composition of the elements in the biochars were evaluated via the XPS technique [16,25,31], which gives detailed and valuable information about the effect of the chemical activation methods (KOH and ZnCl 2 ) on the surface properties of the biochars. Figure 4a (KOH) and b (ZnCl 2 ) show C 1s, O 1s, and N 1s spectra, carbon, oxygen, and nitrogen bonds, respectively.  The asymmetric C 1s spectra could be deconvoluted into four peaks centered at 284.3 and 284.4 eV, which are attributed to C-C and C=C bonds, at 285.4 eV, which is related to C-N, at 286.3 and 286.5 eV (C-O-C), and at 287.4 and 287.5 eV that are related to C=O [16,25,27].
O1s spectra exhibited some differences regarding the chemical activation process. The biochar made with KOH showed O1s spectra deconvoluted to three chemical oxygen states with binding energies at around 530.8 eV, 532.5 eV, and 535.6 eV [16,31]; while the biochar made with KOH deconvoluted into four peaks, 531.2 eV, 532.9 eV, 535.1 eV, and 537.2 eV. The different peaks are related to the following: (i) 531.2 and 530.8-eV oxygen double-bonded with carbon in carbonyl and quinone-like structures, (ii) 532.5 and 532.9 eV-oxygen singly bonded to carbon in aromatic rings, in phenols and ethers, (iii) 535.1 and 535.6 eV-hydroxyl groups, and (iv) 537.2 eV-adsorbed H2O-OH sub-monolayer in which both OH and H2O are hydrogen-bonded to each other (this peak is found only in the ZnCl2 biochar). The presence of this oxygen species can improve the hydrophilicity degree of the sample, which can reflect in better interaction between solid and liquid phase (electrode-electrolyte), characterizing an advantage for permeation of aqueous electrolyte ions into the biochar-based electrode. Figure 4 also show the deconvoluted N 1s spectra for the biochars; a single peak is observed in KOH biochar, which is related to pyrrolic nitrogen (400 eV) [14,16], while for ZnCl2 biochar, two peaks are observed, one at 397.9 eV which corresponds to pyridinic species [14,16] and at 400.5 eV that is related to pyrrolic nitrogen [14,16]. The presence of more N species in the ZnCl2 biochar can improve its electrochemical performances as an electrode for SCs. Nitrogen can act as an electron donor, enhancing the charge exchange with the electrolyte [32,33]. In addition, Hou et al. [33] reported that pyridinic-N boosts the electrochemical performances of the electrodes, which can be considered an essential advantage for ZnCl2-activated biochars.
To further evaluate the chemical composition of the biochar samples, Table 2 show the quantitative analyses for the C, O, and N and the ID/IG ratio (based on Raman analysis). ZnCl2 biochar presented the highest C content, while the oxygen content was much higher in the KOH biochar (see Table 2). The nitrogen content is almost the same in both samples, The asymmetric C 1s spectra could be deconvoluted into four peaks centered at 284.3 and 284.4 eV, which are attributed to C-C and C=C bonds, at 285.4 eV, which is related to C-N, at 286.3 and 286.5 eV (C-O-C), and at 287.4 and 287.5 eV that are related to C=O [16,25,27].
O1s spectra exhibited some differences regarding the chemical activation process. The biochar made with KOH showed O1s spectra deconvoluted to three chemical oxygen states with binding energies at around 530.8 eV, 532.5 eV, and 535.6 eV [16,31]; while the biochar made with KOH deconvoluted into four peaks, 531.2 eV, 532.9 eV, 535.1 eV, and 537.2 eV. The different peaks are related to the following: (i) 531.2 and 530.8 eV-oxygen double-bonded with carbon in carbonyl and quinone-like structures, (ii) 532.5 and 532.9 eV-oxygen singly bonded to carbon in aromatic rings, in phenols and ethers, (iii) 535.1 and 535.6 eV-hydroxyl groups, and (iv) 537.2 eV-adsorbed H 2 O-OH sub-monolayer in which both OH and H 2 O are hydrogen-bonded to each other (this peak is found only in the ZnCl 2 biochar). The presence of this oxygen species can improve the hydrophilicity degree of the sample, which can reflect in better interaction between solid and liquid phase (electrode-electrolyte), characterizing an advantage for permeation of aqueous electrolyte ions into the biocharbased electrode. Figure 4 also show the deconvoluted N 1s spectra for the biochars; a single peak is observed in KOH biochar, which is related to pyrrolic nitrogen (400 eV) [14,16], while for ZnCl 2 biochar, two peaks are observed, one at 397.9 eV which corresponds to pyridinic species [14,16] and at 400.5 eV that is related to pyrrolic nitrogen [14,16]. The presence of more N species in the ZnCl 2 biochar can improve its electrochemical performances as an electrode for SCs. Nitrogen can act as an electron donor, enhancing the charge exchange with the electrolyte [32,33]. In addition, Hou et al. [33] reported that pyridinic-N boosts the electrochemical performances of the electrodes, which can be considered an essential advantage for ZnCl 2 -activated biochars.
To further evaluate the chemical composition of the biochar samples, Table 2 show the quantitative analyses for the C, O, and N and the I D /I G ratio (based on Raman analysis). ZnCl 2 biochar presented the highest C content, while the oxygen content was much higher in the KOH biochar (see Table 2). The nitrogen content is almost the same in both samples, while a residual Zn content is present in the biochar, which could positively affect the electrochemical performance of the material. Raman spectroscopy is considered one of the most informative methods for evaluating the structural perfection and degree of order/graphitization of bio-based carbon materials [16,34]. Raman spectra of the biochars are shown in Figure 5. Both biochars exhibit two typical carbon characteristic diffraction peaks at 1370 cm −1 and 1590 cm −1 , representing the D and G bands, respectively. The D band refers to the degree of chaos or imperfect structure in carbon materials, while the G peak corresponds to the ordered carbon structure [17]. while a residual Zn content is present in the biochar, which could positively affect the electrochemical performance of the material. Raman spectroscopy is considered one of the most informative methods for evaluating the structural perfection and degree of order/graphitization of bio-based carbon materials [16,34]. Raman spectra of the biochars are shown in Figure 5. Both biochars exhibit two typical carbon characteristic diffraction peaks at 1370 cm −1 and 1590 cm −1 , representing the D and G bands, respectively. The D band refers to the degree of chaos or imperfect structure in carbon materials, while the G peak corresponds to the ordered carbon structure [17]. According to Raman analysis, the intensity ratio of D band to G band (ID/IG) can be calculated, which is generally used to appraise the graphitization degree of carbon material [16,21,[34][35][36] (see Table 2). It is well known that graphite has a high conductivity degree and is a very efficient material used as an electrode for ESS. Thus, the degree of graphitization is a valuable tool for understanding the carbon-based material's suitability as electrode material [34][35][36]. The ZnCl2 and KOH biochars presented ID/IG values of 0.94 and 1.16, respectively. Low ID/IG value suggests that the material has closer to perfect and orderly graphite structures with a high graphitization degree; a high ID/IG indicates that the material has more structural defects in its structure [16,21,[34][35][36]. The biochar made via ZnCl2 activation presented a lower ID/IG value (0.94) than KOH activation (1.16); therefore, ZnCl2 biochar had the highest graphitization degree. These results match SSA values because KOH biochar had the highest SSA, suggesting a lot more defects and disordered structure.
The XRD patterns of the biochar samples are shown in Figure 6. The patterns show important differences between both samples. It seems that the different chemical treatments affected the biochar structures. According to Raman analysis, the intensity ratio of D band to G band (I D /I G ) can be calculated, which is generally used to appraise the graphitization degree of carbon material [16,21,[34][35][36] (see Table 2). It is well known that graphite has a high conductivity degree and is a very efficient material used as an electrode for ESS. Thus, the degree of graphitization is a valuable tool for understanding the carbon-based material's suitability as electrode material [34][35][36]. The ZnCl 2 and KOH biochars presented I D /I G values of 0.94 and 1.16, respectively. Low I D /I G value suggests that the material has closer to perfect and orderly graphite structures with a high graphitization degree; a high I D /I G indicates that the material has more structural defects in its structure [16,21,[34][35][36]. The biochar made via ZnCl 2 activation presented a lower I D /I G value (0.94) than KOH activation (1.16); therefore, ZnCl 2 biochar had the highest graphitization degree. These results match SSA values because KOH biochar had the highest SSA, suggesting a lot more defects and disordered structure.
The XRD patterns of the biochar samples are shown in Figure 6. The patterns show important differences between both samples. It seems that the different chemical treatments affected the biochar structures.  The ZnCl2 biochar exhibited a typical diffraction pattern for amorphous biochars 20-30° and three crystalline peaks in 38°, 44°, and 69° (which are assigned to the samp holder of aluminum). It is pointed out that the presence of amorphous material is require for carbon electrodes due to its network pores and vacancies [37]. For KOH-activated b ochar, four evident crystalline peaks at 30°, 38°, 44°, and 69° (with the last three associate with the substrate) and additional and very small peaks at 23°, 36°, 39.5°, and 48.8° can b identified.
The other crystalline peaks in both samples can be related to the high concentratio of calcite in its structures. It is well known that spruce bark is biomass rich in calcium tha when is subjected to pyrolysis, reacts to form calcite [38].
Comparing the XRD of both biochars, it seems that KOH yielded a sample with mo inorganic compounds such as calcite and quartz (electronic inert elements) [37,38], whi can negatively affect the electrochemical properties of the electrode material.
FTIR spectra (see Figure 7) were performed to identify the presence of the function groups on biochar samples. It is possible to observe that the different chemical treatmen affected the chemical functionalities on the biochar surfaces. The band at 3467 cm −1 repr sents the O-H stretching vibration in carboxyl and phenol groups [10][11][12]15]. . It is pointed out that the presence of amorphous material is required for carbon electrodes due to its network pores and vacancies [37]. For KOHactivated biochar, four evident crystalline peaks at 30 • , 38 • , 44 • , and 69 • (with the last three associated with the substrate) and additional and very small peaks at 23 • , 36 • , 39.5 • , and 48.8 • can be identified.
The other crystalline peaks in both samples can be related to the high concentration of calcite in its structures. It is well known that spruce bark is biomass rich in calcium that, when is subjected to pyrolysis, reacts to form calcite [38].
Comparing the XRD of both biochars, it seems that KOH yielded a sample with more inorganic compounds such as calcite and quartz (electronic inert elements) [37,38], which can negatively affect the electrochemical properties of the electrode material.
FTIR spectra (see Figure 7) were performed to identify the presence of the functional groups on biochar samples. It is possible to observe that the different chemical treatments affected the chemical functionalities on the biochar surfaces. The band at 3467 cm −1 represents the O-H stretching vibration in carboxyl and phenol groups [10][11][12]15]. The ZnCl2 biochar exhibited a typical diffraction pattern for amorphous biochars in 20-30° and three crystalline peaks in 38°, 44°, and 69° (which are assigned to the sample holder of aluminum). It is pointed out that the presence of amorphous material is required for carbon electrodes due to its network pores and vacancies [37]. For KOH-activated biochar, four evident crystalline peaks at 30°, 38°, 44°, and 69° (with the last three associated with the substrate) and additional and very small peaks at 23°, 36°, 39.5°, and 48.8° can be identified.
The other crystalline peaks in both samples can be related to the high concentration of calcite in its structures. It is well known that spruce bark is biomass rich in calcium that, when is subjected to pyrolysis, reacts to form calcite [38].
Comparing the XRD of both biochars, it seems that KOH yielded a sample with more inorganic compounds such as calcite and quartz (electronic inert elements) [37,38], which can negatively affect the electrochemical properties of the electrode material.
FTIR spectra (see Figure 7) were performed to identify the presence of the functional groups on biochar samples. It is possible to observe that the different chemical treatments affected the chemical functionalities on the biochar surfaces. The band at 3467 cm −1 represents the O-H stretching vibration in carboxyl and phenol groups [10][11][12]15].  Small peaks at 1252, 792, and 646 cm −1 can be observed only in ZnCl 2 biochar as well as others in the area highlighted by the circle inside the figure, suggesting that the ZnCl 2 activation generated more functionalities on its surface. The presence of more functionalities on the ZnCl 2 biochar surface can be related to the different activation mechanisms previously discussed. The existence of a high number of functional groups on biochar surfaces is often related to better electrochemical properties since it increases the electrode-electrolyte interactions [2,13,14].

Electrochemical Characterization
Electrochemical impedance spectroscopy (EIS) is a non-steady-state method that provides relevant information about several mechanisms at interfaces between the electrolyte and electrode [39]. In particular, the direct relationship between the time-dependent voltage (V) and current (I) defines the impedance (Z = V/I) that can be converted in terms of the complex capacitance C (with j = √ −1) From the definition of current I and capacitance C (I = dQ/dt and C = Q/V), both in terms of the charge Q, it is possible to write that (2) can be finally written in terms of the real and imaginary parts of the complex capacitance, as follows: where C is the capacitance at steady-state and C" is related to the dielectric loss. In addition to the information provided by the complex capacitance, the frequency-response analysis (obtained from Nyquist plots) and response-time data (phase vs. frequency plot data) [40] are relevant information concerning diffusive properties, internal resistance, and resistive-capacitive transitions. Figure 8 summarize EIS-based curves, revealing the relevant electrochemical properties of the electrodes. Nyquist plots in Figure 8a are composed of a small semicircle at a higher frequency followed by a straight line at a low frequency. The capacitive behavior of samples can be explored from the relative variation in the linear line slope at a low frequency, while the intersection with the x-axis provides the estimative about the internal resistance. Results indicate lower internal resistance for ZnCl 2 biochar (R = 0.55 Ω) against 0.86 Ω for KOH biochar. Regarding the slope in the low-frequency region, the inset of Figure 8a confirm a similar slope for both devices, indicating a minimal difference for diffusive transport along with the structures. Relative to the phase versus frequency dependence in the Bode plot (Figure 8b), an important parameter to be considered is the value of the phase angle that intercepts the y-axis. The values for ZnCl 2 -and KOH-based biochars are −77.13 • and −71.93 • , respectively, (the value of −90 • is expected for ideal capacitors), indicating that ZnCl 2 -based samples obtain the best properties for a capacitor. In addition, the typical behavior for the real part of capacitance was observed for both experimental systems with an increase from almost zero at higher frequencies to a maximum value at lower frequencies-characterizing a typical transition from resistive to capacitive behavior confirmed from the peak in the imaginary part of the capacitance. As shown in Figure 8c, confirming previous results from internal resistance and phase angle, the best performance in terms of the real part of capacitance at the quasi-stationary limit of frequency was observed for ZnCl2-based biochar with capacitance in order of 295 mF cm −2 in comparison with 143 mF cm −2 obtained for sample activated by KOH. The imaginary part of capacitance confirmed a breaking frequency established in the transition from resistive to capacitive behavior (values of 0.29 Hz and 0.62 Hz for ZnCl2 and KOH, respectively). The value of frequency at a maximum of C" was explored to estimate the time constant for charge/discharge-the calculated values were 3.44 s for ZnCl2-based biochar and 1.61 s for KOH-based biochar.
Based on the previous results, it was possible to observe that the best performance is attributed to samples prepared via ZnCl2, as indicated by lower internal resistance and higher modulus of phase angle at low frequency, which justifies the good performance in terms of the areal capacitance.
Complementary and standard characterizations were evaluated (cyclic voltammogram, charge-discharge curves, and impedance spectrum), which returned data to calculate the areal capacitance, power density, and energy density for experimental systems. Cyclic voltammograms for ZnCl2-SC and KOH-SC are shown in Figure 9a,b, respectively. From these curves, it is possible to note that the corresponding current observed for ZnCl2-SC devices at the same scan rate is higher than the observed for KOH-SC devices. It introduces direct consequences on the area enclosed in the curve, affecting the calculus of the resulting capacitance. For both experimental systems, a quasi-rectangular behavior was observed at a low scan rate. At increasing values of the scan rates, an evident change can be seen in the curve format that acquires a prolate behavior with a cone-shaped response at a high limit (200 mVs −1 ). According to Liu et al. [41], the abundance of oxygenated functional groups (OH, C=O, COOH) may enhance the pseudocapacitive of biochar-based electrodes, which justifies the prolate behavior in CV curves. In addition, the typical behavior for the real part of capacitance was observed for both experimental systems with an increase from almost zero at higher frequencies to a maximum value at lower frequencies-characterizing a typical transition from resistive to capacitive behavior confirmed from the peak in the imaginary part of the capacitance. As shown in Figure 8c, confirming previous results from internal resistance and phase angle, the best performance in terms of the real part of capacitance at the quasi-stationary limit of frequency was observed for ZnCl 2 -based biochar with capacitance in order of 295 mF cm −2 in comparison with 143 mF cm −2 obtained for sample activated by KOH. The imaginary part of capacitance confirmed a breaking frequency established in the transition from resistive to capacitive behavior (values of 0.29 Hz and 0.62 Hz for ZnCl 2 and KOH, respectively). The value of frequency at a maximum of C" was explored to estimate the time constant for charge/discharge-the calculated values were 3.44 s for ZnCl 2 -based biochar and 1.61 s for KOH-based biochar.
Based on the previous results, it was possible to observe that the best performance is attributed to samples prepared via ZnCl 2 , as indicated by lower internal resistance and higher modulus of phase angle at low frequency, which justifies the good performance in terms of the areal capacitance.
Complementary and standard characterizations were evaluated (cyclic voltammogram, charge-discharge curves, and impedance spectrum), which returned data to calculate the areal capacitance, power density, and energy density for experimental systems. Cyclic voltammograms for ZnCl 2 -SC and KOH-SC are shown in Figure 9a,b, respectively. From these curves, it is possible to note that the corresponding current observed for ZnCl 2 -SC devices at the same scan rate is higher than the observed for KOH-SC devices. It introduces direct consequences on the area enclosed in the curve, affecting the calculus of the resulting capacitance. For both experimental systems, a quasi-rectangular behavior was observed at a low scan rate. At increasing values of the scan rates, an evident change can be seen in the curve format that acquires a prolate behavior with a cone-shaped response at a high limit (200 mVs −1 ). According to Liu et al. [41], the abundance of oxygenated functional groups (OH, C=O, COOH) may enhance the pseudocapacitive of biochar-based electrodes, which justifies the prolate behavior in CV curves. The response of the devices at distinct current density was evaluated from galvanostatic charge-discharge, summarized in Figure 9c,d for samples ZnCl2-SC and KOH-SC, respectively. It is worth mentioning that the format and limiting values from these curves reveal important working mechanisms from respective devices [42][43][44]. Quasi-linear behavior was observed in the response of the supercapacitors, with a longer time interval for a complete charge-discharge cycle at lower current densities, as expected [42][43][44]. It is worth mentioning that a negligible IR drop was observed in the change from charge-discharge cycles, characterizing the low level of ohmic loss, an essential advantage in the overall energy storage process.
The reduced IR drop in both experimental systems can be confirmed from the low internal resistance of samples, as described in Figure 9a, with corresponding values of 0.55 Ω for ZnCl2-based and 0.86 Ω for KOH-based samples.
Data from CV and GCD curves were applied in Equations (5)- (7) to return values of areal capacitance (Car) and the Ragone plot, calculated as follows: From Equation (5), Dar is calculated from the area under the discharge curve, I is the current under the discharge process, V is the voltage window for the discharge curve, and A is the area of the device. The energy density (ED), given by Equation (6), is calculated from areal capacitance and the voltage window, while the power density (PD) considers the resulting energy density and the total time involved in the device's discharge.
Based on Equations (5)- (7) and the data in Figure 9, curves of areal capacitance and Ragone plot were obtained. As shown in Figure 10a, the areal capacitance for samples The response of the devices at distinct current density was evaluated from galvanostatic charge-discharge, summarized in Figure 9c,d for samples ZnCl 2 -SC and KOH-SC, respectively. It is worth mentioning that the format and limiting values from these curves reveal important working mechanisms from respective devices [42][43][44]. Quasi-linear behavior was observed in the response of the supercapacitors, with a longer time interval for a complete charge-discharge cycle at lower current densities, as expected [42][43][44]. It is worth mentioning that a negligible IR drop was observed in the change from charge-discharge cycles, characterizing the low level of ohmic loss, an essential advantage in the overall energy storage process.
The reduced IR drop in both experimental systems can be confirmed from the low internal resistance of samples, as described in Figure 9a, with corresponding values of 0.55 Ω for ZnCl 2 -based and 0.86 Ω for KOH-based samples.
Data from CV and GCD curves were applied in Equations (5)- (7) to return values of areal capacitance (C ar ) and the Ragone plot, calculated as follows: From Equation (5), D ar is calculated from the area under the discharge curve, I is the current under the discharge process, V is the voltage window for the discharge curve, and A is the area of the device. The energy density (E D ), given by Equation (6), is calculated from areal capacitance and the voltage window, while the power density (P D ) considers the resulting energy density and the total time involved in the device's discharge.
Based on Equations (5)- (7) and the data in Figure 9, curves of areal capacitance and Ragone plot were obtained. As shown in Figure 10a, the areal capacitance for samples ZnCl 2 -SC returned a better performance than the corresponding KOH-SC, with higher values for capacitance for all of the current densities. In the same direction, the areal capacitance calculated from the area under the CV curves confirmed that the best performance in the capacitance was observed for ZnCl 2 -based biochars for all scan rates (Figure 10b). The superior electrochemical performance was confirmed from the Ragone plot (see Figure 10c), in which it was possible to observe higher values for both energy density and power density for ZnCl 2 -based samples in comparison with corresponding KOH-based electrodes. In addition, points with different colors were introduced in Figure 10c to compare these values with those reported in the literature for corresponding experimental systems. As can be seen, our samples present good power density and competitive energy density in comparison with data in the literature. ZnCl2-SC returned a better performance than the corresponding KOH-SC, with higher values for capacitance for all of the current densities. In the same direction, the areal capacitance calculated from the area under the CV curves confirmed that the best performance in the capacitance was observed for ZnCl2-based biochars for all scan rates ( Figure  10b). The superior electrochemical performance was confirmed from the Ragone plot (see Figure 10c), in which it was possible to observe higher values for both energy density and power density for ZnCl2-based samples in comparison with corresponding KOH-based electrodes. In addition, points with different colors were introduced in Figure 10c to compare these values with those reported in the literature for corresponding experimental systems. As can be seen, our samples present good power density and competitive energy density in comparison with data in the literature. Degradation assays were evaluated for both experimental systems, in successive GCD assays in which a current of 5 mA was applied in symmetric supercapacitors (KOH-SC and ZnCl2-SC) with results summarized in Figure 10d. As can be seen, due to the prevailing contribution of carbon derivatives in both systems, a high retention degree in the capacitance was observed for ZnCl2-SC and KOH with increasing retention degree (negligible degradation) after 1000 cycles of charge/discharge at a high current density. Denmark observed a similar effect in supercapacitors based on molasses-based co-doped carbon with KOH as the electrolyte [42]. In the literature, this process is attributed to the delayed activation of the electrochemical properties of the device, since the electrochemical charge-discharge reactions progressively activated mechanisms in extra non-accessible sites being favored by the increasing wettability at the electrode/electrolyte interface (higher activation degree is observed for sample ZnCl2-as expected). These data confirm the high stability degree of the device in a basic electrolyte.  [45], purple circle-Ref. [46] and blue down triangle-Ref. [47]), (d) capacitive retention for ZnCl 2 −SC and KOH−SC at GCD curves acquired at a current of 5 mA.
Degradation assays were evaluated for both experimental systems, in successive GCD assays in which a current of 5 mA was applied in symmetric supercapacitors (KOH-SC and ZnCl 2 -SC) with results summarized in Figure 10d. As can be seen, due to the prevailing contribution of carbon derivatives in both systems, a high retention degree in the capacitance was observed for ZnCl 2 -SC and KOH with increasing retention degree (negligible degradation) after 1000 cycles of charge/discharge at a high current density. Denmark observed a similar effect in supercapacitors based on molasses-based co-doped carbon with KOH as the electrolyte [42]. In the literature, this process is attributed to the delayed activation of the electrochemical properties of the device, since the electrochemical charge-discharge reactions progressively activated mechanisms in extra non-accessible sites being favored by the increasing wettability at the electrode/electrolyte interface (higher activation degree is observed for sample ZnCl 2 -as expected). These data confirm the high stability degree of the device in a basic electrolyte.
The electrochemical characterization strongly indicated that the bark biochars exhibited satisfactory supercapacitor application performance. Although the nature of each carbon electrode is different, and each one of them has its advantages and drawbacks, here, we provided comparison data with other published works. Table 3 show the areal capacitance values for our bark biochar electrodes compared with other reported electrodes in the literature. According to Gou et al. [43], it is challenging to produce biomass carbon anodes for supercapacitors with high areal capacitance because many biomass precursors provide carbon anodes with areal capacitance lesser than 28 mF cm −2 . Therefore, developing economically feasible carbon materials with high areal capacitance is imperative to meet the demand of future applications in energy storage.
By Table 3, which compares the areal capacitance of some electrode material, it is possible to see that the areal capacitance for ZnCl 2 biochar is the second-highest among the listed electrodes in Table 3, showing to be very competitive biochar for employment in supercapacitors and perhaps in other electrochemical systems. ZnCl 2 biochar displayed an areal capacitance of 342 mF cm −2 at 5 A g −1 , while some graphene materials presented much less areal capacitance [44][45][46]. It is worth highlighting that the production costs for graphene are incredibly higher when compared to that of ZnCl 2 biochar. Consequently, if the production cost is added to the desirable properties, ZnCl 2 -activated spruce biochar could be classified as an excellent electrode material for supercapacitors with high areal capacitance.
Therefore, the valorization of spruce bark as a sustainable and green strategy to obtain porous and efficient anodes materials for high-performance supercapacitors represents a remarkable example of constructing highly sustainable energy storage devices.
The best performance of ZnCl 2 -based SCs in comparison with KOH-based can be considered as a conjunction of the several factors, described as follows: (i) The measured residual zinc in samples of ZnCl 2 Biochar, even at a small quantity, might influence the capacitance of the electrodes since Zn metal has a high theoretical capacity (820 mAh g −1 ) [51], which is more than double the theoretical capacity of graphite (372 mAh g −1 ); (ii) The morphology of ZnCl 2 -based biochars with a rich distribution of cavities and holes are driven forces that facilitate the permeation of electrolytes along with the electrodes, contributing to a more effective process of charge separation.
In addition to these aspects, the low internal resistance of material associated with the higher phase angle measured of ZnCl 2 -based biochar contributes to the overall best performance in areal capacitances and energy storage. It is a consequence of the higher mesoporosity of ZnCl 2 that facilitates the electrolyte permeation and charge accumulation in assembled supercapacitors.

Conclusions
The chemical activation of biochars for carbon derivatives is a critical step in developing more effective electrodes for supercapacitors. As commonly used activators, the electrochemical properties of biochars based on ZnCl 2 and KOH were evaluated, and the data was compared with the microstructure of the resulting materials. The higher mesoporosity degree was observed for samples activated by ZnCl 2 while widening micropore was obtained with KOH activation. Consequently, better capacitive properties associated with lower internal resistance were obtained for ZnCl 2 -based biochar that returned an areal capacitance in order of 342 mF cm −2 in comparison with 138.49 mF cm −2 for KOH-based biochar. The doping process with a residual zinc element and higher hydrophilic behavior for ZnCl 2 -based samples can be considered positive aspects that improve the performance of the mesopore-type supercapacitors. The results obtained in this work strongly suggest that the spruce bark can be considered a high-efficiency precursor for biobased electrode preparation to be employed in SCs.