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- Blidberg, Andreas, 1987-, et al.
(författare)
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Electronic changes in poly(3,4-ethylenedioxythiophene)-coated LiFeSO4F during electrochemical lithium extraction
- 2019
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Ingår i: Journal of Power Sources. - : ELSEVIER SCIENCE BV. - 0378-7753 .- 1873-2755. ; 418, s. 84-89
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Tidskriftsartikel (refereegranskat)abstract
- The redox activity of tavorite LiFeSO4F coated with poly (3,4-ethylenedioxythiophene), i.e. PEDOT, is investigated by means of several spectroscopic techniques. The electronic changes and iron-ligand redox features of this LiFeSO4F-PEDOT composite are probed upon delithiation through X-ray absorption spectroscopy. The PEDOT coating, which is necessary here to obtain enough electrical conductivity for the electrochemical reactions of LiFeSO4F to occur, is electrochemically stable within the voltage window employed for cell cycling. Although the electronic configuration of PEDOT shows also some changes in correspondence of its reduced and oxidized forms after electrochemical conditioning in Li half-cells, its p-type doping is fully retained between 2.7 and 4.1 V with respect to Li+/Li during the first few cycles. An increased iron-ligand interaction is observed in LixFeSO4F during electrochemical lithium extraction, which appears to be a general trend for polyanionic insertion compounds. This finding is crucial for a deeper understanding of a series of oxidation phenomena in Li-ion battery cathode materials and helps paving the way to the exploration of new energy storage materials with improved electrochemical performances.
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- Blidberg, Andreas, 1987-, et al.
(författare)
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Identifying the Electrochemical Processes in LiFeSO4F Cathodes for Lithium Ion Batteries
- 2017
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Ingår i: ChemElectroChem. - : Wiley. - 2196-0216. ; 4:8, s. 1896-1907
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- The electrochemical performance of tavorite LiFeSO4F can be considerably improved by coating the material with a conducting polymer (poly(3,4-ethylenedioxythiophene); PEDOT). Herein, the mechanisms behind the improved performance are studied systematically by careful electrochemical analysis. It is shown that the PEDOT coating improves the surface reaction kinetics for the Li-ion insertion into LiFeSO4F. For such coated materials no kinetic limitations remain, and a transition from solid state to solution-based diffusion control was observed at 0.6 mA cm−2 (circa C/2). Additionally, the quantity of PEDOT is optimized to balance the weight added by the polymer and the improved electrochemical function. Post mortem analysis shows excellent stability for the LiFeSO4F-PEDOT composite, and maintaining the electronic wiring is the most important factor for stable electrochemical cycling of LiFeSO4F. The insights and the methodology used to determine the rate-controlling steps are readily transferable to other ion-insertion-based electrodes, and the findings are important for the development of improved battery electrodes.
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- Blidberg, Andreas, 1987-, et al.
(författare)
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Monitoring LixFeSO4F (x = 1, 0.5, 0) Phase Distributions in Operando To Determine Reaction Homogeneity in Porous Battery Electrodes
- 2017
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Ingår i: Chemistry of Materials. - : American Chemical Society. - 0897-4756 .- 1520-5002. ; 29:17, s. 7159-7169
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Tidskriftsartikel (refereegranskat)abstract
- Increasing the energy and power density simultaneously remains a major challenge for improving electrochemical energy storage devices such as Li-ion batteries. Understanding the underlying processes in operating electrodes is decisive to improve their performance. Here, an extension of an in operando X-ray diffraction technique is presented, wherein monitoring the degree of coexistence between crystalline phases in multiphase systems is used to investigate reaction homogeneity in Li-ion batteries. Thereby, a less complicated experimental setup using commercially available laboratory equipment could be employed. By making use of the intrinsic structural properties of tavorite type LiFeSO4F, a promising cathode material for Li-ion batteries, new insights into its nonequilibrium behavior are gained. Differences in the reaction mechanism upon charge and discharge are shown; the influence of adequate electronic wiring for the cycling stability is demonstrated, and the effect of solid state transport on rate performance is highlighted. The methodology is an alternative and complementary approach to the expensive and demanding techniques commonly employed for time-resolved studies of structural changes in operating battery electrodes. The multiphase behavior of LiFeSO4F is commonly observed for other insertion type electrode materials, making the methodology transferable to other new energy storage materials. By expanding the possibilities for investigating complex processes in operating batteries to a larger community, faster progress in both electrode development and fundamental material research can be realized.
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- Hedman, Jonas, et al.
(författare)
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Fiber Optic Monitoring of Composite Lithium Iron Phosphate Cathodes in Pouch Cell Batteries
- 2022
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Ingår i: ACS Applied Energy Materials. - : American Chemical Society (ACS). - 2574-0962. ; 5:1, s. 870-881
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Tidskriftsartikel (refereegranskat)abstract
- - Developing techniques for real-time monitoring of the complex and dynamic environment in lithium-ion batteries is crucial for optimal use of the cells and to develop the next generation of batteries. In this work, we demonstrate the use of fiber optic evanescent wave (FOEW) sensors for monitoring lithium iron phosphate (LFP) composite cathodes in pouch cells. The fiber optic sensors were placed on top of the LFP electrodes, and the pouch cells were found to cycle well with significantly improved electrochemical performance compared to fully embedded fibers in Swagelok cells. Galvanostatic, voltammetric, and pulsed current techniques demonstrated that the optical response correlated well with the capacity, and a clear difference in sensor response was seen when the sensors were placed at the surface of composite electrodes compared to fibers embedded in the cathode. The optical response from LFP at different rates was also investigated, but no apparent influence on intensity output was found even though polarization was observed in the voltage profiles at higher currents. It was also demonstrated that the electrolyte itself functioned as a fiber cladding and that the salt concentration in the electrolyte did not influence the optical signal. In addition, given the short penetration depth of the evanescent waves, the sensor response is most likely dominated by the surface conditions of electrode particles near the sensing region. These findings provide further insight into the application and performance of FOEW sensors integrated into batteries, as well as the possibility of developing low-cost fiber optic sensors for battery monitoring under working conditions.
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