Literatura académica sobre el tema "Multiscale structure/ionic transport properties correlations"
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Artículos de revistas sobre el tema "Multiscale structure/ionic transport properties correlations"
Thomas, Elayne M., Phong H. Nguyen, Seamus D. Jones, Michael L. Chabinyc y Rachel A. Segalman. "Electronic, Ionic, and Mixed Conduction in Polymeric Systems". Annual Review of Materials Research 51, n.º 1 (26 de julio de 2021): 1–20. http://dx.doi.org/10.1146/annurev-matsci-080619-110405.
Texto completoSilva, Wagner, Marcileia Zanatta, Ana Sofia Ferreira, Marta C. Corvo y Eurico J. Cabrita. "Revisiting Ionic Liquid Structure-Property Relationship: A Critical Analysis". International Journal of Molecular Sciences 21, n.º 20 (19 de octubre de 2020): 7745. http://dx.doi.org/10.3390/ijms21207745.
Texto completoDong, Dengpan, Weiwei Zhang, Adam Barnett, Jibao Lu, Adri van Duin, Valeria Molinero y Dmitry Bedrov. "Multiscale Modeling of Structure, Transport and Reactivity in Alkaline Fuel Cell Membranes: Combined Coarse-Grained, Atomistic and Reactive Molecular Dynamics Simulations". Polymers 10, n.º 11 (20 de noviembre de 2018): 1289. http://dx.doi.org/10.3390/polym10111289.
Texto completoGautam, Ajay y Marnix Wagemaker. "Lithium Distribution and Site Disorder in Halide-Substituted Lithium Argyrodites: A Structural and Transport Study". ECS Meeting Abstracts MA2023-02, n.º 8 (22 de diciembre de 2023): 3325. http://dx.doi.org/10.1149/ma2023-0283325mtgabs.
Texto completoSacci, Robert L., Tyler H. Bennett, Kee Sung Han, Hong Fang, Puru Jena, Vijay Murugesan y Jagjit Nanda. "How Halide Sub-Lattice Affects Li Ion Transport in Antiperovskites". ECS Meeting Abstracts MA2022-02, n.º 4 (9 de octubre de 2022): 467. http://dx.doi.org/10.1149/ma2022-024467mtgabs.
Texto completoQi, Yue. "(Invited) Modeling the Charge Transfer Reactions at Li/SEI/Electrolyte Interfaces in Lithium-Ion Batteries". ECS Meeting Abstracts MA2023-01, n.º 45 (28 de agosto de 2023): 2452. http://dx.doi.org/10.1149/ma2023-01452452mtgabs.
Texto completoDehghan Khalili, A., J. Y. Y. Arns, F. Hussain, Y. Cinar, W. V. V. Pinczewski y C. H. H. Arns. "Permeability Upscaling for Carbonates From the Pore Scale by Use of Multiscale X-Ray-CT Images". SPE Reservoir Evaluation & Engineering 16, n.º 04 (10 de octubre de 2013): 353–68. http://dx.doi.org/10.2118/152640-pa.
Texto completoEikerling, Michael. "(Invited) Decoding the Symbiotic Relationship between Ionomer and Water in Cathode Catalyst Layers of PEM Fuel Cells". ECS Meeting Abstracts MA2022-02, n.º 45 (9 de octubre de 2022): 1696. http://dx.doi.org/10.1149/ma2022-02451696mtgabs.
Texto completovan der Heijden, Maxime, Marit Kroese, Zandrie Borneman y Antoni Cuenca. "Investigating Mass Transfer Relationships in Stereolithography-Based 3D Printed Electrodes for Redox Flow Batteries". ECS Meeting Abstracts MA2023-01, n.º 55 (28 de agosto de 2023): 2658. http://dx.doi.org/10.1149/ma2023-01552658mtgabs.
Texto completoKhan, Md Sharif, Ambroise Van Roekeghem, Stefano Mossa, Flavien Ivol, Laurent Bernard, Lionel Picard y Natalio Mingo. "Ionic Liquid Crystals As Solid Organic Electrolytes for Li-Ion Batteries: Experiments and Modeling". ECS Meeting Abstracts MA2022-01, n.º 2 (7 de julio de 2022): 183. http://dx.doi.org/10.1149/ma2022-012183mtgabs.
Texto completoTesis sobre el tema "Multiscale structure/ionic transport properties correlations"
Pung, Hélène. "Cristaux liquides ioniques thermotropes : Relations structure/propriétés de transport ionique". Electronic Thesis or Diss., Université Grenoble Alpes, 2024. http://www.theses.fr/2024GRALV007.
Texto completoDeveloping multi-scale spatial (nano/meso/micro-macroscopic) and temporal studies is crucial to understand, control, and pilot the relationships linking the structure to the ionic transport properties of hierarchically self-assembled functional materials. It is along these research lines that this exploratory work is positioned to meet their associated scientific challenges. It aims in particular to bring together elements of understanding for designing families of electrolytes with tuneable-by-design (cat/an)ionic conductivity levels and that can be implemented by reliable manufacturing processes to authorize their scalable integration into more efficient electrochemical energy conversion and storage devices. The scrutinized model families of soft-matter electrolytes are Thermotropic Ionic Liquid Crystals (TILCs), which synergistically combine dynamic hierarchical self-assembly with self-healing functionalities to encode dimensionality (quasi-1D/ quasi-2D/3D) controlled ionic transport. This research work presents and discusses the molecular engineering, syntheses and detailed studies of these model stimuli-responsive (An/Cat)ionic (A/C)-TILCs conductors.The study of the supramolecular organization of a model family of K+ and Na+ cation-conducting C-TILCs has unravelled i) a monotropic (i.e. which develops only during of the first heating scan) bicontinuous Cubic mesophase (Cubbi) with an Ia3d symmetry and ii) a hexagonal Columnar mesophase (Colhex), encoding 3D and quasi-1D transport processes, respectively. Polar ionic sub-domains are localized at the heart of the columns decorated at their periphery by aliphatic chains. The experimental study and modelling of the confinement of charge carriers within a model family of C18C18Im+/X- (X= Br-, I-, N(CN)2-) A-TILCs forming interdigitated Smectic A mesophases (SmAd are hosting quasi-2D anisotropic ionic transport) reveals a regime of nanoconfinement of anions subjected to electrostatic interactions within the ca. 1 nm-"thick" polar sub-layers within their lamellar organizations. The study of these TILCs thus addresses the functional impact of mosaicity, i.e. how the coexistence of mesomorphic domains presenting different orientations and sizes is impacting ionic transport.A first direct experimental description allows to describe the role of this dynamic mosaicity both i) on the long-range organization of mesomorphic domains and ii) onto ion transport at the meso-/macro-scopic scale. Within mesophases formed by the K+-cation conducting C-TILC, the Cubbi mesophase presents conductivity values two orders of magnitude greater than those associated to the Colhex mesophase. As the Cubbi mesophase does not require specific defect management strategies (low density of defects/homophasic interfaces), it turns out that polar subdomains can thus percolate efficiently according to an intrinsically 3D mechanism. In contrast, the long-range ordering of the (dynamic) SmAd mesomorphic domains of the C18C18Im+/N(CN)2- A-TILC, induced by the application of an external stimulus (here, a magnetic field of 1 T), results in a ca. x1.6 increase (from 92 to 145 nm) of the average size of mesomorphic domains at 80°C. Due to the reduction of the disorder and of the number of homophasic interfaces (which can penalize the transport of anions), a natural (expected) increase in conductivity values by a factor ca. x2.6 (9 to 25 µS·cm-1) is observed.Ultimately, TILCs, i.e. 2.0 electrolytic materials encoding ionic transport properties and (bioinspired) dynamic self-assembly/repairing functionalities, are consisting in an original class of stimuli-sensitive functional materials for the electrochemical conversion and storage of energy