| 1. |
- Blidberg, Andreas, 1987-, et al.
(författare)
-
Electronic changes in poly(3,4-ethylenedioxythiophene)-coated LiFeSO4F during electrochemical lithium extraction
- 2019
-
Ingår i: Journal of Power Sources. - : ELSEVIER SCIENCE BV. - 0378-7753 .- 1873-2755. ; 418, s. 84-89
-
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.
|
|
| 2. |
- Blidberg, Andreas, 1987-, et al.
(författare)
-
Identifying the Electrochemical Processes in LiFeSO4F Cathodes for Lithium Ion Batteries
- 2017
-
Ingår i: ChemElectroChem. - : Wiley. - 2196-0216. ; 4:8, s. 1896-1907
-
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.
|
|
| 3. |
- Blidberg, Andreas, 1987-, et al.
(författare)
-
Monitoring LixFeSO4F (x = 1, 0.5, 0) Phase Distributions in Operando To Determine Reaction Homogeneity in Porous Battery Electrodes
- 2017
-
Ingår i: Chemistry of Materials. - : American Chemical Society. - 0897-4756 .- 1520-5002. ; 29:17, s. 7159-7169
-
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.
|
|
| 4. |
|
|
| 5. |
|
|
| 6. |
- JOHANSSON, DAVID, et al.
(författare)
-
Nanoplasmonic sensing of Pb-acid and Li-ion batteries
- 2016
-
Ingår i: Presented at the 2nd International Conference on Sensors and Electronic Instrumental Advances (SEIA), Barcelona, Spain, September 22 – 23, 2016. - : INT FREQUENCY SENSOR ASSOC-IFSA. ; , s. 57-59, s. 57-59
-
Konferensbidrag (refereegranskat)abstract
- The increasing sophistication and performance of batteries are connected with more complex chemical and physical battery processes and increase the need of more direct and informative measurements, both in the R&D phase and for monitoring and control during operation of vehicles. Todays potentiometric based measurement sensors are not sufficiently accurate for optimal battery sensing. To avoid the built in wide safety margins new, more informative monitoring signals are therefore desired or needed. In this study the optical technology NanoPlasmonic Sensing (NPS) has been used to in-situ monitor the charge and discharge processes of lead-acid and Li-ion batteries. The optical signals were found to correlate well with charging/discharging of both battery technologies.
|
|
