Institution
Rensselaer Polytechnic Institute
Education•Troy, New York, United States•
About: Rensselaer Polytechnic Institute is a education organization based out in Troy, New York, United States. It is known for research contribution in the topics: Terahertz radiation & Finite element method. The organization has 19024 authors who have published 39922 publications receiving 1414699 citations. The organization is also known as: RPI & Rensselaer Institute.
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Papers
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01 Oct 2007TL;DR: Terahertz (THz) radiation, which occupies a relatively unexplored portion of the electromagnetic spectrum between the mid-infrared and microwave bands, offers innovative sensing and imaging technologies that can provide information unavailable through conventional methods such as microwave and X-ray as discussed by the authors.
Abstract: Terahertz (THz) radiation, which occupies a relatively unexplored portion of the electromagnetic spectrum between the mid-infrared and microwave bands, offers innovative sensing and imaging technologies that can provide information unavailable through conventional methods such as microwave and X-ray techniques. With the advancement of THz technologies, THz sensing and imaging will impact a broad range of interdisciplinary fields, including chemical and biological detections and identifications. In particular, THz radiation offers the opportunity for transformational advances in defense and security. Recent work shows that THz technologies are promising for the standoff detection and identification of explosive targets.
479 citations
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TL;DR: A new class of both p- and n-type bulk nanomaterials with room-temperature ZT as high as 1.1 is demonstrated using a combination of sub-atomic-per-cent doping and nanostructuring to address the challenge of obtaining thermoelectric materials with high figure of merit ZT in thin films.
Abstract: In the quest for more efficient thermoelectrics, a common strategy has been to introduce nanostructures in bulk crystals, thus reducing the thermal conductivity without affecting the electrical transport properties. A route is now presented in which the aggregation of nanoplatelets creates nanostructured materials that have higher thermoelectric efficiencies than their bulk counterparts.
479 citations
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TL;DR: In this article, the electrocatalytic reduction of dissolved oxygen (important H2±O2 fuel cell reaction), using microelectrodes constructed from multiwalled nanotubes, is reported.
Abstract: The closed topology and tubular structure of carbon nanotubes make them unique among different carbon forms and provide pathways for chemical studies. A number of investigations have been carried out to find applications of nanotubes in catalysis, hydrogen storage, intercalation, etc. Since carbon-electrode-based fuel cells have been experimented with for decades, it is of importance to learn the electrodic performance of these new carbon structures. We report here results of the electrocatalytic reduction of dissolved oxygen (important H2±O2 fuel cell reaction), using microelectrodes constructed from multiwalled nanotubes. In parallel, ab initio calculations were performed for oxygen deposited on the lattice and defect sites of nanotube surfaces to determine the charge transfer during oxygen reduction and compared with similar reactions on planar graphite. The microelectrodes were constructed in the following way (see Fig. 1). Multiwalled nanotubes (10 mg) prepared by the electric arc discharge process and liquid paraffin (4 mL) were intimately mixed, placed in the narrow cylindrical slot of a Perspex holder and then packed by smooth vibration. The assembly was cured at 50 C for 30 min. From the inner side of the Perspex, contact to a copper lead was made through conducting paint. Carbon paste electrodes (based on commercially available graphite powder) were prepared similarly. Carbon nanotube electrodes were prepared earlier by similar techniques to probe bioelectrochemical reactions. The need for oxygen reduction at catalytic surfaces has been recognized in fuel cells, batteries, and many other electrodic applications. Hence, oxygen reduction at nanotube surfaces is of great interest. Electrochemical reduction of dissolved oxygen is carried out in aqueous acidic (H2SO4) and neutral media (1 M KNO3). The solution is first degassed by bubbling nitrogen gas for about 15± 30 min in order to record the background current±voltage curves. Under these conditions, no cyclic voltammetric peak in the potential range 0 to ±0.8 V were observed. The same solutions were then saturated with oxygen by bubbling oxygen gas for 15 min. The cyclic voltammetric curve showed a well-defined peak at Epc = ±0.31 V vs. SCE (saturated calomel electrode) in H2SO4 solution (pH 2) at the carbon nanotube electrodes. At the carbon paste electrodes only an ill-defined peak is seen at Epc = ±0.48 V. In the KNO3 medium (pH 6.2), the reduction of dissolved oxygen is observed at Epc = ±0.51 V at the carbon nanotube electrode. This peak is shifted at the carbon paste electrode by about 30 mV. The shift of the peaks, corresponding to the reaction on the nanotube electrodes, is a strong indication of the electrocatalysis on this electrode (see discussion below). The shift may be considered as an overpotential, which indicates a more facile reaction occurring at the nanotubes compared to other carbons. The electrochemical reduction of oxygen is a function of pH of the medium as proton participation occurs as described by Equation 1.
478 citations
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TL;DR: In this article, the authors found that although Sony was as fast as any of its chief competitors in getting new models to market, an important explanation for the wide variety of models offered by the firm is the greater longevity of its key models.
477 citations
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TL;DR: In this article, the incorporation of 23 nm titanium dioxide nanoparticles into an epoxy matrix to form a nanocomposite structure is described, and it is shown that the use of nanometric particles results in a substantial change in the behavior of the composite, which can be traced to the mitigation of internal charge when a comparison is made with conventional TiO2 fillers.
Abstract: The incorporation of 23 nm titanium dioxide nanoparticles into an epoxy matrix to form a nanocomposite structure is described. It is shown that the use of nanometric particles results in a substantial change in the behaviour of the composite, which can be traced to the mitigation of internal charge when a comparison is made with conventional TiO2 fillers. A variety of diagnostic techniques (including dielectric spectroscopy, electroluminescence, thermally stimulated current, photoluminescence) have been used to augment pulsed electro-acoustic space charge measurement to provide a basis for understanding the underlying physics of the phenomenon. It would appear that, when the size of the inclusions becomes small enough, they act co-operatively with the host structure and cease to exhibit interfacial properties leading to Maxwell-Wagner polarization. It is postulated that the particles are surrounded by high charge concentrations in the Gouy-Chapman-Stern layer. Since nanoparticles have very high specific areas, these regions allow limited charge percolation through nano-filled dielectrics. The practical consequences of this have also been explored in terms of the electric strength exhibited. It would appear that there was a window in which real advantages accrue from the nano-formulated material. An optimum loading of about 10% (by weight) is indicated.
477 citations
Authors
Showing all 19133 results
Name | H-index | Papers | Citations |
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Pulickel M. Ajayan | 176 | 1223 | 136241 |
Zhenan Bao | 169 | 865 | 106571 |
Murray F. Brennan | 161 | 925 | 97087 |
Ashok Kumar | 151 | 5654 | 164086 |
Joseph R. Ecker | 148 | 381 | 94860 |
Bruce E. Logan | 140 | 591 | 77351 |
Shih-Fu Chang | 130 | 917 | 72346 |
Michael G. Rossmann | 121 | 594 | 53409 |
Richard P. Van Duyne | 116 | 409 | 79671 |
Michael Lynch | 112 | 422 | 63461 |
Angel Rubio | 110 | 930 | 52731 |
Alan Campbell | 109 | 687 | 53463 |
Boris I. Yakobson | 107 | 443 | 45174 |
O. C. Zienkiewicz | 107 | 455 | 71204 |
John R. Reynolds | 105 | 607 | 50027 |