| 1. |
- Karlsson, Christoffer, et al.
(författare)
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Stable Deep Doping of Vapor-Phase Polymerized Poly(3,4-ethylenedioxythiophene)/Ionic Liquid Supercapacitors.
- 2016
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Ingår i: ChemSusChem. - : Wiley. - 1864-5631 .- 1864-564X. ; 9:16, s. 2112-2121
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Tidskriftsartikel (refereegranskat)abstract
- Liquid-solution polymerization and vapor-phase polymerization (VPP) have been used to manufacture a series of chloride- and tosylate-doped poly(3,4-ethylenedioxythiophene) (PEDOT) carbon paper electrodes. The electrochemistry, specific capacitance, and specific charge were determined for single electrodes in 1-ethyl-3-methylimidazolium dicyanamide (emim dca) ionic liquid electrolyte. VPP-PEDOT exhibits outstanding properties with a specific capacitance higher than 300 F g(-1) , the highest value reported for a PEDOT-based conducting polymer, and doping levels as high as 0.7 charges per monomer were achieved. Furthermore, symmetric PEDOT supercapacitor cells with the emim dca electrolyte exhibited a high specific capacitance (76.4 F g(-1) ) and high specific energy (19.8 Wh kg(-1) ). A Ragone plot shows that the VPP-PEDOT cells combine the high specific power of conventional ("pure") capacitors with the high specific energy of batteries, a highly sought-after target for energy storage.
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| 2. |
- Berthomier, M., et al.
(författare)
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Alfven : magnetosphere-ionosphere connection explorers
- 2012
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Ingår i: Experimental astronomy. - Dordrecht : Springer. - 0922-6435 .- 1572-9508. ; 33:2-3, s. 445-489
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Tidskriftsartikel (refereegranskat)abstract
- The aurorae are dynamic, luminous displays that grace the night skies of Earth's high latitude regions. The solar wind emanating from the Sun is their ultimate energy source, but the chain of plasma physical processes leading to auroral displays is complex. The special conditions at the interface between the solar wind-driven magnetosphere and the ionospheric environment at the top of Earth's atmosphere play a central role. In this Auroral Acceleration Region (AAR) persistent electric fields directed along the magnetic field accelerate magnetospheric electrons to the high energies needed to excite luminosity when they hit the atmosphere. The "ideal magnetohydrodynamics" description of space plasmas which is useful in much of the magnetosphere cannot be used to understand the AAR. The AAR has been studied by a small number of single spacecraft missions which revealed an environment rich in wave-particle interactions, plasma turbulence, and nonlinear acceleration processes, acting on a variety of spatio-temporal scales. The pioneering 4-spacecraft Cluster magnetospheric research mission is now fortuitously visiting the AAR, but its particle instruments are too slow to allow resolve many of the key plasma physics phenomena. The Alfv,n concept is designed specifically to take the next step in studying the aurora, by making the crucial high-time resolution, multi-scale measurements in the AAR, needed to address the key science questions of auroral plasma physics. The new knowledge that the mission will produce will find application in studies of the Sun, the processes that accelerate the solar wind and that produce aurora on other planets.
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| 3. |
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| 4. |
- De Spiegeleer, Alexandre, 1990-
(författare)
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There and back again... An Earth magneto-tale : understanding plasma flows in the magnetotail
- 2020
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- On average, the Earth's magnetotail plasma sheet seems to be a calm region of the magnetosphere where the plasma moves slowly towards Earth. However, the plasma sheet actually hosts many phenomena, some of which can affect Earth. For example, high-speed flows of plasma with speed larger than 400 km/s are observed in the plasma sheet and they can lead to aurorae. Such dynamical phenomena and the impact they may have on Earth naturally makes the plasma sheet an important region of study. Even though these high-speed flows can affect Earth, they are observed less than 5% of the time, meaning that most of the time, other disturbances take place in the plasma sheet. Our aim is to investigate and better understand the plasma dynamics in the plasma sheet.The plasma above and below the cross-tail current sheet was previously thought to convect in the same direction. However, we find that under clearly non-zero Interplanetary Magnetic Field (IMF)By (dawn-dusk component), the plasma has a tendency to convect in opposite dawn-dusk direction across the current sheet near the midnight sector depending on the sign of IMF By.The high-speed plasma flows are known to be associated with an increase of the northward component of the magnetic field as they propagate toward Earth. Using simulations, we notice that the magnetic field lines are bent by the high-speed flows and dents can appear. The deformation of the magnetic field is such that it may be directed towards the tail above the cross-tail current sheet and towards the Earth below it. This is opposite to the expected orientation of the magnetic field thus making this feature important in order to properly identify the region in which a spacecraft is located.At times, the plasma can be seen to move back and forth in an oscillatory manner. We investigate statistically such oscillatory behaviour and compare them to high-speed flows and to time periods when the plasma is calm. These oscillatory flows are observed about 8% of the time in the plasma sheet. They typically have a frequency of about 1.7 mHz (~10 min period) and usually last about 41 min.Some oscillations of the plasma velocity are observed along the magnetic field. The particles measured by the satellite initially have a velocity parallel to the magnetic field and towards Earth. Gradually with time, the measured velocity of the particles turns around to first become more perpendicular to the magnetic field and then be along the magnetic field but away from Earth. These signatures are interpreted simply as being due to mirroring particles injected tailward of the satellite and move toward Earth. The particles are then reflected, and move away from Earth. We investigate the general features of such oscillations along the magnetic field and find that the source of the particles is typically located less than 25 RE (Earth's radii) tailward of the satellite.
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| 5. |
- Every, Hayley A, et al.
(författare)
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Room temperature fast-ion conduction in imidazolium halide salts
- 2001
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Ingår i: Journal of Materials Chemistry Articles. - : Royal Society of Chemistry (RSC). - 0959-9428 .- 1364-5501. ; 11:3031-6
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Tidskriftsartikel (refereegranskat)abstract
- Fast-ion conduction has been observed in the iodide and bromide salts of 1-methyl-3-ethylimidazolium at ambient temperatures. The melting point of these two compounds is above 350 K and even at 273 K the ionic conductivity in the solid-state is greater than 10–3S cm–1. Cation diffusion coefficients have been measured using fringe field gradient and/or pulse field gradient 1H NMR techniques, which indicated cation diffusion coefficients of the order of 10–10 m2 s–1 in the solid-state. Remarkably, these values are up to an order of magnitude higher than the cation diffusion coefficient in the supercooled liquid at 293 K. The activation energy for diffusion in the solid-state is extremely small, as is typical of solid-state fast-ion conductors and indicates a change in transport mechanism from the melt to the crystal. The inability to detect an 127I signal together with the modelling of the conductivity using the Nernst–Einstein equation suggests that the solid-state conduction is primarily due to cation diffusion. The solid-state fast-ion conduction is most likely related to vacancy diffusion along the cation layers in the crystal. The temperature dependence of the NMR signal intensity indicates that the number of mobile species is increasing with increasing temperature with an activation energy of approximately 20–30 kJ mol–1.
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| 6. |
- Ferry, Anders, et al.
(författare)
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Connectivity, ionic interactions, and migration in a fast-ion-conducting polymer-in-salt electrolyte based on poly(acrylonitrile) and LiCF3SO3
- 1999
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Ingår i: Journal of Applied Physics. - : American Institute of Physics (AIP). - 0021-8979 .- 1089-7550. ; 86:4, s. 2346-2348
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Tidskriftsartikel (refereegranskat)abstract
- The ionic conductivity of a polymeric fast-ion-conductor based on LiCF3SO3 salt and poly(acrylonitrile), [CH2CH(CN)]n), is enhanced by ∼5 orders of magnitude when the composition approaches the "polymer-in-salt" regime; i.e., when the salt content increases from N:Li=12:1 to 1.2:1 (or ∼70 wt % of salt). This is in contrast to common salt-in-polymer electrolytes where a conductivity maximum typically is encountered at intermediate compositions. We suggest that connectivity effects in a microscopically phase segregated material may influence the long-range migration of charge carriers. Conductivity data are augmented with Raman spectroscopic investigations, thus probing microscopic details regarding the state of the dissolved salt.
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| 7. |
- Ferry, Anders, et al.
(författare)
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NMR and Raman studies of a novel fast-ion-conducting polymer-in-salt electrolyte based on LiCF3SO3 and PAN
- 2000
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Ingår i: Electrochimica Acta. - : Elsevier. - 0013-4686 .- 1873-3859. ; 45:8-9, s. 1237-1242
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Tidskriftsartikel (refereegranskat)abstract
- We report spectroscopic results from investigations of a novel solid polymeric fast-ion-conductor based on poly(acrylonitrile), (PAN, of repeat unit [CH2CH(CN)]n), and the salt LiCF3SO3. From NMR studies of the temperature and concentration dependencies of 7Li- and 1H-NMR linewidths, we conclude that significant ionic motion occurs at temperatures close to the glass transition temperature of these polymer-in-salt electrolytes, in accordance with a recent report on the ionic conductivity. In the dilute salt-in-polymer regime, however, ionic motion appears mainly to be confined to local salt-rich domains, as determined from the dramatic composition dependence of the ionic conductivity. FT-Raman spectroscopy is used to directly probe the local chemical anionic environment, as well as the Li+-PAN interaction. The characteristic δs(CF3) mode of the CF3SO3- anion at ∼ 750-780 cm-1 shows that the ionic substructure is highly complex. Notably, no spectroscopic evidence of free anions is found even at relatively salt-depleted compositions (e.g. N:Li ∼ 60-10:1). A strong Li+-PAN interaction is manifested as a pronounced shift of the characteristic polymer C=N stretching mode, found at ∼2244 cm-1 in pure PAN, to ∼ 2275 cm-1 for Li+-coordinated C=N moieties. Our proton-NMR data suggest that upon complexation of PAN with LiCF3SO3, the glass transition occurs at progressively lower temperatures.
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| 8. |
- Garcia-Quintana, Laura, et al.
(författare)
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Stabilisation of the superoxide anion in bis(fluorosulfonyl)imide (FSI) ionic liquid by small chain length phosphonium cations: Voltammetric, DFT modelling and spectroscopic perspectives
- 2021
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Ingår i: Electrochemistry Communications. - : Elsevier BV. - 1388-2481. ; 127
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Tidskriftsartikel (refereegranskat)abstract
- Ionic liquids (ILs) containing the bis(fluorosulfonyl)imide anion, FSI, have been investigated as electrolytes for metal-air batteries. Full chemical reversibility is found for the reduction of oxygen to superoxide at 60 degrees C under short time scale conditions of cyclic voltammetry at a glassy carbon electrode when the IL contains the small chain length triisobutyl(methyl)phosphonium rather than a pyrrolidinium cation. DFT calculations suggest that this is a consequence of the higher ion pair association energy and shorter intermolecular distance associated with the interaction of the superoxide anion with the phosphonium cation. Stabilization on longer timescales was also established by spectroscopic techniques when the phosphonium based ILs were exposed to KO2. Studies on superoxide stability in related ionic liquids containing the triisobutyl(methyl)phosphonium cation with the fluorosulfonyl(trifluoromethanesulfonyl)imide, FTFSI, or bis(trifluoromethanesulfonyl)imide, TFSI, anions are also reported.Y
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| 9. |
- Li, Hua, et al.
(författare)
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Addition of low concentrations of an ionic liquid to a base oil reduces friction over multiple length scales : a combined nano- and macrotribology investigation
- 2016
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Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry. - 1463-9076 .- 1463-9084. ; 18:9, s. 6541-6547
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Tidskriftsartikel (refereegranskat)abstract
- The efficacy of ionic liquids (ILs) as lubricant additives to a model base oil has been probed at the nanoscale and macroscale as a function of IL concentration using the same materials. Silica surfaces lubricated with mixtures of the IL trihexyl(tetradecyl) phosphonium bis(2,4,4-trimethylpentyl)phosphinate and hexadecane are probed using atomic force microscopy (AFM) (nanoscale) and ball-on-disc tribometer (macroscale). At both length scales the pure IL is a much more effective lubricant than hexadecane. At the nanoscale, 2.0 mol% IL (and above) in hexadecane lubricates the silica as well as the pure IL due to the formation of a robust IL boundary layer that separates the sliding surfaces. At the macroscale the lubrication is highly load dependent; at low loads all the mixtures lubricate as effectively as the pure IL, whereas at higher loads rather high concentrations are required to provide IL like lubrication. Wear is also pronounced at high loads, for all cases except the pure IL, and a tribofilm is formed. Together, the nano- and macroscales results reveal that the IL is an effective lubricant additive - it reduces friction - in both the boundary regime at the nanoscale and mixed regime at the macroscale.
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| 10. |
- Li, Hua, et al.
(författare)
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Ionic Liquid Adsorption and Nanotribology at the Silica-Oil Interface : Hundred-Fold Dilution in Oil Lubricates as Effectively as the Pure Ionic Liquid
- 2014
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Ingår i: The Journal of Physical Chemistry Letters. - : American Chemical Society (ACS). - 1948-7185. ; 5:23, s. 4095-4099
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Tidskriftsartikel (refereegranskat)abstract
- The remarkable physical properties of ionic liquids (ILs) make them potentially excellent lubricants. One of the challenges for using ILs as lubricants is their high cost. In this article, atomic force microscopy (AFM) nanotribology measurements reveal that a 1 mol % solution of IL dissolved in an oil lubricates the silica surface as effectively as the pure IL. The adsorption isotherm shows that the IL surface excess need only be approximately half of the saturation value to prevent surface contact and effectively lubricate the sliding surfaces. Using Its in this way makes them viable for large-scale applications.
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| 11. |
- Makhlooghiazad, Faezeh, et al.
(författare)
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Electrolytes for sodium batteries
- 2021
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Ingår i: Na-ion Batteries. - : Wiley. ; , s. 205-241
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Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
- This chapter presents an overview of different liquid and solid electrolytes employed for sodium batteries. It covers the basics in more depth and discusses the current status of ionic liquid (IL)-based electrolytes. The chapter outlines the challenges that remain to be solved to enable the realization of sodium batteries based on such electrolytes. Organic liquid electrolytes for sodium batteries typically consist of one or more sodium salts dissolved in one or more organic solvents. Organic ionic plastic crystals, the solid-state analogues of ILs, are emerging solid-state electrolytes that have advantageous properties, similar to ILs. ILs-based electrolytes present some unique properties that endows significant safety enhancements in comparison with conventional organic solvents, mostly related to higher decomposition temperatures. The IL-based electrolytes must also show an economic viability in comparison with conventional organic liquid electrolytes.
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| 12. |
- Nakamura, R., et al.
(författare)
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Low- altitude electron acceleration due to multiple flow bursts in themagnetotail
- 2014
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Ingår i: Geophysical Research Letters. - 0094-8276 .- 1944-8007. ; 41:3, s. 777-784
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Tidskriftsartikel (refereegranskat)abstract
- At 10:00 UT on 25 February 2008, Cluster 1 spacecraft crossed the near-midnight auroral zone, at about 2R(E) altitude, while two of the Time History of Events and Macroscale Interactions During Substorms (THEMIS) spacecraft, THD and THE, observed multiple flow bursts on the near-conjugate plasma sheet field lines. The flow shear pattern at THEMIS was consistent with the vortical motion at duskside of a localized flow channel. Coinciding in time with the flow bursts, Cluster 1 observed bursts of counterstreaming electrons with mostly low energies (441eV), accompanied by short time scale (<5s) magnetic field disturbances embedded in flow-associated field-aligned current systems. This conjugate event not only confirms the idea that the plasma sheet flows are the driver of the kinetic Alfven waves accelerating the low-energy electrons but is a unique observation of disturbances in the high-altitude auroral region relevant to the multiple plasma sheet flows. Key Points First observation of multiple flow signatures on near-conjugate flux tubes Low-energy electron profile suggests Alfvenic acceleration due to fast flow Multiple flow bursts are obtained to extend over large radial distance in tail
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| 13. |
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| 14. |
- Shah, Faiz Ullah, et al.
(författare)
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Halogen-free chelated orthoborate ionic liquids and organic ionic plastic crystals
- 2012
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Ingår i: Journal of Materials Chemistry. - 0959-9428 .- 1364-5501. ; 22:14, s. 6928-6938
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Tidskriftsartikel (refereegranskat)abstract
- Five halogen-free orthoborate salts comprised of three different cations (cholinium, pyrrolidinium and imidazolium) and two orthoborate anions, bis(mandelato)borate and bis(salicylato)borate, were synthesised and characterised by DSC, X-ray diffraction and NMR. DSC measurements revealed that glass transition points of these orthoborate salts are in the temperature range from −18 to −2 °C. In addition, it was found that [EMPy][BScB] and [EMIm][BScB] salts have solid–solid phase transitions below their melting points, i.e. they exhibit typical features of plastic crystals. Salts of the bis(salicylato)borate anion [BScB]− have higher melting points compared with corresponding salts of the bis(mandelato)borate anion [BMB]−. Single crystal X-ray diffraction crystallography (for [Chol][BScB] crystals) and solid-state multinuclear (13C, 11B and 15N) NMR spectroscopy were employed for the structural characterisation of [Chol][BScB], [EMPy][BScB] and [EMIm][BScB], which are solids at room temperature: a strong interaction between [BScB]− anions and [Chol]+ cations was identified as (i) hydrogen bonding between OH of [Chol]+ and carbonyl groups of [BScB]− and (ii) as the inductive C–Hπ interaction. In the other salt, [EMIm][BScB], anions exhibit ππ stacking in combination with C–Hπ interactions with [EMIm]+ cations. These interactions were not identified in [EMPy][BScB] probably because of the lack of aromaticity in cations of the latter system. Our data on the formation of a lanthanum complex with bis(salicylato)borate in the liquid mixture of La3+(aq) with [Chol][BScB] suggest that this class of novel ILs can be potentially used in the extraction processes of metal ions of rare earth elements.
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| 15. |
- Shah, Faiz Ullah, et al.
(författare)
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Novel halogen-free chelated orthoborate-phosphonium ionic liquids : synthesis and tribophysical properties
- 2011
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Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 13:28, s. 12865-12873
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Tidskriftsartikel (refereegranskat)abstract
- We report on the synthesis, characterisation, and physical and tribological properties of halogen-free ionic liquids based on various chelated orthoborate anions with different phosphonium cations, both without halogen atoms in their structure. Important physical properties of the ILs including glass transition temperatures, density, viscosity and ionic conductivity were measured and are reported here. All of these new halogen-free orthoborate ionic liquids (hf-BILs) are hydrophobic and hydrolytically stable liquids at room temperature. As lubricants, these hf-BILs exhibit considerably better antiwear and friction reducing properties under boundary lubrication conditions for steel–aluminium contacts as compared with fully formulated (15W-50 grade) engine oil. Being halogen free these hf-BILs offer a more environmentally benign alternative to ILs being currently developed for lubricant applications.
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| 16. |
- Wang, Guang, et al.
(författare)
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Evolution of structural dimensions in mesoporous template precursor from hexagonal lyotropic liquid crystals
- 2020
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Ingår i: Journal of Physics. - : Institute of Physics (IOP). - 0953-8984 .- 1361-648X. ; 32:7
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Tidskriftsartikel (refereegranskat)abstract
- Producing nanopores from hexagonal lyotropic liquid crystals (LLCs) templates requires not only retaining phase morphology of the templates but also precisely controlling structural dimensions of unit cells. In this study, SAXS and H-2 NMR are used to investigate dimensional evolutions of ternary systems consisting of polymerizable species, (ethylene glycol) diacrylate (PEGDA) and/or 2-hydroxyethyl methacrylate (HEMA), in a LLCs template of hexagonally packed cylinders formed from dodecyl trimethylammonium bromide (DTAB) and water. With the addition of those polymerizable species, the system rearranges into a new hexagonal system with a smaller aggregation number, smaller pores and a thicker pore wall thickness. The hexagonal system will coexist with an aqueous-rich phase containing isotropically distributed DTAB if sufficient PEGDA is applied but the single hexagonal system could be restored by partially replacing the PEGDA with HEMA. The mobility of DTAB molecules within the aggregates varies depending on monomer compositions. The changes in structural dimensions of the unit cells and phase behaviors after adding polymerizable monomers allow dimensional control of mesochannels and potentially enable the control of selectivity and robustness of polymerized nanomaterials via molecular design.
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| 17. |
- Wang, Zhiyu, et al.
(författare)
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Interfacial Modification of Lithium Metal Anode by Boron Nitride Nanosheets
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Ingår i: ACS Nano. - 1936-086X. ; 18:4, s. 3531-3541
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Tidskriftsartikel (refereegranskat)abstract
- Metallic lithium (Li) is the most attractive anode for Li batteries because it holds the highest theoretical specific capacity (3860 mA h g -1) and the lowest redox potential (-3.040 V vs SHE). However, the poor interface stability of the Li anode, which is caused by the high reactivity and dendrite formation of metallic Li upon cycling, leads to undesired electrochemical performance and safety issues. While two-dimensional boron nitride (BN) nanosheets have been utilized as an interfacial layer, the mechanism on how they stabilize the Li-electrolyte interface remains elusive. Here, we show how BN nanosheet interlayers suppress Li dendrite formation, enhance Li ion transport kinetics, facilitate Li deposition, and reduce electrolyte decomposition. We show through both simulation and experimental data that the desolvation process of a solvated Li ion within the interlayer nanochannels kinetically favors Li deposition. This process enables long cycling stability, reduced voltage polarization, improved interface stability, and negligible volume expansion. Their application as an interfacial layer in symmetric cells and full cells that display significantly improved electrochemical properties is also demonstrated. The knowledge gained in this study provides both critical insights and practical guidelines for designing a Li metal anode with significantly improved performance.
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| 18. |
- Zhang, Heng, et al.
(författare)
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From Solid-Solution Electrodes and the Rocking-Chair Concept to Today's Batteries
- 2020
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Ingår i: Angewandte Chemie - International Edition. - : Wiley. - 1433-7851 .- 1521-3773. ; 59:2, s. 534-538
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Tidskriftsartikel (refereegranskat)abstract
- Lithium-ion batteries (LIBs) have become ubiquitous power sources for small electronic devices, electric vehicles, and stationary energy storage systems. Despite the success of LIBs which is acknowledged by their increasing commodity market, the historical evolution of the chemistry behind the LIB technologies is laden with obstacles and yet to be unambiguously documented. This Viewpoint outlines chronologically the most essential findings related to today's LIBs, including commercial electrode and electrolyte materials, but furthermore also depicts how the today popular and widely emerging solid-state batteries were instrumental at very early stages in the development of LIBs.
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