| 1. |
- Calcagno, Giulio, 1990, et al.
(författare)
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Fast charging negative electrodes based on anatase titanium dioxide beads for highly stable Li-ion capacitors
- 2020
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Ingår i: Materials Today Energy. - : Elsevier BV. - 2468-6069. ; 16
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Tidskriftsartikel (refereegranskat)abstract
- Hybrid energy storage systems aim to achieve both high power and energy densities by combining supercapacitor-type and battery-type electrodes in tandem. The challenge is to find sustainable materials as fast charging negative electrodes, which are characterized by high capacity retention. In this study, mesoporous anatase beads are synthetized with tailored morphology to exploit fast surface redox reactions. The TiO2-based electrodes are properly paired with a commercial activated carbon cathode to form a Li-ion capacitor. The titania electrode exhibits high capacity and rate performance. The device shows extremely stable performance with an energy density of 27 mWh g-1 at a specific current of 2.5 A g−1 for 10,000 cycles. The remarkable stability is associated with a gradual shift of the potential during cycling as result of the formation of cubic LiTiO2 on the surface of the beads. This phenomenon renews the interest in using TiO2 as negative electrode for Li-ion capacitors.
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| 2. |
- Vavra, Szilvia, 1990, et al.
(författare)
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An imidazolium ionic liquid as effective structure-directing agent for the fabrication of silica thin films with vertically aligned nanochannels
- 2020
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Ingår i: Microporous and Mesoporous Materials. - : Elsevier BV. - 1387-1811. ; In Press
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Tidskriftsartikel (refereegranskat)abstract
- In parallel to the increasing variety of ionic liquids that show different kinds of nanometer-scale structuration in their pure and solved forms, there is a raising interest in exploring the possibility of using ionic liquids as soft-templates for the synthesis of mesoporous materials. We report the case of 1-hexadecyl-3-methylimidazolium chloride (C16MIMCl), a surface active ionic liquid (SAIL), here used as an excellent soft-template for the formation of vertically aligned, uniform mesochannels, with a well defined pore width of 2.5 nm in silica thin films deposited with the electrochemically assisted self-assembly (EASA) method. The obtained mesochannels run through the entire thickness of the films and after removal of the ionic liquid the emptied mesochannels ensure a thorough mass transport to the substrate, here monitored by the redox-active electrochemical probe Ru(II)/Ru(III) during cyclic voltammetry (CV). Moreover, the mechanism of pore formation is explained; unlike the mechanisms reported for short chain imidazolium ionic liquid silica templates, in the case of C16MIMCl the dominating so-called cooperative interaction is the electrostatic attraction between the C16MIM+ and the network-forming negatively charged silicate oligomers. Therefore, this study provides a better understanding of the templating behavior of long chain imidazolium ionic liquids and motivates further research on the synthesis of ionic liquid-based functional hybrid materials.
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| 3. |
- Örn Simonarson, Gunnar, 1986, et al.
(författare)
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Electrochemical and structural characterization of lithiation in spray deposited ordered mesoporous titania as an anode for Li ion batteries
- 2020
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Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 10:34, s. 20279-20287
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Tidskriftsartikel (refereegranskat)abstract
- Ordered mesoporous titania, preparedvialow-temperature spray deposition, was examined as an anode material for lithium ion batteries. The material exhibits an exceptionally high electrochemical capacity of 680 mA h g-1during the first discharge, which rapidly decreases over the following cycles. The capacity stabilizes at around 170 mA h g-1after 50 cycles and the material delivers 83 mA h g-1at high charge/discharge rates (10C). A combination of electrochemical and structural characterization techniques were used to study the charge/discharge behavior of the material and the origin of the irreversible capacity. To determine the effect of cycling on the structure of the material, X-ray absorption spectroscopy (XAS) and energy filtered TEM were carried out on pristine and cycled samples in intercalated and deintercalated states. Titanium K-edge XAS measurements showed that intercalated lithium affects the NEXAFS region. By comparing peak intensity ratios, we propose a method to quantify the amount of lithium inserted into the titania structure and to differentiate between lithium bound in close proximity to titanium, and lithium bound further away from titanium. Additionally, we suggest that the irreversible loss in capacity is due to the formation of phases that are stable, and thereby electrochemically inactive, over the electrochemical cycling conditions applied.
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