73 72 Principal Scientist Profiles Volker Deckert Volker Deckert Principal Scientist Profiles VOLKER DECKERT RESEARCH AREAS Prof. Deckert research interest in general covers fundamentals, method developments, and application of near-field optical spectroscopy. The main target is to use the optical properties of nanoscale metallic structures to reveal the structural conformation and composition of molecules at the highest possible spatial resolution and also understand the underlying principles of high spatial resolution spectroscopy. Research interests include: • Near-field optics • Electromagnetic and chemical interactions on the nanometer scale • Raman spectroscopy • Structural investigation of proteins and protein aggregations • Membrane-protein interaction • Virus surface characterisation • Single-site catalysis • Limits of lateral resolution TEACHING FIELDS Prof. Deckert is involved in the teaching of general physical chemistry and advanced characterization tools. RESEARCH METHODS Prof. Deckert’s laboratories are dedicated to the molecularlevel investigation of surface structures, in particular of biomolecules and heterogeneous catalysis using ultra-high resolution: • Tip-enhanced Raman scattering (TERS) microscopy • Scanning probe microscopy (standard, force-distance, high speed, PiFM, …) • Fabrication of thin layers (evaporation/sputtering/ALD) • AFM-coupled transient absorption spectroscopy • Non-linear optical spectroscopy PROFESSOR OF NANOSCALE STRUCTURAL INVESTIGATIONS OF BIOLOGICAL AND BIOMEDICAL SYSTEMS, INSTITUTE OF PHYSICAL CHEMISTRY Professor Deckert holds a joint position at the Institute of Physical Chemistry and the Leibniz Institute of Photonic Technology where he heads the Nanoscopy Department. His main research field deals with investigations of molecular structures within the nanometer range. In 2020, he received the Ellis R. Lippincott Award Spectroscopy for his achievements in high resolution Raman spectroscopy and the realization of tip-enhanced Raman spectroscopy. RECENT RESEARCH RESULTS Recent experimental evidence made clear that the generally assumed lateral resolution limits in near-field optics have to be revisited. In cooperation with other groups we developed two models to explain tip based nearfield spectroscopy results that demonstrate sub molecular resolution recently. Both models are based on the fact that a plasmonically active nanoparticle can never be a perfect sphere but eventually must show atomic scale features at edges and corners. Such a model is well accepted and used in scanning tunneling microscopy. As for near-field optics, firstly, we could theoretically demonstrate that such features affect the plasmon resonance dramatically in terms of enhancement and field confinement, i.e. lateral resolution. [1] Secondly, if an atomic sized probe is scanning across a molecule, it affects the electronic structure of the molecule depending on the exact location of the probe with respect to the molecule. This so-called chemical effect predicts probe site dependent changes in the vibrational structure of the molecule that are readily detected experimentally as“intensity and spectral position fluctuations”but eventually are related to lateral resolution.[2] Our group also develops new methods to exploit either new information on a specimen, or to improve near-field optical techniques regarding speed or sensitivity. Recent developments are related to laser mode dependent enhancement optimization using a correlated photoinduced force microscopy, a TERS approach and the direct and simultaneous assessment of the tips plasmon resonance and actual temperature directly from a Stokes/anti-Stokes comparison.[3,4] In terms of applications, our main interest is related to bio-related specimen and soft-matter. Based on the experience on bio-spectroscopy with nanometer resolution, the long-term research focus lies on the investigations of dynamic systems, i.e. protein-lipid interactions, immobilized photocatalysts, and drug release of core-shell particles. The latter is a nice example to show how the combined application of different scanning probe techniques provides fast and also structurally specific information about block-copolymer structures used as potential drug carriers.[5] Particularly the correlation of mechanic (force-distance spectroscopy) and near-field Raman (TERS) data allows for a rapid surface precharacterization based on elasticity and adhesion parameters while subsequent specifically targeted TERS experiments result in nanometer resolved structural sensitive information about surface composition, compound mixing ,and even unexpected reaction products. This also a good example how specific experimental requirements drive the method development and ultimately also the fundamentals of the underlying theoretical concepts. NANOSCALE STRUCTURE BASED VIRUS DISCRIMINATION Based on previous high-resolution Raman data on protein crystals and single virions we demonstrate that the direct distinction of mixed virus particles is possible via TERS experiments. The results demonstrate that a near-field spectroscopy-based classification is possible also for specimen sizes below the diffraction limit. Furthermore, also specific virus properties like the presence of a lipid shell can be clearly observed. To address the potential pitfalls by a “too high” lateral resolution a resolution decrease was achieved by spectral acquisition during scanning. This ensures that the entire virion surface contributes to the spectra and consequently dramatically improves reproducibility. Figure: Scheme of nanometer scale plasmon and temperature assessment via modelling Stokes/anti-Stokes ratios [1] Trautmann et al., Nanoscale. 9, 391 (2017). [2] Latorre et al., Nanoscale. 8, 10229 (2016). [3] Meyer et al., ACS Photonics. 6, 1191 (2019). [4] Richard-Lacroix et al., Light Sci Appl. 9, 3922 (2020). [5] Höppener et al., Small. 112, 1907418 (2020). Contact: Phone: +49 3641 9-48347 Email: volker.deckert@uni-jena.de
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