Publikationen

Platelets are activated immediately when contacting with non-physiological surfaces. Minimization of surface-induced platelet activation is important not only for platelet storage but also for other blood-contacting devices and implants. Chemical surface modification tunes the response of cells to contacting surfaces, but it requires a long process involving many regulatory challenges to transfer into a marketable product. Biophysical modification overcomes these limitations by modifying only the surface topography of already approved materials. The available large and random structures on platelet storage bags do not cause a significant impact on platelets because of their smallest size (only 1-3 μm) compared to other cells. We have recently demonstrated the feasibility of the mask-free nanoprint fluid force microscope (FluidFM) technology for writing dot-grid and hexanol structures. Here, we demonstrated that the technique allows the fabrication of nanostructures of varying features. Characteristics of nanostructures including height, width, and cross-line were analyzed and compared using atomic force microscopy imaging. Based on the results, we identified several technical issues, such as the printing direction and shape of structures that directly altered nanofeatures during printing. We confirmed that FluidFM is a powerful technique to precisely fabricate a variety of desired nanostructures for the development of platelet/blood-contacting devices if technical issues during printing are well controlled.

Scanning tunneling microscopy and spectroscopy experiments on surface-localized electron states confined to nanometer-scaled resonators are reviewed from the first observations to the recently discovered novel reflection mechanism of electron de Broglie waves. The focus of the presented work is on lateral confinement and on processes leading to finite decay rates of the confined states.

With the development of the energy system transformation the quality and efficiency of the rechargeable batteries, particularly the Li ion technology, gain major importance. In spite of the enormous advances, along with many other technological challenges corrosion of the metallic battery parts is often a difficult obstacle for producers and researchers. Li-metal batteries and especially the “anode-free” battery concept could significantly increase the energy density. However, contact corrosion of the Li anode, can occur in this cell configuration since there is a high probability of a three-phase contact between Li-metal, current collector and electrolyte, a condition triggering an intensive Li corrosion. In this work, a new in-situ analytical methodology based on combining electrochemical (ZRA) and microgravimetric (QCM) techniques is proposed for studying the galvanic corrosion. The applicability of this approach is explored in three different electrolyte compositions. Beside the analysis of the conventional electrochemical parameters an in-situ gravimetric detection of the deposited electrolyte decomposition products on the cathode surface is demonstrated. Adsorbed polymer layer on the Cu surface is applied for cathodic inhibition of the galvanic corrosion process, which is studied by means of the novel ZRA-QCM approach.

Sodium-carbon dioxide (Na-CO2) batteries are regarded as promising energy storage technologies because of their impressive theoretical energy density and CO2 reutilization, but their practical applications are restricted by uncontrollable sodium dendrite growth and poor electrochemical kinetics of CO2 cathode. Constructing suitable multifunctional electrodes for dendrite-free anodes and kinetics-enhanced CO2 cathodes is considered one of the most important ways to advance the practical application of Na-CO2 batteries. Herein, RuO2 nanoparticles encapsulated in carbon paper (RuCP) are rationally designed and employed as both Na anode host and CO2 cathode in Na-CO2 batteries. The outstanding sodiophilicity and high catalytic activity of RuCP electrodes can simultaneously contribute to homogenous Na+ distribution and dendrite-free sodium structure at the anode, as well as strengthen discharge and charge kinetics at the cathode. The morphological evolution confirmed the uniform deposition of Na on RuCP anode with dense and flat interfaces, delivering enhanced Coulombic efficiency of 99.5% and cycling stability near 1500 cycles. Meanwhile, Na-CO2 batteries with RuCP cathode demonstrated excellent cycling stability (>350 cycles). Significantly, implementation of a dendrite-free RuCPNa anode and catalytic-site-rich RuCP cathode allowed for the construction of a symmetric Na-CO2 battery with long-duration cyclability, offering inspiration for extensive practical uses of Na-CO2 batteries.

The limit point and limit circle classification of real Sturm-Liouville problems by H. Weyl more than 100 years ago was extended by A.R. Sims around 60 years ago to the case when the coefficients are complex. Here the main result is a collection of various criteria which allow us to decide to which class of Sims' scheme a given Sturm-Liouville problem with complex coefficients belongs. This is subsequently applied to a second order differential equation defined on a ray in C which is motivated by the recent intensive research connected with PT-symmetric Hamiltonians.