Mohamed Rahmane
General Electric
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Featured researches published by Mohamed Rahmane.
Journal of Applied Physics | 2005
Loucas Tsakalakos; Mohamed Rahmane; Michael Larsen; Yan Gao; Lauraine Denault; Paul Stuart Wilson; Joleyn Balch
Transition-metal carbides in bulk form have historically been of technological interest primarily due to their excellent mechanical and refractory properties. As electronic materials these ceramic compounds are also particularly intriguing in that their electrical resistivity is relatively low compared to other ceramics and shows metallic temperature-dependent behavior. Some compositions also have superconducting transitions temperatures above 10°K. However, the synthesis of such materials in the form of one-dimensional nanostructures, which may be of interest for various nanoelectronic applications, is relatively difficult due to their refractory nature (Tmelt⩾2000°C). Here we report the synthesis of well-defined Mo2C nanowires and ribbons using a two-step approach in which we catalytically grow metal oxide nanostructures followed by in situ carburization. The growth mechanisms, microstructure, and initial electrical property measurements are discussed.
ASME 2004 3rd Integrated Nanosystems Conference | 2004
Loucas Tsakalakos; Lauraine Denault; Michael Larsen; Mohamed Rahmane; Yan Gao; Joleyn Balch; Paul Stuart Wilson
Transition metal carbides are an interesting class of electronic materials owing to their high electrical conductivity at room temperature, which is only slightly lower than that of their constituent transition metal elements. For example, the room temperature electrical resistivity of bulk Mo2 C is ∼70 μΩ-cm compared to that of Mo (4.85 μΩ-cm), whereas that of NbC is ∼50 μΩ-cm as compared to 15.2 μΩ-cm for Nb. Indeed, the temperature dependent resistivity of many transition metal carbides suggests metallic-like conduction. Furthermore, certain transition metal carbides are known to become superconducting, with transition temperatures ranging from 1.15 °K for TiC1−x to 14 °K for NbC. [1] They are also able to withstand high temperatures and are chemically stable. Initial synthesis of metal carbide nanorods was demonstrated using the carbon nanotube (CNT) confined reaction mechanism by Lieber and co-workers [2] and subsequent superconducting behavior was shown by Fukunaga et al. [3]. Vapor-liquid-solid growth was employed by Johnson et al. [4] to synthesize micron-sized carbide whiskers. Here, we have successfully synthesized Mo2 C nanorods and ribbons on Si substrates using a novel two-step catalytic approach, which allows for synthesis of such high temperature nanostructures at manufacturable temperatures (≤ 1000 °C) and time scales (≤ 60 min). In the first step we utilize a catalytic vapor phase process to grow Mo and/or molybdenum oxide nanostructures, which are subsequently carburized in situ to form the desired Mo2 C nanostructures. Unlike true VLS growth of carbides, in which high temperature (≤ 1100–1200 °C) is required to adequately dissolve carbon into the catalyst particles, our strategy is to react the nanostructures along their entire length with a carbon vapor source after creating the oxide/metal nanostructures, which for Mo2 C can be achieved at relatively low temperatures. (≤ 1000 °C). The nanorods and ribbons are polycrystalline, with a mean grain size of 20–50 nm and 50–150 nm, respectively. We hypothesize that the growth mechanism is a complex mixture of VLS, VSS, and auto-catalytic growth, in which molten catalyst nanoparticles enter a three phase region once the metal precursor is supplied. The growth then presumably continues via a vapor-solid-solid process and is possible assisted by the presence of various molybdenum oxide species on the surface. Initial single nanowire electrical measurements yield a higher resistivity than in the bulk, which is attributed to the fine grain sizes and/or the presence of an oxide layer. A discussion of the growth mechanism will be presented along with issues relating to single nanowire device fabrication and control of nanowire orientation.Copyright
MRS Proceedings | 2006
Loucas Tsakalakos; Jody Fronheiser; Larry Burton Rowland; Mohamed Rahmane; Michael Larsen; Yan Gao
Polycrystalline SiC nanowires and composite Si nanowire-SiC nanograin structures have been synthesized using a combined catalytic chemical vapor deposition and carburization method. Si nanowires are grown at low temperature (550-650 C) and subsequently carburized at 1100-1200 C in a methane/hydrogen or propane/hydrogen environment. Thermochemical calculations showed that the Si carburization is thermodynamically favorable over a wide tempareture range, whereas our studies showed that the Si nanowire carburization is kinetically limited below ∼1100 °C. Partially carburized nanowires contained distinct SiC nanosized grains on the Si nanowire surface, whereas fully carburized nanowires were polycrystalline 3C SiC with grain sizes of ∼ 50-100 nm.
Archive | 2004
Mohamed Rahmane; Eric Croquesel; Svetlana Selezneva
Archive | 2008
Bernard Patrick Bewlay; Bruce Alan Knudsen; James Anthony Brewer; James Scott Vartuli; Dennis Joseph Dalpe; Mohamed Rahmane
Archive | 2010
Sundeep Kumar; Mohamed Rahmane; Mohandas Nayak; Arunabh Basak; Kalaga Murali Krishna; Atanu Saha
Archive | 2008
Timothy David Russell; Mohamed Rahmane; Peter Joel Meschter; Gary W. Utterback
Archive | 2007
Mohamed Rahmane; Agoston Boroczki; James Anthony Brewer; Sergiy Zalyubovskiy; Gabor Farkas; Steven Charles Aceto
Archive | 2010
Mohamed Rahmane; Darren Michael Stohr; James Anthony Brewer; Dong-Sil Park
Archive | 2007
Bernard Patrick Bewlay; Michael Francis Xavier Gigliotti; Thomas Joseph Kelly; Mohamed Rahmane; Stephen Francis Rutkowski; Michael James Weimer; Sairam Sundaram