Mildred S. Dresselhaus

Bio: Mildred S. Dresselhaus is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Carbon nanotube & Raman spectroscopy. The author has an hindex of 136, co-authored 762 publications receiving 112525 citations. Previous affiliations of Mildred S. Dresselhaus include University of California, Los Angeles & Universidade Federal de Minas Gerais.

Pulsed Laser Melting of Graphite

Abstract: Experimental evidence for laser melting of graphite, by irradiation with 30ns pulses from a ruby laser, is presented. RBS-channeling analysis, Raman scattering and TEM measurements reveal that the surface of graphite melts at a threshold energy density of about 0.6 J/cm2. For laser pulse energy densities above 0.6 J/cm2, the melt front penetration depth increases nearly linearly with increasing energy density. An intense emission of carbon particles during and after irradiation is observed. The thickness of the carbon layer removed in this process also increases nearly linearly with increasing pulse fluence. A dramatic redistribution of ion implanted impurities is also observed. Furthermore, the crystalline structure of the resolidified material is shown to depend on the energy density of the laser pulse. In order to explain these phenomena, a model for laser melting of graphite at high temperatures to form liquid carbon has been developed in which a free electron gas approximation is used to describe the properties of liquid carbon. The model is solved numerically to give the time and depth dependences of the temperature as a function of the laser pulse energy density. Very good agreement is found between the observed melt depth dependence on laser pulse energy density, as determined by RBS-channeling, and the model calculations. The redistribution of ion implanted impurities and the modification of the crystalline structure, caused by the pulsed laser irradiation, are also consistent with the model and permit the determination, for the first time, of interfacial segregation coefficients for impurities in liquid carbon. The model also predicts that liquid carbon at low pressure (p < 1 kbar) has metallic properties.

A Band Structure Phase Diagram Calculation of 2D BiSb Films

Abstract: Ever since the birth of thermoelectrics, it has been well known that semiconductors (materials with a relative small bandgap) give the best thermoelectric performance. From quantum mechanics, it is also well known that low dimension quantum confinement leads to changes in the band alignment of a material. Thus, a semimetallic material can be made semiconducting by using low dimensionality quantum confinement effects. BiSb alloys have been of particular interest for thermoelectric application in the temperature range of 70K to 100K. In bulk form, BiSb alloys can either be semimetal or semiconductor, depending on the alloy composition. Moreover, semimetallic BiSb alloys can be made semiconducting by using the low dimensionality quantum confinement concept. With these two previous concepts in mind, it is valuable to further explore the dependence of the band alignment for different alloy concentrations and different confinement conditions for BiSb alloys. Following the study of the effect of the Sb concentration and of the wire diameter on the semimetallic or semiconducting phase of BiSb alloy nanowires, we now examine the corresponding effect of the Sb concentration and the film thickness on the properties of BiSb alloy films. A band structure phase diagram is calculated, giving the details on the dependence of the relative band edge position on the film thickness and the Sb concentration. This phase diagram gives a first hand guideline for choosing the film thickness and the Sb concentration to better improve the thermoelectric performance of BiSb alloy films.

Electric Field Effect in Atomically Thin Carbon Films

Abstract: We describe monocrystalline graphitic films, which are a few atoms thick but are nonetheless stable under ambient conditions, metallic, and of remarkably high quality. The films are found to be a two-dimensional semimetal with a tiny overlap between valence and conductance bands, and they exhibit a strong ambipolar electric field effect such that electrons and holes in concentrations up to 10 13 per square centimeter and with room-temperature mobilities of ∼10,000 square centimeters per volt-second can be induced by applying gate voltage.

Helical microtubules of graphitic carbon

Abstract: THE synthesis of molecular carbon structures in the form of C60 and other fullerenes1 has stimulated intense interest in the structures accessible to graphitic carbon sheets. Here I report the preparation of a new type of finite carbon structure consisting of needle-like tubes. Produced using an arc-discharge evaporation method similar to that used for fullerene synthesis, the needles grow at the negative end of the electrode used for the arc discharge. Electron microscopy reveals that each needle comprises coaxial tubes of graphitic sheets, ranging in number from 2 up to about 50. On each tube the carbon-atom hexagons are arranged in a helical fashion about the needle axis. The helical pitch varies from needle to needle and from tube to tube within a single needle. It appears that this helical structure may aid the growth process. The formation of these needles, ranging from a few to a few tens of nanometres in diameter, suggests that engineering of carbon structures should be possible on scales considerably greater than those relevant to the fullerenes. On 7 November 1991, Sumio Iijima announced in Nature the preparation of nanometre-size, needle-like tubes of carbon — now familiar as 'nanotubes'. Used in microelectronic circuitry and microscopy, and as a tool to test quantum mechanics and model biological systems, nanotubes seem to have unlimited potential.

The rise of graphene

Abstract: Graphene is a rapidly rising star on the horizon of materials science and condensed-matter physics. This strictly two-dimensional material exhibits exceptionally high crystal and electronic quality, and, despite its short history, has already revealed a cornucopia of new physics and potential applications, which are briefly discussed here. Whereas one can be certain of the realness of applications only when commercial products appear, graphene no longer requires any further proof of its importance in terms of fundamental physics. Owing to its unusual electronic spectrum, graphene has led to the emergence of a new paradigm of 'relativistic' condensed-matter physics, where quantum relativistic phenomena, some of which are unobservable in high-energy physics, can now be mimicked and tested in table-top experiments. More generally, graphene represents a conceptually new class of materials that are only one atom thick, and, on this basis, offers new inroads into low-dimensional physics that has never ceased to surprise and continues to provide a fertile ground for applications.

Fast parallel algorithms for short-range molecular dynamics

Abstract: Three parallel algorithms for classical molecular dynamics are presented. The first assigns each processor a fixed subset of atoms; the second assigns each a fixed subset of inter-atomic forces to compute; the third assigns each a fixed spatial region. The algorithms are suitable for molecular dynamics models which can be difficult to parallelize efficiently—those with short-range forces where the neighbors of each atom change rapidly. They can be implemented on any distributed-memory parallel machine which allows for message-passing of data between independently executing processors. The algorithms are tested on a standard Lennard-Jones benchmark problem for system sizes ranging from 500 to 100,000,000 atoms on several parallel supercomputers--the nCUBE 2, Intel iPSC/860 and Paragon, and Cray T3D. Comparing the results to the fastest reported vectorized Cray Y-MP and C90 algorithm shows that the current generation of parallel machines is competitive with conventional vector supercomputers even for small problems. For large problems, the spatial algorithm achieves parallel efficiencies of 90% and a 1840-node Intel Paragon performs up to 165 faster than a single Cray C9O processor. Trade-offs between the three algorithms and guidelines for adapting them to more complex molecular dynamics simulations are also discussed.

The electronic properties of graphene

Abstract: This article reviews the basic theoretical aspects of graphene, a one-atom-thick allotrope of carbon, with unusual two-dimensional Dirac-like electronic excitations. The Dirac electrons can be controlled by application of external electric and magnetic fields, or by altering sample geometry and/or topology. The Dirac electrons behave in unusual ways in tunneling, confinement, and the integer quantum Hall effect. The electronic properties of graphene stacks are discussed and vary with stacking order and number of layers. Edge (surface) states in graphene depend on the edge termination (zigzag or armchair) and affect the physical properties of nanoribbons. Different types of disorder modify the Dirac equation leading to unusual spectroscopic and transport properties. The effects of electron-electron and electron-phonon interactions in single layer and multilayer graphene are also presented.