||Jul. 2018: hot-electrons-induced atomic disorder in Au nanoclusters.|
Researchers of the
Structural and Electronic Surface Dynamics group of the FHI Department of Physical Chemistry, Berlin,
in cooperation with colleagues at the
Nanoscale Physics Research Laboratory of the University of Birmingham and the
College of Engineering of the University of Swansea,
have published a joint article in
observing various forms of atomic motion, such as thermal vibrations, thermal expansion, and lattice disordering on size-selected Au nanoclusters
on thin-film substrates as distinct and reciprocal-space manifestations.
Thermal equilibration proceeds through intrinsic heat flow between electrons and lattice, and extrinsic heat flow between the nanoclusters
and the substrate. The two-temperature model was extended to 0D/2D heterostructures so as to describe energy flow among various subsystems,
to quantify interfacial coupling contents and to elucidate the role of optical and thermal substrate properties.
At lattice heating of the nanoclusters dominated by intrinsic heat flow, a reversible disordering of atomic positions occurs,
which is absent when heat is injected as hot substrate phonons.
The analysis suggests that hot electrons can distort the lattice of nanoclusters, even at lattice temperatures below the equilibrium threshold for surface premelting,
and this is interpreted as activation of surface diffusion due to modifications of the potential energy surface at high electronic temperatures.
Impact of crystal-lattice vibrations on magnetic properties.|
Heating a ferromagnet beyond some critical temperature leads to loss of magnetic properties.
The precise mechanism and time-scale of the process remained undescribed.
A team of scientists from Berlin (Fritz Haber Inst., FU Physics Dept., TU Inst. for Optics & Atomic Physics, Max Born Inst.),
Dresden (Helmholtz Center), Uppsala (Dept. of Physics and Astronomy), St. Petersburg (Ioffe Inst.), and Sendai, Japan (inst. of Materials Research)
have now revealed the elementary steps of this process.
The researchers have directly probed the flow of energy and angular momentum in the model insulating ferrimagnet yttrium iron garnet.
After ultrafast resonant lattice excitation, one
could observe that magnetic order reduces on distinct
time scales of 1 ps and 100 ns. Temperature-dependent
measurements, a spin-coupling analysis, and simulations show
that the two dynamics directly reflect wo stages of spin-
On the 1-ps scale, spins and phonons reach quasi-equilibrium in terms of energy through phonon-induced modulation of the exchange interaction.
This mechanism leads to identical demagnetization of the ferrimagnets two spin sublattices and to a ferrimagnetic state of
increased temperature yet unchanged total magnetization. Finally, on the much slower, 100-ns scale,
These findings are relevant for all insulating ferrimagnets and indicate that spin manipulation by phonons,
including the spin Seebeck effect, can be extended to anti- ferromagnets and into the terahertz frequency range.
This has been published in
|See further details in
the Fritz Haber Institute public information site,|
Jul. 2017: Laurenz Rettig receives a grant of the Emmy Noether Programme.
|The Emmy Noether Programme
of the DFG (Deutsche Forschungsgemeinschaft)) has accorded Laurenz Rettig,
leader of the research group Dynamics of Correlated Materials its support for his research project
Beyond time constants: Quantifying interactions in correlated materials by complementary ultrafast time-domain approaches
Correlated materials are characterised by the variety of interactions between the elementary degrees of freedom, leading to novel ground states
with broken symmetries and often intriguing properties. The quantitative determination of those couplings and their relevance for the formation
of broken-symmetry ground states and phase transitions is a major challenge in solid state physics.
In particular, in thermal equilibrium the various interactions are present simultaneously in a system,
making it difficult to separate them due to their similar energy scale. Studies of those interactions in the time domain in a non-equilibrium system
created after ultrafast optical excitation promise a way to separate such contributions by their intrinsically
||different dynamics. Such an approach, however, is often hindered by the unspecific nature of the employed probes and thus frequently limited to a
qualitative discussion of time constants. The goal of this research project is to combine complementary, quantitative time-resolved
spectroscopies, which directly address the dynamics of specific degrees of freedom, in order to determine the couplings between
the different degrees of freedom and their relevance for a phase transition from their temporal evolution. Combining time- and
angle-resolved photoemission spectroscopy, time-resolved resonant and non-resonant x-ray diffraction and electron diffraction
techniques provides direct and quantitative access to electronic, magnetic and structural ordering phenomena. This approach
will be employed for different selected classes of phase transitions, such as charge-density waves, antiferromagnetically ordered
system and complex charge- and orbitally ordered systems, in order to determine and quantify the couplings between the different
degrees of freedom responsible for the formation of those broken-symmetry states.
||Jul. 2017: Nikolai Paßler receives the Physics-studies Prize.|
The Physikalische Gesellschaft zu Berlin has announced that Nikolai Paßler of the
Lattice Dynamics group
has been awarded the Physics-studies Prize 2017.
The Physics-studies Prize is awarded by the Physikalische Gesellschaft zu Berlin
to outstanding radiates with diploma or masters degree.
||Jul. 2017: photoexcited carriers interact with lattice vibrations in thin films of the layered WSe2.|
A team of researchers from the
Structural and Electronic Surface Dynamics group of the FHI Department of Physical Chemistry, Berlin,
and the MPI for Structure and Dynamics of Matter, Hamburg, have published an outstanding article in
the Physical Review Letters,
investigating the interactions of photoexcited carriers with lattice vibrations in thin films of the layered transition metal dichalcogenide WSe2.
Employing femtosecond electron diffraction with monocrystalline samples and first-principles density functional theory calculations,
a momentum-resolved picture of the energy transfer from excited electrons to phonons is obtained.
The measured momentum-dependent phonon population dynamics are compared to first-principles calculations of the phonon linewidth and
rationalized in terms of electronic phase-space arguments.
The momentum-dependent electron-phonon coupling leads to a nonthermal phonon distribution, which relaxes to a thermal distribution via electron-phonon
and phonon-phonon collisions.
The results provide a basis for monitoring and predicting out of equilibrium electrical and thermal transport properties for nanoscale applications
of transition metal dichalcogenides.
||Feb. 2017: simultaneous probe of electron-lattice interactions in photoexcited antimony.|
Researchers of the
Structural and Electronic Surface Dynamics group of the FHI Department of Physical Chemistry, Berlin,
in cooperation with colleagues at
Theoretical Physics II &
Center for Interdisciplinary Nanostructure Science and Technology of the University of Kassel,
have published a joint article in
the Physical Review B,
demonstrating in the example of photoexcited atimony, that the entire electron-lattice interaction, particularly coherent and incoherent electron-phonon coupling,
can be probed simultaneously.
Femtosecond electron diffraction (FED) with high temporal resolution allowed to simultaneously observe coherent excitation of the
fully symmetric A1g optical phonon mode
as well as energy transfer from electrons to phonons via incoherent electron-lattice scattering.
Oct. 2016: Takashi Kumagai receives PRESTO promotion.
|The PRESTO (Precursory Research for Embryonic
Science and Technology) managed by JST (Japan Science & Technology Agency) has announced that Takashi Kumagai,
leader of the research group Nanoscale Surface Chemistry will be supported in his research topic
Eluciation of microscopic mechanism of catalytic effects via localized plasminon excitation.
||on plasmonic metal nano-structures can enhance chemical reactions. However, the microscopic mechanism of the process
induced via near-field excitation remains poorly understood. This research project investigates near-field induced
chemical reactions using a low-temperature scanning probe microscope and aims at obtaining the detailed reaction
mechanism at the single-molecule level. The application for methane activation via near-field excitation will also be examined.
Sep. 2016: Julia Stähler wins the Edith Flanigen Award 2016.
The Collaborative Research Centre 1109
(CRC 1109) has announced that the winner of the Edith Flanigen Award 2016 is Dr. A Julia Stähler,
leader of the Max Planck Research Group Electron Dynamiχ.
The award is conferred annually by the CRC 1109 to an exceptional female scientist at an early stage of her career
for outstanding results on metal oxide water systems.
The announcement mentions that in her research, the awardee investigates ultrafast non-equilibrium dynamics after
optical excitation in a wide range of fields: Electron- and exciton-transfer processes at inorganic-organic hybrid systems,
photo- and electron-induced chemical reactions at interfaces, elementary excitations at surfaces, and photoinduced phase transitions.
||Sep. 2016: Lutz Waldecker receives prize for his Thesis.|
The Physikalische Gesellschaft zu Berlin has announced that Lutz Waldecker of the
Structural & Electronic Surface Dynamics group
has been awarded the Carl-Ramsauer-Award 2016
for his Thesis Electron-Lattice Interactions and Ultrafast Structural Dynamics of Solids.
Lutz Waldeckers thesis studies the interactions between the atomic cores of solids and their outer
electrons. These interactions determine fundamental material properties such as electric and
thermal conductivity, and are responsible for how a material behaves in extreme conditions. To investigate these interactions,
materials were placed in non-equilibrium states by very short laser pulses. The subsequent relaxation
proceeds within an extremely short period of a few hundred femtoseconds (1 Femtosekunde = 10-15).
Complementary femtosecond optical- and diffraction techniques based on the pump-probe principle were developed,
allowing to observe these processes on their fundamental time scale. Applying these methods it became possible
to elucidate new details of the electron-lattice interactions in simple metals as well as in two-dimensional semiconductors.
Additional experiments with strongly excitated phase-change materials gave new insights into the pathway of
the transition between their two crystallographic states and on what role the electron-lattice interactions play
in this process.
||Apr. 2016: Observing basic interactions in solids.|
Interactions between electrons and vibrations of atomic ions, of which all condensed matter
is composed, and which determine such fundamental features like electron and thermal conductivity of materials, energy dissipation
in electronic devices, and emergence of quantum phenomena like superconductivity, are a central subject in solid-state physics.
Lutz Waldecker and Roman Bertoni of the Max Planck Research Group headed by Ralph Ernstorfer, in coopertion with
Jan Vorberger of the Max-Planck-Institut für Physik komplexer Systeme, Dresden,
have now visualized and quantified electron-lattice interactions after a sudden very short
external disturbance (a 50 femtosecond infrared laser pulse) in aluminum, a proto-typical metal. Due to these interactions, the
excited electrons proceed to equilibrate with the atomic vibrations, and successive snapshots of these latter provide
a movie of the relaxation process. Comparing the experimental findings with state-of-the-art numerical calculations
of atomic mean squared displacements made it possible to revise the existing model of such interactions.
The report of these results has now been published in
Physical Review X vol. 6.
||Feb. 2016: ERC double feature at the PC department.|
Tobias Kampfrath and Ralph Ernstorfer have been successful in the 2015 Call for
Consolidator Grants of the European Research Council (ERC).
ERC Consolidator Grants are awarded to single principal investigators based on the quality of the research proposal and
the scientific track record of the applicant. Tobias Kampfraths and Ralph Ernstorfers projects each have a
duration of 5 years and are funded with 2.0 and 2.6 million Euro, respectively.
In his TERAMAG project, Tobias Kampfrath will implement spintronic operations, i.e. operations utilizing the spin of
electrons, at extremely high frequencies in the elusive terahertz range. This research is not only relevant for
future processing of magnetically stored information, but will also result in novel and highly efficient emitters
of terahertz electromagnetic radiation.
Ralph Ernstorfer will investigate the interaction between electrons, their spin and the vibrations of atoms in semiconductors
with layered crystalline structure. The project FLATLAND aims at obtaining a microscopic understanding of relaxation and
dissipation effects in two-dimensional semiconductors and stacked heterostructures comprised thereof.
Further information on the grantees research and the employed methodology can be found on the websites of the
Terahertz Physics group and the
Max Planck Research Group Structural & Electronic Surface Dynamics.|
|| Dr. Tobias Kampfrath &|
Dr. Ralph Ernstorfer
Jan. 2016: Ultrafast dynamics of elementary processes and many-body effects
at surfaces and in solids.
We are happy to announce that the Deutsche Vakuumgesellschaft (DVG) awarded the
Gaede-Preis 2016 to
Dr. Julia Stähler in recognition of her
outstanding work on ultrafast dynamics of elementary processes and many-body effects at surfaces and in solids.
The prize will be handed over on March 8, 2016 in a Special Ceremonial Session at the 80th Annual Meeting of the DPG in Regensburg.
Order versus disorder: Electrons are diffracted differently in crystalline structured and amorphous
Ge2Sb2Te5 (GST), leading to distinctly different
diffraction images of the crystal (left) and of the amorphous material (right).
© Fritz Haber Institute of the MPG
Jul. 2015: Light switches on a DVD.
A germanium, antimony and tellurium compound, Ge2Sb2Te5, also known by its acronym GST,
has long been used as data storage material, in that its structure is rearranged by laser pulses, switching it between
transparent and non-transparent states A researcher team at the Physical-Chemistry Department of the Fritz Haber Institute (FHI)
in Berlin, in collaboration with colleagues from the Institut de Ciències Fotòniques (ICFO) in Barcelona,
have discovered that the materials optical properties change much faster than the structure, which opens new perspectives
for its use in photonics components. Hence, while DVDs may soon become obsolete, the implemented GST may find applications
other than as storage material.
These findings, together with a video,
have been published in
|MPG research news: Light switches on a DVD
|| (doi: 10.1038/nmat4359)|
Contact person: Dr. Ralph Ersntorfer
Apr. 2015: Solvation of electrons in water.
The behavior in water of naked electrons, i.e. of such which are not attached to atoms or molecules, plays a significant
role in the progress of chemical reactions when water is involved. As a first step, the negatively charged electrons become
solvated, they surround themselves with water molecules by attracting the positive electrical poles of the latter.
A research team of the Department of Physical Chemistry has now obtained detailed information about the solvation process,
determining the energy with which a naked electron is bound directly when immersed in water, when its charge is not yet
buffered off by the water molecules, and has also measured the time it takes until the naked electron begins to gather
water molecules around it. The findings on the immersion process of an electron were made using time-resolved two-photon
The findings have been published as cover story in
Journal of the American Chemical Socierty.
|MPG research news: Diving electrons
||Contact person: Dr. Julia Stähler|
Jun. 2014: Karl Scheel Prize 2014 is awarded to Dr. Tobias Kampfrath.
The Physikalische Gesellschaft zu Berlin (PGzB) has decided to award the Karl Scheel Prize for 2014 to Tobias Kampfrath
in recognition of his outstanding research on manipulation of spins and light at terahertz frequencies.
The prize will be handed over on June 27, 2014, at a meeting of the PGzB in the Magnus House in Berlin, at which occasion
the awardee will present a talk on that subject.
||Every single atom counts.|
The environment of every single molecule is important in any chemical process as it defines the potential energy
landscape in a reaction. A research team at the Fritz-Haber-Institute Berlin (in collaboration with theoreticians from Liverpool
and chemists from Warszaw) could for the first time control a chemical process by single atoms in the vicinity of the molecule.
Porphycene molecules were studied on a copper surface and an intramolecular proton transfer, a process that is important in nature,
was induced by the tip of a scanning tunneling microscope. The researchers then placed very precisely individual copper atoms close
to a porphycene molecule and found a dramatic influence of the atom location on the proton transfer rate in the molecule. It is
thus possible to tune the transfer rate up and down, depending on the atom position.
This surprising effect is caused by the modified potential energy landscape of the molecule in the presence of an atom.
It could be extended to rows of porphycene molecules on the surface. In such an arrangement it was found that even the position of
the protons in the centre of a molecule can modifiy the proton transfer in the neighbour molecule. Hence, positive and negative
cooperativity could be directly imaged in real space. These results show on the one hand the importance of controlling the environment
of molecules with atomic precision and demonstrate on the other hand the potential to regulate processes that occur in a single molecule.
These findings have been published in
Nov. 2013: Carl Ramsauer Award of the German Physical Society Berlin Ceremony at the Technical University Berlin.
The 2013 awards for outstanding PhD theses will be conferred today, November 13, at the Technical University Berlin.
Amongst the awardees are, besides Laurenz Rettig (see below), also
Marc Herzog who defended his thesis
Structural Dynamics of Photoexcited Nanolayered Perovskites Studied by Ultrafast X-ray Diffraction at the
University of Potsdam, but presently is in the Electron Dynamics group of the FHI Physical Chemistry Department.
Aug. 2013: Carl Ramsauer Award of the German Physical Society Berlin for Dr. Laurenz Rettig.
The German Physical Society in Berlin will award the
Carl-Ramsauer-Award 2013 to
Laurenz Rettig for his PhD thesis Ultrafast dynamics of correlated electrons.
recognizes one outstanding PhD thesis in physics at each of the 3 universities in Berlin
and at the University of Potsdam. The award is named after Carl Wilhelm Ramsauer,
who discovered in 1920 the high transmission of slow electrons through gases demonstrating
non-classical behavior of electrons (Ramsauer-Townsend-Effect).
Schematic representation of the experiment.
Left: An extremely short ultraviolet pulse creates hot excited electrons in the semiconductor titanium dioxide.
This changes the spatial distribution of the electrons within the lattice, resulting in a shift of the potentials for the atomic cores,
i.e., their rest position (center). The subsequent cooling of the electrons which takes about 20 femtoseconds
further amplifies this effect (right). The combined effect of electron excitation and cooling leads to a force
on the oxygen atomic cores, resulting in a coherent oscillation within the crystal structure.
||Feb. 2013: Cooling of electrons drives ultrafast lattice dynamics.|
At the atomic scale, solids are made of atomic cores, i.e., nuclei with tightly bound electrons, and weakly bound valence electrons.
The valence electrons strongly interact with each other and thereby act as a kind of glue that holds the atomic cores together
within the crystal. The fundamental properties of a material, e.g., its electrical conductivity, optical properties, or crystal
structure, are the result of the continuous interplay between the positions of the atomic cores and the valence electrons.
The investigation these correlations, in particular for complex materials, manifests one of the central topics of modern solid state
physics. One experimental approach uses extremely short light pulses to excite the material and observes the response of the crystal
lattice to this perturbation. These processes occur on time scales of femtoseconds (1 fs = 1015 s).
The correlations between electronic and atomic structures are particularly strong for transition metal oxides. For some of them it is
even possible to induce a structural phase transition with an optical excitation. A team of researchers from the Fritz Haber Institute,
in collaboration with colleagues from the Max Planck Institute for Quantum Optics, the Technical University of Munich, and the
University of Kassel have now shown that even a small redistribution of electrons can produce a significant force on the atomic cores
in the crystal lattice. They excited the semiconductor titanium dioxide with extremely short ultraviolet light pulses and measured the
subsequent changes of the crystals reflectivity. The excitation initially generates a small number of very hot electrons which thereby
also redistribute spatially within the crystal: the electron concentration is reduced around the oxygen cores while it is increased
around the titanium cores. In consequence, the potential energy surface for the atomic cores, which is due to the valence electron
distribution, changes and the rest position of the oxygen cores is shifted relative to the position of the titanium cores. Since these
changes occur faster than motion of the atom cores in the crystal, each oxygen core experiences the same force, and all of them start
oscillating in phase.
This effect is best understood imagining a ball (oxygen atom core) in a bowl (potential surface of the crystal).
In the ground state, the ball is in the center at the bottom of the bowl. The excitation of the electrons causes a sudden shift
of the bowl, and the ball starts oscillating.
Detailed analysis of the phase of these lattice oscillations and extensive theoretical calculations revealed a surprising effect:
it is not only the initial excitation of the electrons that is important for the new rest position of the atomic cores, but also the
subsequent cooling of the electrons. The initially hot electrons cool down from several thousand Kelvins to room temperature within
about 20 femtoseconds. While the crystals warms up only slightly on those time scales, a significant change of the spatial redistribution
of valence electrons and, in consequence, the rest positions of the atomic cores is observed. Such dependence of the crystal structure
on the electronic temperature has been long predicted, and could now be shown experimentally for the first time. The results show how
the equilibrium state of a crystal can be extremely sensitive to small changes in the electronic structure. The work is another step
towards understanding the complex interactions in transition metal oxides and opens up new ways of designing materials for
|The findings are published in
Physical Review Letters.
Contact person: Dr. Ralph Ersntorfer
| ||Oct. 2012: 2011 Foresight Institute Feynman Prize awarded to Dr. Leonhard Grill.|
Feynman Prize ||
The Foresight Institute at Palo Alto (CA), which awards annual Feynman Prizes for Nanotechnology Theory and Experiment
in the amount of $5,000 each, announced on Oct. 16, 2012, that the winner of the 2011 Feynman Prize
for Experimental work is Leonhard Grill of the Department of Physical Chemistry
of the FHI:
in recognition of his pioneering and continuing work on manipulating and structuring functional matter at the
atomic scale. He has used scanning tunneling microscopy to characterize the electronic and mechanical properties of
single molecules; constructed atomically precise covalent molecular nanostructures from single molecules; and used
an STM tip to roll a 0.8 nanometer molecular wheel on a surface.
Experiment scheme: a single graphen strip is drawn off a gold surface and its conductance is measured.
||Single graphene stripes as molecular wires.|
The transport of electrons and thus electrical current is not only of central importance in modern society,
but also for scientists in fundamental research where it is of interest for biological processes and for
potential applications for future molecular electronics (with single molecules as devices).
A research team at the Fritz-Haber-Institute Berlin (in collaboration with theoreticians from Toulouse and Singapore)
could measure for the first time the electrical current through single molecules at different electrode voltages,
thus characterizing various charge transport regimes. Graphene stripes were chosen, due to their interesting electronic properties,
and assembled directly on the surface by in-situ polymerization.
The central challenge for such measurements is to measure the current thourgh an object at the atomic scale with
macroscopic electrodes, ensuring for a well-defined arrangement.
In this work, a scanning tunneling microscope was used
to pick up single graphene ribbons from a surface and thus realizing the desired geometry. In this way,
the decay of the electric current with the molecular length, the key property for charge transport efficiency,
can be measured in real time. It is shown that the conductance properties of a single molecule can be correlated
with its electronic states. Comparison with calculation reveals that the conductance depends on the precise atomic
structure and bending of the molecule in the junction.
These findings have been published in
Light induced changes in crystal vibrations enable researchers to optically probe changes in atomic structure.
||Mar. 2012: Measuring ultrafast phase transitions with light.|
Short, femtosecond (10-15 s) pulses of intense laser light offer the fastest ways to manipulate material properties.
One active area of research is to investigate how such pulses can be used to trigger ultrafast phase transitions,
which results in colossal changes in a materials properties on very short timescales. During these phase transitions
the structure of the material can evolve extremely rapidly so that conventional probes of the crystal structure,
such as X-ray and electron diffraction, produce blurred images, and the transition pathway cannot be resolved.
Although optical pulses have the required temporal resolution, their wavelength is too long to measure the atomic
positions directly. To overcome this limitation, researchers at the Fritz Haber Institute instead used an optical
technique to measure the forces that dictate the atomic positions, thus enabling an ultrafast optical probe of
the crystal structure.
The technique was used to measure the structural component of the photoinduced insulator-metal phase transition
in VO2, using samples grown and characterized at the Vanderbilt University. When the laser strikes the material,
vibrations, which are characteristic of the insulating phase, are created. By using a high power laser, these
vibrations could be completely eliminated, providing insights into the nature of the timescale and driving mechanism
of the phase transition. These findings have been published in
Nature Communications see elaborate information
in German at the MPG news site.
|Feb. 2012: Modifying the light spectrum with a spectral lens.|
Left: schematic of a spectral lens. A pulse of light modifies the light spectrum of the lens,
so that its initially broad frequency range (shown red) is compressed to a narrower, higher-frequency
Right: experimental realization. When a probe pulse is sent through a light conductor,
the low frequencies infiltrate a wider area of the membrane while the high frequencies
remain concentrated in the middle. An intensive pump pulse then mainly affects the lower frequencies,
while the higher frequencies are protected by a gold stripe.
A conventional optical lens can be used to magnify an image, or to reduce it. Quite different is the effect of a
so-called spectral lens developed by researchers of the Department of Physical Chemistry of the FHI, the Amsterdam
FOM Institute for Atomic and Molecular Physics (AMOLF), and the School of Physics and Astronomy at the University
of St. Andrews (Scotland, UK). It narrows or widens the spectral range of a light beam.|
Its construction, and mode of functioning, is of course quite different from that of an optical lens. To narrow the
spectral range of a light beam, the frequencies are shifted to higher frequencies such, that the frequency increase
is dependent of the initial frequency. The lower the initial frequency, the greater the upwards shift.
This is achieved in a so-called photonic crystal, that is a solid with a periodic structural modulation, for example
a regularly repeating pattern of tiny holes. This influences the index of refraction of the solid, and hence the
dispersal of light in it.
|The photonic crystal of the researchers around Tobias Kampfrath of the FHI PC Department consists of a 220 nanometer
(a nanometer is a millionth of a millimeter) thin silicon foil with regularly distributed little holes, each a few hundred
nanometer in size. In the middle there is a very thin strip without holes, that serves as light conductor. When a pulse
of light is directed through this strip, the higher (blue) frequencies remain concentrated within it, while the lower
(red) frequencies penetrate far into the perforated part. As a result, only the higher frequencies are influenced by
the perpendicularly incident controlling pump pulse.
The results have been published in
Physical Review Letters see also the elaborate information
in German at the MPG news site,
and in the FHI archives.
||Hierarchical linking of individual molecules into complex structures|
Researchers at the Fritz-Haber-Institute demonstrate the controlled assembly of
nanoscopic building blocks on the path towards novel materials and molecular electronics
A central challenge of nanotechnology, which is crucial to visions such as molecular machines,
novel materials and molecular electronics, lies in the bottom-up connection of molecular building blocks
in a well-defined assembly. One can think of it as similar to LEGO, however at the nanometer scale.
Due to their exceptionally low size, such structures hold the promise of low energy consumption,
high operating speeds and low production costs. However, to date, only simple structures could be formed,
because the assembly process was limited to a single step. A research group at the Fritz Haber Institute, Berlin,
could now, in collaboration with scientists from the Humboldt University, Berlin, and the Laboratorio TASC ,Trieste,
for the first time demonstrate hierarchical growth in several steps by the suitable provision of distinct side groups.
This was performed by sequentially supplying reactive sites on molecular building blocks, which allowed the
formation of considerably more sophisticated structures. With this method the researchers could affect the formation
of networks made of two different molecular building blocks with high selectivity with regard to the connection sites,
which would not have been possible with a non-hierarchical process.
These results have been reported in the journal Nature Chemistry.
Drawing an individual polymer from a surface and applying an
electric tension (potential difference) opens the way to an atomic scale study
of charge transport through molecular wires.
||Can molecular wires become the basis for new computers?|
In their pursuit of ever faster and more efficient processors, the producers of computer chips are approaching
the physical limits of maniaturisation. The tiniest transistors in modern microprocessors, measuring just a few
nanometers (1 nanometer is one billionth of a meter), can no longer be made smaller by conventional techniques
of so-called top-down procedures. For this reason, the semiconductor industry is compelled to place more transistors
on a chip, and to operate them at higher clock frequencies both having the consequence of rising energy
consumption and higher waste heat. A major European project, the Atomic Scale and Single Molecule
Logic Gate Technologies (AtMol), in which researchers of the Fritz Haber Istitute
are taking part, aims for solutions of the problem.
In this, the research group headed by Leonhard Grill at the Department of Physical Chemistry is to play an
important role, in that they will measure the electric conductivity of individual molecular wires, i.e. of
polymers (molecule chains). In cooperation with Stefan Hecht of the Humboldt University, Grill will
implement a jointly developed method to produce the polymers directly on surfaces so as to assemble the first
logical circuit elements with custom-built molecular modules.
||Jun. 2011: Professor Bernhard Heß Lectureship, Regensburg.|
The Bernhard Heß Foundation of the Regensburg University awards an annual
Professor Bernhard Heß Lectureship prize of 2,000.
The award is designed to give external upcoming researchers the opportunity to hold guest lectures at
the Faculty of Physics in Regensburg, so as in this way to widen the range of courses of the University.
The presentation of the award will be in February, on the Physics Day at the Regensburg University.
The awardee for 2011, Dr. Tobias Kampfrath, is preparing a lecture series on the subject
spectroscopy and photonics with a femtosecond laser, that will magnificently
augment the courses offered at the University.
The basic principle: Electrons (blue spheres) carry a spin that can be seen as a persistent rotation
of the electron about its own axis, resulting in a magnetic moment (blue arrows).
In the experiment, spins are kicked by an intense terahertz magnetic transient (orange waveform),
leading to a precession about their equilibrium directions, similar to a spinning top.
||Coherent terahertz control of antiferromagnetic spin waves.|
Researchers of our Department with colleagues from the University of Konstanz
and the Hemlholtz Institute in Bonn have succeeded in
controlling the electron spin direction, which had heretofore been inaccessible. The experiment employs
electromagnetic radiation in the terahertz frequency range (1 THz = 1012 Hz), which is
currently attracting attention because
of its use in body scanners in airports. Like many other applications, these scanners exploit the
electric component of the terahertz wave. The present work shows that the magnetic component of terahertz
radiation has important further potential applications.
Their findings were reported in the journal Nature Photonics.
Turing patterns in a complex network.
Turing patterns in network-organized activatorinhibitor systems.|
Researchers of our Department and the Department of Physics of the Kyoto University
have made an important step towards understanding self-organization
phenomena, extending theoretical analysis to complex networks. Their attention was focused on
patterns under conditons of instblility first proposed in 1952 by the British mathematician
Alan Turing. However, the treatment of Turing instability in networks has so far only been
considered in the example of regular lattices and small networks. The present work studies
Turing patterns in large random networks, which reveal striking differences from the classical behaviour.
Their findings were reported in the journal Nature Physics.
||A new book by Gerhard Ertl: Reactions at Solid Surfaces|
A new book entitled Reactions at Solid Surfaces by Nobel Prize winner
Gerhard Ertl has appeared,
based on Ertls Baker Lectures
at Cornell University in 2007.
The book describes how surface chemistry works and how to probe and understand the dynamics of
reactions at surfaces. The book is a thoughtful and compact introduction to surface reactions for
graduate students and professional scientists alike.
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