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Unravelling the origin of capacity fade in Prussian white hard carbon full cells through operando X-ray diffraction
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.ORCID iD: 0000-0002-6511-8291
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.ORCID iD: 0000-0003-4399-2372
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.ORCID iD: 0000-0003-2538-8104
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2024 (English)In: Journal of Materials Chemistry A, ISSN 2050-7488, E-ISSN 2050-7496, Vol. 12, no 28, p. 17413-17421Article in journal (Refereed) Published
Abstract [en]

Prussian white (PW), Na2−xFe[Fe(CN)6], is an attractive cathode material for sodium-ion batteries due to its porous framework enabling fast sodium-ion extraction and insertion, environmentally safe elements, scalable synthesis, and performance comparable to current lithium-ion technologies. However, PW suffers from large volume changes between rhombohedral and cubic phases during cycling which is suggested to be detrimental over time because of structural degradation and increased ion insertion resistance. In particular, studies on PW hard carbon full cells revealed that most of the capacity is lost from the lower potential plateau, where this phase transition occurs. It is proposed that cycling in a restricted potential range, where the phase transition is avoided, could benefit the cycle lifetime and capacity retention. Here, we show an operando X-ray diffraction study aiming at determining how the structure evolves after prolonged cycling in different restricted potential ranges and how this impacts the cycling stability and capacity fade in PW. No signs of structural degradation were observed independently of the pre-cycling conditions used. In addition, more of the rhombohedral phase and capacity were recovered in the discharged state when a more restricted potential range had been applied. Thus, it was shown that the phase transition and corresponding volume changes have little impact on the capacity fade. Instead, the main source for capacity fade was proved to be sodium inventory loss, especially during the initial cycles, in combination with, to a lesser extent, polarization. This study gives a new perspective on PW-based batteries in that neither volume changes nor phase transitions are detrimental to battery performance. These results aid the development of improved cycling protocols and battery systems comprised of PW where the lifetime of the material is prolonged.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2024. Vol. 12, no 28, p. 17413-17421
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:uu:diva-540933DOI: 10.1039/d4ta02325kISI: 001249037900001OAI: oai:DiVA.org:uu-540933DiVA, id: diva2:1907857
Funder
Swedish Foundation for Strategic Research, GSn15-0008Swedish Research Council, 2018-07152Vinnova, 2018-04969Swedish Research Council Formas, 2019-02496Available from: 2024-10-23 Created: 2024-10-23 Last updated: 2025-08-15Bibliographically 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, IdaHall, Charles AramMattsson, Agnes-MatildaYounesi, RezaEk, GustavBrant, William

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