| 1. |
- Fretz, Samuel Joseph, 1987, et al.
(författare)
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Amine- and Amide-Functionalized Mesoporous Carbons: A Strategy for Improving Sulfur/Host Interactions in Li-S Batteries
- 2020
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Ingår i: Batteries and Supercaps. - : Wiley. - 2566-6223. ; 3:8, s. 757-765
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Tidskriftsartikel (refereegranskat)abstract
- Lithium-sulfur (Li-S) batteries are of great interest due to their potentially high energy density, but the low electronic conductivity of both the sulfur (S-8) cathode active material and the final discharge product lithium sulfide (Li2S) require the use of a conductive host. Usually made of relatively hydrophobic carbon, such hosts are typically ill-suited to retain polar discharge products such as the intermediate lithium polysulfides (LiPs) and the final Li2S. Herein, we propose a route to increase the sulfur utilization by functionalizing the surface of ordered mesoporous carbon CMK3 with polar groups. These derivatized CMK3 materials are made using a simple two-step procedure of bromomethylation and subsequent nucleophilic substitution with amine or amide nucleophiles. We demonstrate that, compared to the unfunctionalized control, these modified CMK3 surfaces have considerably larger binding energies with LiPs and Li2S, which are proposed to aid the electrochemical conversion between S-8 and Li2S by keeping the LiPs species in close proximity to the carbon surface during Li-S battery cycling. As a result, the functionalized cathodes exhibit significantly improved specific capacities relative to their unmodified precursor.
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| 2. |
- Lindberg, Simon, 1985, et al.
(författare)
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A VO2 based hybrid super-capacitor utilizing a highly concentrated aqueous electrolyte for increased potential window and capacity
- 2020
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Ingår i: Electrochimica Acta. - : Elsevier BV. - 0013-4686. ; 345
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Tidskriftsartikel (refereegranskat)abstract
- In this work we demonstrate the application of a highly concentrated aqueous electrolyte to a hybrid supercapacitor cell. We combine an 8 m Sodium bis(trifluoromethanesulfonyl)imide (NaTFSI) aqueous electrolyte with a nanostructured VO2-cathode to enhance the voltage widow up to 2.4 V in a full cell. With the enhanced potential window, we are able to exploit the full contribution of the VO2 material, where a part is outside the stability window of standard alkaline aqueous electrolytes. We show that the VO2 material in the highly concentrated electrolyte provides a faradaic contribution even at the highest current density (25 A/g) and in this way increases the energy content also in high power conditions. The full cell shows a good efficiency but also a capacity fade over 500 cycles (39%) which is most likely related to dissolution of VO2.
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| 3. |
- Lindberg, Simon, 1987, et al.
(författare)
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Charge storage mechanism of α-MnO2 in protic and aprotic ionic liquid electrolytes
- 2020
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Ingår i: Journal of Power Sources. - : Elsevier BV. - 0378-7753 .- 1873-2755. ; 460
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Tidskriftsartikel (refereegranskat)abstract
- In this work we have investigated the charge storage mechanism of MnO2 electrodes in ionic liquid electrolytes. We show that by using an ionic liquid with a cation that has the ability to form hydrogen bonds with the active material (MnO2) on the surface of the electrode, a clear faradaic contribution is obtained. This situation is found for ionic liquids with cations that have a low pKa, i.e. protic ionic liquids. For a protic ionic liquid, the specific capacity at low scan rate rates can be explained by a densely packed layer of cations that are in a standing geometry, with a proton directly interacting through a hydrogen bond with the surface of the active material in the electrode. In contrast, for aprotic ionic liquids there is no interaction and only a double layer contribution to the charge storage is observed. However, by adding an alkali salt to the aprotic ionic liquid, a faradaic contribution is obtained from the insertion of Li+ into the surface of the MnO2 electrode. No effect can be observed when Li+ is added to the protic IL, suggesting that a densely packed cation layer in this case prevent Li-ions from reaching the active material surface.
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| 4. |
- Lindberg, Simon, 1985, et al.
(författare)
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Electrochemical Behaviour of Nb-Doped Anatase TiO2 Microbeads in an Ionic Liquid Electrolyte
- 2020
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Ingår i: Batteries and Supercaps. - : Wiley. - 2566-6223. ; 3:11, s. 1233-1238
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Tidskriftsartikel (refereegranskat)abstract
- TiO(2)is a promising material for high-power battery and supercapacitor applications. However, in general TiO(2)suffers from an initial irreversible capacity that limits its use in different applications. A combination of a microbead morphology, Nb-doping, and the use of an ionic liquid electrolyte is shown to significantly decrease the irreversible capacity loss. A change in the electrochemical response in the first cycles indicates formation of a solid-electrolyte interphase (SEI) or a modification of the structure of the surface layer of the TiO2/Nb microbeads, which apparently stabilises the performance. The change in the response is manifested in an increased charge transfer resistance and the presence of two charge transfer contributions. During prolonged cycling the TiO2/Nb electrode shows an excellent stability over 5000 cycles. Ex situ analysis after cycling shows that the overall microbead morphology is intact and that there are no changes in the crystal structure. However, a decrease in the intensity of the XRD pattern can point to a decrease in size of the nanocrystals building up the microbeads or the formation of amorphous phases.
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