Showing papers on "Graphene oxide paper published in 2008"
TL;DR: Graphene is established as the strongest material ever measured, and atomically perfect nanoscale materials can be mechanically tested to deformations well beyond the linear regime.
Abstract: We measured the elastic properties and intrinsic breaking strength of free-standing monolayer graphene membranes by nanoindentation in an atomic force microscope. The force-displacement behavior is interpreted within a framework of nonlinear elastic stress-strain response, and yields second- and third-order elastic stiffnesses of 340 newtons per meter (N m(-1)) and -690 Nm(-1), respectively. The breaking strength is 42 N m(-1) and represents the intrinsic strength of a defect-free sheet. These quantities correspond to a Young's modulus of E = 1.0 terapascals, third-order elastic stiffness of D = -2.0 terapascals, and intrinsic strength of sigma(int) = 130 gigapascals for bulk graphite. These experiments establish graphene as the strongest material ever measured, and show that atomically perfect nanoscale materials can be mechanically tested to deformations well beyond the linear regime.
18,008 citations
TL;DR: It is reported that chemically converted graphene sheets obtained from graphite can readily form stable aqueous colloids through electrostatic stabilization, making it possible to process graphene materials using low-cost solution processing techniques, opening up enormous opportunities to use this unique carbon nanostructure for many technological applications.
Abstract: Graphene sheets offer extraordinary electronic, thermal and mechanical properties and are expected to find a variety of applications. A prerequisite for exploiting most proposed applications for graphene is the availability of processable graphene sheets in large quantities. The direct dispersion of hydrophobic graphite or graphene sheets in water without the assistance of dispersing agents has generally been considered to be an insurmountable challenge. Here we report that chemically converted graphene sheets obtained from graphite can readily form stable aqueous colloids through electrostatic stabilization. This discovery has enabled us to develop a facile approach to large-scale production of aqueous graphene dispersions without the need for polymeric or surfactant stabilizers. Our findings make it possible to process graphene materials using low-cost solution processing techniques, opening up enormous opportunities to use this unique carbon nanostructure for many technological applications.
8,534 citations
TL;DR: Graphene dispersions with concentrations up to approximately 0.01 mg ml(-1), produced by dispersion and exfoliation of graphite in organic solvents such as N-methyl-pyrrolidone are demonstrated.
Abstract: Fully exploiting the properties of graphene will require a method for the mass production of this remarkable material. Two main routes are possible: large-scale growth or large-scale exfoliation. Here, we demonstrate graphene dispersions with concentrations up to approximately 0.01 mg ml(-1), produced by dispersion and exfoliation of graphite in organic solvents such as N-methyl-pyrrolidone. This is possible because the energy required to exfoliate graphene is balanced by the solvent-graphene interaction for solvents whose surface energies match that of graphene. We confirm the presence of individual graphene sheets by Raman spectroscopy, transmission electron microscopy and electron diffraction. Our method results in a monolayer yield of approximately 1 wt%, which could potentially be improved to 7-12 wt% with further processing. The absence of defects or oxides is confirmed by X-ray photoelectron, infrared and Raman spectroscopies. We are able to produce semi-transparent conducting films and conducting composites. Solution processing of graphene opens up a range of potential large-area applications, from device and sensor fabrication to liquid-phase chemistry.
5,600 citations
TL;DR: Transparent, conductive, and ultrathin graphene films, as an alternative to the ubiquitously employed metal oxides window electrodes for solid-state dye-sensitized solar cells, are demonstrated and show high chemical and thermal stabilities and an ultrasmooth surface with tunable wettability.
Abstract: Transparent, conductive, and ultrathin graphene films, as an alternative to the ubiquitously employed metal oxides window electrodes for solid-state dye-sensitized solar cells, are demonstrated. These graphene films are fabricated from exfoliated graphite oxide, followed by thermal reduction. The obtained films exhibit a high conductivity of 550 S/cm and a transparency of more than 70% over 1000−3000 nm. Furthermore, they show high chemical and thermal stabilities as well as an ultrasmooth surface with tunable wettability.
4,314 citations
TL;DR: A solution-based method is reported that allows uniform and controllable deposition of reduced graphene oxide thin films with thicknesses ranging from a single monolayer to several layers over large areas, which could represent a route for translating the interesting fundamental properties of graphene into technologically viable devices.
Abstract: The integration of novel materials such as single-walled carbon nanotubes and nanowires into devices has been challenging, but developments in transfer printing and solution-based methods now allow these materials to be incorporated into large-area electronics1,2,3,4,5,6. Similar efforts are now being devoted to making the integration of graphene into devices technologically feasible7,8,9,10. Here, we report a solution-based method that allows uniform and controllable deposition of reduced graphene oxide thin films with thicknesses ranging from a single monolayer to several layers over large areas. The opto-electronic properties can thus be tuned over several orders of magnitude, making them potentially useful for flexible and transparent semiconductors or semi-metals. The thinnest films exhibit graphene-like ambipolar transistor characteristics, whereas thicker films behave as graphite-like semi-metals. Collectively, our deposition method could represent a route for translating the interesting fundamental properties of graphene into technologically viable devices.
4,174 citations
TL;DR: Only the alternating pattern of single-double carbon bonds within the sp2 carbon ribbons provides a satisfactory explanation for the experimentally observed blue shift of the G band of the Raman spectra relative to graphite.
Abstract: We investigate Raman spectra of graphite oxide and functionalized graphene sheets with epoxy and hydroxyl groups and Stone−Wales and 5−8−5 defects by first-principles calculations to interpret our experimental results. Only the alternating pattern of single−double carbon bonds within the sp2 carbon ribbons provides a satisfactory explanation for the experimentally observed blue shift of the G band of the Raman spectra relative to graphite. To obtain these single−double bonds, it is necessary to have sp3 carbons on the edges of a zigzag carbon ribbon.
4,000 citations
TL;DR: The work presented here will not only open a new way for preparing water-soluble graphene dispersions but also provide a general route for fabricating conducting films based on graphene.
Abstract: Flexible graphene films were prepared by the filtration of water-soluble noncovalently functionalized graphene sheets with pyrenebutyrate. The work presented here will not only open a new way for preparing water-soluble graphene dispersions but also provide a general route for fabricating conducting films based on graphene.
3,079 citations
TL;DR: These experiments demonstrate solution-processed GO films have potential as transparent electrodes and sheet resistance and optical transparency using different reduction treatments.
Abstract: Processable, single-layered graphene oxide (GO) is an intriguing nanomaterial with tremendous potential for electronic applications. We spin-coated GO thin-films on quartz and characterized their sheet resistance and optical transparency using different reduction treatments. A thermal graphitization procedure was most effective, producing films with sheet resistances as low as 102 −103 Ω/square with 80% transmittance for 550 nm light. Our experiments demonstrate solution-processed GO films have potential as transparent electrodes.
3,011 citations
TL;DR: This pressurized graphene membrane is the world's thinnest balloon and provides a unique separation barrier between 2 distinct regions that is only one atom thick.
Abstract: We demonstrate that a monolayer graphene membrane is impermeable to standard gases including helium. By applying a pressure difference across the membrane, we measure both the elastic constants and the mass of a single layer of graphene. This pressurized graphene membrane is the world's thinnest balloon and provides a unique separation barrier between 2 distinct regions that is only one atom thick.
2,648 citations
TL;DR: A facile and scalable preparation of aqueous solutions of isolated, sparingly sulfonated graphene is reported, and NMR and FTIR spectra indicate that the bulk of the oxygen-containing functional groups was removed from graphene oxide.
Abstract: A facile and scalable preparation of aqueous solutions of isolated, sparingly sulfonated graphene is reported. 13C NMR and FTIR spectra indicate that the bulk of the oxygen-containing functional groups was removed from graphene oxide. The electrical conductivity of thin evaporated films of graphene (1250 S/m) relative to similarly prepared graphite (6120 S/m) implies that an extended conjugated sp2 network is restored in the water soluble graphene.
2,577 citations
TL;DR: In all of these solvents, full exfoliation of the graphite oxide material into individual, single-layer graphene oxide sheets was achieved by sonication, and graphene oxide dispersions exhibited long-term stability and were made of sheets between a few hundred nanometers and a few micrometers large.
Abstract: The dispersion behavior of graphene oxide in different organic solvents has been investigated. As-prepared graphite oxide could be dispersed in N,N-dimethylformamide, N-methyl-2-pyrrolidone, tetrahydrofuran, and ethylene glycol. In all of these solvents, full exfoliation of the graphite oxide material into individual, single-layer graphene oxide sheets was achieved by sonication. The graphene oxide dispersions exhibited long-term stability and were made of sheets between a few hundred nanometers and a few micrometers large, similar to the case of graphene oxide dispersions in water. These results should facilitate the manipulation and processing of graphene-based materials for different applications.
TL;DR: The photocatalytic methodology not only provides an on-demand UV-assisted reduction technique but also opens up new ways to obtain photoactive graphene-semiconductor composites.
Abstract: Graphene oxide suspended in ethanol undergoes reduction as it accepts electrons from UV-irradiated TiO2 suspensions. The reduction is accompanied by changes in the absorption of the graphene oxide, as the color of the suspension shifts from brown to black. The direct interaction between TiO2 particles and graphene sheets hinders the collapse of exfoliated sheets of graphene. Solid films cast on a borosilicate glass gap separated by gold-sputtered terminations show an order of magnitude decrease in lateral resistance following reduction with the TiO2 photocatalyst. The photocatalytic methodology not only provides an on-demand UV-assisted reduction technique but also opens up new ways to obtain photoactive graphene-semiconductor composites.
TL;DR: It is shown that epitaxy on Ru(0001) produces arrays of macroscopic single-crystalline graphene domains in a controlled, layer-by-layer fashion, and demonstrates a route towards rational graphene synthesis on transition-metal templates for applications in electronics, sensing or catalysis.
Abstract: Graphene has been used to explore the fascinating electronic properties of ideal two-dimensional carbon, and shows great promise for quantum device architectures. The primary method for isolating graphene, micromechanical cleavage of graphite, is di cult to scale up for applications. Epitaxial growth is an attractive alternative, but achieving large graphene domains with uniform thickness remains a challenge, and substrate bonding may strongly a ect the electronic properties of epitaxial graphene layers. Here, we show that epitaxy on Ru(0001) produces arrays of macroscopic single-crystalline graphene domains in a controlled, layer-by-layer fashion. Whereas the first graphene layer indeed interacts strongly with the metal substrate, the second layer is almost completely detached, shows weak electronic coupling to the metal, and hence retains the inherent electronic structure of graphene. Our findings demonstrate a route towards rational graphene synthesis on transition-metal templates for applications in electronics, sensing or catalysis.
TL;DR: It is reported that the exfoliation-reintercalation-expansion of graphite can produce high-quality single-layer graphene sheets stably suspended in organic solvents that exhibit high electrical conductance at room and cryogenic temperatures.
Abstract: Graphene is an intriguing material with properties that are distinct from those of other graphitic systems1,2,3,4,5. The first samples of pristine graphene were obtained by ‘peeling off’2,6 and epitaxial growth5,7. Recently, the chemical reduction of graphite oxide was used to produce covalently functionalized single-layer graphene oxide8,9,10,11,12,13,14,15. However, chemical approaches for the large-scale production of highly conducting graphene sheets remain elusive. Here, we report that the exfoliation–reintercalation–expansion of graphite can produce high-quality single-layer graphene sheets stably suspended in organic solvents. The graphene sheets exhibit high electrical conductance at room and cryogenic temperatures. Large amounts of graphene sheets in organic solvents are made into large transparent conducting films by Langmuir–Blodgett assembly in a layer-by-layer manner. The chemically derived, high-quality graphene sheets could lead to future scalable graphene devices. The first samples of pristine graphene were obtained by 'peeling off' and epitaxial growth, but chemical approaches are more suited to large-scale production. Exfoliation, reintercalation and expansion of graphite can produce high-quality single-layer graphene sheets suspended in organic solvents, and these sheets can be made into large transparent films by Langmuir–Blodgett assembly.
TL;DR: In this paper, a study was conducted to demonstrate that highly ordered graphene paper can be prepared by directional flow-induced assembly of graphene sheets that are well dispersed in solution, which can enhance its mechanical stiffness and strength, and also electrical conductivity.
Abstract: A study was conducted to demonstrate that highly ordered graphene paper can be prepared by directional flow-induced assembly of graphene sheets that are well dispersed in solution. Moderate thermal annealing can enhance its mechanical stiffness and strength, and also electrical conductivity. Scanning electron microscopy (SEM) analysis reveals that the surface of the graphene paper is quite smooth and the fracture edges of the papers exhibit a layered structure through the entire cross-section. The study has also shown the results of cell culture experiments, which indicate that graphene paper may be biocompatible and therefore suitable for biomedical applications. The combination of the exceptional mechanical strength, thermal stability, high electrical conductivity, and biocompatibility makes graphene paper a promising material for many technological applications, such as inclusion in heart valves.
TL;DR: Graphene nanosheets were produced in large quantity via a soft chemistry synthetic route involving graphite oxidation, ultrasonic exfoliation, and chemical reduction in this paper.
Abstract: Graphene nanosheets were produced in large quantity via a soft chemistry synthetic route involving graphite oxidation, ultrasonic exfoliation, and chemical reduction. X-ray diffraction and transmission electron microscopy (TEM) observations show that graphene nanosheets were produced with sizes in the range of tens to hundreds of square nanometers and ripple-like corrugations. High resolution TEM (HRTEM) and selected area electron diffraction (SAED) analysis confirmed the ordered graphite crystal structure of graphene nanosheets. The optical properties of graphene nanosheets were characterized by Raman spectroscopy.
TL;DR: In this article, a new green route for the synthesis of processable graphene on a large scale was reported by heating an exfoliated graphite oxide (GO) suspension under strongly alkaline conditions at moderate temperatures (50-90 8C).
Abstract: Graphene – a flat monolayer of carbon atoms tightly packed into a two-dimensional (2D) honeycomb lattice – is the basal building block in all graphitic materials. Since it was first reported in 2004, graphene has attracted great interest because of the unique electronic, thermal, and mechanical properties arising from its strictly 2D structure, and to its potential technical applications. However, producing graphene on a large scale using existing mechanical methods is still unfeasible. Searching for alternative chemical approaches is an urgent matter. However, the hydrophobic nature of graphene and its strong tendency to agglomerate in solvents present a great challenge to the development of fabrication methods, and severely restrict its promising applications. Although the mechanism involved remains unproven, the chemical reduction of readily available exfoliated graphite oxide (GO) with reducing agents such as hydrazine and dimethylhydrazine is a promising strategy in the large-scale production of graphene. Unfortunately, the reducing agents involved are very hazardous, and the graphene obtained presents irreversibly agglomerated features in solvents that do not contain polymer surfactants. Here, we report a new green route for the synthesis of processable graphene on a large scale. We observed that a stable graphene suspension could be quickly prepared by simply heating an exfoliated-GO suspension under strongly alkaline conditions at moderate temperatures (50–90 8C) (Figure 1a). Our initial purpose was to introduce functional groups to exfoliated GO by free-radical addition. Surprisingly, the addition of NaOH to the GO suspension – to improve the solubility of the alkyl free-radical initiator, which is carboxyl-terminated – was accompanied by a fast, unexpected color change (from yellow-brown to homogeneous black). Careful experiments revealed that exfoliated GO can undergo fast deoxygenation in strongly alkaline solutions, resulting in stable aqueous graphene suspensions
TL;DR: Significant enhancement in mechanical stiffness and fracture strength of graphene oxide paper, a novel paperlike material made from individual graphene oxide sheets, can be achieved upon modification with a small amount of Mg(2+) and Ca(2+).
Abstract: Significant enhancement in mechanical stiffness (10–200%) and fracture strength (∼50%) of graphene oxide paper, a novel paperlike material made from individual graphene oxide sheets, can be achieved upon modification with a small amount (less than 1 wt %) of Mg2+ and Ca2+. These results can be readily rationalized in terms of the chemical interactions between the functional groups of the graphene oxide sheets and the divalent metals ions. While oxygen functional groups on the basal planes of the sheets and the carboxylate groups on the edges can both bond to Mg2+ and Ca2+, the main contribution to mechanical enhancement of the paper comes from the latter.
TL;DR: Reduced graphene oxide is demonstrated as the active material for high-performance molecular sensors fabricated from exfoliated graphene oxide platelets that are deposited to form an ultrathin continuous network.
Abstract: We demonstrate reduced graphene oxide as the active material for high-performance molecular sensors. Sensors are fabricated from exfoliated graphene oxide platelets that are deposited to form an ultrathin continuous network. These graphene oxide networks are tunably reduced toward graphene by varying the exposure time to a hydrazine hydrate vapor. The conductance change of the networks upon exposure to trace levels of vapor is measured as a function of the chemical reduction. The level of reduction affects both the sensitivity and the level of 1/f noise. The sensors are capable of detecting 10 s exposures to simulants of the three main classes of chemical-warfare agents and an explosive at parts-per-billion concentrations.
TL;DR: In this article, a general approach for the preparation of graphene−metal particle nanocomposites in a water−ethylene glycol system using graphene oxide as a precursor and metal nanoparticles (Au, Pt and Pd) as building blocks.
Abstract: Graphene sheets, which possess unique nanostructure and a variety of fascinating properties, can be considered as promising nanoscale building blocks of new composites, for example, a support material for the dispersion of nanoparticles. Here, we present a general approach for the preparation of graphene−metal particle nanocomposites in a water−ethylene glycol system using graphene oxide as a precursor and metal nanoparticles (Au, Pt and Pd) as building blocks. These metal nanoparticles are adsorbed on graphene oxide sheets and play a pivotal role in catalytic reduction of graphene oxide with ethylene glycol, leading to the formation of graphene−metal particle nanocomposites. The typical methanol oxidation of graphene−Pt composites in cyclic voltammograms analyses indicated its potential application in direct methanol fuel cells, bringing graphene−particle nanocomposites close to real technological applications.
TL;DR: In this article, a metal nanoparticle-graphene composite with a partially exfoliated graphene morphology derived from drying aqueous dispersions of platinum nanoparticles adhered to graphene is presented.
Abstract: Aggregation of isolated graphene sheets during drying graphene dispersions leads to a loss of its ultrahigh surface area advantage as a two-dimensional nanomaterial. We report a metal nanoparticle-graphene composite with a partially exfoliated graphene morphology derived from drying aqueous dispersions of platinum nanoparticles adhered to graphene. Platinum nanoparticles with diameters spanning several nanometers are adhered to graphene by a chemical route involving the reduction of metal precursors in a graphene dispersion. Face-to-face aggregation of graphene sheets is arrested by 3−4 nm fcc Pt crystallites on the graphene surfaces, and in the resulting jammed Pt−graphene composite, the Pt acts as spacers resulting in mechanically exfoliated, high-surface-area material of potential interest for supercapacitors and fuel cells.
TL;DR: In this paper, chemically modified graphene sheets are obtained through solvothermal reduction of colloidal dispersions of graphite oxide in various solvents, where reduction occurs at relatively low temperatures (120-200°C) and self-generated pressure in the sealed reaction vessel and the reducing power of the solvent influences the extent of reduction.
TL;DR: In this article, a mild, one-step electrochemical approach for the preparation of ionic-liquid-functionalized graphite sheets with the assistance of an ionic liquid and water is presented.
Abstract: Graphite, inexpensive and available in large quantities, unfortunately does not readily exfoliate to yield individual graphene sheets. Here a mild, one-step electrochemical approach for the preparation of ionic-liquid-functionalized graphite sheets with the assistance of an ionic liquid and water is presented. These ionic-liquid-treated graphite sheets can be exfoliated into functionalized graphene nanosheets that can not only be individuated and homogeneously distributed into polar aprotic solvents, but also need not be further deoxidized. Different types of ionic liquids and different ratios of the ionic liquid to water can influence the properties of the graphene nanosheets. Graphene nanosheet/polystyrene composites synthesized by a liquid-phase blend route exhibit a percolation threshold of 0.1 vol % for room temperature electrical conductivity, and, at only 4.19 vol %, this composite has a conductivity of 13.84 S m(-1), which is 3-15 times that of polystyrene composites filled with single-walled carbon nanotubes.
TL;DR: In this paper, solution-processed graphene thin films can serve as transparent conductive anodes for organic photovoltaic cells, and the graphene electrodes were deposited on quartz substrates by spin coating of an aqueous dispersion of functionalized graphene.
Abstract: We demonstrate that solution-processed graphene thin films can serve as transparent conductive anodes for organic photovoltaic cells. The graphene electrodes were deposited on quartz substrates by spin coating of an aqueous dispersion of functionalized graphene, followed by a reduction process to reduce the sheet resistance. Small molecular weight organic solar cells can be directly deposited on such graphene anodes. The short-circuit current and fill factor of these devices on graphene are lower than those of control device on indium tin oxide due to the higher sheet resistance of the graphene films. We anticipate that further optimization of the reduction conditions will improve the performance of these graphene anodes.
TL;DR: In this paper, a solution-based approach of chemical reduction of AuCl4- ions in graphene suspensions is explored, where gold particles anchored on octadecylamine functionalized graphene are readily suspendable in THF medium.
Abstract: Renewed interest in graphene architectures has opened up new avenues to utilize them in electronic and optoelectronic applications. The desire to design graphene−metal nanohybrid assemblies has led us to explore a solution-based approach of chemical reduction of AuCl4- ions in graphene suspensions. The gold particles anchored on octadecylamine functionalized graphene are readily suspendable in THF medium. The dependence of particle stability on the graphene concentration and SEM analysis indicate that the gold nanoparticles are well dispersed on graphene sheets. Transient absorption spectroscopy measurements suggest that the ultrafast disappearance of plasmon absorption and its recovery are unaffected by the presence of graphene.
TL;DR: It is found that O 2 etching kinetics vary strongly with the number of graphene layers in the sample, and three-layer-thick samples show etching similar to bulk natural graphite.
Abstract: Patterned graphene shows substantial potential for applications in future molecular-scale integrated electronics. Environmental effects are a critical issue in a single-layer material where every atom is on the surface. Especially intriguing is the variety of rich chemical interactions shown by molecular oxygen with aromatic molecules. We find that O2 etching kinetics vary strongly with the number of graphene layers in the sample. Three-layer-thick samples show etching similar to bulk natural graphite. Single-layer graphene reacts faster and shows random etch pits in contrast to natural graphite where nucleation occurs at point defects. In addition, basal plane oxygen species strongly hole dope graphene, with a Fermi level shift of ∼0.5 eV. These oxygen species desorb partially in an Ar gas flow, or under irradiation by far UV light, and readsorb again in an O2 atmosphere at room temperature. This strongly doped graphene is very different from “graphene oxide” made by mineral acid attack.
TL;DR: Composite films of graphene and polystyreneslufonate doped poly(3,4-ethylenedioxythiophene) (graphene/PEDOT-PSS) were deposited on indium tin oxide (ITO) substrates by spin coating at room temperature and applied as counter electrodes of dye-sensitized solar cells.
TL;DR: It is shown experimentally that multilayer graphene grown on the carbon terminated SiC(0001[over ]) surface contains rotational stacking faults related to the epitaxial condition at the graphene-SiC interface, and via first-principles calculation, that such faults produce an electronic structure indistinguishable from an isolated single graphene sheet in the vicinity of the Dirac point.
Abstract: We show experimentally that multilayer graphene grown on the carbon terminated SiC(0001[over ]) surface contains rotational stacking faults related to the epitaxial condition at the graphene-SiC interface. Via first-principles calculation, we demonstrate that such faults produce an electronic structure indistinguishable from an isolated single graphene sheet in the vicinity of the Dirac point. This explains prior experimental results that showed single-layer electronic properties, even for epitaxial graphene films tens of layers thick.
TL;DR: The functionalization method could be used to integrate ultrathin high-kappa dielectrics in future graphene electronics and to decorate and probe single defect sites in graphene planes.
Abstract: We investigate atomic layer deposition (ALD) of metal oxide on pristine and functionalized graphene. On pristine graphene, ALD coating can only actively grow on edges and defect sites, where dangling bonds or surface groups react with ALD precursors. This affords a simple method to decorate and probe single defect sites in graphene planes. We used perylene tetracarboxylic acid (PTCA) to functionalize the graphene surface and selectively introduced densely packed surface groups on graphene. Uniform ultrathin ALD coating on PTCA graphene was achieved over a large area. The functionalization method could be used to integrate ultrathin high-κ dielectrics in future graphene electronics.
TL;DR: In this article, the effect of substrate on the atomic/electronic structures of monolayer graphene is investigated and it is shown that the Raman features are independent of the substrate used.
Abstract: Graphene has attracted a lot of interest for fundamental studies as well as for potential applications. Till now, micromechanical cleavage (MC) of graphite has been used to produce high-quality graphene sheets on different substrates. Clear understanding of the substrate effect is important for the potential device fabrication of graphene. Here we report the results of the Raman studies of micromechanically cleaved monolayer graphene on standard SiO2 (300 nm)/Si, single crystal quartz, Si, glass, polydimethylsiloxane (PDMS), and NiFe. Our data suggests that the Raman features of monolayer graphene are independent of the substrate used; in other words, the effect of substrate on the atomic/electronic structures of graphene is negligible for graphene made by MC. On the other hand, epitaxial monolayer graphene (EMG) on SiC substrate is also investigated. Significant blueshift of Raman bands is observed, which is attributed to the interaction of the graphene sheet with the substrate, resulting in the change o...