Rodney S. Ruoff | |
---|---|
Nationality | American |
Alma mater | University of Illinois-Urbana, University of Texas at Austin |
Awards | Clarivate Citation Laureate, James C. McGroddy Prize for New Materials |
Scientific career | |
Fields | Carbon and related materials |
Institutions | Ulsan National Institute of Science and Technology, Center for Multidimensional Carbon Materials |
Thesis | Fourier-Transform Microwave Spectroscopy of Hydrogen-bonded Trimers and of Conformer Relaxation in Free Jets (1988) |
Doctoral advisor | Herbert S. Gutowsky |
Website | http://cmcm.ibs.re.kr |
Rodney S. "Rod" Ruoff is an American physical chemist and nanoscience researcher. He is one of the world experts on carbon materials including carbon nanostructures such as fullerenes, nanotubes, graphene, diamond, and has had pioneering discoveries on such materials and others. Ruoff received his B.S. in chemistry from the University of Texas at Austin (1981) and his Ph.D. in chemical physics at the University of Illinois-Urbana (1988). After a Fulbright Fellowship at the MPI fuer Stroemungsforschung in Goettingen, Germany (1989) and postdoctoral work at the IBM T. J. Watson Research Center (1990–91), Ruoff became a staff scientist in the Molecular Physics Laboratory at SRI International (1991–1996). He is currently UNIST Distinguished Professor at the Ulsan National Institute of Science and Technology (UNIST), and the director of the Center for Multidimensional Carbon Materials, an Institute for Basic Science Center located at UNIST.
Rod Ruoff and his research groups have made seminal contributions to developing new synthesis techniques and improving our understanding of properties of novel materials including nanostructures and 2D materials, especially novel carbon materials (graphene, diamond, nanotubes, sp3-sp2 hybrids, negative curvature carbon, carbon nanofoams, boron nitride allotropes, fullerenes, etc.). Some examples of pioneering studies, among others, include:(i) of the mechanics of C60, [1] and of nanotubes, [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] including pullout of inner shell with respect to outer shell of the nanotube, [12] and of a connection between mechanical deformation and structure on the one hand, and chemical reactivity on the other; [13] [14] (ii) of solubility phenomena of fullerenes, nanotubes, and graphene; [15] [16] [17] [18] [19] [20] (iii) of carbon-encapsulated metal nanoparticles; [21] [22] (iv) of patterned graphite and thus micromechanically exfoliated graphene-like flakes; [23] [24] (v) of scaled growth of graphene on copper and copper-nickel foils; [25] [26] [27] [28] [29] [30] [31] [32] (vi) of isotopically labeled graphites (graphite oxide) and graphene; [33] [34] [35] [36] (vii) of graphene oxide and reduced graphene oxide and composites and paper-like films composed of them; [37] [38] [39] [40] [41] [42] (viii) of the use of chemically modified graphene and graphite foam for electrode materials in electrical energy storage; [43] [44] [45] [46] [47] (ix) of graphene as a support film for biological TEM; [48] (x) of graphene as a protective coating against oxidation (and corrosion) (please also note Appl. Phys. Lett. 92, 052506 (2008) and Appl. Phys. Lett. 93, 022509 (2008)). [49] Ruoff provided some personal perspectives on graphene and new carbon materials ‘on the horizon’ in 2012. [50] As a graduate student at the University of Illinois-Urbana, Ruoff and colleagues published seminal papers on the structure of weakly bound clusters formed in supersonic jets, [51] and of relaxation processes in supersonic jets. [52]
His predictions with A. L. Ruoff about the mechanical response of fullerite under high pressure, [1] and his work with colleagues on the unique solvation phenomena of C60 in various solvent systems, [15] [16] and of synthesis and structural characterization of supergiant fullerenes containing single crystal metal ‘encapsulates’, [21] have demonstrated to the scientific community the novel properties of closed-shell carbon structures. He also co-developed a new in-situ mechanical testing device for measuring the tensile response of bundles of SWCNTs and individual MWCNTs inside of a scanning electron microscope. [4] [5] [6] [12] This work has yielded important insights into the mechanics and tribology of these systems, and suggested the possibility of very low friction linear bearings. [12] Similarly, Ruoff and collaborators were the first to use solubility parameters to rationalize the solubility of fullerenes, [15] of single-walled nanotubes, [18] and of chemically modified graphenes. [20] Furthermore, Rod is credited with first creating graphene by lithographic patterning to make single crystal graphite micropillars; he and his team achieved thereby single crystal multilayer graphene platelets. [23] [24]
From 2009, Ruoff and collaborators have demonstrated synthesis of large area monolayer graphene on copper foil by chemical vapor deposition, [25] [27] [28] [29] for which relatively high carrier mobilities have been obtained, and subsequently have used isotopic labeling and micro-Raman mapping to map grains and grain boundaries in such atom thick layers and to elucidate growth mechanisms, [30] and studied their performance as transparent conductive electrodes. [26] Ruoff and his collaborators have also made a series of advances in novel composite systems comprising chemically modified graphene platelets. [38] [40] [41]
Ruoff and his team were the first to use graphene as electrodes of electrochemical capacitors, reporting on graphene supercapacitors in 2008. [43] In 2011, Ruoff and his group reported on a new carbon, potentially having regions of ‘negative curvature carbon’ (NCC) with a remarkably high specific surface area of 3100 m2 g−1, and atom-thick carbon sp2-bonded walls that define pores varying in diameter from about 0.6 to 5 nm. They showed that this type of porous carbon (‘a-MEGO’) works very well as an electrode material for double-layer supercapacitors, a very exciting advance. [44]
Rod and his team continue to make contributions at the Institute for Basic Science Center for Multidimensional Carbon Materials with a focus on carbon and related materials but also in some other research topics. [53]
Rod has a Hirsch factor of 156. [54] He is inventor or co-inventor on 60 issued patents. [55]
A carbon nanotube (CNT) is a tube made of carbon with a diameter in the nanometre range (nanoscale). They are one of the allotropes of carbon.
Graphene is an allotrope of carbon consisting of a single layer of atoms arranged in a hexagonal lattice nanostructure. The name is derived from "graphite" and the suffix -ene, reflecting the fact that the graphite allotrope of carbon contains numerous double bonds.
James Mitchell Tour is an American chemist and nanotechnologist. He is a Professor of Chemistry, Professor of Materials Science and Nanoengineering at Rice University in Houston, Texas.
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Carbon nanotubes (CNTs) are cylinders of one or more layers of graphene (lattice). Diameters of single-walled carbon nanotubes (SWNTs) and multi-walled carbon nanotubes (MWNTs) are typically 0.8 to 2 nm and 5 to 20 nm, respectively, although MWNT diameters can exceed 100 nm. CNT lengths range from less than 100 nm to 0.5 m.
Graphene nanoribbons are strips of graphene with width less than 100 nm. Graphene ribbons were introduced as a theoretical model by Mitsutaka Fujita and coauthors to examine the edge and nanoscale size effect in graphene.
Alex K. Zettl is an American experimental physicist, educator, and inventor.
Linear acetylenic carbon (LAC), also known as carbyne or Linear Carbon Chain (LCC), is an allotrope of carbon that has the chemical structure (−C≡C−)n as a repeat unit, with alternating single and triple bonds. It would thus be the ultimate member of the polyyne family.
The optical properties of carbon nanotubes are highly relevant for materials science. The way those materials interact with electromagnetic radiation is unique in many respects, as evidenced by their peculiar absorption, photoluminescence (fluorescence), and Raman spectra.
Graphite oxide (GO), formerly called graphitic oxide or graphitic acid, is a compound of carbon, oxygen, and hydrogen in variable ratios, obtained by treating graphite with strong oxidizers and acids for resolving of extra metals. The maximally oxidized bulk product is a yellow solid with C:O ratio between 2.1 and 2.9, that retains the layer structure of graphite but with a much larger and irregular spacing.
Carbide-derived carbon (CDC), also known as tunable nanoporous carbon, is the common term for carbon materials derived from carbide precursors, such as binary (e.g. SiC, TiC), or ternary carbides, also known as MAX phases (e.g., Ti2AlC, Ti3SiC2). CDCs have also been derived from polymer-derived ceramics such as Si-O-C or Ti-C, and carbonitrides, such as Si-N-C. CDCs can occur in various structures, ranging from amorphous to crystalline carbon, from sp2- to sp3-bonded, and from highly porous to fully dense. Among others, the following carbon structures have been derived from carbide precursors: micro- and mesoporous carbon, amorphous carbon, carbon nanotubes, onion-like carbon, nanocrystalline diamond, graphene, and graphite. Among carbon materials, microporous CDCs exhibit some of the highest reported specific surface areas (up to more than 3000 m2/g). By varying the type of the precursor and the CDC synthesis conditions, microporous and mesoporous structures with controllable average pore size and pore size distributions can be produced. Depending on the precursor and the synthesis conditions, the average pore size control can be applied at sub-Angstrom accuracy. This ability to precisely tune the size and shapes of pores makes CDCs attractive for selective sorption and storage of liquids and gases (e.g., hydrogen, methane, CO2) and the high electric conductivity and electrochemical stability allows these structures to be effectively implemented in electrical energy storage and capacitive water desalinization.
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Graphene is the only form of carbon in which every atom is available for chemical reaction from two sides. Atoms at the edges of a graphene sheet have special chemical reactivity. Graphene has the highest ratio of edge atoms of any allotrope. Defects within a sheet increase its chemical reactivity. The onset temperature of reaction between the basal plane of single-layer graphene and oxygen gas is below 260 °C (530 K). Graphene combusts at 350 °C (620 K). Graphene is commonly modified with oxygen- and nitrogen-containing functional groups and analyzed by infrared spectroscopy and X-ray photoelectron spectroscopy. However, determination of structures of graphene with oxygen- and nitrogen- functional groups requires the structures to be well controlled.
A graphene morphology is any of the structures related to, and formed from, single sheets of graphene. 'Graphene' is typically used to refer to the crystalline monolayer of the naturally occurring material graphite. Due to quantum confinement of electrons within the material at these low dimensions, small differences in graphene morphology can greatly impact the physical and chemical properties of these materials. Commonly studied graphene morphologies include the monolayer sheets, bilayer sheets, graphene nanoribbons and other 3D structures formed from stacking of the monolayer sheets.
Andrea Carlo Ferrari is a professor of nanotechnology at the University of Cambridge.
Professor Ruoff is the director of the Center for Multidimensional Carbon Materials, established in November 2013.