Xinbo Xua,
Jiafeng Ruana,
Yuepeng Pangab,
Tao Yuanab and
Shiyou Zheng*ab
aSchool of Materials Science and Engineering, University of Shanghai for Science and Technology, Shanghai 200093, China. E-mail: syzheng@usst.edu.cn
bShanghai Innovation Institute for Materials, Shanghai 200444, China
First published on 31st January 2018
Rechargeable Li–S batteries are receiving ever-increasing attention due to their high theoretical energy density and inexpensive raw sulfur materials. However, their practical applications have been hindered by short cycle life and limited power density owing to the poor electronic conductivity of sulfur species, diffusion of soluble polysulfide intermediates (Li2Sn, n = 4–8) and the large volume change of the S cathode during charge/discharge. Optimizing the carbon framework is considered as an effective approach for constructing high performance S/carbon cathodes because the microstructure of the carbon host plays an important role in stabilizing S and restricting the “shuttle reaction” of polysulfides in Li–S batteries. In this work, reduced graphite oxide (rGO) materials with different oxidation degree were investigated as the matrix to load the active material by an in situ thermally reducing graphite oxide (GO) and intercalation strategy under vacuum at 600 °C. It has been found that the loaded amount of S embedded in the rGO layer for the S/carbon cathode and its electrochemical performance strongly depended on the oxidation degree of GO. In particular, on undergoing CS2 treatment, the rGO–S cathode exhibits extraordinary performances in Li–S batteries. For instance, at a current density of 0.2 A g−1, the optimized rGO–S cathode shows a columbic efficiency close to 100% and retains a capacity of around 750 mA h g−1 with progressive cycling up to over 250 cycles.
In order to alleviate the above issues, many efforts have been made to explore novel structures and materials for the S cathode, interlayer, electrolyte, and separator for Li–S batteries. The electrolyte materials have been modified to improve the stability of electrochemical reactions.5–7 New materials have been developed as interlayers and separators that can help the restrained polysulfide shuttling to large extents by preventing polysulfides from diffusing to the anode.8–12 The vast majority of the above studies were focused on sulfur cathode materials. In the studies of cathode materials, attempts have been made with progress on caging the active material in different matrices, such as carbon-based materials, conducting polymers, and metal oxides.13–21
Among the carbon materials, graphene has become one of research hotspots in the recent years owing to its superior electronic conductivity, large surface area, and intriguing mechanical properties, etc.22–24 Thus it can be applied as an ideal candidate for loading active materials in battery applications. Usually, graphene was prepared by a Hummers oxidation method. It was reported that oxygen functional groups on the graphene oxide could anchor S species to the nanosheets through chemical adsorption, which resulting in the improvement of cycle performance of the sulfur based cathode in Li–S cathodes.25–27 There have been a lot of works focusing on fabricating graphene–S composite cathodes for Li–S batteries. Ji et al. coated the uniform sulfur layers on graphene oxide sheets by a simple chemical reaction. Benefited from the reactive functional groups, polysulfides and sulfur could be binded strongly on the carbon sheets, which enabled a high reversible capacity and stable cycling performance for 50 cycles at 0.1C.28 Wang et al. prepared functionalized reduced graphene oxide as substrate structure for S, especially, after being modified in ethylenediamine, carbon showed much stronger covalent binding energy to sulfur and its discharge products, and the reduced graphene oxide–S composites showed stable capacity retention of 80% after 350 cycles and high-rate capacity of 480 mA h g−1 at 4C.29 To further improve the interface kinetic structure between sulfur and graphene sheets, Zhang et al. prepared a layer structure S/PPy/graphene composite cathode which showed high S utilization and interfacial stabilization.30 Zhang et al. obtained an S–reduced graphene oxide hybrid by bubbling concentrated H2S gas into a graphene oxide aqueous suspension at 70 °C.31 This method could realize the reduction of graphene oxide and form the graphene–S hybrid in one step. Although grapheme oxide is the most frequently used precursor for the preparation of graphene and its derived materials, it suffers from poor conductivity due to the destruction of the continuous sp2 hybridized network by abundant O-containing groups. Functionalization of graphene is an efficient way to enhance the conductivity and hence the electrochemical performance of the sulfur/graphene cathode. Zu et al. applied hydroxylated graphene nanosheets as a substrate for capturing amorphous S nanoparticles by an in situ deposition method at room temperature.32 In the synthesis of the S–hydroxylated graphene composite, graphene sheets were firstly grafted with hydroxyl groups by a modified hydrothermal treatment. With similar precursor of reduced graphite oxide, Zhou et al. use sealing thermal method to embed S8 molecule into graphite oxide at 155 °C for 4 h, the rGO–S composite delivers an initial discharge capacity of 792 mA h g−1 and the coulombic efficiency was 65.8%, retains capacity of 392 mA h g−1 after 200 cycles.33
It is well known that the graphite oxide is an isolated multilayer graphene oxide. The multilayer structures are more suitable for sulfur carrier. Herein, a facile one-step solid-state method was employed to prepare the reduced graphite oxide/sulfur (rGO–S) composite. We directly heat the ground mixture of sulfur powder with graphite oxides. After heat treatment process, graphite oxide (GO) was reduced, and a homogeneous composite containing sulfur simultaneously formed. In this work, a series of graphite oxides with different oxidation degree were prepared successfully by using Hummer method through adjustment of dose of oxidant. The rGO with different oxidation degree were investigated as matrix to load active material by in situ thermal-reducing graphite oxide (GO) and intercalating strategy under vacuum at 600 °C. It has been found that the loading amount of S embedded in the rGO layer for the S–carbon cathode and its electrochemical performance were strongly affected by the oxidation degree of GO. The reversible capacity of the optimized rGO–S cathode with a high S content (∼80%) retains around 820 mA h g−1 after 100 charge/discharge cycles and the coulombic efficiency is close to 100% at a current density of 0.2 A g−1. The structural features of GO were characterized by Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, wide-angle X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM).
Raman spectra further provide additional evidences of the reduction of GO. As shown in Fig. 2. The Raman spectra of all for samples display two prominent peaks, corresponding to the G and D bands. The G band is usually assigned to the E2g phonon of C sp2 atoms, while the D band originates from a breathing κ-point phonon with A1g symmetry and related to local defects and disorder.35 Raman spectra show that both GO2 and rGO2–S exhibit two broad peaks at 1336 cm−1 and 1591 cm−1, which in accordance with those of graphite, respectively. The D band is attributed to the defects or imperfections, reflecting the presence of disordered edges or boundaries in the rGO domains.35 The higher D/G band intensity ratio (ID/IG) in rGO2–S (ID/IG = 1.14) than that in GO2 (ID/IG = 0.91) means that most of the oxygen functional groups intercalated into the interlayer spacing of GO have been removed and a larger number of defects and disordered edge sites are introduced during heating treatment.36
The S contents in the rGOn–S (n = 1–5) were determined by TG measurement and shown in Fig. 3. The weight losses of rGO1–S, rGO2–S, rGO3–S were 69.3 wt%, 82.0 wt% and 82.4 wt%, respectively. However, with higher oxidation degree, the rGO4–S and rGO5–S showed lower sulfur contents with 71.6 wt% and 70.5 wt%, respectively. The high S content in this may be related to the microstructure and appropriate interplanar space. It is reported that part of S (S8) may be deposited on the external surface of the carbon matrix through high-temperature vapor S infusion method. Therefore, the rGO2–S composite was washed by CS2. After undergoing treatment with CS2, the S content remains around 40% for the rGO2–S–CS2.
Fig. 3 TG curves for rGOn–S (n = 1–5) and rGO2–S–CS2 samples from room temperature to 600 °C at a heating rate of 10 °C min−1 under N2 atmosphere. |
The scanning electron microscopy (SEM) images of GO are presented in Fig. 4. The GO1 has large, agglomerated graphite-like particles with a deeply connected lamellar morphology (Fig. 4a). With higher oxidation, the samples from GO2 to GO5 have more loose morphology and there are more defects on surface. Cross-section of GO2 film is depicted in Fig. 4f, it can easy to see that GO is comprised of stacked sheets with a layer by layer structure, which favors to load S inside.
Fig. 4 SEM images of GO1 (a), GO2 (b), GO3 (c), GO4 (d), GO5 (e), and cross-section of GO2 film (f). |
The morphologies of the rGOn–S (n = 1–5) composites were also investigated by SEM as shown in Fig. 5. From the SEM images of rGOn–S (n = 1–5) composite, it seems that most of sulfur particles were enveloped by graphite sheets, but some of them were uncovered. The microstructure of rGO2–S was also characterized by TEM. As seen in Fig. 5f, GO sheets are large and transparent, demonstrating that GO consists of a few graphene layers. And TEM picture of the black particles reveals the clear crystal lattice, which proves that there are many individual sulfur nanoparticles interlate between layers of graphene. The EDX mapping for rGO2–S was shown in Fig. 5g–i. The elemental distribution maps of C and S clearly demonstrate that the S is homogeneously distributed in the rGO layer.
Fig. 5 SEM images of rGOn–S (n = 1–5) (a–e), and TEM image of rGO2–S (f) and its corresponding elemental mapping of rGO2–S (g) for C (h) and S (i). |
Fourier transform infrared (FTIR) was used to analyze GO and rGO–S samples, as shown in Fig. 6. Similar spectra were obtained for all the oxidized GOs with the distinct oxygen containing functional groups. The spectra of GO exhibit strong peaks throughout the entire wave number range, located at 3442, 1750, 1622, 1372, 1222, 1040 cm−1, which are due to the vibration and deformation bands of O–H and CO stretching vibrations from carbonyl groups, CC configurable vibrations from the aromatic zooms, C–O vibrations from epoxy groups and alkoxy groups. After undergoing 600 °C thermal reduction, these peaks related to the oxygen containing functional groups vanish in the FTIR spectrum of rGO2–S composites, which suggests that all of the oxygen-containing functional groups of the GO have been removed during the preparation process of rGO–S composite.
The surface chemical composition and functional groups of the rGO2–S were identified by XPS in Fig. 7. The deconvoluted C 1s spectra of rGO2–S shows five peaks at 285.5 eV for C–S, 285.6 eV for C–C, 286.5 eV for C–O, 288.3 eV for C–CO, respectively. The fraction of carbon–carbon and carbon–sulfur bonding can be attributed to the efficient removal of oxygen functional groups from the GO by the one-step heat treating process and demonstrates the formation of rGO–S. The successful loading of sulfur on rGO is also depicted by the S 2p spectrum of the rGO2–S (Fig. 7b). The S 2p exhibits one strong peak at about 164.6 eV along with a broad peak centered at 167.03 eV. Further fitting indicates that the strong peak can be split into two peaks for 165.13 and 164 eV, respectively, which are assigned to S 2p1/2 and 2p3/2 due to spin orbit coupling, but the binding energies are slightly higher than those of the characteristic peaks of elemental S, which is mainly related to the signals come from the S confined in the rGO.37,38 In addition, there exists a broad high binding energy peak positioned between 164 and 170 eV, which is an evidence of the strong interaction of sulfur and carbon.39 The C 1s spectra of rGO1–S, rGO3–S show similar peak positions in Fig. S1(a and c),† which indicates that there is no obvious change for the functional groups on GO of different oxide degree after reducing process. The atomic ratio for rGO (1–3)–S samples is shown in Fig. S2.† It can be seen that the values of the O atomic ratio are almost around 16% for all samples, suggesting that the rGOs in the composites have a close oxidation degree. On the contrary, S/C atomic ratio of increased from 0.18 of rGO1–S to 0.48 of rGO3–S, which was an important evidence to prove the enhancement of S element load is related to the oxidation of GO precursor.
Fig. 8 (a–e) Cyclic voltammograms of the rGOn–S (n = 1–5) composite electrode in the first three cycles within the voltage window of 1.0–3.0 V at a scan rate of 0.2 mV s−1. |
From the discharge/charge galvanostatic profiles of rGO–S series composite, two distinct discharge plateaus are observed at around 2.4 and 1.9 V (only rGO2–S exhibits in Fig. 9a), which agrees with the reduction peaks of CV curves. When discharging below 1.9 V, the curve become kinetically slow and normally suffers high polarization, which could be attributed to the nonconductive nature of Li2S2 and Li2S.40,41 Fig. 9b and c display the cycling performance of the rGO–S electrodes at 200 mA g−1 and the rate capability at the current density from 0.1 A g−1 to 4.0 A g−1. It can be seen that the coulombic efficiencies of rGOn–S (n = 1–5) remain 98% except the initial several cycles, by comparison, rGO2–S composite shows relatively higher specific capacity than other four composites, especially, the first discharge capacity can be reached 1142 mA h g−1. On the whole, the rGO2–S composite exhibits the best comprehensive electrochemical performance among the rGO–S cathodes without the use of LiNO3 in electrolyte.
To further investigate the difference of electrochemical performance for the rGOn–S (n = 1–5) composites, electrochemical impedance spectra (EIS) of the rGOn–S (n = 1–5) composites as cathodes in Li–S cells in the initial states were measured and compared in Fig. 9d. The diameter of the semicircular portion of the curve represents the charge transfer resistance Rct. The Rct values of the rGO–S composites are 102, 220, 285, 171 and 64 Ω cm−2, respectively. It is obvious that the Rct values of rGO–S are directly relevant with the oxidation degree of the pristine GO. The rGO1–S and rGO5–S composite electrode exhibited a much lower charge transfer resistance than that of the rGO3–S and rGO2–S composite, which could be attributed to the higher sulfur loading of rGO3–S and rGO2–S composite.
Similar to other carbon–S and graphene–S composite cathodes reported in literatures,42–44 the capacity gradually decay in the first 50–100 cycles and then stabilize at a capacity range. The initial capacity decay is attributed to the dissolution of high-order polysulfides formed from S8 that is coated on the outside surface of carbon matrixs. Therefore, we should expect much higher reversible capacities to be obtained for these rGO–S composite cathodes if the S8 in the rGO–S composites can be removed, i.e., reducing the irreversible capacity. Herein, CS2 was use to wash the surface of rGO2–S sample. From TG results, there are around 40% S in the rGO2–S–CS2 composite. The electrochemical performances of the rGO2–S–CS2 composite were also evaluated as cathodes for Li–S batteries in coin cells and displayed in Fig. 10. The rGO2–S–CS2 cathode exhibits coulombic efficiency over 100% in the initial several cycles, which is attributed to the formation of solid electrolyte interface (SEI) on surface of lithium anode, i.e., a fraction of lithium-ion lose in charging process. The loss results in that charge capacity is lower than discharge capacity. After about 10 cycles, the coulombic efficiency is close to 100%, demonstrating better cycle stability. Even cycling up to more than 250 cycles, the discharge capacities of the electrode still remain about 750 mA h g−1 at 0.2 A g−1. The cycling test of the Li–S cell is still under way.
In summary, the flexible structure of two dimensional rGO sheets and the strong interaction between S and rGO sheets in rGO–S series composites are beneficial to efficiently prevent volume expansion/contraction and aggregation of S during Li+ insertion and extraction process. As a carrier of sulfur, the GO matrix with different oxidation degree shows different effect. Such a series of rGO–S composite is capable of effectively utilizing the mesoporous, good conductivity, mechanical flexibility and good conductivity of rGO. Among them, rGO2–S cathode shows relatively good electrochemical performance.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c7ra12694h |
This journal is © The Royal Society of Chemistry 2018 |