Martin Aeschlimann

Bio: Martin Aeschlimann is an academic researcher from Kaiserslautern University of Technology. The author has contributed to research in topics: Femtosecond & Angle-resolved photoemission spectroscopy. The author has an hindex of 56, co-authored 291 publications receiving 12034 citations. Previous affiliations of Martin Aeschlimann include University of Kiel & University of Rochester.

Explaining the paradoxical diversity of ultrafast laser-induced demagnetization

Abstract: Demagnetization in metals occurs on very different timescales depending on the material. It is now shown that electron–phonon-mediated spin scattering describes the process of demagnetization well in every case, and the differences in timescale are mainly determined by the ratio between Curie temperature and the atomic magnetic moment.

All-optical control of ferromagnetic thin films and nanostructures

Abstract: The interplay of light and magnetism allowed light to be used as a probe of magnetic materials. Now the focus has shifted to use polarized light to alter or manipulate magnetism. Here, we demonstrate optical control of ferromagnetic materials ranging from magnetic thin films to multilayers and even granular films being explored for ultra-high-density magnetic recording. Our finding shows that optical control of magnetic materials is a much more general phenomenon than previously assumed and may have a major impact on data memory and storage industries through the integration of optical control of ferromagnetic bits.

Engineered materials for all-optical helicity-dependent magnetic switching.

Abstract: A promising strategy for achieving information storage devices with low energy consumption is to avoid using applied magnetic fields as a means to manipulate the magnetization of materials. Now, the class of materials that can be switched by all-optical means is shown to extend beyond alloys consisting of rare earths and transition metals.

Topological states on the gold surface

Abstract: Gold surfaces host special electronic states that have been understood as a prototype of Shockley surface states. These surface states are commonly employed to benchmark the capability of angle-resolved photoemission spectroscopy (ARPES) and scanning tunnelling spectroscopy. Here we show that these Shockley surface states can be reinterpreted as topologically derived surface states (TDSSs) of a topological insulator (TI), a recently discovered quantum state. Based on band structure calculations, the Z2-type invariants of gold can be well-defined to characterize a TI. Further, our ARPES measurement validates TDSSs by detecting the dispersion of unoccupied surface states. The same TDSSs are also recognized on surfaces of other well-known noble metals (for example, silver, copper, platinum and palladium), which shines a new light on these long-known surface states. The surfaces of noble metals possess Shockley states which exhibit Rashba-type spin splitting and spin-momentum locking. Here, the authors use ab initiomethods and photoemission spectroscopy to demonstrate how such Shockley states may be reinterpreted as topologically protected surface states.

Adaptive subwavelength control of nano-optical fields.

Abstract: The size of mechanical tools limits their spatial resolution. In the case of a drill, for instance, its diameter determines the size of the smallest hole that it can make, with 1-mm holes from 10-mm drills an obvious impossibility. But in the world of optics, the 'impossible' can happen. Aeschlimann et al. demonstrate a light-based tool that not only 'drills holes' smaller than its own size (its wavelength), but does so in selectable positions that can be changed at the speed of light. The experiment combines adaptive control with nano-optics, to control interactions between light and matter with sub-wavelength resolution and femtosecond timing. Adaptive shaping of the phase and amplitude of femtosecond laser pulses has been developed into an efficient tool for the directed manipulation of interference phenomena, thus providing coherent control over various quantum-mechanical systems1,2,3,4,5,6,7,8,9,10. Temporal resolution in the femtosecond or even attosecond range has been demonstrated, but spatial resolution is limited by diffraction to approximately half the wavelength of the light field (that is, several hundred nanometres). Theory has indicated11,12 that the spatial limitation to coherent control can be overcome with the illumination of nanostructures: the spatial near-field distribution was shown to depend on the linear chirp of an irradiating laser pulse. An extension of this idea to adaptive control, combining multiparameter pulse shaping with a learning algorithm, demonstrated the generation of user-specified optical near-field distributions in an optimal and flexible fashion13. Shaping of the polarization of the laser pulse14,15 provides a particularly efficient and versatile nano-optical manipulation method16,17. Here we demonstrate the feasibility of this concept experimentally, by tailoring the optical near field in the vicinity of silver nanostructures through adaptive polarization shaping of femtosecond laser pulses14,15 and then probing the lateral field distribution by two-photon photoemission electron microscopy18. In this combination of adaptive control1,2,3,4,5,6,7,8,9,10 and nano-optics19, we achieve subwavelength dynamic localization of electromagnetic intensity on the nanometre scale and thus overcome the spatial restrictions of conventional optics. This experimental realization of theoretical suggestions11,12,13,16,17,20 opens a number of perspectives in coherent control, nano-optics, nonlinear spectroscopy, and other research fields in which optical investigations are carried out with spatial or temporal resolution.

疟原虫var基因转换速率变化导致抗原变异[英]／Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1（PfPMP1）与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用，在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员，通过启动转录不同的var基因变异体为抗原变异提供了分子基础。

Chemistry and properties of nanocrystals of different shapes.

Abstract: The interest in nanoscale materials stems from the fact that new properties are acquired at this length scale and, equally important, that these properties * To whom correspondence should be addressed. Phone, 404-8940292; fax, 404-894-0294; e-mail, mostafa.el-sayed@ chemistry.gatech.edu. † Case Western Reserve UniversitysMillis 2258. ‡ Phone, 216-368-5918; fax, 216-368-3006; e-mail, burda@case.edu. § Georgia Institute of Technology. 1025 Chem. Rev. 2005, 105, 1025−1102

Spectral properties and relaxation dynamics of surface plasmon electronic oscillations in gold and silver nanodots and nanorods

Abstract: The field of nanoparticle research has drawn much attention in the past decade as a result of the search for new materials. Size confinement results in new electronic and optical properties, possibly suitable for many electronic and optoelectronic applications. A characteristic feature of noble metal nanoparticles is the strong color of their colloidal solutions, which is caused by the surface plasmon absorption. This article describes our studies of the properties of the surface plasmon absorption in metal nanoparticles that range in size between 10 and 100 nm. The effects of size, shape, and composition on the plasmon absorption maximum and its bandwidth are discussed. Furthermore, the optical response of the surface plasmon absorption due to excitation with femtosecond laser pulses allowed us to follow the electron dynamics (electron−electron and electron−phonon scattering) in these metal nanoparticles. It is found that the electron−phonon relaxation processes in nanoparticles, which are smaller than t...

Multiferroics: progress and prospects in thin films.

Abstract: Multiferroic materials, which show simultaneous ferroelectric and magnetic ordering, exhibit unusual physical properties — and in turn promise new device applications — as a result of the coupling between their dual order parameters. We review recent progress in the growth, characterization and understanding of thin-film multiferroics. The availability of high-quality thin-film multiferroics makes it easier to tailor their properties through epitaxial strain, atomic-level engineering of chemistry and interfacial coupling, and is a prerequisite for their incorporation into practical devices. We discuss novel device paradigms based on magnetoelectric coupling, and outline the key scientific challenges in the field.

Molecular self-assembly and nanochemistry: A chemical strategy for the synthesis of nanostructures

Abstract: Molecular self-assembly is the spontaneous association of molecules under equilibrium conditions into stable, structurally well-defined aggregates joined by noncovalent bonds. Molecular self-assembly is ubiquitous in biological systems and underlies the formation of a wide variety of complex biological structures. Understanding self-assembly and the associated noncovalent interactions that connect complementary interacting molecular surfaces in biological aggregates is a central concern in structural biochemistry. Self-assembly is also emerging as a new strategy in chemical synthesis, with the potential of generating nonbiological structures with dimensions of 1 to 10(2) nanometers (with molecular weights of 10(4) to 10(10) daltons). Structures in the upper part of this range of sizes are presently inaccessible through chemical synthesis, and the ability to prepare them would open a route to structures comparable in size (and perhaps complementary in function) to those that can be prepared by microlithography and other techniques of microfabrication.