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Local structure of hydrated and dehydrated Prussian white cathode materials
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.ORCID iD: 0000-0002-6511-8291
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2025 (English)In: Journal of Materials Chemistry C, ISSN 2050-7526, E-ISSN 2050-7534Article in journal (Refereed) Epub ahead of print
Abstract [en]

The sodium iron hexacyanoferrate compound with chemical formula Na2.04(2)Fe[Fe(CN)6]·2.24(2)H2O, also known as Prussian white (PW), contains disordered and dynamic water molecules that have a dualistic effect on its battery performance. Furthermore, the material exhibits severe strain when dehydrated, which over time diminishes the performance. To understand the complex role of water on the sodium ion conduction and the structural changes happening upon dehydration, local structural characterization is needed. Here, we report the first neutron total scattering study of PW. Reverse Monte Carlo (RMC) fitting reveals that local octahedral distortion of the nitrogen-bound iron octahedra contributes to the disorder of the framework. The strain observed in the dehydrated material comes from a combination of the Fe–N bond elongation and a disordered distribution of sodium throughout the larger structure. In the hydrated material, the sodium exhibits more order due to the presence of water, which constrains the sodium movement. However, the sodium ordering affects the orientation of the water molecules. In the low temperature P21/n phase, sodium orders into planes with the oxygen atoms in the water molecules being in the plane, while the hydrogen atoms are pointing away from the sodium plane. In the room temperature R phase, the sodium and water are less ordered despite similar frameworks. Sodium can take a wide range of positions, especially if no water molecule blocks its way, to obtain optimal bonding conditions. These results show that the relationship between sodium and water is co-dependent, and demonstrate that the local structure of framework materials has a crucial link to their properties.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2025.
National Category
Materials Chemistry
Research subject
Chemistry with specialization in Materials Chemistry
Identifiers
URN: urn:nbn:se:uu:diva-565111DOI: 10.1039/D5TC03143EISI: 001631384900001OAI: oai:DiVA.org:uu-565111DiVA, id: diva2:1989298
Available from: 2025-08-15 Created: 2025-08-15 Last updated: 2026-02-03Bibliographically approved
In thesis
1. Water in Prussian blue analogues: A blessing or a curse?
Open this publication in new window or tab >>Water in Prussian blue analogues: A blessing or a curse?
2025 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Prussian blue analogues (PBAs), AxM[M’(CN)6]1–y·zG, are used in many different applications, such as energy storage, due to their tunable composition and structural diversity. To understand the material properties, it is important to accurately determine the composition and atomic structure of these materials. However, this is challenging due to the interdependent relationship between the three compositional parameters: the alkali cation (Ax), water (z), and [M’(CN)6]n– (y) vacancy content. Furthermore, the atomic structure depends on the composition, which leads to a rich structural landscape that further influences the material properties. This thesis presents a comprehensive strategy for characterizing the composition and atomic structure of iron- and sodium-based PBAs. To accurately determine the composition of iron-based PBAs, it was found that a combination of multiple characterization techniques is needed; especially Mössbauer spectroscopy proved vital for accurately determining the vacancy content. Neutron diffraction, neutron total scattering, quasi-elastic neutron scattering, and inelastic neutron scattering were applied to probe the local and average structures as well as the dynamics of the water in PBAs as a function of sodium content and temperature. It was found that the PBA system is more dynamic than previously thought, and that the sodium and water can occupy a broad range of positions, which change with temperature. The material becomes more disordered upon dehydration or when the sodium content is lowered. Additionally, distortions of the PBA framework proved to be an inherent property of these materials. This work also demonstrates that neutron diffraction alone is insufficient to describe sodium and water positions, confirming the need for local probes such as total scattering and inelastic neutron scattering. These findings highlight the importance of proper compositional, structural, and dynamical characterization using multiple techniques and lay the groundwork for further development of new PBAs.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2025. p. 63
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 2571
Keywords
Prussian blue analogues, neutron scattering, sodium-ion batteries, crystallography, spectroscopy, structural dynamics.
National Category
Materials Chemistry
Identifiers
urn:nbn:se:uu:diva-565121 (URN)978-91-513-2558-3 (ISBN)
Public defence
2025-10-03, Siegbahnsalen, Ångströmlaboratoriet, Regementsvägen 10, Uppsala, 09:15 (English)
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Available from: 2025-09-11 Created: 2025-08-15 Last updated: 2025-09-11

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Nielsen, IdaBrant, William R.

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