@misc{45455,
  author       = {{Claes, Leander and Meihost, Lars and Jurgelucks, Benjamin}},
  title        = {{{Inverse procedure for the identification of piezoelectric material parameters supported by dense neural networks}}},
  year         = {{2023}},
}

@misc{45456,
  author       = {{Jurgelucks, Benjamin}},
  title        = {{{Parameter Identification of Piezoelectrics improved by Neural Networks}}},
  year         = {{2023}},
}

@misc{45457,
  author       = {{Kuess, Raphael}},
  title        = {{{Parameter identification in piezoelectricity based on all-at-once and reduced regularization}}},
  year         = {{2023}},
}

@inproceedings{57086,
  author       = {{Kuhlmann, Michael and Meise, Adrian Tobias and Seebauer, Fritz and Wagner, Petra and Häb-Umbach, Reinhold}},
  booktitle    = {{Speech Communication; 15th ITG Conference}},
  pages        = {{121–125}},
  title        = {{{Investigating Speaker Embedding Disentanglement on Natural Read Speech}}},
  year         = {{2023}},
}

@article{62675,
  abstract     = {{<jats:title>Abstract</jats:title>
                  <jats:p>
                    Materials dictate carbon neutral industrial chemical processes. Visible‐light photoelectrocatalysts from abundant resources will play a key role in exploiting solar irradiation. Anionic doping via pre‐organization of precursors and further co‐polymerization creates tuneable semiconductors. Triazole derivative‐purpald, an unexplored precursor with sulfur (S) container, combined in different initial ratios with melamine during one solid‐state polycondensation with two thermal steps yields hybrid S‐doped carbon nitrides (C
                    <jats:sub>3</jats:sub>
                    N
                    <jats:sub>4</jats:sub>
                    ). The series of S‐doped/C
                    <jats:sub>3</jats:sub>
                    N
                    <jats:sub>4</jats:sub>
                    ‐based materials show enhanced optical, electronic, structural, textural, and morphological properties and exhibit higher performance in organic benzylamine photooxidation, oxygen evolution, and similar energy storage (capacitor brief investigation). 50M‐50P exhibits the highest photooxidation conversion (84 ± 3%) of benzylamine to imine at 535 nm – green light for 48 h, due to a discrete shoulder (≈700) nm, high sulfur content, preservation of crystal size, new intraband energy states, structural defects by layer distortion, and 10–16 nm pores with arbitrary depth. This work innovates by studying the concomitant relationships between: 1) the precursor decomposition while C
                    <jats:sub>3</jats:sub>
                    N
                    <jats:sub>4</jats:sub>
                    is formed, 2) the insertion of S impurities, 3) the S‐doped C
                    <jats:sub>3</jats:sub>
                    N
                    <jats:sub>4</jats:sub>
                    property‐activity relationships, and 4) combinatorial surface, bulk, structural, optical, and electronic characterization analysis. This work contributes to the development of disordered long‐visible‐light photocatalysts for solar energy conversion and storage.
                  </jats:p>}},
  author       = {{Jerigova, Maria and Markushyna, Yevheniia and Teixeira, Ivo F. and Badamdorj, Bolortuya and Isaacs, Mark and Cruz, Daniel and Lauermann, Iver and Muñoz‐Márquez, Miguel Ángel and Tarakina, Nadezda V. and Lopez Salas, Nieves and Savateev, Oleksandr and Jimenéz‐Calvo, Pablo}},
  issn         = {{2198-3844}},
  journal      = {{Advanced Science}},
  number       = {{13}},
  publisher    = {{Wiley}},
  title        = {{{Green Light Photoelectrocatalysis with Sulfur‐Doped Carbon Nitride: Using Triazole‐Purpald for Enhanced Benzylamine Oxidation and Oxygen Evolution Reactions}}},
  doi          = {{10.1002/advs.202300099}},
  volume       = {{10}},
  year         = {{2023}},
}

@article{62671,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Carbonaceous electrocatalysts offer advantages over metal‐based counterparts, being cost‐effective, sustainable, and electrochemically stable. Their high surface area increases reaction kinetics, making them valuable for environmental applications involving contaminant removal. However, their rational synthesis is challenging due to the applied high temperatures and activation steps, leading to disordered materials with limited control over doping. Here, a new synthetic pathway using carbon oxide precursors and tin chloride as a p‐block metal salt melt is presented. As a result, highly porous oxygen‐rich carbon sheets (with a surface area of 1600 m<jats:sup>2</jats:sup> g<jats:sup>−1</jats:sup>) are obtained at relatively low temperatures (400 °C). Mechanistic studies reveal that Sn(II) triggers reductive deoxygenation and concomitant condensation/cross‐linking, facilitated by the Sn(II) → Sn(IV) transition. Due to their significant surface area and oxygen doping, these materials demonstrate exceptional electrocatalytic activity in the nitrate‐to‐ammonia conversion, with an ammonia yield rate of 221 mmol g<jats:sup>−1</jats:sup> h<jats:sup>−1</jats:sup> and a Faradic efficiency of 93%. These results surpass those of other carbon‐based electrocatalysts. In situ Raman studies reveal that the reaction occurs through electrochemical hydrogenation, where active hydrogen is provided by water reduction. This work contributes to the development of carbonaceous electrocatalysts with enhanced performance for sustainable environmental applications.</jats:p>}},
  author       = {{Zheng, Xinyue and Tian, Zhihong and Bouchal, Roza and Antonietti, Markus and Lopez Salas, Nieves and Odziomek, Mateusz}},
  issn         = {{0935-9648}},
  journal      = {{Advanced Materials}},
  number       = {{13}},
  publisher    = {{Wiley}},
  title        = {{{Tin (II) Chloride Salt Melts as Non‐Innocent Solvents for the Synthesis of Low‐Temperature Nanoporous Oxo‐Carbons for Nitrate Electrochemical Hydrogenation}}},
  doi          = {{10.1002/adma.202311575}},
  volume       = {{36}},
  year         = {{2023}},
}

@article{62672,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Functionalized porous carbons are central to various important applications such as energy storage and conversion. Here, a simple synthetic route to prepare oxygen‐rich carbon nitrides (CNOs) decorated with stable Ni and Fe‐nanosites is demonstrated. The CNOs are prepared via a salt templating method using ribose and adenine as precursors and CaCl<jats:sub>2</jats:sub>·2H<jats:sub>2</jats:sub>O as a template. The formation of supramolecular eutectic complexes between CaCl<jats:sub>2</jats:sub>·2H<jats:sub>2</jats:sub>O and ribose at relatively low temperatures facilitates the formation of a homogeneous starting mixture, promotes the condensation of ribose through the dehydrating effect of CaCl<jats:sub>2</jats:sub>·2H<jats:sub>2</jats:sub>O to covalent frameworks, and finally generates homogeneous CNOs. As a specific of the recipe, the condensation of the precursors at higher temperatures and the removal of water promotes the recrystallization of CaCl<jats:sub>2</jats:sub> (<jats:italic>T</jats:italic> &lt; <jats:italic>T<jats:sub>m</jats:sub></jats:italic> = 772 °C), which then acts as a hard porogen. Due to salt catalysis, CNOs with oxygen and nitrogen contents as high as 12 and 20 wt%, respectively, can be obtained, while heteroatom content stayed about unchanged even at higher temperatures of synthesis, pointing to the extraordinarily high stability of the materials. After decorating Ni and Fe‐nanosites onto the CNOs, the materials exhibit high activity and stability for electrochemical oxygen evolution reaction with an overpotential of 351 mV.</jats:p>}},
  author       = {{Li, Chun and Lepre, Enrico and Bi, Min and Antonietti, Markus and Zhu, Junwu and Fu, Yongsheng and Lopez Salas, Nieves}},
  issn         = {{2198-3844}},
  journal      = {{Advanced Science}},
  number       = {{22}},
  publisher    = {{Wiley}},
  title        = {{{Oxygen‐Rich Carbon Nitrides from an Eutectic Template Strategy Stabilize Ni, Fe Nanosites for Electrocatalytic Oxygen Evolution}}},
  doi          = {{10.1002/advs.202300526}},
  volume       = {{10}},
  year         = {{2023}},
}

@article{62673,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Self‐templating is a facile strategy for synthesizing porous carbons by direct pyrolysis of organic metal salts. However, the method typically suffers from low yields (&lt;4%) and limited specific surface areas (SSA&lt;2000 m<jats:sup>2</jats:sup> g<jats:sup>−1</jats:sup>) originating from low activity of metal cations (e.g., K<jats:sup>+</jats:sup> or Na<jats:sup>+</jats:sup>) in promoting construction and activation of carbon frameworks. Here we use cesium acetate as the only precursor of oxo‐carbons with large SSA of the order of 3000 m<jats:sup>2</jats:sup> g<jats:sup>−1</jats:sup>, pore volume approaching 2 cm<jats:sup>3</jats:sup> g<jats:sup>−1</jats:sup>, tunable oxygen contents, and yields of up to 15 %. We unravel the role of Cs<jats:sup>+</jats:sup> as an efficient promoter of framework formation, templating and etching agent, while acetates act as carbon/oxygen sources of carbonaceous frameworks. The oxo‐carbons show record‐high CO<jats:sub>2</jats:sub> uptake of 8.71 mmol g<jats:sup>−1</jats:sup> and an ultimate specific capacitance of 313 F g<jats:sup>−1</jats:sup> in the supercapacitor. This study helps to understand and rationally tailor the materials design by a still rare organic solid‐state chemistry.</jats:p>}},
  author       = {{Li, Jiaxin and Kossmann, Janina and Zeng, Ke and Zhang, Kun and Wang, Bingjie and Weinberger, Christian and Antonietti, Markus and Odziomek, Mateusz and Lopez Salas, Nieves}},
  issn         = {{1433-7851}},
  journal      = {{Angewandte Chemie International Edition}},
  number       = {{26}},
  publisher    = {{Wiley}},
  title        = {{{When High‐Temperature Cesium Chemistry Meets Self‐Templating: Metal Acetates as Building Blocks of Unusual Highly Porous Carbons}}},
  doi          = {{10.1002/anie.202217808}},
  volume       = {{62}},
  year         = {{2023}},
}

@unpublished{47447,
  abstract     = {{Sodium-ion capacitors (SICs) have great potential in energy storage due to their low cost, the abundance of Na, and the potential to deliver high energy and power simultaneously. This paper demonstrates a template-assisted method to induce graphitic nanodomains and micro-mesopores into nitrogen-doped carbons. This study elucidates that these graphitic nanodomains are beneficial for Na+ storage. The obtained N-doped carbon (As8Mg) electrode achieved a reversible capacity of 254 mA h g−1 at 0.1 A g−1. Moreover, the As8Mg-based SIC device achieves high combinations of power/energy densities (52 W kg−1 at 204 Wh kg−1 and 10,456 W kg−1 at 51 Wh kg−1) with outstanding cycle stability (99.7% retention over 10000 cycles at 0.2 A g−1). Our findings provide insights into optimizing carbon’s microstructure to boost sodium storage in the pseudo-capacitive mode. }},
  author       = {{Lopez Salas, Nieves and Li, Chun  and Song, Zihan and Liu, Minliang and Lepre, Enrico and Antonietti, Markus and Zhu, Junwu and Liu, Jian and Fu, Yongsheng}},
  keywords     = {{sodium ion capacitor, anode, template, N-doped carbons, graphitic nanodomains}},
  title        = {{{Template-induced graphitic nanodomains in nitrogen-doped carbons enable high-performance sodium-ion capacitors - ACCEPTED MANUSCRIPT}}},
  year         = {{2023}},
}

@article{42648,
  abstract     = {{In real photonic quantum systems losses are an unavoidable factor limiting the scalability to many modes and particles, restraining their application in fields as quantum information and communication. For this reason, a considerable amount of engineering effort has been taken in order to improve the quality of particle sources and system components. At the same time, data analysis and collection methods based on post-selection have been used to mitigate the effect of particle losses. This has allowed for investigating experimentally multi-particle evolutions where the observer lacks knowledge about the system's intermediate propagation states. Nonetheless, the fundamental question how losses affect the behaviour of the surviving subset of a multi-particle system has not been investigated so far. For this reason, here we study the impact of particle losses in a quantum walk of two photons reconstructing the output probability distributions for one photon conditioned on the loss of the other in a known mode and temporal step of our evolution network. We present the underlying theoretical scheme that we have devised in order to model controlled particle losses, we describe an experimental platform capable of implementing our theory in a time multiplexing encoding. In the end we show how localized particle losses change the output distributions without altering their asymptotic spreading properties. Finally we devise a quantum civilization problem, a two walker generalisation of single particle recurrence processes.}},
  author       = {{Pegoraro, Federico and Held, Philip and Barkhofen, Sonja and Brecht, Benjamin and Silberhorn, Christine}},
  issn         = {{0031-8949}},
  journal      = {{Physica Scripta}},
  number       = {{3}},
  publisher    = {{IOP Publishing}},
  title        = {{{Dynamic conditioning of two particle discrete-time quantum walks}}},
  doi          = {{10.1088/1402-4896/acbcaa}},
  volume       = {{98}},
  year         = {{2023}},
}

@techreport{49295,
  author       = {{Heinemann-Heile, Vanessa and Maiterth, Ralf and Sureth-Sloane, Caren}},
  title        = {{{Umfrage: Beurteilung Investitionsfördernder Maßnahmen durch Unternehmen aus Handel, Dienstleistung und Industrie}}},
  doi          = {{doi.org/10.52569/JCNY6589}},
  year         = {{2023}},
}

@misc{52427,
  author       = {{Schlüter, Alexander}},
  publisher    = {{Marcus Nettelbeck}},
  title        = {{{2050 - The Future Podcast, Folge The Energy Systems of the Future}}},
  year         = {{2023}},
}

@inproceedings{58793,
  author       = {{Wirth, Robert}},
  booktitle    = {{Aktuelle Politische Bildung im Englischunterricht: Mitdenken! Mitreden! Mitgestalten! }},
  title        = {{{Letting ‘someone else rule your land’? – the Scottish Quandary" / "Putting the ‘Great’ Back Into Great Britain}}},
  year         = {{2023}},
}

@inproceedings{58794,
  author       = {{Wirth, Robert}},
  booktitle    = {{Fachreferententagung}},
  title        = {{{Letting ‘someone else rule your land’? – the Scottish Quandary}}},
  year         = {{2023}},
}

@article{64893,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>The synthesis of three novel imidazolyl‐substituted sulfur‐containing heteroacenes is reported. These heteroacenes consisting of annelated benzo‐ and naphthothiophenes serve as precursors for the generation of open‐shell quinoid heteroacenes by oxidation with alkaline ferric cyanide. Spectroscopic and computational experiments support the formation of reactive open‐shell quinoids, which, however, quickly produce paramagnetic polymeric material.</jats:p>}},
  author       = {{Hou, Peng and Peschtrich, Sebastian and Feuerstein, Wolfram and Schoch, Roland and Hohloch, Stephan and Breher, Frank and Paradies, Jan}},
  issn         = {{2191-1363}},
  journal      = {{ChemistryOpen}},
  number       = {{11}},
  publisher    = {{Wiley}},
  title        = {{{Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids}}},
  doi          = {{10.1002/open.202300003}},
  volume       = {{12}},
  year         = {{2023}},
}

@article{45112,
  author       = {{Beverungen, Daniel and Kundisch, Dennis and Mirbabaie, Milad and Müller, Oliver and Schryen, Guido and Trang, Simon Thanh-Nam and Trier, Matthias}},
  journal      = {{Business & Information Systems Engineering}},
  number       = {{4}},
  pages        = {{463 -- 474}},
  title        = {{{Digital Responsibility – a Multilevel Framework for Responsible Digitalization}}},
  doi          = {{10.1007/s12599-023-00822-x}},
  volume       = {{65}},
  year         = {{2023}},
}

@article{48262,
  author       = {{Jacke, Christoph and Flath, Beate}},
  journal      = {{Kulturpolitische Mitteilungen}},
  number       = {{Nr. III/2023}},
  pages        = {{84--85}},
  title        = {{{Popmusik- und Medienkulturen verstehen, erforschen und reflektieren. Studiengang "Populäre Musik und Medien" und Gründung des Forschungszentrums "C:POP".}}},
  volume       = {{182}},
  year         = {{2023}},
}

@inbook{64937,
  author       = {{Mersch, Katharina Ulrike}},
  booktitle    = {{A companion to the abbey of Quedlinburg in the Middle Ages}},
  editor       = {{Blough, Karen}},
  pages        = {{15--46}},
  title        = {{{Quedlinburg abbey’s medieval history in ever-changing political and religious frameworks: a survey}}},
  volume       = {{29}},
  year         = {{2023}},
}

@inbook{64938,
  author       = {{Mersch, Katharina Ulrike}},
  booktitle    = {{Women and monastic reform in the medieval west, c. 1000-1500. Debating identities, creating communities}},
  editor       = {{Hotchin, Julie and Thibaut, Jirki}},
  pages        = {{227--248}},
  title        = {{{Who made reform visible? Male and female agency in changing visual culture}}},
  volume       = {{44}},
  year         = {{2023}},
}

@inbook{64940,
  author       = {{Mersch, Katharina Ulrike}},
  booktitle    = {{1100 Jahre Quedlinburg. Einblicke in das Leben auf der Königspfalz}},
  editor       = {{Freund, Stephan}},
  pages        = {{41--64}},
  title        = {{{Pfalz und Stift Quedlinburg in Konflikten des 10. bis 12. Jahrhunderts}}},
  volume       = {{9}},
  year         = {{2023}},
}

