PKPhilipp Ksoll

Philipp Ksoll

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Philipp Ksoll has a total of 9 co-authors. Here are the top co-authors by number of shared publications:

  • C. Meyer

    Erstes Physikalisches Institut, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany

    1 shared publication
  • Christoph Meyer

    Erstes Physikalisches Institut, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany

    1 shared publication
  • L. Schüler

    Erstes Physikalisches Institut, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany

    1 shared publication
  • Leonard Schüler

    Erstes Physikalisches Institut, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany

    1 shared publication
  • Rajesh Mandal

    Erstes Physikalisches Institut, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany

    1 shared publication
  • V. Moshnyaga

    Erstes Physikalisches Institut, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany

    1 shared publication

Latest Publications

  • Open Access

    B-Site Cation Ordering in Films, Superlattices, and Layer-by-Layer-Grown Double Perovskites

    by Philipp Ksoll, Christoph Meyer, Leonard Schüler, Vladimir Roddatis, Vasily Moshnyaga

    The preparation of cation-ordered thin films of correlated oxides is of great interest for both fundamental and applied research. The scientific long-term vision is strongly motivated by the perspective of studying electronic correlations in condensed matter without the presence of chemical or quenched disorder. A promising material platform provides double perovskite A2BB’O6 bulk samples with different types of B/B’ ordering. However, the growth of A- and/or B-site-ordered correlated oxide thin films is known to be a challenging task. In this review, we evaluate the growth of double perovskite A2BB’O6 thin films by means of well-elaborated physical vacuum deposition techniques, such as pulsed laser deposition (PLD) and sputtering and compare them with a close-to-equilibrium growth with the metalorganic aerosol deposition (MAD) technique. The latter was further developed to grow an emergent interfacial double perovskite phase in LaNiO3/LaMnO3 superlattices, and finally, by way of a layer-by-layer route. The growth of La2CoMnO6 films on SrTiO3(111) substrates by sequential deposition of single perovskite layers of LaCoO3/LaMnO3/LaCoO3/… was demonstrated and the film properties were compared to those obtained within the state-of-the art growth mode.


  • Emergent double perovskite phase at LaMnO3/LaNiO3 interfaces: Coupled charge transfer and structural reconstruction

    by P. Ksoll, R. Mandal, C. Meyer, L. Schüler, V. Roddatis, V. Moshnyaga

    We report [(LaNiO3)n/(LaMnO3)n]M/SrTiO3(111) superlattices [n=20, 10, 5, 2, and 1 unit cells (u.c.)] as “precursor” heterostructures for a double perovskite La2NiMnO6. A charge transfer at the LaNiO3/LaMnO3 interfaces and formation of the emergent La2NiMnO6 phase with Ni2+ and Mn4+ oxidation states was evidenced by in situ optical ellipsometry and supported by magnetic and Raman measurements. The 10/10 and 5/5 superlattices revealed a complex magnetic behavior with two ferromagnetic phase transitions with TC−low=170K and TC−high∼250–280K, originating from the ferromagnetic LaMnO3 and the emergent interfacial La2NiMnO6 phase, respectively. With decreasing thickness of individual layers, the magnetism of 2/2 and 1/1 superlattices transforms into that of the ordered double perovskite La2NiMnO6. Furthermore, a structural reconstruction into a monoclinic (P12) structure of the ordered La2NiMnO6 at the interface, evidenced by Raman spectroscopy, goes ahead with the charge transfer and magnetic La2NiMnO6 behavior.