- Open Access
The application of graphene in lithium ion battery electrode materials
© Zhu et al.; licensee Springer. 2014
Received: 22 July 2014
Accepted: 30 September 2014
Published: 8 October 2014
Graphene is composed of a single atomic layer of carbon which has excellent mechanical, electrical and optical properties. It has the potential to be widely used in the fields of physics, chemistry, information, energy and device manufacturing. In this paper, we briefly review the concept, structure, properties, preparation methods of graphene and its application in lithium ion batteries. A continuous 3D conductive network formed by graphene can effectively improve the electron and ion transportation of the electrode materials, so the addition of graphene can greatly enhance lithium ion battery’s properties and provide better chemical stability, higher electrical conductivity and higher capacity. In this review, some recent advances in the graphene-containing materials used in lithium ion batteries are summarized and future prospects are highlighted.
Nowadays, ever-increasing demands on energy have driven many countries to invest heavily in finding new sources of energy or investigating new ways/devices to store energy (Zhu et al.2014). A kind of energy storage device is lithium ion batteries, which have many unique advantages in comparison to conventional batteries. These merits include high open-circuit voltage, high energy density, long useful life, no memory effect, no pollution and low self-discharge rate. The advantageous properties of lithium ion batteries make them quickly become the new generation of secondary batteries in recent years and they are now widely used in mobile phones, laptops and other portable electronic devices (Tarascon & Armand2001). In lithium ion batteries, lithium ions move from the negative electrode to the positive electrode during discharge, and this is reversed during the charging process. Cathode materials commonly used are lithium intercalation compounds, such as LiCoO2, LiMn2O4 and LiFePO4; anode materials commonly used are graphite, tin-based oxides and transition metal oxides. However, these materials have some drawbacks that limit their use. For example, carbon materials have good cycle performance but low initial charge and discharge efficiency; tin-based oxides have good cycle but high irreversible capacity loss in the first cycle (Simon & Gogotsi2008). One of the potential solutions to these problems is to develop new electrode materials for lithium ion batteries. Graphene, a miracle material, is chemically stable and has high electrical conductivity. So it has naturally been considered as a suitable electrode alternative in the battery applications (Atabaki & Kovacevic2013).
2 Preparation methods of graphene
Graphene are currently produced by several different methods: micromechanical exfoliation of highly oriented pyrolytic graphite with or without previous processing of the surface (Tang & Hu2012; Lu et al.1999; Fredriksson et al.2009), epitaxial growth (Yu et al.2011; Berger et al.2006), chemical vapor deposition (CVD) (An et al.2011; Wintterlin & ML2009) and reduction of graphene oxide (GO) (Li et al.2008; Gómez-Navarro et al.2007; Stankovich et al.2007; Mattevi et al.2009; Fernandez-Merino et al.2010). The graphene produced by micromechanical exfoliation and chemical vapor deposition shows good monolayer morphology. However these methods are complex and can only produce small amounts of grapheme, hence are not suitable for mass production and application. Chemical reduction of graphene oxide is currently the most suitable method for large-scale graphene production. So graphene used in the vast majority of lithium ion battery electrode materials is obtained by reducing GO.
Graphene oxide is produced from natural graphite through the Hummers method (Fan et al.2008; Gómez-Navarro et al.2007), Brodie method (Brodie & Chim1860) or Staudenmaie method (Staudenmaier & Deut1898). The Hummers method is most commonly used. Once GO is produced, hydrazine hydrate, NaBH4 (Shin et al.2009) or other reducing agents are used to produce graphene. This mode of preparation is simple and will enable mass production of graphene. The shortfall of this method is that introduced oxygen will affect the produced graphene’s electrochemical properties, resulting in deterioration of graphene. Despite these drawbacks, chemical reduction of GO is still the primary method used by researchers, owing to its simplicity and lower equipment burden.
3 Graphene in lithium ion battery cathode materials
Some of the most commonly studied cathode materials used in lithium ion batteries (LIBs) are LiCoO2, LiMn2O4, LiFePO4 and Li3V2(PO4)3. These materials have electronic conductivities of 10-4 S/cm (Dokko et al.2001; Barker et al.1996; Levasseur et al.2002), 10-6 S/cm (Marzec et al.2002; Cao & Prakash2002), 10-9 S/cm (Prosini et al.2002; Shi et al.2003) and 2.4 × 10-7 S/cm (Pan et al.2011) respectively. These electronic conductivity values are fairly low when high battery performance is required, so electron conducting additives are frequently added to such materials in order to improve their electrochemical properties.
Existing studies show that pure graphene can’t become a direct substitute for current carbon-based commercial electrode materials in lithium ion batteries due to its low coulombic efficiency, high charge–discharge platform and poor cycle stability (Atabaki & Kovacevic2013). However, when used as a matrix in the composite electrode materials, graphene can play a very important role.
In recent years, researchers have begun to study graphene modified for use as a cathode material and have found that it can significantly improve cathode electrochemical performance (Geim & Novoselov2007). For example, the two-dimensional large surface area and superior electron transfer capability of graphene can effectively improve the transmission and diffusion abilities of electron and ion in cathode materials.
3.1 Lithium metal oxide-graphene composites as cathode materials for LIBs
LiMn2O4 is used as cathode electrode material, owing to its low cost, environmental friendliness and high abundance (Manev et al.1995). However, its low electrical conductivity results in a low-rate capacity. Published papers have demonstrated that graphene sheets are effective agents for improving their conductivity and rate capacity. LiMn2O4-graphene composites with high rate capacity were synthesized by a microwave assisted hydrothermal method (Bak et al.2011). The composites exhibited reversible capacities of 117 mAh/g and 101 mAh/g at 50C and 100C. In another study, LiMn2O4-graphene composites were synthesized by self-assembly approach combined with a solid-state lithiation method (Zhao et al.2011). The enhancement in electrochemical properties is attributed to the superior Li+ diffusion kinetics and improved stability across a wide voltage range in crystalline LiMn2O4-graphene composites. Furthermore, their capacities approached the theoretical value and the cycling stability was enhanced.
LiNi1/3Mn1/3Co1/3O2 is a promising candidate for cathode electrode materials. It shows high energy density, good stability, enhanced safety and can be produced at low cost (Zhu et al.2012). However, cation disorder occurs during calcination and results in deterioration of its kinetic properties. To improve its electrochemical performance, LiNi1/3Mn1/3Co1/3O2-graphene composites are prepared as cathode materials for LIBs. Jiang and coworkers reported that LiNi1/3Mn1/3Co1/3O2-graphene composites prepared by mechanical mixing could deliver a capacity of 115 mAh/g at 6C (Jiang et al.2012). LiNi1/3Mn1/3Co1/3O2-graphene composites prepared by micro-emulsion and ball-milling route could deliver a reversible capacity of 150 mAh/g at 5C, much higher than that of bare LiNi1/3Mn1/3Co1/3O2 (Rao et al.2011). The improved performance is attributed to grain connectivity and high electronic conductivity.
3.2 LiMPO4-graphene composites as cathode materials for LIBs
In comparison to LiFePO4, Li3V2(PO4)3 is an attractive cathode material for LIBs, because its average extraction/reinsertion voltage is about 4.0 V, and its theoretical capacity is 197 mAh/g (Huang et al.2009; Yu et al.2012). Li3V2(PO4)3 forms a monoclinic structure and has a high operating voltage and shows a good performance at high discharge currents. However, its intrinsic low electronic conductivity (240 nS/cm at 25°C) limits its rate capacity, so graphene is added to improve its electrochemical performance. Li3V2(PO4)3/graphene cathode material has been prepared by sol–gel, solid state and spray-drying synthesis methods (Huang et al.2009; Yu et al.2012). The product which was prepared by a sol–gel route shows excellent rate capacity and cycling stability (Yu et al.2012).
4 Graphene in lithium ion battery anode materials
Graphene has opened new possibilities in the field of lithium ion battery materials due to its light weight, high electrical conductivity, superior mechanical flexibility, and chemical stability (Su et al.2012). These properties prove advantageous when graphene is used in the anode. The addition of graphene to anode materials has lead to superior electrical conductivity, high surface area (2620 m2g-1), high surface-to-volume ratio, ultra-thin thickness which can shorten the diffusion distance of ions, structural flexibility that paves the way for constructing flexible electrodes, thermal and chemical stability which guarantee its durability in harsh environments.
Summary of LIB anode materials (non-carbon) containing graphene
Capacity and cycle performance
First discharge capacity 1588 mAhg-1, after 40 cycles remain 730 mAh/g
(Zhu et al.2011)
Cubic diamond type
First discharge capacity 2753 mAhg-1, after 50 cycles remain 590 mAh/g
First discharge capacity 1826 mAhg-1, after 40 cycles maintain 1310 mAh/g
(Lian et al.2010a)
First discharge capacity 900 mAhg-1, after 100 cycles maintain 390 mAh/g
(Tao et al.2012)
N-methyl-2-p yrrolidone solvent
First discharge capacity 640 mAhg-1, after 50 cycles maintain 583.5 mAh/g.
(Wang et al.2010b)
First discharge capacity 1426 mAhg-1, after 100 cycles maintain 580 mAh/g
(Kim et al.2012)
Gas/liquid interface reaction
First discharge capacity 499 mAhg-1, after 10 cycles maintain 150 mAh/g
(Tung et al.2009)
First discharge capacity 1469 mAhg-1, after 100 cycles maintain 605 mAh/g
(Cai et al.2012a)
Hexagonal crystal structure
Solution phase method
First discharge capacity 1664 mAhg-1, after 500 cycles maintain 600 mAh/g
(Wang et al.2011a)
Gas–liquid interfacial reaction
First discharge capacity 1740 mAhg-1, after 115 cycles maintain 1198 mAh/g
(Chang et al.2012)
First discharge capacity 430 mAhg-1, after 35cycles maintain 150 mAh/g
4.1 Graphene modified tin-based oxide
Sn and their oxides such as SnO2 are exclusively studied as lithium ion battery anode materials. However, their use is limited by a defect, in that chemical reduction will often bring in electronic barriers to Li+ repulsion. Lithiation and delithiation reactions (Sn + 4.4Li++ 4.4e-↔Li4.4Sn) can cause large volume changes. This leads to the pulverization of the particles and the electrical disconnection of the electrode. In order to circumvent this, new anode materials with graphene have been examined in many recent studies. For example, the performance of anode electrode was improved when tin nanoparticles embedded in grapheme was used (Liang et al.2011).
The graphene matrix not only can accommodate the volume change of Sn during charge–discharge, but also facilitate electron transport because of its high electronic conductivity. To prepare this type of anode, it is essential to use hydrothermal synthesis and subsequent annealing. It is reported that the reversible specific capacity of the nanocomposite is 662 mAhg-1 at a specific current of 100 mAg-1 after 100 cycles, and 417 mAhg-1 at the high current of 1000 mAg-1(Liang et al.2011).
4.2 Graphene-modified silicon-based materials
As an anode material, silicon and lithium ions can form Li 4.4 Si. The theoretical charge capacity of this compound is up to 4200 mAh/g, it also has a low discharge voltage. However, a limitation to its use is its charge volume effect. During the discharge process, silicon and lithium form Li3.75Si. As a result, Si volume increased up to 270%. This leads to poor circulation stability (Wolfenstine1999). The addition of Silicon nanomaterials and carbon-coating can buffer this volume expansion to some extent. When graphene is introduced, it can not only prevent silicon nanoparticles gathering but also improve the electron and lithium ions transport capability.
Yushin etc. (Evanoff et al.2011) used a vapor deposition method to form a continuous Si film on the graphene sheet surface. Following that, a high temperature treatment in propylene allowed the silicon surface to be coated with carbon. The obtained composite material showed enhanced conductivity as well as oxidation resistance. This composite has 3D porous structure, which buffer Si volume change during charge and discharge, owing to the presence of a stable solid electrolyte interface film. Furthermore, this composite has more than 1000 mAh/g specific delithiated capacity and good cycle stability under 1400 mA/g current density.
4.3 Graphene modified transition metal-based materials
Transition metal oxides which have high lithium storage capacity are known as potential alternative anode materials for high capacity lithium ion batteries. Owing to the presence of volume changes during charge and discharge and their low conductivity, graphene can also be used to improve their electrochemical properties.
Co3O4 has a high theoretical capacity of 890mAh/g. However, the processes of charging and discharging cause large volume expansion. The addition of graphene can effectively improve Co3O4 electrochemical properties (Kim et al.2011; Li et al.2011; Yan et al.2010; Wu et al.2010; Yang et al.2010). For example, at 200 mA/g of current density, Co(OH)2’s first cycle off-lithium specific capacity is 660 mAh/g. Through synchronizing hydrothermal reduction with graphene, the material’s delithiated specific capacity increases up to 1120mAh/g. After 30 cycles, the reversible capacity of the composite material remains 82% of the initial capacity.
Mn3O4 has a 936 mAh/g theoretical capacity. However, due to its poor electrical conductivity (about 10- 7-10- 8 S/cm), the actual capacity with Co doped can only reach a maximum of 400 mAh/g. When the composite with graphene formed through a two-step liquid method, followed by hydrothermal synthesis, the delithiated ratio capacity of this compound is about 900 mAh/g at low current density (40 mA/g), closing to the theoretical capacity. When current density reaches 1600 mA/g, the specific capacity of this compound maintains 390 mAh/g (Wang et al. 2010c).
CuO has low band gap energy and high catalytic activity. However, as an anode material, it has a low conductive performance and large volume expansion effect. These shortcomings can be improved by forming CuO/graphene composites (Mai et al.2011). First CuO and graphite oxide are used to produce CuO/graphene composite by hydrothermal synthesis, followed by a reduction process. After 50 cycles, the composite material’s inverse capacity reached 583.5 mAh/g and the capacity retention ratio was 75.5%.
Fe3O4/graphene composites have excellent high-rate performance, except when prepared by gas–liquid interface method (Lian et al.2010b). At 35 mA/g current density, the specific reversible capacity holds at 1026 mAh/g (30 cycles). At 700 mA/g current density, the capacity is still 580 mAh/g after 100 cycles. Fe2O3 is used as anode material owing to its high theoretical capacity (1005 mAh/g) and low price (Choucair et al.2009a). (Wang et al.2011b) prepared Fe2O3/graphene composites by a hydrothermal method. The addition of graphene prevented Fe2O3 from aggregation and also buffered material’s volume expansion. At l160 mA/g current density, the reversible capacity of the composite remains 660 mAh/ g after 100 cycles.
TiO2 with graphene is another nanocomposite that can be synthesized by a facile gas/liquid interface reaction (Cai et al.2012a). The electrochemical performance tests show that the composite’s specific charge capacity is 499 mAh g-1 at a current density of 100 mAg-1. This specific charge capacity drops to 150 mAhg-1at a high current density of 3000 mAg-1. The advantage of this nanocomposite is that the oxygen-containing groups on the graphene sheets can be reduced after the heat treatment and residual functional groups including the OH and COOH on the surface of graphene sheets can strongly interact with the metal ions during the synthesis process .The random hybridization of TiO2 nanoparticles and ultrathin graphene sheets form a three-dimensional porous structure of the TiO2-graphene nanocomposite. The small nanoparticles provide a short mean-free-path for electron and lithium ion to travel during the lithium ion insertion/extraction process, resulting in excellent rate capability.
Compared to traditional carbon electrode materials, graphene, due to its low initial coulombic efficiency, high charge and discharge platform and other shortcomings, cannot directly replace traditional graphite as an anode material. However, graphene does demonstrate high electrical conductivity, good mechanical strength, excellent flexibility, great chemical stability and high specific surface area. This is especially noticeable when graphene is chemically converted with a greater proportion of functional groups, proving that it is suited for use as a base composite electrode material. When used as electrode material, graphene can effectively reduce the size of the active material, prevent agglomeration of nanoparticles, improve electrons and ions transmission capacity, as well as enhancing the electrode’s mechanical stability. As a result, graphene-containing electrode materials have high capacity and good rate performance. Lithium metal oxide-graphene, LiMPO4-graphene, Tin-based, Si-based and transition metal based electrode materials with graphene have been extensively studied in this paper. The composite materials’ advantages can be summarized as following. Firstly, graphene’s flexibility makes it an ideal material to buffer metal electrode’s volume expansion and contraction during the charge–discharge process. This improves the electrode material’s cycle life performance. Further, the excellent electrical properties of graphene can enhance the conductivity of metal electrode material. Moreover, the addition of graphene can control the growth of metal oxide particles. Smaller particles means the diffusion distance of lithium ions and electrons is reduced, this improves the material’s rate performance. Finally, the lithium storage capacity for most metal oxide composite materials with graphene has improved greatly.
In addition, various approaches are taken to prepare graphene. These vary from simple mechanical mixing to the well controlled in situ reactions and interfacial reactions, which result in better graphene morphology and structure. Developing easily replicable methods for producing graphene is the key to future application of graphene in lithium ion batteries.
We thank the national natural science foundations of China (No. 21373074), Anhui province science and technology plan (No. 11010202133) for their financial support.
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