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Naar aanleiding van het advies van de commissie Terlouw heeft het college van bestuur besloten dat het Debye Instituut for NanoMaterials Science zijn naam mag blijven gebruiken. Onderstaand persbericht zal vanochtend door de Universiteit Utrecht worden uitgebracht. Hierbij als pdf het advies van de commissie Terlouw.
17 januari 2008 Commissie Terlouw: ‘Handhaaf naamgebruik Debye’
De commissie Terlouw heeft de colleges van bestuur van de universiteiten van Utrecht en Maastricht geadviseerd het gebruik van de naam van Peter Debye voor de aanduiding van het chemisch-fysisch instituut in Utrecht, en de wetenschappelijke prijs in Maastricht te handhaven. De Universiteit Utrecht volgt dit advies, de Universiteit Maastricht niet.
De commissie is in het voorjaar 2007 door beide universiteiten ingesteld met de vraag om schriftelijk advies uit te brengen over het naamgebruik van Debye na het te verschijnen NIOD-rapport over Peter Debye ten tijde van de periode 1933-1945. In februari 2006 besloten de universiteiten van Utrecht en Maastricht af te zien van het naamgebruik van Debye. De universiteiten vonden het destijds opgeroepen beeld van Debye niet langer verenigbaar met de voorbeeldfunctie die gekoppeld was aan instituut en prijs.
De opdracht aan de commissie Terlouw was te adviseren over de wenselijkheid of onwenselijkheid ten aanzien van het gebruik van de naam van Debye voor aanduiding van activiteiten, gebouwen of onderdelen door de Universiteit Utrecht, dan wel het meewerken aan de toekenning en uitreiking van een wetenschappelijke prijs, die de naam heeft van Debye, door de Universiteit Maastricht.
De commissie geeft in haar advies aan begrip te hebben voor de beslissing van de universiteiten destijds, maar stelt op grond van het NIOD rapport dat “nu geen kwade trouw van Debye is bewezen, er moet worden uitgegaan van diens goede trouw”. De commissie concludeert: ‘Wij zijn van oordeel dat er onvoldoende reden is Debye zijn wetenschappelijke lauweren te ontnemen’..
Het college van bestuur van de Universiteit Utrecht volgt het advies en noemt haar organisatie voor chemisch-fysisch onderzoek weer het Debye Institute for NanoMaterials Science. Het college van bestuur van de universiteit Maastricht blijft bij haar eerdere oordeel.
Samenstelling adviescommissie
Meer informatie:
Ludo Koks, woordvoerder Universiteit Utrecht, 06 23 90 72 96,
L.Koks@uu.nl.
The Summer School, 14-25 August 2006, in pictures Utrecht Summer School![]() “Nanomaterials: science and applications”Debye Institute, Utrecht University, The Netherlands August 14-25, 2006
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The fields of nanoscience and nanotechnology depend on materials with critical dimensions in the nanometre range. Examples include organic macromolecules, inorganic catalyst particles, and size-quantized metal and semiconductor structures. Nanomaterials find and promise applications in a wide range of fields such as device technology (nanophotonics, solar energy conversion, opto-electronics), medicine (sensors, labelling) and chemical synthesis (catalysis). The emphasis in this school will be on:
The school will combine theory (lectures, tu- torials) with experiment and laboratory visits.
Master course: Computational
Materials Science by Dr. M. Dijkstra and Dr.ir. T.J.H. Vlugt
Debye Lecture 2005
On March 16 2005, prof. dr. ir. Bert Weckhuysen of the Debye Institute
research programme Inorganic Chemistry and Catalysis was among the first 40
young scientists (17 female, 23 male) who were nominated as members of THE
YOUNG ACADEMY of the Royal Dutch Academy of Sciences. Her Excellency mrs.
Maria van der Hoeven, minister of Education, performed the official
inauguration. The new Young Academy members were challenged by mrs. Van der
Hoeven to supply her with new and unconventional proposals to face upcoming
societal problems in the field of health, environmental protection, energy
supply, new technologies etc. The chair woman of the Young Academy gave
instant promising replies to the minister. |
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"MANIPULATION OF MOLECULES WITH ELECTRIC FIELDS" by Prof. Gerard Meijer
Fritz-Haber-Institut der Max-Planck-Gesellschaft Getting full control over both the internal and external degrees of freedom of molecules has been an important goal in molecular physics during the last decades. This control is essential in the presently very active field of Cold Molecules. Trapped samples of neutral molecules have been created by means of buffer gas cooling in a magnetic trap, by using deceleration of a molecular beam in combination with an electrostatic trap, and by pairing cold atoms to form molecules in optical or magnetic traps. Recently, spectacular progress has been made with association of ultra-cold atoms assisted by magnetically induced Feshbach resonances, resulting in the first molecular Bose-Einstein condensates. In the field of Cold Molecules there is a particular interest in cold dipolar molecules which stems from the presence of the anisotropic, long-range dipole-dipole interaction in these samples, which is predicted to lead to interesting physics and novel applications. In this presentation I will give an overview of the various experiments that we have performed during the last few years to explore the possibilities of manipulating neutral polar molecules with electric fields [1]. Arrays of time-varying, inhomogeneous electric fields have been used to reduce in a stepwise fashion the forward velocity of molecules in a beam. With this so-called 'Stark decelerator', the equivalent of a LINear ACcelerator (LINAC) for charged particles, one can transfer the high phase-space density that is present in the moving frame of a pulsed molecular beam to a reference frame at any desired velocity; molecular beams with a computer-controlled (calibrated) velocity and with a narrow velocity distribution, corresponding to sub-mK longitudinal temperatures, can be produced. These decelerated beams offer new possibilities for collision studies, for instance, and enable spectroscopic studies with an improved spectral resolution; first proof-of-principle high-resolution spectroscopic studies have been performed. These decelerated beams have also been used to load ground-state OH radicals in an electrostatic trap at a density of (better than) 107 mol/cm3 and at temperatures of around 50 mK. In another experiment, a decelerated beam of ammonia molecules is injected in an electrostatic storage ring. The package of molecules in the ring can be observed for more than 50 distinct round trips, corresponding to 40 meter in circular orbit and almost 0.5 sec. storage time. By miniaturizing the electrode geometries, high electric fields can be produced using only modest voltages. A micro-structured mirror for neutral molecules that can rapidly be switched on and off has been constructed and used to retro-reflect a beam of ammonia molecules with a forward velocity of about 30 m/s. This holds great promise for miniaturizing the whole decelerator, trap and storage ring for future applications.
[1]
H.L. Bethlem and G. Meijer, Int. Rev. Phys. Chem. 22, 73 (2003) SUCCESFULL INTERNATIONAL HOT-WIRE CVD CONFERENCE IN AUGUST 2004 ORGANISED BY THE RESEARCH PROGRAMME SURFACES, INTERFACES AND DEVICES OF THE DEBYE INSTITUTE. For a review see www.hwcvd.nl
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DEBYE PROFESSOR 2004 DESIGNING NANOSCALE MATERIALS Lecture 1. Why smaller, really is different; A survey of
finite size effects in nanomaterials. Lecture 2. General routes to nanoparticle production. Lecture 3. Semiconductor nanocrystals Part 1: Preparation
and properties. Lecture 4. Semiconductor nanocrystals , Part 2:
Applications of Quantum dots. Lecture 5. Nanowires; Lecture 6. Nanostructured magnetic materials for
information technology Lecture 7. Nanomagnetic for bio-applications and beyond. Lecture 8. Self-assembled nanocrystal superlattices:
preparation and properties. Lecture 9. Binary nanocrystal assembly a route to
multifunctional nanomaterials. Lecture 10. Nanoporous materials: Lecture 11. Part1 Ethics and issues for nanomaterials
research: Lecture dates: LECTURES 1+2: Wednesday September 8 10.00-12.30 ROOM 106 Buys Ballot Laboratory LECTURES 3+4: Wednesday September 15 10.00-12.30 ROOM 106 Buys Ballot Laboratory LECTURE 5: Monday September 20 11.00-12.30 ROOM 160 Buys Ballot Laboratory LECTURE 6+7: Wednesday September 29 10.00-12.30 ROOM C010 Aardwetenschappen LECTURE 8+9: Wednesday October 6 10.00-12.30 ROOM 160 Buys Ballot Laboratory LECTURE 10+11: Wednesday October 13 10.00-12.30 ROOM 106 Buys Ballot Laboratory This lecture series will provide an overview of progress in the synthesis and characterization of nanoscale building blocks and their assembly into functional materials and devices. The perspective of this course is that of a synthetic chemist/ colloid scientist although a variety of materials preparation techniques will the discussed and compared. An effort will be made to balance the excitement of materials discovery with the challenges of developing viable technologies based of nanomaterials. An introductory lecture will survey the origin of a collection of finite size effects that are being exploited to engineer materials properties. Where possible the "threats to continued scaling" of conventional technology will be highlighted along with the potential for new applications. General routes to the preparation of nanoparticles will be surveyed in lecture 2 while detailed examples of progress in the synthesis of semiconductor nanocrystals (quantum dots) and the development of applications base on these systems will comprise lectures 3 and 4. In lecture 5 we will move from zero dimensional to one dimensional semiconductors as progress in the preparation and characterization of semiconductor nanowires and their integration in to devices is explored. Lectures 6 and 7 will switch in focus to nanomagentic materials, exploring their preparation, properties and the applications that are driving intense interest in these systems. Lecture 8 will focus on conditions that allow an ensemble of monodisperse nanocrystals to organize themselves in extended ordered structures. We will draw-upon understanding developed from classic studies of micron scale colloidal systems and explore the development of new delocalized "collective phenomena" in nanocrystal assemblies. Lecture 9 will move one notch in complexity as we investigate routes to induce different types of nanocrystals to organize into binary colloidal crystals providing a route of multifunctional nanomaterials. Furthermore we will attempt to develop a systematic approach to structurally characterizing these fascinating systems. In lecture 10 we will survey some developments in nanoporous materials and then focus on opportunities to harness these materials as templates for the fabrication of nanoscale devices. The final lecture in the series will be reserved for a discussion of some of the most promising new areas and opportunities in nanomaterials research. With the benefit of an audience engaged and enabled by concepts from lectures 1-10 we will move to the most interactive of the sessions lecture 11. In lecture 11 be composed of 2 parts. The first section we will discus some of the ethical, environmental, and health issues surrounding nanotechnology. Serious attention must be paid now to the possible implication of the dissemination, use and disposal of these materials. Researchers must develop a more proactive stance to full social and environmental impacts of these developments if these materials are to reach their full beneficial potential. In the final part of lecture 11 discussing the next "hot areas" to pursue We will also discuss how we as members of the scientific community can critically navigate the hype surrounding nanomaterials research. ABOUT DR. MURRAY: |
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Award Recipients of the PHONONS Award (with year and conference site)
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The engraved text reads: To Harold de Wijn - for outstanding contributions to phonon physics - Phonons 2004 S. Petersburg |
The Opening of the XXS-exhibition in Utrecht University Museum
from March 25, 2004 t/m October31, 2004
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| On February 2, 2004, Prof. Daniel Vanmaekelbergh gave his inaugural address entiteld "Feynmans's Dream: about dream and reality in the nanosciences", because he was appointed as a new professor on the chair "Chemistry and Physics of Nanostructures". | |
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On March 12, 2004, Prof. Frans B. van Duijneveldt en dr. Jeanne van Duijneveldt-van de Rijdt retired with a plenary lecture by prof. Van Duijneveldt and subsequently a reception. The added pictures give an impression of this event. |
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With the beginning of 2004 we have a new scientific director:
Professor, scientific director of the Debye Institute
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Mesostructured
Solids: From Self-Assembly to Nanocasting Max-Planck-Institut für Kohlenforschung, Mülheim an der Ruhr Mesostructured and mesoporous solids entered the scientific world on a larger scale with the 1992 Mobil publication on MCM-41 type materials. Since then, numerous other ordered mesoporous materials have been described, with different pore structure and different chemical composition. Most of the pathways used to synthesize such solids are cooperative, that is, inorganic species assemble in solution with surfactants to form organic-inorganic liquid crystals. After removal of the surfactant part, accessible pore systems result. The surface of the pores can be modified over wide ranges, and different types of other materials can be deposited in the pores in a controlled manner. Since few years, an alternative access to ordered mesoporous materials has been opened, initiated by the synthesis of CMK-type carbon materials by Ryong Ryoo. This synthesis relies on the use of ordered mesoporous silica as “mold” to generate another ordered mesoporous material. Thus, by filling the voids of MCM-48 or SBA-15 with a carbon precursor, pyrolyzing the precursor to generate carbon, and then leaching the silica with HF or NaOH one obtains a carbon negative from the original silica. One can even take this one step further, since now the carbon in turn can be used as the “mold” to be filled with another solids precursor, such as tetraethoxysilane. After hydrolysis and condensation of the silica, the carbon can be removed by combustion and the negative of the negative is obtained, i.e. again an ordered mesoporous silica, which very closely resembles the starting material with respect to pore system and morphology. Thus, over the last ten years an unprecedented control over structures in the size range of several nanometers has been achieved with rather straightforward and simple chemical means. | ||||||||||||||||||||||||||||||
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DEBYE PROFESSOR 2003 |
LASER
COOLING AND TRAPPING
A series of lectures by Prof. Dr. Harold J. Metcalf , Ornstein Laboratory (entrance via Buys Ballot Laboratory, Princetonplein 5) Room 260
Thursdays 9-11 o’clock |
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