There is Plenty of Room at the Bottom （ 1918~ 1988 ） R.P.Feynman
The Origin and Development of Nanotechnology Feynman—— 《 There is Plenty of Room at the Bottom 》 The Invention of the Scanning Tunneling Microscope(STM) The Nanotechnology Developed Rapidly in1990s, and the New Words Came Fast One of the 9 Major Key Technologies in the Future Global Technology Development
Why?--a materials perspective Image of reconstruction on a clean Gold(100) surface, as visualized using scanning tunneling microscopy. The positions of the individual atoms composing the surface are visiblereconstruction Gold100 scanning tunneling microscopyatoms “quantum size effect” ： dominant when the nanometer size range is reached. a number of physical (mechanical, electrical, optical, etc.) properties change when compared to macroscopic systems. For example: opaque substances become transparent (copper); stable materials turn combustible (aluminum); insoluble materials become soluble (gold). A material such as gold, which is chemically inert at normal scales, can serve as a potent chemical catalyst at nanoscales.
Why?--Simple to complex: a molecular perspective Molecular self-assembly: automatically arrange themselves into some useful conformation. through a bottom-up approach to prepare small molecules to almost any structure The DNA structure at left (schematic shown) will self-assemble into the structure visualized by atomic force microscopy at right. Image from Strongatomic force microscopy
How?--Tools and techniques Tools: The atomic force microscope (AFM) and the Scanning Tunneling Microscope (STM) are two early versions of scanning probes that launched nanotechnology Typical AFM setup. A microfabricated cantilever with a sharp tip is deflected by features on a sample surface, much like in a phonograph but on a much smaller scale. A laser beam reflects off the backside of the cantilever into a set of photodetectors, allowing the deflection to be measured and assembled into an image of the surfaceAFMmicrofabricatedcantileverphonographlaser photodetectors They can be used to look at surfaces and to move atoms around. By designing different tips for these microscopes, they can be used for carving out structures on surfaces and to help guide self-assembling structures.
Bottom-up approaches Molecular self-assembly seeks to use concepts of supremolecular chemistry, and molecular recognition in particular, to cause single-molecule components to automatically arrange themselves into some useful conformation. Sarfus image of a DNA biochip elaborated by bottom-up approach. These seek to arrange smaller components into more complex assemblies
Top-down approaches These seek to create smaller devices by using larger ones to direct their assembly. This device transfers energy from nano-thin layers of quantum wells to nanocrystals above them, causing the nanocrystals to emit visible light.  quantum wellsnanocrystals  Solid-state techniques can be used to create devices known as nanoelectromechanical systems or NEMS, which are related to microelectromechanical systems or MEMS. Solid-state silicon methods for fabricating microprocessors
The Self-Cleanliness on the Surface of Lotus Flower
Fullerene Introduction of Fullerene family (what is?) Fullerene (discovery, naming) Types of Fullerene and related structures Properties Synthesis (to fabricate) Potential and current applications
A Fullerene is any molecule composed entirely of carbon, in the form of a hollow sphere, ellipsoid, or tube. Spherical fullerenes are also called buckyballs, and cylindrical ones are called carbon nanotubes or buckytubes.sphereellipsoidtubecarbon nanotubes What is Fullerene? C 60 in solution Buckminster fullerene C 60 (left) and carbon nanotubes (right) are two examples of structures in the fullerene family.
Allotropes of carbon Allotropes of carbon: Diamond (hardest natural mineral)mineral Graphite(dry lubrican t, graphene)lubrican t graphene Amorphous carbon (coal and soot)coalsoot Fullerene family (C 60, carbon nanotubes etc) Allotropes : different structural modifications of an element; the atoms of the element are bonded together in a different manner.atoms bonded Diamond and graphite are two allotropes of carbon: pure forms of the same element that differ in structure.
Fullerene-History The existence of C 60 was predicted by Eiji Osawa of Toyohashi University of Technology in a Japanese magazine in 1970Toyohashi University of Technology With mass spectrometry, discrete peaks were observed corresponding to molecules with the exact mass of sixty or seventy or more carbon atoms. In 1985, Harold Kroto etc ， discovered C 60, and shortly thereafter came to discover the fullerenes. Kroto, Curl, and Smalley were awarded the 1996 Nobel Prize in Chemistry for their roles in the discovery of this class of compounds.mass spectrometryHarold Kroto Nobel Prize in Chemistry Minute quantities of the fullerenes, in the form of C 60, C 70, C 76, and C 84 molecules, are produced in nature, hidden in soot and formed by lightning discharges in the atmosphere.soot Buckminsterfullerene C 60 The Icosahedral Fullerene C 540Icosahedral
Discovery of Carbon C 60 1985, Robert F. Curl, … discovered a new form of carbon ， that 60 or 70 carbon atoms could cluster together to form a cage-like molecule. The molecular structure resembled the pattern of a soccer ball or the geodesic designs of Buckminster Fullerenes. Thus the name buckyballs or fullerenes. Since then the discovery has led to new research in polymers, semiconductors, and other various areas. Nobel Prize to their finders in 1996
Existence in the nature In 1992, fullerenes were found in a family of minerals known as Shungites in Karelia, Russia.ShungitesKarelia In 2010, fullerenes (C60) have been discovered in a cloud of cosmic dust surrounding a distant star 6500 light years away. Using NASA's Spitzer infrared telescope the scientists spotted the molecules' unmistakable infrared signature. Sir Harry Kroto, who shared the 1996 Nobel Prize in Chemistry for the discovery of buckyballs commented: "This most exciting breakthrough provides convincing evidence that the buckyball has, as I long suspected, existed since time immemorial in the dark recesses of our galaxy” Spitzer
Naming--Fullerene The substance of the Fullerene was named after the American inventor, architects and philosophers Richard Buckminster Fuller (1895 till 1983). As an architect, R.B.Fuller designed the constructions which exist of 5-corners and 6- corners, for example, the American pavilion to the Expo in '67 in Montréal(geodesic dome).geodesic dome Fullerenes are similar in structure to graphite, which is composed of stacked graphene sheets of linked hexagonal rings; but they may also contain pentagonal (or sometimes heptagonal) rings.graphitegraphene
Buckminster Fuller Richard Buckminster Fuller, c. 1917. BornJuly 12, 1895 Milton, Massachusetts, United States Milton, Massachusetts DiedJuly 1, 1983 (aged 87) Los Angeles, United States Los Angeles OccupationVisionaryVisionary, designer,architect, author, inventordesignerarchitectinventor SpouseAnne Fuller Children2: Allegra Fuller Snyder and Alexandra who died in childhood Buckminster Fuller The Montreal Biosphère by Buckminster Fuller, 1967Montreal Biosphère Richard Buckminster Fuller, c. 1917
After the IUPAC nomenclature the C60 has the following name: [220.127.116.11.2,14.03,12. 04,59.05,10.06,58. 07,55.08,53.09,21. 011,20.013,18.015,30. 016,28.017,25.019,24. 022,52. 023.50.026,49.027,47. 029,45.032,44.033,60. 034,57.035,43.036,56. 037,41.038,54.039,51. 040,48.042,46]hexaconta- 1,3,5(10),6,8,11,13(18), 14,16,19,21,23,25,27,29(45),30,32(44),33,35(43), 36,38(54),39(51),40(48),41,46,49,52,55,57,59-triacont IUPAC--International Union of Pure and Applied Chemistry
Another fairly common fullerene is C 70, but fullerenes with 72, 76, 84 and even up to 100 carbon atoms are commonly obtained. In mathematical terms, the structure of a fullerene is a trivalent convex polyhedron with pentagonal and hexagonal faces. In graph theory, the term fullerene refers to any 3-regular, planar graph with all faces of size 5 or 6 (including the external face). It follows from Euler's polyhedron formula, V − E + F = 2, (where V, E, F are the numbers of vertices, edges, and faces), that there are exactly 12 pentagons in a fullerene and V/2 − 10 hexagons. mathematicaltrivalentpolyhedrongraph theoryregularplanar graphEuler's polyhedron formula C20 C26 C60 C70 Different structure buckyballs
Fullerene Family Fig. 3.1: A schematic representation of the structures of graphite, diamond and fullerenes. While the two-dimensional sheets formed by hexagons are packed one over another in graphite, the diamond structure is three-dimensional. Only two fullerenes are shown. The smaller one is buckminsterfullerene, C 60. structure. The double bonds are localized exocyclic to the pentagons giving  radialene character to the pentagons and cyclohexa-1,3,5-triene character to the hexagons.
Synthesis(discover) of C60 Fig. 3.2: The experimental set-up used to discover C 60. The graphite disk is evaporated with a Nd:YAG laser and the evaporated carbon plasma is cooled by a stream of helium coming from a pulsed valve. The clusters of carbon are produced in the integration cup and are expanded into vacuum. The ions are detected by time of flight mass spectrometry
synthesis and purification of fullerenes Fig. 3.4: Schematic illustration of the processed involved in the synthesis and purification of fullerenes. Graphite rods are evaporated in an arc, under He atmosphere. The soot collected is extracted with toluene and subjected to chromatography.
Properties & Applications In April 2003, fullerenes were under study for potential medicinal use: binding specific antibiotics to the structure to target resistant bacteria and even target certain cancer cells potential medicinal use antibiotics bacteriacancer use of fullerenes as light-activated antimicrobial agentsantimicrobial Fullerenes are stable, but not totally unreactive. Solubility C 60 in solution Fullerenes are sparingly soluble in many solventssolvents Solutions of pure buckminsterfullerene have a deep purple color. Solutions of C 70 are a reddish brown. The higher fullerenes C 76 to C 84 have a variety of colors
Properties & Applications Fig. 3.6: (Bottom) Mass spectrum of a laser evaporated C 60 film showing coalescence of fullerenes. Mass peaks are seen at (C 60 ) n (Ref.64). (Top) Collision of high energy ions on C 60 results in the addition of C 2 s to C 60. The mass spectrum here shows the addition of a number of such species (Ref.65). Combined figure originally published in, T. Pradeep, Current Science, 72 (1997) 124.
Hydrated Fullerene C 60 HyFn water solution with a C 60 concentration of 0.22 mg/mL Hydrated fullerene C 60 HyFn is a stable, highly hydrophilic, supra-molecular complex consisting of С 60 fullerene molecule enclosed into the first hydrated shell that contains 24 water molecules: C 60 @(H 2 O) 24. that intercalation of alkali-metal atoms in solid C 60 leads to metallic behavior. In 1991, it was revealed that potassium-doped C 60 becomes superconducting at 18 K. This was the highest transition temperature for a molecular superconductor. Since then, superconductivity has been reported in fullerene doped with various other alkali metals superconducting Superconductivity Properties & Applications
Fig. 3.8: Normalized DC electrical resistivity ρ （ T ） of a K 3 C 60 single crystal. The T c observed is 19.8K. ρ 0 is the resistivity at T=280K. Reprinted with permission from Xiang, et al. (Ref.95). Copyright (1992) AAAS.
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