@article{57625,
  author       = {{Giesselmann, Frank and Kitzerow, Heinz-Siegfried and Zentel, Rudolf}},
  issn         = {{1358-314X}},
  journal      = {{Liquid Crystals Today}},
  number       = {{1}},
  pages        = {{2--9}},
  publisher    = {{Informa UK Limited}},
  title        = {{{Fifty years of liquid crystal research in the mirror of the German Liquid Crystal Conference}}},
  doi          = {{10.1080/1358314x.2024.2415787}},
  volume       = {{33}},
  year         = {{2024}},
}

@article{56947,
  abstract     = {{<jats:p>Pore engineering is commonly used to alter the properties of metal–organic frameworks. This is achieved by incorporating different linker molecules (L) into the structure, generating isoreticular frameworks. CPO-27, also named MOF-74, is a prototypical material for this approach, offering the potential to modify the size of its one-dimensional pore channels and the hydrophobicity of pore walls using various linker ligands during synthesis. Thermal activation of these materials yields accessible open metal sites (i.e., under-coordinated metal centers) at the pore walls, thus acting as strong primary binding sites for guest molecules, including water. We study the effect of the pore size and linker hydrophobicity within a series of Ni2+-based isoreticular frameworks (i.e., Ni2L, L = dhtp, dhip, dondc, bpp, bpm, tpp), analyzing their water sorption behavior and the water interactions in the confined pore space. For this purpose, we apply water vapor sorption analysis and Fourier transform infrared spectroscopy. In addition, defect degrees of all compounds are determined by thermogravimetric analysis and solution 1H nuclear magnetic resonance spectroscopy. We find that larger defect degrees affect the preferential sorption sites in Ni2dhtp, while no such indication is found for the other materials in our study. Instead, strong evidence is found for the formation of water bridges/chains between coordinating water molecules, as previously observed for hydrophobic porous carbons and mesoporous silica. This suggests similar sorption energies for additional water molecules in materials with larger pore sizes after saturation of the primary binding sites, resulting in more bulk-like water arrangements. Consequently, the sorption mechanism is driven by classical pore condensation through H-bonding anchor sites instead of sorption at discrete sites.</jats:p>}},
  author       = {{Kloß, Marvin and Schäfers, Lara and Zhao, Zhenyu and Weinberger, Christian and Egold, Hans and Tiemann, Michael}},
  issn         = {{2079-4991}},
  journal      = {{Nanomaterials}},
  number       = {{22}},
  pages        = {{1791}},
  publisher    = {{MDPI AG}},
  title        = {{{Water Sorption on Isoreticular CPO-27-Type MOFs: From Discrete Sorption Sites to Water-Bridge-Mediated Pore Condensation}}},
  doi          = {{10.3390/nano14221791}},
  volume       = {{14}},
  year         = {{2024}},
}

@article{56080,
  abstract     = {{CPO‐27 is a metal‐organic framework (MOF) with coordinatively unsaturated metal centers (open metal sites). It is therefore an ideal host material for small guest molecules, including water. This opens up numerous possible applications, such as proton conduction, humidity sensing, water harvesting, or adsorption‐driven heat pumps. For all of these applications, profound knowledge of the adsorption and desorption of water in the micropores is mandatory. The hydration and water structure in CPO‐27‐M (M = Zn or Cu) is investigated using water vapor sorption, Fourier transform infrared (FTIR) spectroscopy, density functional theory (DFT) calculations, and molecular dynamics simulation. In the pores of CPO‐27‐Zn, water binds as a ligand to the Zn center. Additional water molecules are stepwise incorporated at defined positions, forming a network of H‐bonds with the framework and with each other. In CPO‐27‐Cu, hydration proceeds by an entirely different mechanism. Here, water does not coordinate to the metal center, but only forms H‐bonds with the framework; pore filling occurs mostly in a single step, with the open metal site remaining unoccupied. Water in the pores forms clusters with extensive intra‐cluster H‐bonding.}},
  author       = {{Kloß, Marvin and Beerbaum, Michael and Baier, Dominik and Weinberger, Christian and Zysk, Frederik and Elgabarty, Hossam and Kühne, Thomas D. and Tiemann, Michael}},
  issn         = {{2196-7350}},
  journal      = {{Advanced Materials Interfaces}},
  number       = {{35}},
  pages        = {{2400476}},
  publisher    = {{Wiley}},
  title        = {{{Understanding Hydration in CPO‐27 Metal‐Organic Frameworks: Strong Impact of the Chemical Nature of the Metal (Cu, Zn)}}},
  doi          = {{10.1002/admi.202400476}},
  volume       = {{11}},
  year         = {{2024}},
}

@article{58612,
  author       = {{Luis-Sunga, Maximina and González-Orive, Alejandro and Calderón, Juan Carlos and Gamba, Ilaria and Ródenas, Airán and de los Arcos de Pedro, Maria Teresa and Hernández-Creus, Alberto and Grundmeier, Guido and Pastor, Elena and García, Gonzalo}},
  issn         = {{2574-0970}},
  journal      = {{ACS Applied Nano Materials}},
  title        = {{{Nickel-Induced Reduced Graphene Oxide Nanoribbon Formation on Highly Ordered Pyrolytic Graphite for Electronic and Magnetic Applications}}},
  doi          = {{10.1021/acsanm.3c05949}},
  year         = {{2024}},
}

@article{58611,
  abstract     = {{AFM-IR investigation of thin PECVD SiOx films on a polypropylene substrate in the surface-sensitive mode}},
  author       = {{Müller, Hendrik and Stadler, Hartmut and de los Arcos de Pedro, Maria Teresa and Keller, Adrian and Grundmeier, Guido}},
  issn         = {{2190-4286}},
  journal      = {{Beilstein Journal of Nanotechnology}},
  number       = {{1}},
  pages        = {{603–611}},
  title        = {{{AFM-IR investigation of thin PECVD SiO x films on a polypropylene substrate in the surface-sensitive mode}}},
  doi          = {{10.3762/bjnano.15.51}},
  volume       = {{15}},
  year         = {{2024}},
}

@article{56075,
  abstract     = {{An isostructural series of FeII, FeIII, and Fe(IV)complexes [Fe(ImP)2]0/+/2+ utilizing the ImP 1,1′-(1,3-phenylene)-bis(3-methyl-1-imidazol-2-ylidene) ligand, combining N-heterocy-clic carbenes and cyclometalating functions, is presented. The strong donor motif stabilizes the high-valent Fe(IV) oxidation state yet keeps the FeII oxidation state accessible from the parent Fe(III)compound. Chemical oxidation of [Fe(ImP)2]+ yields stable [FeIV(ImP)2]2+. In contrast, [FeII(ImP)2]0, obtained by reduction,is highly sensitive toward oxygen. Exhaustive ground state characterization by single-crystal X-ray diffraction, 1H NMR,Mössbauer spectroscopy, temperature-dependent magnetic measurements, a combination of X-ray absorption near edge structureand valence-to-core, as well as core-to-core X-ray emission spectroscopy, complemented by detailed density functional theory (DFT) analysis, reveals that the three complexes[Fe(ImP)2]0/+/2+ can be unequivocally attributed to low-spin d6, d5, and d4 complexes. The excited state landscape of the Fe(II) and Fe(IV) complexes is characterized by short-lived 3MLCT and 3LMCT states, with lifetimes of 5.1 and 1.4 ps, respectively. In the FeII-compound, an energetically low-lying MC state leads to fast deactivation of the MLCT state. The distorted square-pyramidal state, where one carbene is dissociated, can not only relax into the ground state, but also into a singlet dissociated state. Its formation was investigated with time-dependent optical spectroscopy, while insights into its structure were gained by NMR spectroscopy.}},
  author       = {{Steube, Jakob and Fritsch, Lorena and Kruse, Ayla and Bokareva, Olga S. and Demeshko, Serhiy and Elgabarty, Hossam and Schoch, Roland and Alaraby, Mohammad and Egold, Hans and Bracht, Bastian Johannes and Schmitz, Lennart and Hohloch, Stephan and Kühne, Thomas D. and Meyer, Franc and Kühn, Oliver and Lochbrunner, Stefan and Bauer, Matthias}},
  issn         = {{0020-1669}},
  journal      = {{Inorganic Chemistry}},
  keywords     = {{Photo}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Isostructural Series of a Cyclometalated Iron Complex in Three Oxidation States}}},
  doi          = {{10.1021/acs.inorgchem.4c02576}},
  year         = {{2024}},
}

@article{56074,
  abstract     = {{Effective photoinduced charge transfer makes molecular bimetallic assemblies attractive for applications as active light‐induced proton reduction systems. Developing competitive base metal dyads is mandatory for a more sustainable future. However, the electron transfer mechanisms from the photosensitizer to the proton reduction catalyst in base metal dyads remain so far unexplored. A Fe─Co dyad that exhibits photocatalytic H2 production activity is studied using femtosecond X‐ray emission spectroscopy, complemented by ultrafast optical spectroscopy and theoretical time‐dependent DFT calculations, to understand the electronic and structural dynamics after photoexcitation and during the subsequent charge transfer process from the Fe(II) photosensitizer to the cobaloxime catalyst. This novel approach enables the simultaneous measurement of the transient X‐ray emission at the iron and cobalt K‐edges in a two‐color experiment. With this methodology, the excited state dynamics are correlated to the electron transfer processes, and evidence of the Fe→Co electron transfer as an initial step of proton reduction activity is unraveled.}},
  author       = {{Nowakowski, Michał and Huber‐Gedert, Marina and Elgabarty, Hossam and Kalinko, Aleksandr and Kubicki, Jacek and Kertmen, Ahmet and Lindner, Natalia and Khakhulin, Dmitry and Lima, Frederico A. and Choi, Tae‐Kyu and Biednov, Mykola and Schmitz, Lennart and Piergies, Natalia and Zalden, Peter and Kubicek, Katerina and Rodriguez‐Fernandez, Angel and Salem, Mohammad Alaraby and Canton, Sophie E. and Bressler, Christian and Kühne, Thomas D. and Gawelda, Wojciech and Bauer, Matthias}},
  issn         = {{2198-3844}},
  journal      = {{Advanced Science}},
  keywords     = {{Photo, Xray}},
  publisher    = {{Wiley}},
  title        = {{{Ultrafast Two‐Color X‐Ray Emission Spectroscopy Reveals Excited State Landscape in a Base Metal Dyad}}},
  doi          = {{10.1002/advs.202404348}},
  year         = {{2024}},
}

@article{52346,
  abstract     = {{Promising cathode materials for fluoride-ion batteries (FIBs) are 3d transition metal containing oxides with Ruddlesden-Popper-type structure. So far, multi-elemental compositions were not investigated, but could alternate electrochemical performance similar to what has been found for cathode materials for lithium-ion batteries. Within this study, we investigate RP type La2Ni0.75Co0.25O4.08 as an intercalation-based active cathode material for all-solid-state FIBs. We determine the structural changes of La2Ni0.75Co0.25O4.08 during fluoride intercalation / de-intercalation by ex-situ X-ray diffraction, which showed that F- insertion leads to transformation of the parent phase to three different phases. Changes in Ni and Co oxidation states and coordination environment were examined by X-ray absorption spectroscopy and magnetic measurements in order to understand the complex reaction behaviour of the phases in detail, showing that the two transition metals behave differently in the charging and discharging process. Under optimized operating conditions, a cycle life of 120 cycles at a critical cut-off capacity of 40 mAh g-1 against Pb/PbF2 was obtained, which is one of the highest observed for intercalation electrode materials in FIBs so far. The average Coulombic efficiencies ranged from 85% to 90%. Thus, La2Ni0.75Co0.25O4.08 could be a promising candidate for cycling-stable high-energy cathode materials for all-solid-state FIBs}},
  author       = {{Vanita, Vanita and Waidha, Aamir Iqbal and Vasala, Sami and Puphal, Pascal and Schoch, Roland and Glatzel, Pieter and Bauer, Matthias and Clemens, Oliver}},
  issn         = {{2050-7488}},
  journal      = {{Journal of Materials Chemistry A}},
  keywords     = {{Xray}},
  number       = {{12}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Insights into the First Multi-Transition-Metal Containing Ruddlesden Popper-Type Cathode for all-solid-state Fluoride Ion Batteries}}},
  doi          = {{10.1039/d4ta00704b}},
  year         = {{2024}},
}

@article{60216,
  abstract     = {{Hydride donors such as DIBAL or CuH react with ZnO and ZrO2 via hydrogen spillover. This suggests that hydrogen spillover in catalysts based on these metal oxides may take place via initial hydride transfer and not via proton–electron transfer.}},
  author       = {{Benz, Michael and Bunjaku, Osman and Nowakowski, Michał and Allgaier, Alexander and Biswas, Indro and van Slageren, Joris and Bauer, Matthias and Estes, Deven P.}},
  issn         = {{2044-4753}},
  journal      = {{Catalysis Science & Technology}},
  keywords     = {{Xray}},
  number       = {{20}},
  pages        = {{5854--5863}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Hydrogen spillover through hydride transfer: the reaction of ZnO and ZrO2 with strong hydride donors}}},
  doi          = {{10.1039/d4cy00504j}},
  volume       = {{14}},
  year         = {{2024}},
}

@article{54024,
  abstract     = {{Transition metal complexes, particularly copper hydrides, play an important role in various catalytic processes and molecular inorganic chemistry. This study employs synchrotron hard X‐ray spectroscopy to gain insights into the geometric and electronic properties of copper hydrides as potential catalysts for CO2 hydrogenation. The potential of high energy resolution X‐ray absorption near‐edge structure (HERFD‐XANES) and valence‐to‐core X‐ray emission (VtC‐XES) is demonstrated with measurement on Stryker's reagent (Cu6H6) and [Cu3(μ3‐H)(dpmppe)2](PF6)2 (Cu3H), alongside a non‐hydride copper compound (Cu‐I). The XANES analysis reveals that coordination geometries strongly influence the spectra, providing only indirect details about hydride coordination. The VtC‐XES analysis exhibits a distinct signal around 8975 eV, offering a diagnostic tool to identify hydride ligands. Theoretical calculations support and extend these findings by comparing hydride‐containing complexes with their hydride‐free counterparts.}},
  author       = {{Fritsch, Lorena and Rehsies, Pia and Barakat, Wael and Estes, Deven P. and Bauer, Matthias}},
  issn         = {{0947-6539}},
  journal      = {{Chemistry – A European Journal}},
  keywords     = {{Xray}},
  number       = {{36}},
  publisher    = {{Wiley}},
  title        = {{{Detection and Characterization of Hydride Ligands in Copper Complexes by Hard X‐ray Spectroscopy}}},
  doi          = {{10.1002/chem.202400357}},
  volume       = {{30}},
  year         = {{2024}},
}

@article{54969,
  abstract     = {{This work presents a new and facile route for the preparation of iron oxide-based catalysts supported on alumina, which enables the targeted synthesis of catalysts with an increased amount of isolated tetrahedrally coordinated iron centers compared to a conventional impregnation procedure, and therefore leads to an increase in activity for CO oxidation reaction. By a multi-step impregnation–calcination protocol, the catalysts were synthesized with iron loadings of between 1 and 10 wt%, and their catalytic activity was then compared with a 10 wt% loaded catalyst prepared by conventional single impregnation. With a loading of 8 wt%, the presented catalysts showed an improved catalytic activity regarding light-off and full conversion temperatures compared to this reference. Through the application of several analytical methods (PXRD, PDF, DRUVS, SEM, XAFS), the improved catalytic activity can be correlated with an increased amount of isolated iron centers and a significantly reduced fraction of agglomerates or particles.}},
  author       = {{Schlicher, Steffen and Schoch, Roland and Prinz, Nils and Zobel, Mirijam and Bauer, Matthias}},
  issn         = {{2073-4344}},
  journal      = {{Catalysts}},
  keywords     = {{Catalysis}},
  number       = {{7}},
  publisher    = {{MDPI AG}},
  title        = {{{New and Facile Preparation Method for Highly Active Iron Oxide Catalysts for CO Oxidation}}},
  doi          = {{10.3390/catal14070416}},
  volume       = {{14}},
  year         = {{2024}},
}

@article{35657,
  abstract     = {{The controlled delivery of active pharmaceutical ingredients to the site of disease represents a major challenge in drug therapy. Particularly when drugs have to be transported across biological barriers, suitable drug delivery systems are of importance. In recent years responsive delivery systems have been developed which enable a controlled drug release depending on internal or external stimuli such as changes in pH, redox environment or light and temperature. In some studies delivery systems with reactivity against two different stimuli were established either to enhance the response by synergies of the stimuli or to broaden the window of possible trigger events. In the present review numerous exciting developments of pH-, light- and redox-cleavable polymers suitable for the preparation of smart delivery systems are described. The review discusses the different stimuli that can be used for a controlled drug release of polymer-based delivery systems. It puts a focus on the different polymers described for the preparation of stimuli-sensitive systems, their preparation techniques as well as their stimuli-responsive degradation. © 2022 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry.}},
  author       = {{Rust, Tarik and Jung, Dimitri and Langer, Klaus and Kuckling, Dirk}},
  issn         = {{0959-8103}},
  journal      = {{Polymer International}},
  keywords     = {{drug delivery system, stimuli, polymer, cleavable}},
  number       = {{1}},
  pages        = {{5--19}},
  publisher    = {{Wiley}},
  title        = {{{Stimuli‐accelerated polymeric drug delivery systems}}},
  doi          = {{10.1002/pi.6474}},
  volume       = {{72}},
  year         = {{2023}},
}

@article{45826,
  author       = {{Niemann, Valerie A. and Huck, Marten and Steinrück, Hans-Georg and Toney, Michael F. and Tarpeh, William A. and Bone, Sharon E.}},
  issn         = {{2690-0637}},
  journal      = {{ACS ES&T Water}},
  keywords     = {{Water Science and Technology, Environmental Chemistry, Chemistry (miscellaneous), Chemical Engineering (miscellaneous)}},
  pages        = {{2627--2637}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{X-ray Absorption Spectroscopy Reveals Mechanisms of Calcium and Silicon Fouling on Reverse Osmosis Membranes Used in Wastewater Reclamation}}},
  doi          = {{10.1021/acsestwater.3c00144}},
  volume       = {{3}},
  year         = {{2023}},
}

@article{47589,
  author       = {{Krämer, Felix and Paradies, Jan and Fernández, Israel and Breher, Frank}},
  issn         = {{1755-4330}},
  journal      = {{Nature Chemistry}},
  keywords     = {{General Chemical Engineering, General Chemistry}},
  publisher    = {{Springer Science and Business Media LLC}},
  title        = {{{A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media}}},
  doi          = {{10.1038/s41557-023-01340-9}},
  year         = {{2023}},
}

@article{48013,
  author       = {{Liu, Ping and Schumann, Nils and Abele, Fabian and Ren, Fazheng and Hanke, Marcel and Xin, Yang and Hartmann, Andreas and Schlierf, Michael and Keller, Adrian and Lin, Weilin and Zhang, Yixin}},
  issn         = {{2574-0970}},
  journal      = {{ACS Applied Nano Materials}},
  keywords     = {{General Materials Science}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Thermophoretic Analysis of Biomolecules across the Nanoscales in Self-Assembled Polymeric Matrices}}},
  doi          = {{10.1021/acsanm.3c03623}},
  year         = {{2023}},
}

@article{48588,
  abstract     = {{<jats:p>Bacterial colonization and biofilm formation on abiotic surfaces are initiated by the adhesion of peptides and proteins. Understanding the adhesion of such peptides and proteins at a molecular level thus represents an important step toward controlling and suppressing biofilm formation on technological and medical materials. This study investigates the molecular adhesion of a pilus‐derived peptide that facilitates biofilm formation of Pseudomonas aeruginosa, a multidrug‐resistant opportunistic pathogen frequently encountered in healthcare settings. Single‐molecule force spectroscopy (SMFS) was performed on chemically etched ZnO surfaces to gather insights about peptide adsorption force and its kinetics. Metal‐free click chemistry for the fabrication of peptide‐terminated SMFS cantilevers was performed on amine‐terminated gold cantilevers and verified by X‐ray photoelectron spectroscopy (XPS) and polarization‐modulated infrared reflection absorption spectroscopy (PM‐IRRAS). Atomic force microscopy (AFM) and XPS analyses reveal stable topographies and surface chemistries of the substrates that are not affected by SMFS. Rupture events described by the worm‐like chain model (WLC) up to 600 pN were detected for the non‐polar ZnO(11‐20) surfaces. The dissociation barrier energy at zero force ΔG(0), the transition state distance xb and bound‐unbound dissociation rate at zero force koff(0) for the single crystalline substrate indicate that coordination and hydrogen bonds dominate the peptide/surface interaction.</jats:p>}},
  author       = {{Prüßner, Tim and Meinderink, Dennis and Zhu, Siqi and Orive, Alejandro G. and Kielar, Charlotte and Huck, Marten and Steinrück, Hans-Georg and Keller, Adrian and Grundmeier, Guido}},
  issn         = {{0947-6539}},
  journal      = {{Chemistry – A European Journal}},
  keywords     = {{General Chemistry, Catalysis, Organic Chemistry}},
  publisher    = {{Wiley}},
  title        = {{{Molecular Adhesion of a Pilus‐derived Peptide Involved in Pseudomonas aeruginosa Biofilm Formation on non‐polar ZnO Surfaces}}},
  doi          = {{10.1002/chem.202302464}},
  year         = {{2023}},
}

@article{48602,
  abstract     = {{This article presents the results of the implementation of the Erasmus Plus project (KA203 financed by the European Union, contract number 2019-1-NL01-KA203-060339) Research in Teacher Education (RiTE). The aim of the project was to promote and facilitate pre-service teachers to create and undertake evidence-based practices in teaching science, technology, engineering, and mathematics (STEM). In the RiTE project, pre-service teachers were encouraged to use evidence from educational and scientific research and to experiment and introduce didactic innovations in teaching and learning processes. Although it has its justification in the tradition of thinking about science, evidence-based practice is not yet consciously applied in school practice. In the article, we present both the theoretical framework for such practices, and the results of qualitative research – an analysis of interviews conducted with students, future teachers, and novice teachers involved in the project. The presented results show changes in the context of an understanding of evidence and what evidence-based practices are in the teaching process and the vision of such teaching presented by the respondents.}},
  author       = {{Rybska, Eliza and Dudziak, Renata and Pollmeier, Pascal}},
  issn         = {{2451-2230}},
  journal      = {{Problemy Wczesnej Edukacji}},
  number       = {{1}},
  pages        = {{89--108}},
  publisher    = {{Uniwersytet Gdanski}},
  title        = {{{Evidence-based practices in teaching}}},
  doi          = {{10.26881/pwe.2023.56.06}},
  volume       = {{56}},
  year         = {{2023}},
}

@article{49356,
  author       = {{Moffitt, Stephanie L. and Cao, Chuntian and Van Hest, Maikel F. A. M. and Schelhas, Laura T. and Steinrück, Hans-Georg and Toney, Michael F.}},
  issn         = {{1932-7447}},
  journal      = {{The Journal of Physical Chemistry C}},
  keywords     = {{Surfaces, Coatings and Films, Physical and Theoretical Chemistry, General Energy, Electronic, Optical and Magnetic Materials}},
  number       = {{47}},
  pages        = {{23099–23108}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Heterogeneous Structural Evolution of In–Zn–O Thin Films during Annealing}}},
  doi          = {{10.1021/acs.jpcc.3c06410}},
  volume       = {{127}},
  year         = {{2023}},
}

@article{49609,
  abstract     = {{<jats:p>The alignment of liquid crystals on surfaces plays a central role in optimizing their performances. In this work, a cutting-edge nano-lithography-based method to control the local orientation of a thermotropic liquid crystal is applied to easily available commercial standard materials and evaluated. Parallel nanogrooves on a substrate, created through 3D nanoprinting in a negative-tone photoresin optimized for two-photon polymerization are used for this purpose. Azimuthal anchoring energies of the order from 10<jats:sup>−6</jats:sup> J/m<jats:sup>2</jats:sup> to 10<jats:sup>−5</jats:sup> J/m<jats:sup>2</jats:sup> are found, depending on the spacing, width and depth of the grooves. In part, these values are larger than those reported previously for another photopolymer. Both uniform alignment and spatial patterns of different alignment directions can be realized. Electro-optic studies confirm the suitability of the method for electrically addressable photonic applications and indicate strong polar anchoring.</jats:p>}},
  author       = {{Zhang, Bingru and Plidschun, Malte and Schmidt, Markus A. and Kitzerow, Heinz-Siegfried}},
  issn         = {{2159-3930}},
  journal      = {{Optical Materials Express}},
  keywords     = {{Electronic, Optical and Magnetic Materials}},
  number       = {{12}},
  publisher    = {{Optica Publishing Group}},
  title        = {{{Anchoring and electro-optic switching of liquid crystals on nano-structured surfaces fabricated by two-photon based nano-printing}}},
  doi          = {{10.1364/ome.503100}},
  volume       = {{13}},
  year         = {{2023}},
}

@article{43440,
  author       = {{Zhang, Bingru and Nguyen, Linh and Martens, Kevin and Heuer-Jungemann, Amelie and Philipp, Julian and Kempter, Susanne and Rädler, Joachim O. and Liedl, Tim and Kitzerow, Heinz-Siegfried}},
  issn         = {{0267-8292}},
  journal      = {{Liquid Crystals}},
  keywords     = {{Condensed Matter Physics, General Materials Science, General Chemistry}},
  number       = {{7-10}},
  pages        = {{1243--1251}},
  publisher    = {{Informa UK Limited}},
  title        = {{{Luminescent DNA-origami nano-rods dispersed in a lyotropic chromonic liquid crystal}}},
  doi          = {{10.1080/02678292.2023.2188494}},
  volume       = {{50}},
  year         = {{2023}},
}