Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2024Advancements in Quasi-Solid-State Li Batteries: A Rigid Hybrid Electrolyte Using LATP Porous Ceramic Membrane and Infiltrated Ionic Liquidcitations
  • 2023Using Metal-Organic Framework HKUST-1 for the Preparation of High-Conductive Hybrid Membranes Based on Multiblock Copolymers for Fuel Cells6citations
  • 2023All-solid-state sodium-ion batteries operating at room temperature based on NASICON-type NaTi2(PO4)3 cathode and ceramic NASICON solid electrolyte42citations
  • 2023All-solid-state sodium-ion batteries operating at room temperature based on NASICON-type NaTi 2 (PO 4 ) 3 cathode and ceramic NASICON solid electrolyte:A complete in situ synchrotron X-ray study42citations
  • 2018Additive-free Li<sub>4</sub>Ti<sub>5</sub>O<sub>12</sub> thick electrodes for Li-ion batteries with high electrochemical performance37citations

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Chart of shared publication
Torre, Carmen De La
1 / 1 shared
Reinoso, Deborath Mariana
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Varez, Alejandro
5 / 13 shared
Fernández-Ropero, Antonio J.
1 / 1 shared
Río, Carmen Del
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Gorban, Ivan
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Soldatov, Mikhail
1 / 2 shared
Ureña, Maria De Las Nieves
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Teresa, Pérez Prior María
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Andersen, Bettina P.
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Ravnsbæk, Dorthe Bomholdt
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Martínez-Cisneros, Cynthia S.
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Johansen, Morten
2 / 3 shared
Pandit, Bidhan
2 / 10 shared
Ravnsbæk, Dorthe B.
1 / 4 shared
Torre-Gamarra, C. De La
1 / 1 shared
Bucheli, W.
1 / 5 shared
Sotomayor, M. E.
1 / 3 shared
Alvarez, Jose Manuel Amarilla
1 / 1 shared
Sanchez, J.-Y.
1 / 1 shared
Chart of publication period
2024
2023
2018

Co-Authors (by relevance)

  • Torre, Carmen De La
  • Reinoso, Deborath Mariana
  • Varez, Alejandro
  • Fernández-Ropero, Antonio J.
  • Río, Carmen Del
  • Gorban, Ivan
  • Soldatov, Mikhail
  • Ureña, Maria De Las Nieves
  • Teresa, Pérez Prior María
  • Andersen, Bettina P.
  • Ravnsbæk, Dorthe Bomholdt
  • Martínez-Cisneros, Cynthia S.
  • Johansen, Morten
  • Pandit, Bidhan
  • Ravnsbæk, Dorthe B.
  • Torre-Gamarra, C. De La
  • Bucheli, W.
  • Sotomayor, M. E.
  • Alvarez, Jose Manuel Amarilla
  • Sanchez, J.-Y.
OrganizationsLocationPeople

article

All-solid-state sodium-ion batteries operating at room temperature based on NASICON-type NaTi2(PO4)3 cathode and ceramic NASICON solid electrolyte

  • Varez, Alejandro
  • Andersen, Bettina P.
  • Levenfeld, Belen
  • Ravnsbæk, Dorthe Bomholdt
  • Martínez-Cisneros, Cynthia S.
  • Johansen, Morten
  • Pandit, Bidhan
Abstract

<p>All-solid-state sodium-ion batteries that work at ambient temperature are a potential approach for large-scale energy storage systems. Nowadays, ceramic solid electrolytes are gaining attention because of their good ionic conductivity and excellent mechanical and chemical stabilities. Furthermore, a good interface between electrode and solid electrolyte is also required to achieve successful cell performances. In this work, sintered ceramic layer electrolyte Na<sub>3.16</sub>Zr<sub>1.84</sub>Y<sub>0.16</sub>Si<sub>2</sub>PO<sub>12</sub>, with high ionic conductivity (0.202 mS/cm at room temperature), are prepared by using uniaxial pressing followed by a sintering process. The conductive carbon coated NASICON material (NaTi<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub>/C) exhibits, as cathode material, enhanced rate capability and stability for sodium ion batteries for high carbon (18.95 %) coated sample. At C/10, the optimized cathode (with higher carbon content) achieves a remarkable initial discharge capacity of 107.3 mAh/g (reversible capacity of 101.4 mAh/g), a sufficient rate capability up to a rate of 10C, and a long cycle life (capacity retention of 58% after 950 cycles). The one-stage reversible biphasic reaction mechanism and potential-dependent structure–property of NaTi<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> can be explained by employing in situ X-ray synchrotron method. Sequential Rietveld refinements of the in situ data show the evolution of the Na-poor NaTi<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> and Na-rich Na<sub>3</sub>Ti<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> phase fractions (wt%), unit cell characteristics, and unit cell volume. The design of an all-solid-state sodium ion half-cell with a NaTi<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub>/C cathode and a Na<sub>3.16</sub>Zr<sub>1.84</sub>Y<sub>0.16</sub>Si<sub>2</sub>PO<sub>12</sub> solid-state electrolyte interface results in stable capacity of 83.6 mAh/g at C/10 and excellent reversible capacity at high C-rate. The results show that sintered NASICON-based electrolytes can significantly contribute for the fabrication of all-solid-state sodium-ion battery due to the superior conductivity and stability.</p>

Topics
  • impedance spectroscopy
  • Carbon
  • phase
  • Sodium
  • mass spectrometry
  • ceramic
  • sintering
  • carbon content