Monday, 2 May 2011

Graphene - Wikipedia, the free encyclopedia

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Not to be confused with Grapheme.

Graphene is an atomic-scale honeycomb lattice made of carbon atoms.

Graphene is an allotrope of carbon, whose structure is one-atom-thick planar sheets of sp2-bonded carbon atoms that are densely packed in a honeycomb crystal lattice.[1] The term graphene was coined as a combination of graphite and the suffix -ene by Hanns-Peter Boehm,[2][3] who described single-layer carbon foils in 1962.[4] Graphene is most easily visualized as an atomic-scale chicken wire made of carbon atoms and their bonds. The crystalline or "flake" form of graphite consists of many graphene sheets stacked together.

The carbon-carbon bond length in graphene is about 0.142 nanometers.[5] Graphene sheets stack to form graphite with an interplanar spacing of 0.335 nm, which means that a stack of 3 million sheets would be only one millimeter thick. Graphene is the basic structural element of some carbon allotropes including graphite, charcoal, carbon nanotubes and fullerenes. It can also be considered as an indefinitely large aromatic molecule, the limiting case of the family of flat polycyclic aromatic hydrocarbons.

The Nobel Prize in Physics for 2010 was awarded to Andre Geim and Konstantin Novoselov "for groundbreaking experiments regarding the two-dimensional material graphene".[6]

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[edit] Description

One definition given in a recent review on graphene is:

Graphene is a flat monolayer of carbon atoms tightly packed into a two-dimensional (2D) honeycomb lattice, and is a basic building block for graphitic materials of all other dimensionalities. It can be wrapped up into 0D fullerenes, rolled into 1D nanotubes or stacked into 3D graphite.[1]

A previous definition is:

A single carbon layer of the graphitic structure can be considered as the final member of the series naphthalene, anthracene, coronene, etc. and the term graphene should therefore be used to designate the individual carbon layers in graphite intercalation compounds. Use of the term "graphene layer" is also considered for the general terminology of carbons.[7]

The IUPAC compendium of technology states: "previously, descriptions such as graphite layers, carbon layers, or carbon sheets have been used for the term graphene...it is not correct to use for a single layer a term which includes the term graphite, which would imply a three-dimensional structure. The term graphene should be used only when the reactions, structural relations or other properties of individual layers are discussed." In this regard, graphene has been referred to as an infinite alternant (only six-member carbon ring) polycyclic aromatic hydrocarbon (PAH). The largest known isolated molecule of this type consists of 222 atoms and is 10 benzene rings across.[8] It has proven difficult to synthesize even slightly bigger molecules, and they still remain "a dream of many organic and polymer chemists".[9] Furthermore, ab initio calculations show that a graphene sheet is thermodynamically unstable with respect to other fullerene structures if its size is less than about 20 nm (“graphene is the least stable structure until about 6000 atoms” and becomes the most stable one (as within graphite) only for sizes larger than 24,000 carbon atoms).[10] The flat graphene sheet is also known to be unstable with respect to scrolling i.e. curling up, which is its lower energy state.[11] Also, a definition of "isolated or free standing graphene" has recently been proposed: "graphene is a single atomic plane of graphite, which—and this is essential—is sufficiently isolated from its environment to be considered free-standing."[12] This definition is narrower than the definitions given above and refers to cleaved, transferred and suspended graphene monolayers. Other forms of graphene, such as graphene grown on various metals, can also become free-standing if, for example, suspended or transferred to silicon dioxide (SiO2). A new example of isolated graphene is graphene on silicon carbide (SiC) after its passivation with hydrogen.[13]

[edit] Occurrence and production

In essence, graphene is an isolated atomic plane of graphite. From this perspective, graphene has been known since the invention of X-ray crystallography. Graphene planes become even better separated in intercalated graphite compounds. In 2004 physicists at the University of Manchester and the Institute for Microelectronics Technology, Chernogolovka, Russia, first isolated individual graphene planes by using Scotch tape.[14] They also measured electronic properties of the obtained flakes and showed their unique properties.[15] In 2005 the same Manchester Geim group together with the Philip Kim group from Columbia University (see the History section) demonstrated that quasiparticles in graphene were massless Dirac fermions. These discoveries led to an explosion of interest in graphene.

Since then, hundreds of researchers have entered the area, resulting in an extensive search for relevant earlier papers. Manchester researchers themselves published the first literature review.[1] They cite several papers in which graphene or ultra-thin graphitic layers were epitaxially grown on various substrates. Also, they note a number of pre-2004 reports in which intercalated graphite compounds were studied in a transmission electron microscope. In the latter case, researchers occasionally observed extremely thin graphitic flakes ("few-layer graphene" and possibly even individual layers). An early detailed study on few-layer graphene dates back to 1962.[16] The earliest TEM images of few-layer graphene were published by G. Ruess and F. Vogt in 1948.[17] However, already D.C. Brodie was aware of the highly lamellar structure of thermally reduced graphite oxide in 1859[citation needed]. It was studied in detail by V. Kohlschütter and P. Haenni in 1918, who also described the properties of graphite oxide paper.[18]

It is now well known that tiny fragments of graphene sheets are produced (along with quantities of other debris) whenever graphite is abraded, such as when drawing a line with a pencil.[14] There was little interest in this graphitic residue before 2004/05 and, therefore, the discovery of graphene is often attributed to Andre Geim and colleagues [19] who introduced graphene in its modern incarnation.

In 2008 graphene produced by exfoliation was one of the most expensive materials on Earth, with a sample that can be placed at the cross section of a human hair costing more than $1,000 as of April 2008 (about $100,000,000/cm2).[14] Since then, exfoliation procedures have been scaled up, and now companies sell graphene by the ton.[20] On the other hand, the price of epitaxial graphene on SiC is dominated by the substrate price, which is approximately $100/cm2 as of 2009. Even cheaper graphene has been produced by transfer from nickel by Korean researchers,[21] with wafer sizes up to 30 inches (760 mm) reported.[22]

In 2011 the Institute of Electronic Materials Technology, and Department of Physics, Warsaw University announced a joint development of acquisition technology of large pieces of graphene with the best quality so far. In April the same year, Polish scientists with support from the Polish Ministry of Economy began the procedure for granting a patent to their discovery around the world.

In the literature, specifically that of the surface science community, graphene has also been commonly referred to as monolayer graphite. This community has intensely studied epitaxial graphene on various surfaces (over 300 articles prior to 2004). In some cases, these graphene layers are coupled to the surfaces weakly enough (by Van der Waals forces) to retain the two dimensional electronic band structure of isolated graphene,[23][24] as also happens[15] with exfoliated graphene flakes with regard to SiO2. An example of weakly coupled epitaxial graphene is the one grown on SiC (see below).

[edit] Drawing method

In 2004, the Manchester group obtained graphene by mechanical exfoliation of graphite. They used cohesive tape to repeatedly split graphite crystals into increasingly thinner pieces. The tape with attached optically transparent flakes was dissolved in acetone, and, after a few further steps, the flakes including monolayers were sedimented on a silicon wafer. Individual atomic planes were then hunted in an optical microscope. A year later, the researchers simplified the technique and started using dry deposition, avoiding the stage when graphene floated in a liquid. Relatively large crystallites (first, only a few micrometres in size but, eventually, larger than 1 mm and visible by a naked eye) were obtained by the technique. It is often referred to as a scotch tape or drawing method. The latter name appeared because the dry deposition resembles drawing with a piece of graphite.[25] The key for the success probably was the use of high-throughput visual recognition of graphene on a properly chosen substrate, which provides a small but noticeable optical contrast. The Optical properties section below has a photograph of what graphene looks like.

The isolation of graphene led to the current research boom. Previously, free-standing atomic planes were often "presumed not to exist"[15] because they are thermodynamically unstable on a nm scale[10] and, if unsupported, have a tendency to scroll and buckle.[9] It is currently believed that intrinsic microscopic roughening on the scale of 1 nm could be important for the stability of purely 2D crystals.[26]

There were a number of previous attempts to make atomically thin graphitic films by using exfoliation techniques similar to the drawing method. Multilayer samples down to 10 nm in thickness were obtained. These efforts were reviewed in 2007.[1] Furthermore, a couple of very old papers were recently unearthed[16] in which researchers tried to isolate graphene starting with intercalated compounds (see History and experimental discovery). These papers reported the observation of very thin graphitic fragments (possibly monolayers) by transmission electron microscopy. Neither of the earlier observations was sufficient to "spark the graphene gold rush", until the Science paper did so by reporting not only macroscopic samples of extracted atomic planes but, importantly, their unusual properties such as the bipolar transistor effect, ballistic transport of charges, large quantum oscillations, etc. The discovery of such interesting qualities intrinsic to graphene gave an immediate boost to further research and several groups quickly repeated the initial result and moved further. These breakthroughs also helped to attract attention to other production techniques, such as epitaxial growth of ultra-thin graphitic films. In particular, it has later been found that graphene monolayers grown on SiC and Ir are weakly coupled to these substrates (how weakly remains debated) and the graphene-substrate interaction can be passivated further.[13]

Not only graphene but also free-standing atomic planes of boron nitride, mica, dichalcogenides and complex oxides were obtained by using the drawing method.[27] Unlike graphene, the other 2D materials have so far attracted surprisingly little attention.

[edit] Epitaxial growth on silicon carbide

Another method of obtaining graphene is to heat silicon carbide (SiC) to high temperatures (>1100 °C) to reduce it to graphene.[28] This process produces epitaxial graphene with dimensions dependent upon the size of the SiC substrate (wafer). The face of the SiC used for graphene formation, silicon- or carbon-terminated, highly influences the thickness, mobility and carrier density of the graphene.

Many important graphene properties have been identified in graphene produced by this method. For example, the electronic band-structure (so-called Dirac cone structure) has been first visualized in this material.[29][30][31] Weak anti-localization is observed in this material and not in exfoliated graphene produced by the pencil trace method.[32] Extremely large, temperature independent mobilities have been observed in SiC epitaxial graphene. They approach those in exfoliated graphene placed on silicon oxide but still much lower than mobilities in suspended graphene produced by the drawing method. It was recently shown that even without being transferred graphene on SiC exhibits the properties of massless Dirac fermions such as the anomalous quantum Hall effect.[33][34][35][36][37]

The weak van der Waals force that provides the cohesion of multilayer graphene stacks does not always affect the electronic properties of the individual graphene layers in the stack. That is, while the electronic properties of certain multilayered epitaxial graphenes are identical to that of a single graphene layer,[38] in other cases the properties are affected [29][30] as they are for graphene layers in bulk graphite. This effect is theoretically well understood and is related to the symmetry of the interlayer interactions.[38]

Epitaxial graphene on SiC can be patterned using standard microelectronics methods. The possibility of large integrated electronics on SiC epitaxial graphene was first proposed in 2004,[39] and a patent for graphene-based electronics was filed provisionally in 2003 and issued in 2006.[40] Since then, important advances have been made. In 2008, researchers at MIT Lincoln Lab produced hundreds of transistors on a single chip[41] and in 2009, very high frequency transistors were produced at the Hughes Research Laboratories on monolayer graphene on SiC.[42]

[edit] Epitaxial growth on metal substrates

This method uses the atomic structure of a metal substrate to seed the growth of the graphene (epitaxial growth). Graphene grown on ruthenium doesn't typically yield a sample with a uniform thickness of graphene layers, and bonding between the bottom graphene layer and the substrate may affect the properties of the carbon layers.[43] Graphene grown on iridium on the other hand is very weakly bonded, uniform in thickness, and can be made highly ordered. Like on many other substrates, graphene on iridium is slightly rippled. Due to the long-range order of these ripples, generation of minigaps in the electronic band-structure (Dirac cone) becomes visible.[44] High-quality sheets of few layer graphene exceeding 1 cm2 (0.2 sq in) in area have been synthesized via chemical vapor deposition on thin nickel films. These sheets have been successfully transferred to various substrates, demonstrating viability for numerous electronic applications.[22][33]

An improvement of this technique has been found in copper foil; at very low pressure, the growth automatically stops after a single graphene layer forms, and arbitrarily large graphene films can be created.[22][45] However, in atmospheric-pressure CVD growth, multilayer graphene may form on copper (similar to that seen on nickel films).[46]

[edit] Graphite oxide reduction

Graphite oxide reduction was probably historically first method of graphene synthesis. P.Boehm reported monolayer flakes of reduced graphene oxide already in 1962.[47] In this early work existence of monolayer reduced graphene oxide flakes was demonstrated. The contribution of Boehm was recently acknowledged by Nobel prize winner for graphene research, Andre Geim: (Many Pioneers in Graphene Discovery). Graphite oxide exfoliation can be achieved by rapid heating and yields highly dispersed carbon powder with few percents of graphene flakes. Reduction of graphite oxide monolayer films e.g. by hydrazine, annealing in argon/hydrogen was reported to yield graphene films. However, quality of graphene produced by graphite oxide reduction is lower compared to e.g. scotch tape graphene due to incomplete removal of various functional groups by existing reduction methods.

[edit] Growth from metal-carbon melts

The general idea in this process is to dissolve carbon atoms inside a transition metal melt at a certain temperature, and then allowing the dissolved carbon to precipitate out at lower temperatures as single layer graphene (SLG).[48] The metal is first melted in contact with a carbon source. This source could be the graphite crucible inside which the melting process is carried out or it could be the graphite powder or chunk sources which are simply placed in contact with the melt. Keeping the melt in contact with carbon source at a given temperature will give rise to dissolution and saturation of carbon atoms in the melt based on the binary phase diagram of metal-carbon. Upon lowering the temperature, solubility of the carbon in the molten metal will decrease and the excess amount of carbon will precipitate on top of the melt. The floating layer can be either skimmed or allowed to freeze for removal afterwards. Different morphology including thick graphite, few layer graphene (FLG) and SLG were observed on metal substrate. The Raman spectroscopy proved that SLG has been successfully grown on nickel substrate. The SLG Raman spectrum featured no D and D' band, indicating the pristine and high-quality nature of SLG. Among transition metals, nickel provides a better substrate for growing SLG. Since nickel is not Raman active, the direct Raman spectroscopy of graphene layers on top of the nickel is achievable. The graphene-metal composite could be utilized in thermal interface materials for thermal management applications.[48]

[edit] Pyrolysis of sodium ethoxide

A recent publication has described a process for producing gram-quantities of graphene, by the reduction of ethanol by sodium metal, followed by pyrolysis of the ethoxide product, and washing with water to remove sodium salts.[49]

[edit] From nanotubes

Experimental methods for the production of graphene ribbons are reported consisting of cutting open nanotubes.[50] In one such method multi walled carbon nanotubes are cut open in solution by action of potassium permanganate and sulfuric acid.[51] In another method graphene nanoribbons are produced by plasma etching of nanotubes partly embedded in a polymer film [52]

[edit] From sugar

Sucrose among other substances such as Plexiglas have been turned quickly and easily into graphene via application to a copper or nickel substrate and being subjected to 800 °C under low pressure with exposure to argon and hydrogen gas. The process takes only ten minutes and is scalable for industrial production. It also allows the manufacturer to modulate the purity of the graphene for applications that require electrical switching.[53][54]

[edit] Properties

[edit] Atomic structure

The atomic structure of isolated, single-layer graphene was studied by transmission electron microscopy (TEM) on sheets of graphene suspended between bars of a metallic grid.[26] Electron diffraction patterns showed the expected hexagonal lattice of graphene. Suspended graphene also showed "rippling" of the flat sheet, with amplitude of about one nanometer. These ripples may be intrinsic to graphene as a result of the instability of two-dimensional crystals,[1][55][56] or may be extrinsic, originating from the ubiquitous dirt seen in all TEM images of graphene. Atomic resolution real-space images of isolated, single-layer graphene on SiO2 substrates were obtained[57][58] by scanning tunneling microscopy. Graphene processed using lithographic techniques is covered by photoresist residue, which must be cleaned to obtain atomic-resolution images.[57] Such residue may be the "adsorbates" observed in TEM images, and may explain the rippling of suspended graphene. Rippling of graphene on the SiO2 surface was determined by conformation of graphene to the underlying SiO2, and not an intrinsic effect.[57]

Graphene sheets in solid form (density > 1 g/cm3) usually show evidence in diffraction for graphite's 0.34 nm (002) layering. This is true even of some single-walled carbon nanostructures.[59] However, unlayered graphene with only (hk0) rings has been found in the core of presolar graphite onions.[60] Transmission electron microscope studies show faceting at defects in flat graphene sheets,[61] and suggest a possible role in this unlayered-graphene for two-dimensional crystallization from a melt.

[edit] Electronic properties

GNR band structure for zig-zag orientation. Tightbinding calculations show that zigzag orientation is always metallic.

GNR band structure for arm-chair orientation. Tightbinding calculations show that armchair orientation can be semiconducting or metallic depending on width (chirality).

Graphene differs from most conventional three-dimensional materials. Intrinsic graphene is a semi-metal or zero-gap semiconductor. Understanding the electronic structure of graphene is the starting point for finding the band structure of graphite. It was realized as early as 1947 by P. R. Wallace[62] that the E-k relation is linear for low energies near the six corners of the two-dimensional hexagonal Brillouin zone, leading to zero effective mass for electrons and holes. [63] Due to this linear (or “conical") dispersion relation at low energies, electrons and holes near these six points, two of which are inequivalent, behave like relativistic particles described by the Dirac equation for spin 1/2 particles.[64][65] Hence, the electrons and holes are called Dirac fermions, and the six corners of the Brillouin zone are called the Dirac points.[64] The equation describing the E-k relation is E = \hbar v_F\sqrt{k_x^2+k_y^2}; where the Fermi velocity vF ~ 106 m/s.[65]

[edit] Electronic transport

Experimental results from transport measurements show that graphene has a remarkably high electron mobility at room temperature, with reported values in excess of 15,000 cm2V−1s−1.[1] Additionally, the symmetry of the experimentally measured conductance indicates that the mobilities for holes and electrons should be nearly the same.[63] The mobility is nearly independent of temperature between 10 K and 100 K,[66][67][68] which implies that the dominant scattering mechanism is defect scattering. Scattering by the acoustic phonons of graphene places intrinsic limits on the room temperature mobility to 200,000 cm2V−1s−1 at a carrier density of 1012 cm−2.[68][69] The corresponding resistivity of the graphene sheet would be 10−6 Ω·cm. This is less than the resistivity of silver, the lowest resistivity substance known at room temperature.[70] However, for graphene on SiO2 substrates, scattering of electrons by optical phonons of the substrate is a larger effect at room temperature than scattering by graphene’s own phonons. This limits the mobility to 40,000 cm2 V−1s−1.[68]

Despite the zero carrier density near the Dirac points, graphene exhibits a minimum conductivity on the order of 4e2 / h. The origin of this minimum conductivity is still unclear. However, rippling of the graphene sheet or ionized impurities in the SiO2 substrate may lead to local puddles of carriers that allow conduction.[63] Several theories suggest that the minimum conductivity should be 4e2/πh; however, most measurements are of order 4e2/πh or greater[1] and depend on impurity concentration.[71]

Recent experiments have probed the influence of chemical dopants on the carrier mobility in graphene.[71][72] Schedin et al. doped graphene with various gaseous species (some acceptors, some donors), and found the initial undoped state of a graphene structure can be recovered by gently heating the graphene in vacuum. They reported that even for chemical dopant concentrations in excess of 1012 cm−2 there is no observable change in the carrier mobility.[72] Chen, et al. doped graphene with potassium in ultra high vacuum at low temperature. They found that potassium ions act as expected for charged impurities in graphene,[73] and can reduce the mobility 20-fold.[71] The mobility reduction is reversible on heating the graphene to remove the potassium.

Due to its two-dimensional property, charge fractionalization (where the apparent charge of individual pseudoparticles in low-dimensional systems is less than a single quantum[74]) is thought to occur in graphene. It may therefore be a suitable material for the construction of quantum computers using anyonic circuits.[75][76]

[edit] Optical properties

Photograph of graphene in transmitted light. This one atom thick crystal can be seen with the naked eye because it absorbs approximately 2.3% of white light, which is π times the fine-structure constant.

Graphene's unique electronic properties produce an unexpectedly high opacity for an atomic monolayer, with a startlingly simple value: it absorbs πα ≈ 2.3% of white light, where α is the fine-structure constant.[77] This is "a consequence of the unusual low-energy electronic structure of monolayer graphene that features electron and hole conical bands meeting each other at the Dirac point... [which] is qualitatively different from more common quadratic massive bands".[78] Based on the Slonczewski-Weiss-McClure (SWMcC) band model of graphite, the interatomic distance, hopping value and frequency cancel when the optical conductance is calculated using the Fresnel equations in the thin-film limit.

This has been confirmed experimentally, but the measurement is not precise enough to improve on other techniques for determining the fine-structure constant.[79]

Recently it has been demonstrated that the band gap of graphene can be tuned from 0 to 0.25 eV (about 5 micrometre wavelength) by applying voltage to a dual-gate bilayer graphene field-effect transistor (FET) at room temperature.[80] The optical response of graphene nanoribbons has also been shown to be tunable into the terahertz regime by an applied magnetic field.[81] It has been shown that graphene/graphene oxide system exhibits electrochromic behavior, allowing tuning of both linear and ultrafast optical properties.[82]

[edit] Saturable absorption

It is further confirmed that such unique absorption could become saturated when the input optical intensity is above a threshold value. This nonlinear optical behavior is termed saturable absorption and the threshold value is called the saturation fluence. Graphene can be saturated readily under strong excitation over the visible to near-infrared region, due to the universal optical absorption and zero band gap. This has relevance for the mode locking of fiber lasers, where fullband mode locking has been achieved by graphene-based saturable absorber. Due to this special property, graphene has wide application in ultrafast photonics. Moreover, the ultrafast optical response of graphene/graphene oxide layers can be tuned electrically.[83] [84] [85]

[edit] Spin transport

Graphene is thought to be an ideal material for spintronics due to small spin-orbit interaction and near absence of nuclear magnetic moments in carbon. Electrical spin-current injection and detection in graphene was recently demonstrated up to room temperature.[86][87][88] Spin coherence length above 1 micrometre at room temperature was observed,[86] and control of the spin current polarity with an electrical gate was observed at low temperature.[87]

[edit] Anomalous quantum Hall effect

The quantum Hall effect is relevant for accurate measuring standards of electrical quantities, and in 1985 Klaus von Klitzing received the Nobel prize for its discovery. The effect concerns the dependence of a transverse conductivity on a magnetic field, which is perpendicular to a current-carrying stripe. Usually the phenomenon, the quantization of the so-called Hall conductivity σxy at integer multiples of the basic quantity e2 / h (where e is the elementary electric charge and h is Planck's constant) can be observed only in very clean Si or GaAs solids, and at very low temperatures around 3 K, and at very high magnetic fields.

Graphene in contrast, besides its high mobility and minimum conductivity, and because of certain peculiarities explained in Pseudo-relativistic theory below, shows particularly interesting behavior just in the presence of a magnetic field and just with respect to the conductivity-quantization: it displays an anomalous quantum Hall effect with the sequence of steps shifted by 1/2 with respect to the standard sequence, and with an additional factor of 4. Thus, in graphene the Hall conductivity is \sigma_{xy} = \pm {4\cdot\left(N + 1/2 \right)e^2}/h , where N is the above-mentioned integer "Landau level" index, and the double valley and double spin degeneracies give the factor of 4.[1] Moreover, in graphene these remarkable anomalies can even be measured at room temperature, i.e. at roughly 20 °C.[66] This anomalous behavior is a direct result of the emergent massless Dirac electrons in graphene. In a magnetic field, their spectrum has a Landau level with energy precisely at the Dirac point. This level is a consequence of the Atiyah-Singer index theorem and is half-filled in neutral graphene,[64] leading to the "+1/2" in the Hall conductivity.[89] Bilayer graphene also shows the quantum Hall effect, but with the standard sequence (with \sigma_{xy} = \pm {4\cdot N\cdot e^2}/h ), i.e. with only one of the two anomalies. Interestingly, concerning the second anomaly, the first plateau at N = 0 is absent, indicating that bilayer graphene stays metallic at the neutrality point.[1]

Unlike normal metals, the longitudinal resistance of graphene shows maxima rather than minima for integral values of the Landau filling factor in measurements of the Shubnikov-de Haas oscillations, which show a phase shift of π, known as Berry’s phase.[63][66] The Berry’s phase arises due to the zero effective carrier mass near the Dirac points.[90] Study of the temperature dependence of the Shubnikov-de Haas oscillations in graphene reveals that the carriers have a non-zero cyclotron mass, despite their zero effective mass from the E-k relation.[66]

[edit] Nanostripes: Spin-polarized edge currents

Nanostripes of graphene (in the "zig-zag" orientation), at low temperatures, show spin-polarized metallic edge currents, which also suggests applications in the new field of spintronics. (In the "armchair" orientation, the edges behave like semiconductors.[91])

[edit] Graphene oxide

Further information: Graphite Oxide

By dispersing oxidized and chemically processed graphite in water, and using paper-making techniques, the monolayer flakes form a single sheet and bond very powerfully. These sheets, called graphene oxide paper have a measured tensile modulus of 32 GPa.[92] The peculiar chemical property of graphite oxide is related to the functional groups attached to graphene sheets. They even can significantly change the pathway of polymerization and similar chemical processes.[93] Graphene Oxide flakes in polymers also shown enhanced photo-conducting properties.[94]

[edit] Chemical modification

Photograph of single-layer graphene oxide undergoing high temperature chemical treatment, resulting in sheet folding and loss of carboxylic functionality, or through room temperature carbodiimide treatment, collapsing into star-like clusters.

Soluble fragments of graphene can be prepared in the laboratory[95] through chemical modification of graphite. First, microcrystalline graphite is treated with a strongly acidic mixture of sulfuric acid and nitric acid. A series of steps involving oxidation and exfoliation result in small graphene plates with carboxyl groups at their edges. These are converted to acid chloride groups by treatment with thionyl chloride; next, they are converted to the corresponding graphene amide via treatment with octadecylamine. The resulting material (circular graphene layers of 5.3 angstrom thickness) is soluble in tetrahydrofuran, tetrachloromethane and dichloroethane[disambiguation needed]. Refluxing single-layer graphene oxide (SLGO) in solvents leads to size reduction and folding of the individual sheets as well as loss of carboxylic group functionality, by up to 20%, indicating thermal instabilities of SLGO sheets dependant on their preparation methodology. When using thionyl chloride, acyl chloride groups result, which can then form aliphatic and aromatic amides with a reactivity conversion of around 70-80%.

Boehm titration results for various chemical reactions of single-layer graphene oxide, which reveal reactivity of the carboxylic groups and the resultant stability of the SLGO sheets after treatment.

Hydrazine reflux is commonly used for reducing SLGO to SLG(R), but titrations show that only around 20-30% of the carboxylic groups are lost leaving a significant number of COOH groups available for chemical attachment. Analysis of SLG(R) generated by this route reveals that the system is unstable and using a room temperature stirring with HCl (< 1.0 M) leads to around 60% loss of COOH functionality. Room temperature treatment of SLGO with carbodiimides leads to the collapse of the individual sheets into star-like clusters, which exhibited poor subsequent reactivity with amines (ca. 3-5% conversion of the intermediate to the final amide).[96] It is apparent that conventional chemical treatment of carboxylic groups on SLGO generates morphological changes of individual sheets that leads to a reduction in chemical reactivity, which may potentially limit their use in composite synthesis. Therefore, other types of chemical reactions have been explored. SLGO has also been grafted with polyallylamine, cross-linked through epoxy groups. When filtered into graphene oxide paper, these composites exhibit sheets increased stiffness and strength relative to unmodified graphene oxide paper.[97]

Full hydrogenation from both sides of graphene sheet results in graphane, but partial hydrogenation leads to hydrogenated graphene[98]

[edit] Thermal properties

The near-room temperature thermal conductivity of graphene was recently measured to be between (4.84±0.44) ×103 to (5.30±0.48) ×103 Wm−1K−1. These measurements, made by a non-contact optical technique, are in excess of those measured for carbon nanotubes or diamond. It can be shown by using the Wiedemann-Franz law, that the thermal conduction is phonon-dominated.[99] However, for a gated graphene strip, an applied gate bias causing a Fermi energy shift much larger than kBT can cause the electronic contribution to increase and dominate over the phonon contribution at low temperatures. The ballistic thermal conductance of graphene is isotropic.[100]

Potential for this high conductivity can be seen by considering graphite, a 3D version of graphene that has basal plane thermal conductivity of over a 1000 Wm−1K−1 (comparable to diamond). In graphite, the c-axis (out of plane) thermal conductivity is over a factor of ~100 smaller due to the weak binding forces between basal planes as well as the larger lattice spacing.[101] In addition, the ballistic thermal conductance of a graphene is shown to give the lower limit of the ballistic thermal conductances, per unit circumference, length of carbon nanotubes.[102]

Despite its 2-D nature, graphene has 3 acoustic phonon modes. The two in-plane modes (LA, TA) have a linear dispersion relation, whereas the out of plane mode (ZA) has a quadratic dispersion relation. Due to this, the T2 dependent thermal conductivity contribution of the linear modes is dominated at low temperatures by the T1.5 contribution of the out of plane mode.[102] Some graphene phonon bands display negative Grüneisen parameters.[103] At low temperatures (where most optical modes with positive Grüneisen parameters are still not excited) the contribution from the negative Grüneisen parameters will be dominant and thermal expansion coefficient (which is directly proportional to Grüneisen parameters) negative. The lowest negative Grüneisen parameters correspond to the lowest transversal acoustic ZA modes. Phonon frequencies for such modes increase with the in-plane lattice parameter since atoms in the layer upon stretching will be less free to move in the z direction. This is similar to the behavior of a string which is being stretched will have vibrations of smaller amplitude and higher frequency. This phenomenon, named "membrane effect", was predicted by Lifshitz in 1952.[104]

[edit] Mechanical properties

As of 2009, graphene appears to be one of the strongest materials ever tested. Measurements have shown that graphene has a breaking strength 200 times greater than steel, with a tensile strength of 130GPa (19,000,000 psi).[105] However, the process of separating it from graphite, where it occurs naturally, will require some technological development before it is economical enough to be used in industrial processes,[106] though this may be changing soon.[107]

Graphene paper or GP has recently been developed by a research department from the University of Technology Sydney by Guoxiu Wang, that can be processed, reshaped and reformed from its original raw material state. Researchers have successfully milled the raw graphite by purifying and filtering it with chemicals to reshape and reform it into nano-structured configurations which are then processed into sheets as thin as paper, according to a university statement. Lead researcher Ali Reza Ranjbartoreh said: 'Not only is it lighter, stronger, harder and more flexible than steel, it is also a recyclable and sustainably manufacturable product that is eco-friendly and cost effective in its use.' Ranjbartoreh said the results would allow the development of lighter and stronger cars and planes that use less fuel, generate less pollution, are cheaper to run and ecologically sustainable. He said large aerospace companies such as Boeing have already started to replace metals with carbon fibres and carbon-based materials, and graphene paper with its incomparable mechanical properties would be the next material for them to explore.


Using an atomic force microscope (AFM), the spring constant of suspended graphene sheets has been measured. Graphene sheets, held together by van der Waals forces, were suspended over SiO2 cavities where an AFM tip was probed to test its mechanical properties. Its spring constant was in the range 1–5 N/m and the Young's modulus was 0.5 TPa, which differs from that of the bulk graphite. These high values make graphene very strong and rigid. These intrinsic properties could lead to using graphene for NEMS applications such as pressure sensors and resonators.[108]

As is true of all materials, regions of graphene are subject to thermal and quantum fluctuations in relative displacement. Although the amplitude of these fluctuations is bounded in 3D structures (even in the limit of infinite size), the Mermin-Wagner theorem shows that the amplitude of long-wavelength fluctuations will grow logarithmically with the scale of a 2D structure, and would therefore be unbounded in structures of infinite size. Local deformation and elastic strain are negligibly affected by this long-range divergence in relative displacement. It is believed that a sufficiently large 2D structure, in the absence of applied lateral tension, will bend and crumple to form a fluctuating 3D structure. Researchers have observed ripples in suspended layers of graphene,[26] and it has been proposed that the ripples are caused by thermal fluctuations in the material. As a consequence of these dynamical deformations, it is debatable whether graphene is truly a 2D structure.[1][55][56]

[edit] Casimir effect

The Casimir effect is generated by extremely thin plates of electrically conducting materials.[109] Since graphene fulfils those criteria, it probably can be used for generating a Casimir effect as well.[110][111]

[edit] Potential applications

[edit] Single molecule gas detection

Graphene makes an excellent sensor due to its 2D structure. The fact that its entire volume is exposed to its surrounding makes it very efficient to detect adsorbed molecules. Molecule detection is indirect: as a gas molecule adsorbs to the surface of graphene, the location of absorption experiences a local change in electrical resistance. While this effect occurs in other materials, graphene is superior due to its high electrical conductivity (even when few carriers are present) and low noise which makes this change in resistance detectable.[72]

[edit] Graphene nanoribbons

Graphene nanoribbons (GNRs) are essentially single layers of graphene that are cut in a particular pattern to give it certain electrical properties. Depending on how the un-bonded edges are configured, they can either be in a zigzag or armchair configuration. Calculations based on tight binding predict that zigzag GNRs are always metallic while armchairs can be either metallic or semiconducting, depending on their width. However, recent density functional theory calculations show that armchair nanoribbons are semiconducting with an energy gap scaling with the inverse of the GNR width.[112] Indeed, experimental results show that the energy gaps do increase with decreasing GNR width.[113] However, as of February 2008, no experimental results have measured the energy gap of a GNR and identified the exact edge structure. Zigzag nanoribbons are also semiconducting and present spin polarized edges. Their 2D structure, high electrical and thermal conductivity, and low noise also make GNRs a possible alternative to copper for integrated circuit interconnects. Some research is also being done to create quantum dots by changing the width of GNRs at select points along the ribbon, creating quantum confinement.[114]

[edit] Graphene transistors

Due to its high electronic quality, graphene has also attracted the interest of technologists who see it as a way of constructing ballistic transistors. Graphene exhibits a pronounced response to perpendicular external electric fields, allowing one to build FETs (field-effect transistors). In their 2004 paper,[15] the Manchester group demonstrated FETs with a "rather modest" on-off ratio of ~30 at room temperature. In 2006, Georgia Tech researchers, led by Prof. de Heer, announced that they had successfully built an all-graphene planar FET with side gates.[115] Their devices showed changes of 2% at cryogenic temperatures. The first top-gated FET (on-off ratio of <2) was demonstrated by researchers of AMICA and RWTH Aachen University in 2007.[116] Graphene nanoribbons may prove generally capable of replacing silicon as a semiconductor in modern technology.[117]

Facing the fact that current graphene transistors show a very poor on-off ratio, researchers are trying to find ways for improvement. In 2008 researchers of AMICA and University of Manchester demonstrated a new switching effect in graphene field-effect devices. This switching effect is based on a reversible chemical modification of the graphene layer and gives an on-off ratio of greater than six orders of magnitude. These reversible switches could potentially be applied to nonvolatile memories.[118]

In 2009 researchers at the Politecnico di Milano demonstrated four different types of logic gates, each composed of a single graphene transistor.[119] In the same year, the Massachusetts Institute of Technology researchers built an experimental graphene chip known as a frequency multiplier. It is capable of taking an incoming electrical signal of a certain frequency and producing an output signal that is a multiple of that frequency.[120] Although these graphene chips open up a range of new applications, their practical use is limited by a very small voltage gain (typically, the amplitude of the output signal is about 40 times less than that of the input signal). Moreover, none of these circuits was demonstrated to operate at frequencies higher than 25 kHz.

In February 2010, researchers at IBM reported that they have been able to create graphene transistors with an on and off rate of 100 gigahertz, far exceeding the rates of previous attempts, and exceeding the speed of silicon transistors with an equal gate length. The 240 nm graphene transistors made at IBM were made using extant silicon-manufacturing equipment, meaning that for the first time graphene transistors are a conceivable—though still fanciful—replacement for silicon.[121] [122] [123]

[edit] Integrated circuits

Graphene has the ideal properties to be an excellent component of integrated circuits. Graphene has a high carrier mobility, as well as low noise, allowing it to be used as the channel in a FET. The issue is that single sheets of graphene are hard to produce, and even harder to make on top of an appropriate substrate. Researchers are looking into methods of transferring single graphene sheets from their source of origin (mechanical exfoliation on SiO2 / Si or thermal graphitization of a SiC surface) onto a target substrate of interest.[124] In 2008, the smallest transistor so far, one atom thick, 10 atoms wide was made of graphene.[125] IBM announced in December 2008 that they fabricated and characterized graphene transistors operating at GHz frequencies.[126] In May 2009, an n-type transistor was announced meaning that both n and p-type transistors have now been created with graphene.[127] A functional graphene integrated circuit was also demonstrated – a complementary inverter consisting of one p- and one n-type graphene transistor.[128] However, this inverter also suffered from a very low voltage gain.

According to a January 2010 report,[129] graphene was epitaxially grown on SiC in a quantity and with quality suitable for mass production of integrated circuits. At high temperatures, the Quantum Hall effect could be measured in these samples. See also the 2010 work by IBM in the transistor section above in which they made 'processors' of fast transistors on 2-inch (51 mm) graphene sheets.[121][122]

[edit] Electrochromic devices

Graphene Oxide can be reversibly reduced and oxidized using electrical stimulus. Controlled reduction and oxidation in two-terminal devices containing multilayer graphene oxide films are shown to result in switching between partially reduced graphene oxide and graphene, a process which modifies the electronic and optical properties. Oxidation and reduction are also shown to be related to resistive switching. [130] [131]

[edit] Transparent conducting electrodes

Graphene's high electrical conductivity and high optical transparency make it a candidate for transparent conducting electrodes, required for such applications as touchscreens, liquid crystal displays, organic photovoltaic cells, and organic light-emitting diodes. In particular, graphene's mechanical strength and flexibility are advantageous compared to indium tin oxide, which is brittle, and graphene films may be deposited from solution over large areas.[132][133]

Large-area, continuous, transparent, and highly conducting few-layered graphene films were produced by chemical vapor deposition and used as anodes for application in photovoltaic devices. A power conversion efficiency (PCE) up to 1.71% was demonstrated, which is 55.2% of the PCE of a control device based on indium-tin-oxide.[134]

Organic light-emitting diodes (OLEDs) with graphene anodes have also been demonstrated.[135] The electronic and optical performance of devices based on graphene are shown to be similar to devices made with indium-tin-oxide.

An all carbon-based device called a Light-emitting Electrochemical Cell (LEC) was demonstrated with chemically derived graphene as the cathode and the conductive polymer PEDOT as the anode by Matyba et al.[136] Unlike its predecessors, this device contains no metal, but only carbon-based electrodes. The use of graphene as the anode in LECs was also verified in the same publication.

[edit] Reference material for characterizing electroconductive and transparent materials

One layer of graphene absorbs 2.3 % of white light.[137] This property was used to define the Conductivity of Transparency that combines the sheet resistance and the transparency. This parameter was used to compare different materials without the use of two independent parameters.[138]

[edit] Thermal management materials-Thermal interfacial materials

In 2011, researchers in Georgia Institute of Technology reported that a three-dimensional vertically aligned functionalized multilayer graphene architecture can be an approach for graphene-based thermal interfacial materials (TIMs) with superior equivalent thermal conductivity and ultra-low interfacial thermal resistance between graphene and metal.[139]

[edit] Solar cells

The USC Viterbi School of Engineering lab reported the large scale production of highly transparent graphene films by chemical vapor deposition three years ago. In this process, researchers create ultra-thin graphene sheets by first depositing carbon atoms in the form of graphene films on a nickel plate from methane gas. Then they lay down a protective layer of thermoplastic over the graphene layer and dissolve the nickel underneath in an acid bath. In the final step they attach the plastic-protected graphene to a very flexible polymer sheet, which can then be incorporated into a OPV cell (graphene photovoltaics). Graphene/polymer sheets have been produced that range in size up to 150 square centimeters and can be used to create dense arrays of flexible OPV cells. It may eventually be possible to run printing presses laying extensive areas covered with inexpensive solar cells, much like newspaper presses print newspapers (roll-to-roll)[140][141]

[edit] Ultracapacitors

Due to the extremely high surface area to mass ratio of graphene, one potential application is in the conductive plates of ultracapacitors. It is believed that graphene could be used to produce ultracapacitors with a greater energy storage density than is currently available.[142]

[edit] Graphene biodevices

Graphene's modifiable chemistry, large surface area, atomic thickness and molecularly-gatable structure make antibody-functionalized graphene sheets excellent candidates for mammalian and microbial detection and diagnosis devices.[143]

Energy of the electrons with wavenumber k in graphene, calculated in the Tight Binding-approximation. The unoccupied (occupied) states, colored in blue-red (yellow-green), touch each other without energy gap exactly at the above-mentioned six k-vectors.

The most ambitious biological application of graphene is for rapid, inexpensive electronic DNA sequencing. Integration of graphene (thickness of 0.34 nm) layers as nanoelectrodes into a nanopore[144] can solve one of the bottleneck issues of nanopore-based single-molecule DNA sequencing.

[edit] Anti-bacterial

The Chinese Academy of Sciences has found that sheets of graphene oxide are highly effective at killing bacteria such as Escherichia coli. This means graphene could be useful in applications such as hygiene products or packaging that will help keep food fresh for longer.[145]

[edit] Pseudo-relativistic theory

The electrical properties of graphene can be described by a conventional tight-binding model; in this model the energy of the electrons with wave vector k is[62][64]

E=\pm\sqrt{\gamma_0^2\left(1+4\cos^2{\frac{k_ya}{2}}+4\cos{\frac{k_ya}{2}} \cdot \cos{\frac{k_x\sqrt{3}a}{2}}\right)},

with the nearest-neighbor hopping energy γ0 ≈ 2.8 eV and the lattice constant a ≈ 2.46 Å. Conduction and valence band, respectively, correspond to the different signs in the above dispersion relation; they touch each other in six points, the "K-values". However, only two of these six points are independent, whereas the rest is equivalent by symmetry. In the vicinity of the K-points the energy depends linearly on the wave vector, similar to a relativistic particle. Since an elementary cell of the lattice has a basis of two atoms, the wave function even has an effective 2-spinor structure. As a consequence, at low energies, even neglecting the true spin, the electrons can be described by an equation which is formally equivalent to the massless Dirac equation. Moreover, in the present case this pseudo-relativistic description is restricted to the chiral limit, i.e., to vanishing rest mass M0, which leads to interesting additional features:[64]

v_F\, \vec \sigma \cdot \nabla \psi(\mathbf{r})\,=\,E\psi(\mathbf{r}).

Here vF ~ 106 is the Fermi velocity in graphene which replaces the velocity of light in the Dirac theory; \vec{\sigma} is the vector of the Pauli matrices, \psi(\mathbf{r}) is the two-component wave function of the electrons, and E is their energy.[91]

[edit] History and experimental discovery

The term graphene first appeared in 1987[146] to describe single sheets of graphite as one of the constituents of graphite intercalation compounds (GICs); conceptually a GIC is a crystalline salt of the intercalant and graphene. The term was also used in early descriptions of carbon nanotubes,[147] as well as for epitaxial graphene,[148] and polycyclic aromatic hydrocarbons.[149]

Larger graphene molecules or sheets (so that they can be considered as true isolated 2D crystals) cannot be grown even in principle. An article in Physics Today reads:

Fundamental forces place seemingly insurmountable barriers in the way of creating [2D crystals]... The nascent 2D crystallites try to minimize their surface energy and inevitably morph into one of the rich variety of stable 3D structures that occur in soot.

But there is a way around the problem. Interactions with 3D structures stabilize 2D crystals during growth. So one can make 2D crystals sandwiched between or placed on top of the atomic planes of a bulk crystal. In that respect, graphene already exists within graphite... One can then hope to fool Nature and extract single-atom-thick crystallites at a low enough temperature that they remain in the quenched state prescribed by the original higher-temperature 3D growth.[25]

Single layers of graphite were previously (starting from the 1970s) grown epitaxially on top of other materials.[150] This "epitaxial graphene" consists of a single-atom-thick hexagonal lattice of sp2-bonded carbon atoms, as in free-standing graphene. However, there is significant charge transfer from the substrate to the epitaxial graphene, and, in some cases, hybridization between the d orbitals of the substrate atoms and π orbitals of graphene, which significantly alters the electronic structure of the epitaxial graphene.

Single layers of graphite were also observed by transmission electron microscopy within bulk materials (see section Occurrence), in particular inside soot obtained by chemical exfoliation.[14] There have also been a number of efforts to make very thin films of graphite by mechanical exfoliation (starting from 1990 and continuing until after 2004)[14] but nothing thinner than 50 to 100 layers was produced during these years.

A key advance in the science of graphene came when Andre Geim and Kostya Novoselov at Manchester University managed to extract single-atom-thick crystallites (graphene) from bulk graphite in 2004.[15] The Manchester researchers pulled out graphene layers from graphite and transferred them onto thin SiO2 on a silicon wafer in a process sometimes called micromechanical cleavage or, simply, the Scotch tape technique. The SiO2 electrically isolated the graphene, and was weakly interacting with the graphene, providing nearly charge-neutral graphene layers. The silicon beneath the SiO2 could be used as a "back gate" electrode to vary the charge density in the graphene layer over a wide range.

The micromechanical cleavage technique led directly to the first observation of the anomalous quantum Hall effect in graphene,[66][90] which provided direct evidence of the theoretically predicted pi Berry's phase of massless Dirac fermions in graphene. The anomalous quantum Hall effect in graphene was reported around the same time by Geim and Novoselov and by Philip Kim and Yuanbo Zhang in 2005.

Geim has received several awards for his pioneering research on graphene, including the 2007 Mott medal for the "discovery of a new class of materials – free-standing two-dimensional crystals – in particular graphene", the 2008 EuroPhysics Prize (together with Novoselov) "for discovering and isolating a single free-standing atomic layer of carbon (graphene) and elucidating its remarkable electronic properties", and the 2009 Körber Prize for "develop[ing] the first two-dimensional crystals made of carbon atoms". In 2008 and 2009, Reuters (which also runs a bibliometric service Web of Science) tipped him as one of the front-runners for a Nobel prize in Physics.[151] On October 5, 2010, the Nobel Prize in Physics for the year was awarded to Andre Geim and Konstantin Novoselov from the University of Manchester for their work on graphene.[152]

The theory of graphene was first explored by P. R. Wallace in 1947 as a starting point for understanding the electronic properties of more complex, 3D graphite. The emergent massless Dirac equation was first pointed out by Gordon Walter Semenoff and David P. DeVincenzo and Eugene J. Mele.[153] Semenoff emphasized the occurrence in a magnetic field of an electronic Landau level precisely at the Dirac point. This level is responsible for the anomalous integer quantum Hall effect.[66][89][90] Later, single graphene layers were also observed directly by electron microscopy.[26]

More recently, graphene samples prepared on nickel films, and on both the silicon face and carbon face of silicon carbide, have shown the anomalous quantum Hall effect directly in electrical measurements.[33][34][35][36][37] Graphitic layers on the carbon face of silicon carbide show a clear Dirac spectrum in angle-resolved photoemission experiments, and the anomalous quantum Hall effect is observed in cyclotron resonance and tunneling experiments.[154] Even though graphene on nickel and on silicon carbide have both existed in the laboratory for decades, it was graphene mechanically exfoliated on SiO2 that provided the first proof of the Dirac fermion nature of electrons in graphene.[citation needed]

[edit] See also

[edit] References

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[hide]v · d · eAllotropes of carbon
sp3 forms
sp2 forms
sp forms
mixed sp3/sp2 forms
other forms
C1 • C2 • C3 • C8
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