08 Fakultät Mathematik und Physik

Permanent URI for this collectionhttps://elib.uni-stuttgart.de/handle/11682/9

Browse

Filters

2021 - 20244

Settings

Institute: search.filters.UBSInstitut.Max-Planck-Institut für FestkörperforschungSubject: search.filters.subject.620

Search Results

Now showing 1 - 4 of 4
  • Thumbnail Image
    ItemOpen Access
    High space‐bandwidth‐product (SBP) hologram carriers toward photorealistic 3D holography
    (2024) Li, Jin; Li, Xiaoxun; Huang, Xiangyu; Kaissner, Robin; Neubrech, Frank; Sun, Shuo; Liu, Na
    3D holography capable of reproducing all necessary visual cues is considered the most promising route to present photorealistic 3D images. Three elements involving computer‐generated hologram (CGH) algorithms, hologram carriers, and optical systems are prerequisites to create high‐quality holographic displays for photorealistic 3D holography. Especially, the hologram carrier directly determines the holographic display capability and the design of high space‐bandwidth‐product (SBP) optical systems. Currently, two categories of hologram carriers, i.e., spatial light modulators (SLM) and metasurfaces, are regarded as promising candidates for photorealistic 3D holography. However, most of their SBP capability still cannot match the amount of information generated by the CGH. To address this issue, tremendous efforts are made to improve the capability of hologram carriers. Here, the main hologram carriers (from SLM to metasurfaces) that are widely utilized in holography systems to achieve high SBP capability (high resolution, wide viewing angles, and large sizes) are reviewed. The purpose of this review is to identify the key challenges and future directions of SLM‐based and metasurface‐based holography for photorealistic 3D holographic images.
  • Thumbnail Image
    ItemOpen Access
    Stabilizing γ‐MgH2 at nanotwins in mechanically constrained nanoparticles
    (2021) Kammerer, Jochen A.; Duan, Xiaoyang; Neubrech, Frank; Schröder, Rasmus R.; Liu, Na; Pfannmöller, Martin
    Reversible hydrogen uptake and the metal/dielectric transition make the Mg/MgH2 system a prime candidate for solid‐state hydrogen storage and dynamic plasmonics. However, high dehydrogenation temperatures and slow dehydrogenation hamper broad applicability. One promising strategy to improve dehydrogenation is the formation of metastable γ‐MgH2. A nanoparticle (NP) design, where γ‐MgH2 forms intrinsically during hydrogenation is presented and a formation mechanism based on transmission electron microscopy results is proposed. Volume expansion during hydrogenation causes compressive stress within the confined, anisotropic NPs, leading to plastic deformation of β‐MgH2 via (301)β twinning. It is proposed that these twins nucleate γ‐MgH2 nanolamellas, which are stabilized by residual compressive stress. Understanding this mechanism is a crucial step toward cycle‐stable, Mg‐based dynamic plasmonic and hydrogen‐storage materials with improved dehydrogenation. It is envisioned that a more general design of confined NPs utilizes the inherent volume expansion to reform γ‐MgH2 during each rehydrogenation.
  • Thumbnail Image
    ItemOpen Access
    High-resolution nanoscale NMR for arbitrary magnetic fields
    (2023) Meinel, Jonas; Kwon, MinSik; Maier, Rouven; Dasari, Durga; Sumiya, Hitoshi; Onoda, Shinobu; Isoya, Junichi; Vorobyov, Vadim; Wrachtrup, Jörg
    Nitrogen vacancy (NV) centers are a major platform for the detection of nuclear magnetic resonance (NMR) signals at the nanoscale. To overcome the intrinsic electron spin lifetime limit in spectral resolution, a heterodyne detection approach is widely used. However, application of this technique at high magnetic fields is yet an unsolved problem. Here, we introduce a heterodyne detection method utilizing a series of phase coherent electron nuclear double resonance sensing blocks, thus eliminating the numerous Rabi microwave pulses required in the detection. Our detection protocol can be extended to high magnetic fields, allowing chemical shift resolution in NMR experiments. We demonstrate this principle on a weakly coupled 13 C nuclear spin in the bath surrounding single NV centers, and compare the results to existing heterodyne protocols. Additionally, we identify the combination of NV-spin-initialization infidelity and strong sensor-target-coupling as linewidth-limiting decoherence source, paving the way towards high-field heterodyne NMR protocols with chemical resolution.
  • Thumbnail Image
    ItemOpen Access
    Observation of ultrafast interfacial Meitner-Auger energy transfer in a Van der Waals heterostructure
    (2023) Dong, Shuo; Beaulieu, Samuel; Selig, Malte; Rosenzweig, Philipp; Christiansen, Dominik; Pincelli, Tommaso; Dendzik, Maciej; Ziegler, Jonas D.; Maklar, Julian; Xian, R. Patrick; Neef, Alexander; Mohammed, Avaise; Schulz, Armin; Stadler, Mona; Jetter, Michael; Michler, Peter; Taniguchi, Takashi; Watanabe, Kenji; Takagi, Hidenori; Starke, Ulrich; Chernikov, Alexey; Wolf, Martin; Nakamura, Hiro; Knorr, Andreas; Rettig, Laurenz; Ernstorfer, Ralph
    Atomically thin layered van der Waals heterostructures feature exotic and emergent optoelectronic properties. With growing interest in these novel quantum materials, the microscopic understanding of fundamental interfacial coupling mechanisms is of capital importance. Here, using multidimensional photoemission spectroscopy, we provide a layer- and momentum-resolved view on ultrafast interlayer electron and energy transfer in a monolayer-WSe2/graphene heterostructure. Depending on the nature of the optically prepared state, we find the different dominating transfer mechanisms: while electron injection from graphene to WSe2 is observed after photoexcitation of quasi-free hot carriers in the graphene layer, we establish an interfacial Meitner-Auger energy transfer process following the excitation of excitons in WSe2. By analysing the time-energy-momentum distributions of excited-state carriers with a rate-equation model, we distinguish these two types of interfacial dynamics and identify the ultrafast conversion of excitons in WSe2 to valence band transitions in graphene. Microscopic calculations find interfacial dipole-monopole coupling underlying the Meitner-Auger energy transfer to dominate over conventional Förster- and Dexter-type interactions, in agreement with the experimental observations. The energy transfer mechanism revealed here might enable new hot-carrier-based device concepts with van der Waals heterostructures.