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On the compatibility of high mass loading bismuth anodes for full-cell sodium-ion batteries
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.
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: 0000-0003-2538-8104
2022 (English)In: Dalton Transactions, ISSN 1477-9226, E-ISSN 1477-9234, Vol. 51, no 44, p. 16852-16860Article in journal (Refereed) Published
Abstract [en]

Metallic bismuth is here studied as an anode material for sodium-ion batteries. The details of electrochemical redox reactions, rate performance and cycled life were investigated using relatively high mass loading electrodes in two- and three-electrode full-cells. It demonstrated that the rate capability of bismuth anodes with high mass loading are not as good as indicated in previous literatures where low mass loading electrodes were used. It also indicated that the resistances causing a faltering rate performance may be connected to a loss in particle contact during desodiation. Efforts were also made to study the different electrochemical processes that occur during early cycles. Less advantageous characteristics of bismuth electrodes are also discussed. For example, several different electrolyte solutions were tested for compatibility with the bismuth system, where only glyme-based solutions seemed to facilitate robust cycling.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2022. Vol. 51, no 44, p. 16852-16860
National Category
Inorganic Chemistry
Identifiers
URN: urn:nbn:se:uu:diva-490289DOI: 10.1039/d2dt02686dISI: 000874768700001PubMedID: 36305380OAI: oai:DiVA.org:uu-490289DiVA, id: diva2:1717475
Funder
Swedish Energy Agency, 48198-1StandUp, 20-675EU, Horizon 2020, 963542Available from: 2022-12-08 Created: 2022-12-08 Last updated: 2024-06-25Bibliographically approved
In thesis
1. Developing Electrolyte Solutions for Sodium-Ion Batteries: Challenging the Use of Hexafluorophosphate
Open this publication in new window or tab >>Developing Electrolyte Solutions for Sodium-Ion Batteries: Challenging the Use of Hexafluorophosphate
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The ability to store energy will be critical for achieving a functioning electrified society largely based on renewable energy sources. Batteries are anticipated to be a vital part of the infrastructure required to facilitate this energy storage. Electrolyte solutions are an essential component of most batteries, including sodium-ion batteries, which are emerging as a potentially more sustainable alternative to lithium-ion batteries.

This thesis critically assesses the use of sodium hexafluorophosphate as an electrolyte in sodium-ion batteries. Although widely used in lithium-ion batteries, the suitability of hexafluorophosphate for sodium-ion batteries needs re-evaluation. In this thesis, properties meriting the use of sodium hexafluorophosphate are explored, including its solubility in different organic solvents, conductivity, ability to prevent anodic aluminium dissolution, and cycling performance in battery cells. Sodium bis(oxalato)borate is investigated as an example of a fluorine-free alternative that may better align with the goal of increasing the sustainability of contemporary batteries. The main drawback of sodium bis(oxalato)borate is its significantly lower solubility compared to sodium hexafluorophosphate. However, at the same concentration in a given solvent, both electrolytes exhibit similar conductivities, challenging the notion that hexafluorophosphate enhances conductivity through low ion association.

Both electrolytes also prevent anodic aluminium dissolution. However, the use of sodium hexafluorophosphate does not consistently ensure adequate passivation of the negative electrode, suggesting that solvents or additives are more central for this process in these systems. In contrast, sodium bis(oxalato)borate appear to significantly contribute to the passivation of the negative electrode, even when used as an additive. As a sole electrolyte, sodium bis(oxalato)borate enable promising cycling performance in both lab-scale cells and in cells close to commercial standards. This research indicates that sodium hexafluorophosphate can be replaced with a fluorine-free electrolyte without compromising battery performance. The findings highlight the potential for more sustainable sodium-ion batteries and represent a step towards reducing the environmental impact of an electrified society.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2024. p. 54
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 2417
National Category
Materials Chemistry
Research subject
Chemistry with specialization in Materials Chemistry; Chemistry with specialization in Materials Chemistry
Identifiers
urn:nbn:se:uu:diva-533190 (URN)978-91-513-2169-1 (ISBN)
Public defence
2024-09-06, Lecture hall Heinz-Otto Kreiss, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 09:15 (English)
Opponent
Supervisors
Available from: 2024-08-13 Created: 2024-06-25 Last updated: 2024-08-13

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Colbin, Lars Olow SimonYounesi, Reza

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