| 1. |
- Bitenc, Jan, et al.
(author)
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Concept and electrochemical mechanism of an Al metal anode - organic cathode battery
- 2020
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In: Energy Storage Materials. - : Elsevier BV. - 2405-8297 .- 2405-8289. ; 24, s. 379-383
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Journal article (peer-reviewed)abstract
- Aluminum (Al) batteries are fundamentally a promising future post-Li battery technology. The recently demonstrated concept of an Al-graphite battery represents some significant progress for the technology, but the cell energy density is still very modest and limited by the quantity of the AlCl3 based electrolyte, as it relies on AlCl4- intercalation. For further progress, cathode materials capable of an electrochemical reaction with Al positively charged species are needed. Here such a concept of an Al metal anode - organic cathode battery based on anthraquinone (AQ) electrochemistry with a discharge voltage of 1.1 V is demonstrated. Further improvement of both the cell capacity retention and rate capability is achieved by nano-structured and polymerized cathodes. The intricate electrochemical mechanism is proven to be that the anthraquinone groups undergo reduction of their carbonyl bonds during discharge and become coordinated by AlCl2+ species. Altogether the Al metal anode - AQ cathode cell has almost the double energy density of the state-of-the-art Al-graphite battery.
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| 2. |
- Jonsson, Erlendur, 1983
(author)
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Ionic liquids as electrolytes for energy storage applications – A modelling perspective
- 2020
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In: Energy Storage Materials. - : Elsevier BV. - 2405-8297. ; 25, s. 827-835
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Research review (peer-reviewed)abstract
- Ionic liquids as electrolytes for energy storage devices is a promising field. Here, the various approaches of how ionic liquids can be modelled are discussed along with how the modelling connects to experimental results. Recent theoretical developments are highlighted along with extended discussion of what molecular dynamics simulation options are now available and what key results can be extracted. Ab initio work is also discussed, this includes some of the spectral properties, both of ionic liquids and their electrolyte formulations.
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| 3. |
- Liu, Yangyang, et al.
(author)
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Promoted rate and cycling capability of Li–S batteries enabled by targeted selection of co-solvent for the electrolyte
- 2020
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In: Energy Storage Materials. - : Elsevier BV. - 2405-8297. ; 25, s. 131-136
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Journal article (peer-reviewed)abstract
- Lithium sulfur (Li–S) batteries are considered as promising candidates for high-energy-density battery systems owing to the high theoretical capacity of sulfur (1675 mAh g−1) and low cost of raw materials. However, their practical application is hampered by low rate capability and rapid degradation of capacity, arising from the passivation of the cathode by lithium sulfides (Li2S2/Li2S) deposited during discharge and low interfacial stability of the Li anode. Herein, we report on a comprehensive strategy to select co-solvent to the electrolyte to regulate the deposition of lithium sulfides during charge-discharge process. We show that addition of a co-solvent with high solubility, and strong interaction with Li2S to a conventional electrolyte effectively mitigates the formation of a passivating layer on the sulfur cathode and dramatically improves the interfacial stability of the Li anode. We demonstrate that Sulfolane (SL) has these properties and that a Li–S cell with an electrolyte containing 6 vol% SL exhibits outstanding cyclic performance (0.083% decay per cycle) and rate capability (capacity density of 765 mAh g−1 at rate of 1.0C). Thus, we provide a facile strategy for the selection of co-solvent for improved performance of Li–S batteries, realizing their practical application for high-energy-density battery systems.
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| 4. |
- Zhao, Peiyu, et al.
(author)
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Stable lithium metal anode enabled by high-dimensional lithium deposition through a functional organic substrate
- 2020
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In: Energy Storage Materials. - : Elsevier BV. - 2405-8297. ; 33, s. 158-163
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Journal article (peer-reviewed)abstract
- The growth of lithium dendrites severely restricts the development of lithium metal batteries. In order to achieve the goal of dendrites-free lithium in principle, it is crucial and urgent to control nucleation and growth of lithium. Here, a functional organic layer of perylene-3, 4, 9, 10-tetracarboxydiimide-lithium (PTCDI-Li) is built on the lithium anode surface by in-situ chemical reaction of PTCDI and Li metal. PTCDI-Li, with high surface energy (-10.19 eV) and low diffusion barrier (0.89 eV), efficiently promotes disk-shaped high-dimensional nucleation by regulation of lithium ion flux upon lithium plating, leading to a dendrites-free morphology. When operating under a relatively high current density of 10 mA cm−2, the Li | Li symmetrical cells with PTCDI-Li exhibit outstanding cyclic stability for 300 hours with ultralow overpotential of 400 mV, superior to the most of the reported lithium anode. The corresponding PTCDI-Li batteries show high specific capacity and enhanced cycle life. We anticipate that this strategy of regulation of lithium deposition from one-dimensional to high-dimensional opens a new horizon in the development of dendrites-free Li anodes.
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