Universität Stuttgart

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    Tailored nanocomposites for 3D printed micro-optics
    (2020) Weber, Ksenia; Werdehausen, Daniel; König, Peter; Thiele, Simon; Schmid, Michael; Decker, Manuel; Oliveira, Peter William de; Herkommer, Alois; Giessen, Harald
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    Vibrational quenching of weakly bound cold molecular ions immersed in their parent gas
    (2020) Jachymski, Krzysztof; Meinert, Florian
    Hybrid ion–atom systems provide an excellent platform for studies of state-resolved quantum chemistry at low temperatures, where quantum effects may be prevalent. Here we study theoretically the process of vibrational relaxation of an initially weakly bound molecular ion due to collisions with the background gas atoms. We show that this inelastic process is governed by the universal long-range part of the interaction potential, which allows for using simplified model potentials applicable to multiple atomic species. The product distribution after the collision can be estimated by making use of the distorted wave Born approximation. We find that the inelastic collisions lead predominantly to small changes in the binding energy of the molecular ion.
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    Surface- and tip-enhanced resonant Raman scattering from CdSe nanocrystals
    (2015) Sheremet, Evgeniya; Milekhin, Alexander G.; Rodriguez, Raul D.; Weiss, Thomas; Nesterov, Maxim; Rodyakina, Ekaterina E.; Gordan, Ovidiu D.; Sveshnikova, Larisa L.; Duda, Tatyana A.; Gridchin, Victor A.; Dzhagan, Volodymyr M.; Hietschold, Michael; Zahn, Dietrich R. T.
    Surface- and tip-enhanced resonant Raman scattering (resonant SERS and TERS) by optical phonons in a monolayer of CdSe quantum dots (QDs) is demonstrated. The SERS enhancement was achieved by employing plasmonically active substrates consisting of gold arrays with varying nanocluster diameters prepared by electron-beam lithography. The magnitude of the SERS enhancement depends on the localized surface plasmon resonance (LSPR) energy, which is determined by the structural parameters. The LSPR positions as a function of nanocluster diameter were experimentally determined from spectroscopic micro-ellipsometry, and compared to numerical simulations showing good qualitative agreement. The monolayer of CdSe QDs was deposited by the Langmuir–Blodgett-based technique on the SERS substrates. By tuning the excitation energy close to the band gap of the CdSe QDs and to the LSPR energy, resonant SERS by longitudinal optical (LO) phonons of CdSe QDs was realized. A SERS enhancement factor of 2 × 10 3 was achieved. This allowed the detection of higher order LO modes of CdSe QDs, evidencing the high crystalline quality of QDs. The dependence of LO phonon mode intensity on the size of Au nanoclusters reveals a resonant character, suggesting that the electromagnetic mechanism of the SERS enhancement is dominant. Finally, the resonant TERS spectrum from CdSe QDs was obtained using electrochemically etched gold tips providing an enhancement on the order of 10 4 . This is an important step towards the detection of the phonon spectrum from a single QD.
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    Nearly diffraction limited FTIR mapping using an ultrastable broadband femtosecond laser tunable from 1.33 to 8 µm
    (2017) Mörz, Florian; Semenyshyn, Rostyslav; Steinle, Tobias; Neubrech, Frank; Zschieschang, Ute; Klauk, Hagen; Steinmann, Andy; Giessen, Harald
    Micro-Fourier-transform infrared (FTIR) spectroscopy is a widespread technique that enables broadband measurements of infrared active molecular vibrations at high sensitivity. SiC globars are often applied as light sources in tabletop systems, typically covering a spectral range from about 1 to 20 µm (10 000 - 500 cm−1) in FTIR spectrometers. However, measuring sample areas below 40x40 µm2 requires very long integration times due to their inherently low brilliance. This hampers the detection of ultrasmall samples, such as minute amounts of molecules or single nanoparticles. In this publication we extend the current limits of FTIR spectroscopy in terms of measurable sample areas, detection limit and speed by utilizing a broadband, tabletop laser system with MHz repetition rate and femtosecond pulse duration that covers the spectral region between 1250 - 7520 cm−1 (1.33 - 8 µm). We demonstrate mapping of a 150x150 µm2 sample of 100 nm thick molecule layers at 1430 cm−1 (7 µm) with 10x10 µm2 spatial resolution and a scan speed of 3.5 µm/sec. Compared to a similar globar measurement an order of magnitude lower noise is achieved, due to an excellent long-term wavelength and power stability, as well as an orders of magnitude higher brilliance.
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    Ultrathin monolithic 3D printed optical coherence tomography endoscopy for preclinical and clinical use
    (2020) Li, Jiawen; Thiele, Simon; Quirk, Bryden C.; Kirk, Rodney W.; Verjans, Johan W.; Akers, Emma; Bursill, Christina A.; Nicholls, Stephen J.; Herkommer, Alois; Giessen, Harald; McLaughlin, Robert A.
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    Wafer-scale self-organized InP nanopillars with controlled orientation for photovoltaic devices
    (2015) Sanatinia, Reza; Berrier, Audrey; Dhaka, Veer; Perros, Alexander P.; Huhtio, Teppo; Lipsanen, Harri; Anand, Srinivasan
    A unique wafer-scale self-organization process for generation of InP nanopillars is demonstrated, which is based on maskless ion-beam etching (IBE) of InP developed to obtain the nanopillars, where the height, shape, and orientation of the nanopillars can be varied by controlling the processing parameters. The fabricated InP nanopillars exhibit broadband suppression of the reflectance, ‘black InP,’ a property useful for solar cells. The realization of a conformal p-n junction for carrier collection, in the fabricated solar cells, is achieved by a metalorganic vapor phase epitaxy (MOVPE) overgrowth step on the fabricated pillars. The conformal overgrowth retains the broadband anti-reflection property of the InP nanopillars, indicating the feasibility of this technology for solar cells. Surface passivation of the formed InP nanopillars using sulfur-oleylamine solution resulted in improved solar-cell characteristics. An open-circuit voltage of 0.71 V and an increase of 0.13 V compared to the unpassivated device were achieved.
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    Photo-induced ionization dynamics of the nitrogen vacancy defect in diamond investigated by single-shot charge state detection
    (2013) Aslam, Nabeel; Waldherr, Gerald; Neumann, Philipp; Jelezko, Fedor; Wrachtrup, Jörg
    The nitrogen-vacancy centre (NV) has drawn much attention for over a decade, yet detailed knowledge of the photophysics needs to be established. Under typical conditions, the NV can have two stable charge states, negative (NV-) or neutral (NV0), with photo-induced interconversion of these two states. Here, we present detailed studies of the ionization dynamics of single NV centres in bulk diamond at room temperature during illumination and its dependence on the excitation wavelength and power. We apply a recent method which allows us to directly measure the charge state of a single NV centre, and observe its temporal evolution. We find that the steady-state NV− population is always ⩽75% for 450–610 nm excitation wavelength. In combination with saturation measurements, we show that the optimal excitation wavelength is around 510-540 nm. Furthermore, the relative absorption cross-section of NV- is determined for 540-610 nm, revealing a double-peak structure. Finally, the energy of the NV- ground state of 2.6 eV below the conduction band is measured. These results reveal new insights into the charge state dynamics of the NV centre.
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    Short-range surface plasmonics: localized electron emission dynamics from a 60-nm spot on an atomically flat single-crystalline gold surface
    (2017) Frank, Bettina; Kahl, Philip; Podbiel, Daniel; Spektor, Grisha; Orenstein, Meir; Fu, Liwei; Weiss, Thomas; Horn-von Hoegen, Michael; Davis, Timothy J.; Meyer zu Heringdorf, Frank-Joachim; Giessen, Harald
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    Electron-driven photon sources for correlative electron-photon spectroscopy with electron microscopes
    (2020) Christopher, Joshua; Taleb, Masoud; Maity, Achyut; Hentschel, Mario; Giessen, Harald; Talebi, Nahid
    Electron beams in electron microscopes are efficient probes of optical near-fields, thanks to spectroscopy tools like electron energy-loss spectroscopy and cathodoluminescence spectroscopy. Nowadays, we can acquire multitudes of information about nanophotonic systems by applying space-resolved diffraction and time-resolved spectroscopy techniques. In addition, moving electrons interacting with metallic materials and optical gratings appear as coherent sources of radiation. A swift electron traversing metallic nanostructures induces polarization density waves in the form of electronic collective excitations, i.e., the so-called plasmon polariton. Propagating plasmon polariton waves normally do not contribute to the radiation; nevertheless, they diffract from natural and engineered defects and cause radiation. Additionally, electrons can emit coherent light waves due to transition radiation, diffraction radiation, and Smith-Purcell radiation. Some of the mechanisms of radiation from electron beams have so far been employed for designing tunable radiation sources, particularly in those energy ranges not easily accessible by the state-of-the-art laser technology, such as the THz regime. Here, we review various approaches for the design of coherent electron-driven photon sources. In particular, we introduce the theory and nanofabrication techniques and discuss the possibilities for designing and realizing electron-driven photon sources for on-demand radiation beam shaping in an ultrabroadband spectral range to be able to realize ultrafast few-photon sources. We also discuss our recent attempts for generating structured light from precisely fabricated nanostructures. Our outlook for the realization of a correlative electron-photon microscope/spectroscope, which utilizes the above-mentioned radiation sources, is also described.
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    Extending quantum links : modules for fiber‐ and memory‐based quantum repeaters
    (2020) Loock, Peter van; Alt, Wolfgang; Becher, Christoph; Benson, Oliver; Boche, Holger; Deppe, Christian; Eschner, Jürgen; Höfling, Sven; Meschede, Dieter; Michler, Peter; Schmidt, Frank; Weinfurter, Harald
    Elementary building blocks for quantum repeaters based on fiber channels and memory stations are analyzed. Implementations are considered for three different physical platforms, for which suitable components are available: quantum dots, trapped atoms and ions, and color centers in diamond. The performances of basic quantum repeater links for these platforms are evaluated and compared, both for present‐day, state‐of‐the‐art experimental parameters as well as for parameters that can in principle be reached in the future. The ultimate goal is to experimentally explore regimes at intermediate distances - up to a few 100 km - in which the repeater‐assisted secret key transmission rates exceed the maximal rate achievable via direct transmission. Two different protocols are considered, one of which is better adapted to the higher source clock rate and lower memory coherence time of the quantum dot platform, while the other circumvents the need of writing photonic quantum states into the memories in a heralded, nondestructive fashion. The elementary building blocks and protocols can be connected in a modular form to construct a quantum repeater system that is potentially scalable to large distances.