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Article

Pistachio Shell-Derived Carbon Activated with Phosphoric Acid: A More Efficient Procedure to Improve the Performance of Li–S Batteries

by
Almudena Benítez
,
Julián Morales
and
Álvaro Caballero
*
Departamento de Química Inorgánica e Ingeniería Química, Instituto Universitario de Investigación en Química Fina y Nanoquímica, Facultad de Ciencias, Universidad de Córdoba, 14071 Córdoba, Spain
*
Author to whom correspondence should be addressed.
Nanomaterials 2020, 10(5), 840; https://doi.org/10.3390/nano10050840
Submission received: 9 April 2020 / Revised: 21 April 2020 / Accepted: 23 April 2020 / Published: 27 April 2020
(This article belongs to the Special Issue Novel Nanomaterials for Applications in Energy and Catalysis)
Browse Figures
Versions Notes

Abstract

:
A sustainable and low-cost lithium–sulfur (Li–S) battery was produced by reusing abundant waste from biomass as a raw material. Pistachio shell was the by-product from the agri-food industry chosen to obtain activated carbon with excellent textural properties, which acts as a conductive matrix for sulfur. Pistachio shell-derived carbon activated with phosphoric acid exhibits a high surface area (1345 m2·g−1) and pore volume (0.67 cm3·g−1), together with an interconnected system of micropores and mesopores that is capable of accommodating significant amounts of S and enhancing the charge carrier mobility of the electrochemical reaction. Moreover, preparation of the S composite was carried out by simple wet grinding of the components, eliminating the usual stage of S melting. The cell performance was very satisfactory, both in long-term cycling measurements and in rate capability tests. After the initial cycles required for cell stabilization, it maintained good capacity retention for the 300 cycles measured (the capacity loss was barely 0.85 mAh·g−1 per cycle). In the rate capability test, the capacity released was around 650 mAh·g−1 at 1C, a higher value than that supplied by other activated carbons from nut wastes.

Graphical Abstract

1. Introduction

Current energy challenges involve overcoming growing energy needs, climate change, and the increasing scarcity of resources. In the search for a competitive, clean, safe, and efficient energy storage system, the development of scientific studies of lithium–sulfur (Li–S) batteries for future commercialization is a key issue for many researchers [1]. Sulfur, the active material of the battery, has the following advantages: (i) It is very abundant in the earth’s crust, is an enormous residue from the petrochemical industry, and is a cheap material; (ii) it is non-toxic and environmentally friendly due to the fact that its production process is well-controlled industrially; and (iii) it is highly energetic in its reversible reaction with lithium [2], being able to supply a theoretical specific capacity of 1675 mAh·g−1 (corresponding to an energy density of ~2500 Wh·kg−1). However, Li–S batteries must overcome different obstacles to avoid capacity fading during cycling, such as the following [3]: (a) Sulfur and solid reduction products (Li2S2 and Li2S) are insulators, leading to poor electrochemical utilization of the element; (b) formation of intermediate polysulfide, causing severe changes in the volume on the cathode; and (c) dissolution in the electrolyte of some formed polysulfides (Li2Sx, 2 ≤ x ≤ 8), giving rise to the shuttle phenomenon that causes loss of active material and coulombic efficiency. Several strategies [4,5,6,7] have been investigated to reduce the shuttle effect, such as the use of modified separators [8,9,10,11,12], interlayers [13,14,15], solid-polymer electrolytes [16], or the addition of LiNO3 in the electrolyte that passivates the lithium surface and mitigates the problems that take place in the anode. However, the use of porous carbonaceous materials in the positive electrode constitute an excellent matrix for the immobilization of sulfur and entrapment of polysulfides, such as carbon nanotubes [17], carbon nanofibers [18,19,20], carbon flowers [21], graphene [22,23,24,25,26], graphene doped with heteroatoms [27,28], graphene oxide [29], ordered mesoporous carbons [30,31,32], and metal oxide–carbon composites [33]. Unfortunately, most synthetic procedures for these materials are complex and require expensive and non-renewable raw materials, a drawback for large-scale applications.
Porous or activated carbons (ACs) might be an alternative to these more complex systems [34]. In this context, biomass-derived carbon has been widely studied as a promising sulfur host due to its natural abundance, simple and eco-friendly preparation, and low cost. Furthermore, depending on their origin, these easily accessible active carbons have different morphologies and structural properties [35,36]. Thus, a wide variety of waste materials can be used as a matrix to accommodate sulfur, providing a second life to agri-food waste and, at the same time, improving the performance of Li–S batteries, among which it is worth highlighting peanut shell [37], bamboo [38], coconut shell [39], walnut shell [40] with surface hydroxyl groups, or coffee waste with O- and N-doped groups [41]. In addition, their high surface area, large pore volume, and good conductivity have given these materials the proper characteristics to be used as bio-templates to host sulfur and as a separator for preventing the shuttle effect [35].
Our main goal in meeting the challenge of using a sustainable, economical, and renewable source was to research only abundant, nearby, and non-edible sources to improve energy storage systems by reusing waste without having to rely on primary sources. In previous studies, our group revalued the agri-food residues with the highest production in Spain, such as olive stones [42,43,44], cherry pits [45], and almond shells [46]. However, the cultivation of pistachio is becoming very fashionable, and large amounts of shells are currently also generated after consumption. According to the statistics presented by the Food and Agriculture Organization (FAO), in 2018, a total of approximately 1300 kilotons of pistachio were produced in the world, of which 550 kilotons were harvested in Iran (the largest producer in addition to the USA) [47]. During the processing of this crop, a high quantity of residues in the form of shell is generated (equivalent to 45% by weight on average of its production) [48], giving rise to a total of 585 kilotons of pistachio shells in the world during that year. For these reasons, the valorization of pistachio shells (PSs) is crucial to achieving sustainable processing. Thus, PSs were chemically activated with phosphoric acid to obtain AC with optimal textural properties for application in Li–S batteries. Additionally, its porous structure favors penetration of the electrolyte, the entrapment of polysulfides, and the diffusion of ions through the matrix. Herein, we report the electrochemical results obtained using pistachio shell-derived activated carbon (PSAC) as a conductive and renewable matrix. To our knowledge, the use of PSAC in Li–S cells has recently been reported by Chen et al. [49], using activation by ZnCl2. This activating agent, together with KOH and H3PO4, is the most used in the chemical activation of biomass-derived carbons. However, the use of ZnCl2 usually involves the formation of ZnO as an impurity, and its elimination requires subsequent treatment with HCl [50]. Here, as an activating agent, we used H3PO4, which has been preferably used in the activation of many lignocellulosic materials [51]. The reason for this is the ability of H3PO4 to generate P-containing functional groups in the carbon matrix, which are suitable for inducing the formation of micropores in the carbon, beneficial for use in electrochemical energy storage devices [52]. We previously reported the use of H3PO4 to activate carbon derived from cherry pits and its application in a Li–S battery [45]. The performance of the electrode when the pistachio carbon was activated with H3PO4 was notably better than that already reported for PSAC activated with ZnCl2. The presence of impurities and possibly the different pore systems generated by both agents might be the cause of the differences found.

2. Materials and Methods

2.1. Material and Electrode Preparation

Fresh pistachio shells generated in Spanish crops were used in this study, without any prior treatment. Firstly, pistachio shells were ground in a ball mill (Restch PM100, Retsch GmbH, Haan, Germany) at 500 rpm for 4 h, with reversal of rotation every 15 min. Once a fine powder was obtained, the residue was treated with phosphoric acid (85%, Sigma-Aldrich, San Luis, CA, USA). This treatment was carried out by mixing PS and H3PO4 in a 1:1 ratio by weight. In detail, 10 g of PS were added to 40 mL of a 3 M H3PO4 aqueous solution, and this mixture was maintained under constant stirring at 85 °C until a paste was formed in approximately 3 h. Subsequently, the sample was dried at 120 °C overnight, ground in a manual mortar, and pyrolyzed in a tubular furnace (Carbolite Gero CTF, Parsons Lane, Hope Valley, UK) at 800 °C under a nitrogen atmosphere using a flow of 50 mL·min−1 for 4 h to ensure successful carbonization of this material, as was demonstrated in our previous work [46]. Later, the pyrolyzed sample was washed several times with distilled water until obtaining a neutral pH and dried again at 120 °C for 12 h. After homogenization of the sample, it was denoted as PSAC.
The second step was the preparation of the activated carbon/sulfur composite (PSAC@S) using a simple and easily scalable process. A planetary ball mill (Restch PM100, Retsch GmbH, Haan, Germany) was used to mix PSAC and sulfur in a mass ratio of 3:7 with ethanol as a solvent. The wet milling process was carried out at 300 rpm for 3 h, without rest time, to achieve excellent sulfur impregnation. After this process, the obtained product was dried at 50 °C overnight and then ground in a mortar.
Finally, the positive electrodes were prepared by mixing 80 wt.% of the as-prepared PSAC@S composite, 10 wt.% of the conductive agent (Super P carbon, Timcal, Bironico, Switzerland), and 10 wt.% of polyvinylidene fluoride (PVDF 6020, Solvay, Brussels, Beligum) as a binder in N-methyl-2-pyrrolidone (NMP, Sigma-Aldrich) in a manual mortar until a homogeneous slurry was formed. Then, the slurry was casted on a carbon cloth (GDL, ELAT LT1400W, MTI Corp., Richmond, USA) as a current collector by the doctor blade (MTI Corp.) technique. GDL carbon cloth has been reported as an effective current collector for carbon–sulfur composites of Li–S cells [53]. After drying, the electrodes were punched into 13 mm diameter discs (1.33 cm2 geometric surface). Subsequently, the cathode discs were further dried in a vacuum oven (Buchi, Flawil, Switzerland) at 45 °C for 3 h to guarantee the absence of oxygen and humidity in the electrodes. The sulfur loading was ca. 2.5 mg·cm–2. The diagram shown in Scheme 1 summarises the sequential steps used for the preparation of the Li–S cells based on pistachio shell-derived carbon/sulfur composite.

2.2. Material Characterization

The structural and textural properties of the as-fabricated materials were analyzed by different characterization techniques. X-ray diffraction (XRD) was used to study the structures, and the patterns were obtained through a Bruker D8 Advance diffractometer equipped with a Cu Kα source (λ = 1.5406 Å) at 40 kV and 40 mA over the 2θ range of 5° to 80° at a rate of 1.05 s per step with a step size of 0.04°. Raman spectra were recorded with a confocal Raman spectrometer (alpha500, WITec, Ulm, Germany). A frequency-doubled Nd:YAG laser at 532 nm (second harmonic generation) was used for excitation. The laser beam was focused on the sample using a 20×/0.4 Zeiss objective. Thermogravimetric analysis was carried out using a Mettler Toledo-TGA/DSC with a heating rate of 10 °C min−1 under N2 atmosphere in the range between 30 and 1000 °C for the sample of fresh pistachio shell, in a N2 or O2 atmosphere from 30 to 800 °C for PSAC and in a nitrogen atmosphere in the range of 30–600 °C for the PSAC@S composite. A nitrogen adsorption–desorption isotherm was obtained on an Autosorb iQ/ASiQwin (Quantachrome Instruments, Anton Paar GmbH, Graz, Austria). Specific surface areas were determined by the Brunauer–Emmett–Teller (BET) method. Total pore volumes (VT) were determined according to the amount adsorbed at a relative pressure (P/P0) of 0.995. Pore size distributions were calculated by the density functional theory (DFT) method applied to the adsorption branch of the isotherms. The micropore surface area and volume were estimated by the t-plot method.

2.3. Cell Assembly and Electrochemical Measurements

To explore the electrochemical behavior of the working electrode, coin-type CR2032 cells were assembled inside an Ar-filled glove box (M-Braun 150, M-Braun, Garching, Germany). Lithium metal foil (Li, Gelon Lib, Qingdao, China; 15.6 mm diameter and 0.25 mm thickness) served as the counter and reference electrodes. A polyethylene membrane (PE, 25 µm thick, Celgard 2400, Charlotte, NC, USA) was used as a separator, and it was soaked in 50 μL of the electrolyte solution and dried at 80 °C under vacuum overnight prior to use. The electrolyte was 1 M LiTFSI with 0.4 M LiNO3 in in 1,3-dioxolane (DOL, Sigma Aldrich) and 1,2-dimethoxyethane (DME, Sigma Aldrich) (1:1 v/v). The electrochemical process was studied by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements, which were performed using the Autolab PGSTAT-204 (Metrohm, Herisau, Switzerland) equipment. In order to calculate the lithium-ion diffusion coefficients, additional CV measurements were recorded at variable rates of 0.1, 0.2, 0.4, 0.8, and 1.0 mV·s−1 between 1.8 and 2.8 V vs. Li/Li+. EIS measurements were taken at the open-circuit voltage (OCV) and after five CV cycles in the 500 kHz to 100 mHz frequency range using a 10 mV amplitude signal. Galvanostatic cycling tests were performed on an Arbin BT2143 (Arbin Instruments, College Station, USA) within the potential window of 1.8–2.6 V at a constant current of C/10 (1 C = 1675 mA·gS−1) over 300 cycles. Rate capability tests were performed at C/10, C/8, C/5, C/3, C/2, 1C, and 2C rates.

3. Results and Discussion

Knowledge of the carbon composition was obtained from thermogravimetric measurements carried out under different atmospheres (Figure 1). To prepare the activated carbon, a temperature of 800 °C was selected according to the thermogram registered for the fresh pistachio shell in inert atmosphere (Figure 1a). The weight loss values of AC (Figure 1a) were 94% and 14% when heated to 800 °C in an O2 and N2 atmosphere, respectively. This means that both the ash and functional group content was low and, consequently, the impurity content was relatively low. The functional groups presented in these H3PO4-activated carbons obtained from biomass [54], mainly associated with O and H, would be responsible for the slowness in the weight loss observed (between 400 and 800 °C) compared to the highly graphitized carbons [55] or the graphite itself [56], the weight loss of which is more abrupt and occurs between 550 and 700 °C. The high degree of carbon structural disorder was demonstrated by two complementary techniques: XRD and Raman spectroscopy. The XRD pattern exhibited two broad, weak peaks, typical of highly disordered carbons (Figure 1b). The spacing of the (002) reflection is around 3.68 Å, higher than 3.44 Å, a limit value that allows calculation of the graphitization degree of C [57]. As these carbons are hard carbons, this model would not be applicable. As expected, the XRD of the PSAC@S composite exhibited numerous peaks, all assignable to the S orthorhombic phase. The C signal was barely noticeable because it was found as a minor component. Figure 1c shows the Raman spectra of the PSAC and PSAC@S composite recorded between 200 and 2000 cm−1. Two characteristic peaks could be found for both samples. The D band at 1340 cm−1 can be assigned to the defects and disorder [58], while the G band at 1595 cm−1 corresponds to the presence of sp2 hybridized carbon [59]. This is a typical characteristic of the activated carbon [60]. The peak height ratio of ID/IG was 1.03, indicating that the graphitization phase plays a big role in the as-prepared carbon from the pistachio shell [61], which can promote the electrical conductivity of PSAC [62]. After sulfur permeation, the ID/IG ratio value remained unchanged, indicating that the structure of the activated carbon was modified during the melt-diffusion process. The Raman spectrum of the PSAC@S composite showed no characteristic peaks of sulfur at approximately 200 and 460 cm−1, which implies that crystalline sulfur was successfully embedded into the pore structure of carbon material. The absence of sulfur peaks may be due to interferences of carbon micro-mesopores in the Raman signals of encapsulated S [63], as similarly reported for other sulfur-based composites with highly porous biomass-derived carbons [39,64].
The S content in the PSAC@S composite was obtained from TGA measurements (Figure 1a). Up to around 160 °C, weight loss is attributed to the physisorbed and chemisorbed solvents (e.g., residual water and ethanol). The remainder, around 70%, would correspond to S sublimation. This loss occurs in two steps, as suggested by the change in slope at ca. 273 °C. This behavior is similar to that found in other microporous materials, such as metal–organic frameworks (MOFs) [65] and in ZnCl2-activated pistachio carbon itself [49]. This means that there would be two types of interactions between S and the host matrix. Some authors [65] have suggested that S sublimated at temperatures below 273 °C would be physisorbed S and chemisorbed S of a higher temperature. In the case of microporous carbons, there is an alternative explanation, assigning the loss at low temperature to S deposited on the external surface of C. From 273 °C, nanoparticles confined in the micropores would sublimate [66]. In both cases, additional measurements are necessary to verify these models.
The N2 adsorption/desorption isotherms are shown in Figure 1d. The shape of the adsorption isotherm is typical of microporous solids belonging to type I of the BDDT classification. The presence of a small hysteresis loop in the desorption curve would be due to the presence of mesopores in the C texture. Hence, the PSAC sample possesses a dual pore system that is beneficial both for electrolyte impregnation and for the mobility of Li+ ions between the electrodes. The BET surface was 1345 m2 g–1, and the total pore volume was 0.67 cm3·g−1. The t-plot analysis indicated that a significant fraction of the carbon surface area (973 m2·g−1) and pore volume (0.4 cm3·g−1) was associated with the presence of micropores. Regarding the size of the pores, values of 1.6–3.8 nm were deduced from the DFT representation, indicative of the expected dual pore system. The surface of our carbon was greater than that obtained by Chen et al. [49] (1149 m2·g−1). Although the value of the total pore volume was not given, the pore size was less than 2 nm, even though the representation seems to correspond to the application of the Joyner–Barret–Halenda (JBH) method, which is applicable to mesoporous solids. The differences could be due to both the different activator used, ZnCl2, and the heating temperature, 550 °C.
Cyclic voltammograms recorded at different scan rates (0.1–1 mV·s−1) are shown in Figure 2a. The common feature is the presence of two peaks during the cathodic scan (2.34 and 1.99 V at 0.1 mV·s–1), caused by the reduction of S to high- (Li2Sx, 4 ≤ x ≤ 8) and low-order (Li2S2 and Li2S) polysulfides, respectively. The reaction mechanism has been thoroughly investigated by applying the operando X-ray diffraction and Raman spectroscopy [67,68,69]. The corresponding oxidation peaks appeared at about 2.39 and 2.44 V due to the slight hysteresis of the reversible redox reaction [70,71,72]. As expected, there were small shifts in the peak potential due to the change in scan rate, which form the basis of the Randles–Sevcik equation for calculating the diffusion coefficient of the Li+ ion, as follows:
IP = 2.69 ×105 n3/2 A DLi0.5 υ0.5 CLi
where IP is the peak current, n is the number of electron transfers in the reaction, A is the electrode geometric area, υ is the scan rate, and CLi is the concentration of lithium ions in the electrolyte. The relationship of IP vs. υ0.5 is shown in Figure 2b. From the slope of these plots and Equation (1), the DLi values of the two cathodic peaks were 1.6 × 10–9 (C1) and 2.6 × 10–10 (C2) cm2·s–1, and of the anodic peak, the value was 5.8 × 10–9 (A) cm2·s–1. These values are comparable to those calculated for other systems [73,74] and somewhat lower than those obtained in a semi-liquid cell using a Li2S8 catholyte instead of S as the active material [75].
To shed some additional light on the electrochemical process, EIS spectra of the cell were recorded before and after the 1st cycle. The Nyquist plots are shown in Figure 2a, and, as expected, a similar value for the electrolyte resistance (Re), between 4 and 5 Ω, was deduced from the cut of the x-axis at high frequencies. At high-medium frequencies, a semicircle was observed, related to the electrode/electrolyte interphase, the resistance of which was around 27.2 and 6.5 Ω before and after cycling, respectively. This decrease has been observed in other works [71,74] and has been ascribed to the proper change in the electrode due to cycling. Once the electrode is activated, the low resistance value is consistent with both suitable mobility of the charge carriers at the electrode/electrolyte interphase and satisfactory kinetics of the commented redox reactions. The behavior of our activated carbon was somewhat different from that reported by Chen et al. [49], where carbon was activated with ZnCl2. The Nyquist plot profile for the pristine electrode was similar but with an electrode resistance somewhat higher (40 Ω). However, a more complex Nyquist plot was obtained for the cycled cell. In the high-medium frequency region, two semicircles with resistances of around 31 and 41 Ω were observed. These data are simply an example of the many factors that affect the electrochemical reaction. When the pistachio carbon is not activated [56], the EIS spectrum is more complex, considerably increasing the resistance of the interface, approaching 100 Ω. In addition, this resistance increases as the electrode is cycled.
Figure 3a shows the charge/discharge curves for different cycles recorded at C/10 (C = 1675 mA·g−1) between 2.6 and 1.8 V. Below this voltage, another reduction process begins, probably associated with the electrolyte decomposition. Hence, we have chosen to limit the voltage window at the detriment of the specific capacity values. The two plateaus of the discharge curves, ca. 2.31 and 2.06, reflect the two stages of the conversion of S into Li2S2/Li2S, as was previously discussed for the CV curves. The charge curves also show two plateaus with less polarization between them, corresponding to the inverse reaction (origin of the peak broadening observed for the CV curve). The cycling properties of the electrode are shown in Figure 3b. The delivered capacity in the first discharge, 1193 mAh·g−1, sharply decreased in the first twenty cycles to 808 mAh·g−1. From this cycle, the capacity retention significantly improved, and at the 300th cycle, the last cycle tested, the retention capacity was 570 mAh·g−1, which means an average capacity loss of 0.85 mAh·g−1 per cycle. The fluctuation in the coulombic efficiency values was less, with an average value of around 98%.
The study of the performance of the electrode was complemented with measures of rate capability between C/10 and 2C. A discharge/charge curve at each rate selected as an example is shown in Figure 4a. As expected, a gradual decrease in the delivered capacity was observed with increasing rate (average capacity of 1063, 935, 888, 817, 753, and 646 mAh·g−1 at C/10, C/8, C/5, C/3, C/2, and 1C, respectively). In contrast, at 2C, the drop was abrupt, and the cell barely delivered 70 mAh·g−1 (Figure 4b). The decrease is a consequence of the increased voltage gap (∆E) between the charge and discharge processes, parallel to the increase in the rate caused by the sluggishness of the electrochemical process, especially at high rates. ∆E varied from 0.17 to 0.50 V when changing from C/10 to 1C. For 2C, the value was 0.7 V, which is very close to the voltage window used. Despite the poor performance of the electrode at 2C, when the current was lowered back to the pristine value of C/10 during the rate capability test, the electrode maintained a high average capacity of ca. 808 mAh·g–1.
Throughout this section, we have made several comparisons between the behavior of our activated carbon and that recently published by Chen et al. [49]. We have extended this comparison to the electrochemical data collected in Table 1. Apart from the differences in the preparation method, which leads to different textural properties, two differences directly related to the electrochemical response of the electrode must be highlighted: S loading and the voltage window. The S loading of our electrode was almost three times higher. In contrast, the voltage window was almost half less. A higher S content of the electrode would decrease the specific capacity due to the insulating nature of the element, among other reasons. However, the objective of these investigations was to increase the S content so that the delivered energy by the cell would increase. Expanding the voltage window would increase the specific capacity, but in this option, we must be very cautious due to the presence of side reactions, most likely with electrolyte decomposition. In fact, after finishing the low-voltage plateau, the discharge curves included in the reference [49] fell less steeply than that observed in Figure 3a. From 1.8 to 1.5 V, the calculated discharge overcapacity was ca. 200 mAh·g−1. Something similar occurred in the charge curve between 2.6 and 3.0 V, detecting an overcharge capacity somewhat lower (70 mAh·g−1). Consequently, by making this correction, the capacity values would be lower. Even without this correction, the performance of the electrode made with our activated carbon was better than that obtained by Chen et al. [49], as confirmed by the higher capacity values obtained, not only in the prolonged cycling test (although recorded at different rates) but also in the results of rate capability, which were, in this case, measured at the same current rates. We believe that the cause may lie not only in the different method of preparing the carbon, but also in a higher incidence of other factors related to the electrochemical measurements. It would be very beneficial for the scientific community if we standardized the conditions of the electrochemical measurements, such as the electrode composition, voltage windows, electrolyte concentration, and current collector, to avoid divergent measurements for materials of similar textural and structural characteristics, such as the carbon studied here.
Finally, capacity values derived from rate capability measurements of carbons obtained from different dried fruit shells, specifically nuts, are collected in Figure 5 [46,49,76,77]. The capacity released by our carbon is among the highest, for both low and high current rates. These results show that carbon from pistachio shells combined with the use of H3PO4 as an activating agent can be a promising material for future scaled-up Li–S batteries, with an important contribution from circular economy and sustainability models.

4. Conclusions

In summary, highly porous carbon as an efficient host material for a sulfur cathode was successfully prepared through H3PO4-based activation and simple carbonization of pistachio shells. The hierarchical and bimodal micro-mesoporous structure with high specific surface area and large pore volume, as well as residuary functional groups, can significantly limit the shuttle effect of polysulfide through a combination of physical and chemical adsorptions, which enhances sulfur utilization, promotes the reaction kinetics, and allows for remarkable rate capability and long-cycling stability for the assembled Li–S batteries. This work provides a low-cost, eco-friendly, and simple strategy for the preparation of sustainable host materials for high-performance Li–S batteries using natural biomass as a precursor.

Author Contributions

Conceptualization, Á.C.; methodology, A.B.; investigation, A.B.; writing—original draft preparation, A.B. and J.M.; writing—review and editing, Á.C.; supervision, Á.C. and J.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Ministerio de Economía y Competitividad (Project MAT2017-87541-R) and Junta de Andalucía (Group FQM-175).

Acknowledgments

A. Benítez thanks the financial support from Cordoba University (Plan Propio de Investigación 2019; Sub. 2.4.). The authors wish to acknowledge the technical staff from the Instituto Universitario de Nanoquímica (IUNAN) of the Cordoba University. The authors greatly acknowledge support from Ángela López-Lorente (Department of Analytical Chemistry, UCO) in this work.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Zhu, K.; Wang, C.; Chi, Z.; Ke, F.; Yang, Y.; Wang, A.; Wang, W.; Miao, L. How far away are lithium-sulfur batteries from commercialization? Front. Energy Res. 2019, 7, 1–12. [Google Scholar] [CrossRef]
  2. Xu, J.; Ma, J.; Fan, Q.; Guo, S.; Dou, S. Recent progress in the design of advanced cathode materials and battery models for high-performance lithium-X (X = O2, S, Se, Te, I2, Br2) batteries. Adv. Mater. 2017, 29, 1606454. [Google Scholar] [CrossRef] [PubMed]
  3. Manthiram, A.; Fu, Y.; Chung, S.-H.; Zu, C.; Su, Y.-S. Rechargeable lithium–sulfur batteries. Chem. Rev. 2014, 114, 11751–11787. [Google Scholar] [CrossRef] [PubMed]
  4. Chien, Y.-C.; Pan, R.; Lee, M.-T.; Nyholm, L.; Brandell, D.; Lacey, M.J. Cellulose separators with integrated carbon nanotube interlayers for lithium-sulfur batteries: An investigation into the complex interplay between cell components. J. Electrochem. Soc. 2019, 166, A3235–A3241. [Google Scholar] [CrossRef]
  5. Zhang, M.; Chen, W.; Xue, L.; Jiao, Y.; Lei, T.; Chu, J.; Huang, J.; Gong, C.; Yan, C.; Yan, Y.; et al. Adsorption-catalysis design in the lithium-sulfur battery. Adv. Energy Mater. 2020, 10, 1903008. [Google Scholar] [CrossRef]
  6. He, J.; Manthiram, A. Long-life, high-rate lithium–sulfur cells with a carbon-free VN host as an efficient polysulfide adsorbent and lithium dendrite inhibitor. Adv. Energy Mater. 2020, 10, 1903241. [Google Scholar] [CrossRef]
  7. He, J.; Manthiram, A. A review on the status and challenges of electrocatalysts in lithium-sulfur batteries. Energy Storage Mater. 2019, 20, 55–70. [Google Scholar] [CrossRef]
  8. Song, Y.; Zhao, S.; Chen, Y.; Cai, J.; Li, J.; Yang, Q.; Sun, J.; Liu, Z. enhanced sulfur redox and polysulfide regulation via porous VN-modified separator for Li–S batteries. ACS Appl. Mater. Interfaces 2019, 11, 5687–5694. [Google Scholar] [CrossRef]
  9. Fang, D.; Wang, Y.; Liu, X.; Yu, J.; Qian, C.; Chen, S.; Wang, X.; Zhang, S. Spider-web-inspired nanocomposite-modified separator: Structural and chemical cooperativity inhibiting the shuttle effect in Li-S batteries. ACS Nano 2019, 13, 1563–1573. [Google Scholar] [CrossRef]
  10. Li, N.; Xie, Y.; Peng, S.; Xiong, X.; Han, K. Ultra-lightweight Ti3C2T MXene modified separator for Li–S batteries: Thickness regulation enabled polysulfide inhibition and lithium ion transportation. J. Energy Chem. 2020, 42, 116–125. [Google Scholar] [CrossRef] [Green Version]
  11. Sun, Z.; Wu, X.; Peng, Z.; Wang, J.; Gan, S.; Zhang, Y.; Han, D.; Niu, L. Compactly coupled nitrogen-doped carbon nanosheets/molybdenum phosphide nanocrystal hollow nanospheres as polysulfide reservoirs for high-performance lithium–sulfur chemistry. Small 2019, 15, 1902491. [Google Scholar] [CrossRef]
  12. Wu, F.; Zhao, S.; Chen, L.; Lu, Y.; Su, Y.; Jia, Y.; Bao, L.; Wang, J.; Chen, S.; Chen, R. Metal-organic frameworks composites threaded on the CNT knitted separator for suppressing the shuttle effect of lithium sulfur batteries. Energy Storage Mater. 2018, 14, 383–391. [Google Scholar] [CrossRef]
  13. Paolella, A.; Demers, H.; Chevallier, P.; Gagnon, C.; Girard, G.; Delaporte, N.; Zhu, W.; Vijh, A.; Guerfi, A.; Zaghib, K. A platinum nanolayer on lithium metal as an interfacial barrier to shuttle effect in Li-S batteries. J. Power Sources 2019, 427, 201–206. [Google Scholar] [CrossRef]
  14. Paolella, A.; Laul, D.; Timoshevskii, V.; Zhu, W.; Marras, S.; Bertoni, G.; Wahba, A.S.; Girard, G.; Gagnon, C.; Rodrigue, L.; et al. The role of metal disulfide interlayer in Li–S batteries. J. Phys. Chem. C 2018, 122, 1014–1023. [Google Scholar] [CrossRef]
  15. Yuan, H.; Peng, H.-J.; Li, B.-Q.; Xie, J.; Kong, L.; Zhao, M.; Chen, X.; Huang, J.-Q.; Zhang, Q. Conductive and catalytic triple-phase interfaces enabling uniform nucleation in high-rate lithium-sulfur batteries. Adv. Energy Mater. 2019, 9, 1802768. [Google Scholar] [CrossRef]
  16. Marceau, H.; Kim, C.-S.; Paolella, A.; Ladouceur, S.; Lagacé, M.; Chaker, M.; Vijh, A.; Guerfi, A.; Julien, C.M.; Mauger, A.; et al. In operando scanning electron microscopy and ultraviolet–visible spectroscopy studies of lithium/sulfur cells using all solid-state polymer electrolyte. J. Power Sources 2016, 319, 247–254. [Google Scholar] [CrossRef]
  17. Patel, M.D.; Cha, E.; Kang, C.; Gwalani, B.; Choi, W. High performance rechargeable Li-S batteries using binder-free large sulfur-loaded three-dimensional carbon nanotubes. Carbon 2017, 118, 120–126. [Google Scholar] [CrossRef]
  18. Zeng, L.; Pan, F.; Li, W.; Jiang, Y.; Zhong, X.; Yu, Y. Free-standing porous carbon nanofibers–sulfur composite for flexible Li–S battery cathode. Nanoscale 2014, 6, 9579–9587. [Google Scholar] [CrossRef] [PubMed]
  19. Wei, B.; Shang, C.; Pan, X.; Chen, Z.; Shui, L.; Wang, X.; Zhou, G. Lotus root-like nitrogen-doped carbon nanofiber structure assembled with VN catalysts as a multifunctional host for superior lithium–sulfur batteries. Nanomaterials 2019, 9, 1724. [Google Scholar] [CrossRef] [Green Version]
  20. Liu, Y.; Han, D.; Wang, L.; Li, G.; Liu, S.; Gao, X. NiCo2O4 nanofibers as carbon-free sulfur immobilizer to fabricate sulfur-based composite with high volumetric capacity for lithium–sulfur battery. Adv. Energy Mater. 2019, 9, 1803477. [Google Scholar] [CrossRef]
  21. Moreno, N.; Caballero, A.; Morales, J.; Agostini, M.; Hassoun, J. Lithium battery using sulfur infiltrated in three-dimensional flower-like hierarchical porous carbon electrode. Mater. Chem. Phys. 2016, 180, 82–88. [Google Scholar] [CrossRef]
  22. Zhao, M.-Q.; Liu, X.-F.; Zhang, Q.; Tian, G.-L.; Huang, J.-Q.; Zhu, W.; Wei, F. Graphene/single-walled carbon nanotube hybrids: One-step catalytic growth and applications for high-rate Li–S batteries. ACS Nano 2012, 6, 10759–10769. [Google Scholar] [CrossRef] [PubMed]
  23. Zhang, Y.; Bakenov, Z.; Tan, T.; Huang, J. Three-dimensional hierarchical porous structure of PPy/porous-graphene to encapsulate polysulfides for lithium/sulfur batteries. Nanomaterials 2018, 8, 606. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Li, H.; Sun, L.; Wang, Z.; Zhang, Y.; Tan, T.; Wang, G.; Bakenov, Z. Three-dimensionally hierarchical graphene based aerogel encapsulated sulfur as cathode for lithium/sulfur batteries. Nanomaterials 2018, 8, 69. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Jin, K.; Zhou, X.; Liu, Z. Graphene/sulfur/carbon nanocomposite for high performance lithium-sulfur batteries. Nanomaterials 2015, 5, 1481–1492. [Google Scholar] [CrossRef]
  26. Benítez, A.; Di Lecce, D.; Elia, G.A.; Caballero, Á.; Morales, J.; Hassoun, J. A lithium-ion battery using a 3 D-array nanostructured graphene–sulfur cathode and a silicon oxide-based anode. ChemSusChem 2018, 11, 1512–1520. [Google Scholar] [CrossRef] [Green Version]
  27. Benítez, A.; Di Lecce, D.; Caballero, Á.; Morales, J.; Rodríguez-Castellón, E.; Hassoun, J. Lithium sulfur battery exploiting material design and electrolyte chemistry: 3D graphene framework and diglyme solution. J. Power Sources 2018, 397, 102–112. [Google Scholar] [CrossRef]
  28. Chen, Z.; Sun, Z.; Zhang, Y.; Tan, T.; Tian, Y.; Chen, Z. Novel sulfur/ethylenediamine-functionalized reduced graphene oxide composite as cathode material for high-performance lithium-sulfur batteries. Nanomaterials 2018, 8, 303. [Google Scholar] [CrossRef] [Green Version]
  29. Tian, Y.; Sun, Z.; Zhang, Y.; Wang, X.; Bakenov, Z.; Yin, F. Micro-spherical sulfur/graphene oxide composite via spray drying for high performance lithium sulfur batteries. Nanomaterials 2018, 8, 50. [Google Scholar] [CrossRef] [Green Version]
  30. Moreno, N.; Agostini, M.; Caballero, A.; Morales, J.; Hassoun, J. A long-life lithium ion sulfur battery exploiting high performance electrodes. Chem. Commun. 2015, 51, 14540–14542. [Google Scholar] [CrossRef]
  31. Moreno, N.; Caballero, A.; Hernán, L.; Morales, J.; Canales-Vázquez, J. Ordered mesoporous carbons obtained by a simple soft template method as sulfur immobilizers for lithium–sulfur cells. Phys. Chem. Chem. Phys. 2014, 16, 17332–17340. [Google Scholar] [CrossRef] [PubMed]
  32. Tesio, A.Y.; Arias, A.N.; Morales, J.; Planes, G.A.; Caballero, A. Versatility of a Nitrogen-containing monolithic porous carbon for lithium-based energy storage. ChemistrySelect 2018, 3, 8560–8567. [Google Scholar] [CrossRef] [Green Version]
  33. He, J.; Luo, L.; Chen, Y.; Manthiram, A. Yolk-Shelled C@Fe3O4 Nanoboxes as efficient sulfur hosts for high-performance lithium-sulfur batteries. Adv. Mater. 2017, 29, 1702707. [Google Scholar] [CrossRef]
  34. Díez, N.; Ferrero, G.A.; Sevilla, M.; Fuertes, A.B. A simple and general approach for in situ synthesis of sulfur–porous carbon composites for lithium–sulfur batteries. Sustain. Energy Fuels 2019, 3, 3498–3509. [Google Scholar] [CrossRef] [Green Version]
  35. Yuan, H.; Liu, T.; Liu, Y.; Nai, J.; Wang, Y.; Zhang, W.; Tao, X. A review of biomass materials for advanced lithium–sulfur batteries. Chem. Sci. 2019, 10, 7484–7495. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Liedel, C. Sustainable battery materials from biomass. ChemSusChem 2020, 92, 455–459. [Google Scholar] [CrossRef] [PubMed]
  37. Zhou, J.; Guo, Y.; Liang, C.; Yang, J.; Wang, J.; Nuli, Y. Confining small sulfur molecules in peanut shell-derived microporous graphitic carbon for advanced lithium sulfur battery. Electrochim. Acta 2018, 273, 127–135. [Google Scholar] [CrossRef]
  38. Yan, Y.; Shi, M.; Wei, Y.; Zhao, C.; Carnie, M.; Yang, R.; Xu, Y. Process optimization for producing hierarchical porous bamboo-derived carbon materials with ultrahigh specific surface area for lithium-sulfur batteries. J. Alloys Compd. 2018, 738, 16–24. [Google Scholar] [CrossRef] [Green Version]
  39. Chen, Z.-H.; Du, X.-L.; He, J.-B.; Li, F.; Wang, Y.; Li, Y.-L.; Li, B.; Xin, S. Porous coconut shell carbon offering high retention and deep lithiation of sulfur for lithium–sulfur batteries. ACS Appl. Mater. Interfaces 2017, 9, 33855–33862. [Google Scholar] [CrossRef]
  40. Liu, J.; Liu, B.; Wang, C.; Huang, Z.; Hu, L.; Ke, X.; Liu, L.; Shi, Z.; Guo, Z. Walnut shell – Derived activated carbon: Synthesis and its application in the sulfur cathode for lithium–sulfur batteries. J. Alloys Compd. 2017, 718, 373–378. [Google Scholar] [CrossRef]
  41. Zhao, Y.; Wang, L.; Huang, L.; Maximov, M.; Jin, M.; Zhang, Y.; Wang, X.; Zhou, G. Biomass-derived oxygen and nitrogen Co-doped porous carbon with hierarchical architecture as sulfur hosts for high-performance lithium/sulfur batteries. Nanomaterials 2017, 7, 402. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Moreno, N.; Caballero, A.; Hernán, L.; Morales, J. Lithium–sulfur batteries with activated carbons derived from olive stones. Carbon 2014, 70, 241–248. [Google Scholar] [CrossRef]
  43. Moreno, N.; Caballero, Á.; Morales, J.; Rodríguez-Castellón, E. Improved performance of electrodes based on carbonized olive stones/S composites by impregnating with mesoporous TiO2 for advanced Li—S batteries. J. Power Sources 2016, 313, 21–29. [Google Scholar] [CrossRef]
  44. Luna-Lama, F.; Hernández-Rentero, C.; Caballero, A.; Morales, J. Biomass-derived carbon/γ-MnO2 nanorods/S composites prepared by facile procedures with improved performance for Li/S batteries. Electrochim. Acta 2018, 292, 522–531. [Google Scholar] [CrossRef] [Green Version]
  45. Hernández-Rentero, C.; Córdoba, R.; Moreno, N.; Caballero, A.; Morales, J.; Olivares-Marín, M.; Gómez-Serrano, V. Low-cost disordered carbons for Li/S batteries: A high-performance carbon with dual porosity derived from cherry pits. Nano Res. 2018, 11, 89–100. [Google Scholar] [CrossRef]
  46. Benítez, A.; González-Tejero, M.; Caballero, Á.; Morales, J. Almond shell as a microporous carbon source for sustainable cathodes in lithium-sulfur batteries. Materials 2018, 11, 1428. [Google Scholar] [CrossRef] [Green Version]
  47. Özbek, H.N.; Fockink, D.H.; Yanık, D.K.; Göğüş, F.; Łukasik, R.M. The green biorefinery concept for the valorisation of pistachio shell by high-pressure CO2/H2O system. J. Clean. Prod. 2018, 196, 842–851. [Google Scholar] [CrossRef] [Green Version]
  48. Scholten, J.M.; Spanjer, M.C. Determination of Aflatoxin Bi in pistachio kernels and shells. J. AOAC Int. 1996, 79, 1360–1364. [Google Scholar] [CrossRef] [Green Version]
  49. Chen, H.; Xia, P.; Lei, W.; Pan, Y.; Zou, Y.; Ma, Z. Preparation of activated carbon derived from biomass and its application in lithium–sulfur batteries. J. Porous Mater. 2019, 26, 1325–1333. [Google Scholar] [CrossRef]
  50. Arrebola, J.C.; Caballero, A.; Hernán, L.; Morales, J.; Olivares-Marín, M.; Gómez-Serrano, V. Improving the performance of biomass-derived carbons in Li-ion batteries by controlling the lithium insertion process. J. Electrochem. Soc. 2010, 157, A791. [Google Scholar] [CrossRef]
  51. Srinivasakannan, C. Production of activated carbon from rubber wood sawdust. Biomass Bioenergy 2004, 27, 89–96. [Google Scholar]
  52. Hulicova-Jurcakova, D.; Puziy, A.M.; Poddubnaya, O.I.; Suárez-García, F.; Tascón, J.M.D.; Lu, G.Q. Highly stable performance of supercapacitors from phosphorus-enriched carbons. J. Am. Chem. Soc. 2009, 131, 5026–5027. [Google Scholar] [CrossRef] [PubMed]
  53. Benítez, A.; Caballero, Á.; Rodríguez-Castellón, E.; Morales, J.; Hassoun, J. The role of current collector in enabling the high performance of Li/S battery. ChemistrySelect 2018, 3, 10371–10377. [Google Scholar] [CrossRef]
  54. Hernández-Rentero, C.; Marangon, V.; Olivares-Marín, M.; Gómez-Serrano, V.; Caballero, Á.; Morales, J.; Hassoun, J. Alternative lithium-ion battery using biomass-derived carbons as environmentally sustainable anode. J. Colloid Interface Sci. 2020, 573, 396–408. [Google Scholar] [CrossRef]
  55. Soler-Piña, F.J.; Hernández-Rentero, C.; Caballero, A.; Morales, J.; Rodríguez-Castellón, E.; Canales-Vázquez, J. Highly graphitized carbon nanosheets with embedded Ni nanocrystals as anode for Li-ion batteries. Nano Res. 2020, 13, 86–94. [Google Scholar] [CrossRef]
  56. Barbosa, L.; Luna-Lama, F.; González Peña, Y.; Caballero, A. Simple and eco-friendly fabrication of electrode materials and their performance in high-voltage lithium-ion batteries. ChemSusChem 2020, 13, 838–849. [Google Scholar] [CrossRef]
  57. Seehra, M.S.; Pavlovic, A.S. X-Ray diffraction, thermal expansion, electrical conductivity, and optical microscopy studies of coal-based graphites. Carbon 1993, 31, 557–564. [Google Scholar] [CrossRef]
  58. Wang, S.; Zou, K.; Qian, Y.; Deng, Y.; Zhang, L.; Chen, G. Insight to the synergistic effect of N-doping level and pore structure on improving the electrochemical performance of sulfur/N-doped porous carbon cathode for Li-S batteries. Carbon 2019, 144, 745–755. [Google Scholar] [CrossRef]
  59. Zhu, Q.; Deng, H.; Su, Q.; Du, G.; Yu, Y.; Ma, S.; Xu, B. A free-standing nitrogen-doped porous carbon foam electrode derived from melaleuca bark for lithium-sulfur batteries. Electrochim. Acta 2019, 293, 19–24. [Google Scholar] [CrossRef]
  60. Hu, L.; Lu, Y.; Li, X.; Liang, J.; Huang, T.; Zhu, Y.; Qian, Y. Optimization of microporous carbon structures for lithium-sulfur battery applications in carbonate-based electrolyte. Small 2017, 13, 1603533. [Google Scholar] [CrossRef]
  61. Liu, J.; Liu, W.; Chen, K.; Ji, S.; Zhou, Y.; Wan, Y.; Xue, D.; Hodgson, P.; Li, Y. Facile synthesis of transition-metal oxide nanocrystals embedded in hollow carbon microspheres for high-rate lithium-ion-battery anodes. Chem. Eur. J. 2013, 19, 9811–9816. [Google Scholar] [CrossRef] [PubMed]
  62. Gu, X.; Lai, C.; Liu, F.; Yang, W.; Hou, Y.; Zhang, S. A conductive interwoven bamboo carbon fiber membrane for Li–S batteries. J. Mater. Chem. A 2015, 3, 9502–9509. [Google Scholar] [CrossRef] [Green Version]
  63. Zhang, X.; Zhu, J.; Tiwary, C.S.; Ma, Z.; Huang, H.; Zhang, J.; Lu, Z.; Huang, W.; Wu, Y. Palladium nanoparticles supported on nitrogen and sulfur dual-doped graphene as highly active electrocatalysts for formic acid and methanol oxidation. ACS Appl. Mater. Interfaces 2016, 8, 10858–10865. [Google Scholar] [CrossRef] [PubMed]
  64. Chen, F.; Yang, J.; Bai, T.; Long, B.; Zhou, X. Biomass waste-derived honeycomb-like nitrogen and oxygen dual-doped porous carbon for high performance lithium-sulfur batteries. Electrochim. Acta 2016, 192, 99–109. [Google Scholar] [CrossRef]
  65. Baumann, A.E.; Aversa, G.E.; Roy, A.; Falk, M.L.; Bedford, N.M.; Thoi, V.S. Promoting sulfur adsorption using surface Cu sites in metal–organic frameworks for lithium sulfur batteries. J. Mater. Chem. A 2018, 6, 4811–4821. [Google Scholar] [CrossRef]
  66. Kim, J.; Lee, D.-J.; Jung, H.-G.; Sun, Y.-K.; Hassoun, J.; Scrosati, B. An advanced lithium-sulfur battery. Adv. Funct. Mater. 2013, 23, 1076–1080. [Google Scholar] [CrossRef]
  67. Zhu, W.; Paolella, A.; Kim, C.-S.; Liu, D.; Feng, Z.; Gagnon, C.; Trottier, J.; Vijh, A.; Guerfi, A.; Mauger, A.; et al. Investigation of the reaction mechanism of lithium sulfur batteries in different electrolyte systems by in situ Raman spectroscopy and in situ X-ray diffraction. Sustain. Energy Fuels 2017, 1, 737–747. [Google Scholar] [CrossRef]
  68. Paolella, A.; Zhu, W.; Marceau, H.; Kim, C.; Feng, Z.; Liu, D.; Gagnon, C.; Trottier, J.; Abdelbast, G.; Hovington, P.; et al. Transient existence of crystalline lithium disulfide Li2S2 in a lithium-sulfur battery. J. Power Sources 2016, 325, 641–645. [Google Scholar] [CrossRef]
  69. Zhu, W.; Liu, D.; Paolella, A.; Gagnon, C.; Gariépy, V.; Vijh, A.; Zaghib, K. Application of operando X-ray diffraction and Raman spectroscopies in elucidating the behavior of cathode in lithium-ion batteries. Front. Energy Res. 2018, 6, 1–16. [Google Scholar] [CrossRef] [Green Version]
  70. You, Y.; Zeng, W.; Yin, Y.-X.; Zhang, J.; Yang, C.-P.; Zhu, Y.; Guo, Y.-G. Hierarchically micro/mesoporous activated graphene with a large surface area for high sulfur loading in Li–S batteries. J. Mater. Chem. A 2015, 3, 4799–4802. [Google Scholar] [CrossRef]
  71. Carbone, L.; Coneglian, T.; Gobet, M.; Munoz, S.; Devany, M.; Greenbaum, S.; Hassoun, J. A simple approach for making a viable, safe, and high-performances lithium-sulfur battery. J. Power Sources 2018, 377, 26–35. [Google Scholar] [CrossRef]
  72. Lv, Y.; Shang, M.; Chen, X.; Niu, J. Double-net enclosed sulfur composite as a new cathode in lithium sulfur batteries. J. Phys. Chem. C 2019, 123, 17719–17727. [Google Scholar] [CrossRef]
  73. Kim, H.; Lee, J.; Ahn, H.; Kim, O.; Park, M.J. Synthesis of three-dimensionally interconnected sulfur-rich polymers for cathode materials of high-rate lithium–sulfur batteries. Nat. Commun. 2015, 6, 7278. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Benítez, A.; Caballero, A.; Morales, J.; Hassoun, J.; Rodríguez-Castellón, E.; Canales-Vázquez, J. Physical activation of graphene: An effective, simple and clean procedure for obtaining microporous graphene for high-performance Li/S batteries. Nano Res. 2019, 12, 759–766. [Google Scholar] [CrossRef]
  75. Di Lecce, D.; Marangon, V.; Benitez, A.; Caballero, A.; Morales, J.; Rodríguez-Castellón, E.; Hassoun, J. High capacity semi-liquid lithium sulfur cells with enhanced reversibility for application in new-generation energy storage systems. J. Power Sources 2019, 412, 575–585. [Google Scholar] [CrossRef]
  76. Han, J.; Li, Y.; Li, S.; Long, P.; Cao, C.; Cao, Y.; Wang, W.; Feng, Y.; Feng, W. A low cost ultra-microporous carbon scaffold with confined chain-like sulfur molecules as a superior cathode for lithium–sulfur batteries. Sustain. Energy Fuels 2018, 2, 2187–2196. [Google Scholar] [CrossRef]
  77. Liu, J.; Xiao, S.H.; Zhang, Z.; Chen, Y.; Xiang, Y.; Liu, X.; Chen, J.S.; Chen, P. Naturally derived honeycomb-like N,S-codoped hierarchical porous carbon with MS2 (M = Co, Ni) decoration for high-performance Li–S battery. Nanoscale 2020, 12, 5114–5124. [Google Scholar] [CrossRef]
Nanomaterials 10 00840 sch001 550
Scheme 1. Schematic diagram for the preparation of pistachio shell-derived activated carbon/sulfur (PSAC@S) composite as cathode for lithium–sulfur (Li–S) batteries.
Scheme 1. Schematic diagram for the preparation of pistachio shell-derived activated carbon/sulfur (PSAC@S) composite as cathode for lithium–sulfur (Li–S) batteries.
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Figure 1. (a) Thermogravimetric analysis (TGA) curves of fresh pistachio shell (blue line) in a nitrogen atmosphere, pistachio shell-derived activated carbon (PSAC) in oxygen (dotted black line) and nitrogen (black line) atmospheres, and PSAC@S composite (green line) in a nitrogen atmosphere. (b) X-ray diffraction (XRD) patterns and (c) Raman spectra of PSAC and the PSAC@S composite. (d) N2 adsorption/desorption isotherm and pore size distribution of PSAC.
Figure 1. (a) Thermogravimetric analysis (TGA) curves of fresh pistachio shell (blue line) in a nitrogen atmosphere, pistachio shell-derived activated carbon (PSAC) in oxygen (dotted black line) and nitrogen (black line) atmospheres, and PSAC@S composite (green line) in a nitrogen atmosphere. (b) X-ray diffraction (XRD) patterns and (c) Raman spectra of PSAC and the PSAC@S composite. (d) N2 adsorption/desorption isotherm and pore size distribution of PSAC.
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Figure 2. (a) Cyclic voltammograms recorded at different scan rates (from 0.1 to 1.0 mV·s–1). Electrochemical impedance spectroscopy (EIS) spectra before (black) and after (green) the first cycle, recorded at 0.1 mV·s−1, are shown in the inset. (b) Variation in the peak current with the square root of the scan rate (Randles–Sevcik equation).
Figure 2. (a) Cyclic voltammograms recorded at different scan rates (from 0.1 to 1.0 mV·s–1). Electrochemical impedance spectroscopy (EIS) spectra before (black) and after (green) the first cycle, recorded at 0.1 mV·s−1, are shown in the inset. (b) Variation in the peak current with the square root of the scan rate (Randles–Sevcik equation).
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Figure 3. (a) Galvanostatic charge/discharge curves at different cycles recorded at C/10. (b) Variation in the discharge capacity and coulombic efficiency as a function of the number of cycles.
Figure 3. (a) Galvanostatic charge/discharge curves at different cycles recorded at C/10. (b) Variation in the discharge capacity and coulombic efficiency as a function of the number of cycles.
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Figure 4. (a) Galvanostatic charge/discharge curves at different rates. (b) Rate performance.
Figure 4. (a) Galvanostatic charge/discharge curves at different rates. (b) Rate performance.
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Figure 5. Variation in the specific discharge capacity reported in the literature as a function of the rate.
Figure 5. Variation in the specific discharge capacity reported in the literature as a function of the rate.
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Table
Table 1. Selected properties of lithium–sulfur (Li–S) cells made from activated carbons derived from pistachio shells (reported in the literature). The properties of our carbon are also included for comparison.
Table 1. Selected properties of lithium–sulfur (Li–S) cells made from activated carbons derived from pistachio shells (reported in the literature). The properties of our carbon are also included for comparison.
Preparation MethodSBET
m2·g−1		S Loading
mg·cm−2		Long Term CyclingRate CapabilityReference
Voltage Window
V		CiCfCycleRateRateCaverage
mAh·g−1
mAh·g−1
Activation with ZnCl2, 550 °C
S impregnation by melt diffusion
(70:20:10) 1		11490.843.0–1.5 2980380200C/5C/5
C/2
1C		580
450
320		[24]
Activation with
H3PO4, 800 °C
S impregnation by
wet milling(80:10:10) 1		13452.52.6–1.81193570300C/10C/5
C/2
1C		888
753
646		This work
1 Electrode composition (composite:carbon black:PVDF ratio). 2 Voltage window drawn in the figure. In the text, the indicated voltage window is 1.0–3.0 V.

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Benítez, A.; Morales, J.; Caballero, Á. Pistachio Shell-Derived Carbon Activated with Phosphoric Acid: A More Efficient Procedure to Improve the Performance of Li–S Batteries. Nanomaterials 2020, 10, 840. https://doi.org/10.3390/nano10050840

AMA Style

Benítez A, Morales J, Caballero Á. Pistachio Shell-Derived Carbon Activated with Phosphoric Acid: A More Efficient Procedure to Improve the Performance of Li–S Batteries. Nanomaterials. 2020; 10(5):840. https://doi.org/10.3390/nano10050840

Chicago/Turabian Style

Benítez, Almudena, Julián Morales, and Álvaro Caballero. 2020. "Pistachio Shell-Derived Carbon Activated with Phosphoric Acid: A More Efficient Procedure to Improve the Performance of Li–S Batteries" Nanomaterials 10, no. 5: 840. https://doi.org/10.3390/nano10050840

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