Structure–Capacitance Relationships of Graphene/Ionic Liquid Electrolyte Double Layers

2021 ◽  
Vol 125 (37) ◽  
pp. 20204-20218
Author(s):  
Yi-Jung Tu ◽  
Jesse G. McDaniel
2021 ◽  
Vol 9 ◽  
Author(s):  
Guanchen Li ◽  
Charles W. Monroe

Purely ionic electrolytes—wherein ionic liquids replace neutral solvents—have been proposed to improve lithium-ion-battery performance, on the basis that the unique microscopic characteristics of polarized ionic-liquid/electrode interfaces may improve the selectivity and kinetics of interfacial lithium-exchange reactions. Here we model a “three-ion” ionic-liquid electrolyte, composed of a traditional ionic liquid and a lithium salt with a common anion. Newman's concentrated-solution theory is extended to account for space charging and chemomechanical coupling. We simulate electrolytes in equilibrium and under steady currents. We find that the local conductivity and lithium transference number in the diffuse double layers near interfaces differ considerably from their bulk values. The mechanical coupling causes ion size to play a crucial role in the interface's electrical response. Interfacial kinetics and surface charge on the electrodes both affect the apparent transport properties of purely ionic electrolytes near interfaces. Larger ionic-liquid cations and anions may facilitate interfacial lithium-exchange kinetics.


2020 ◽  
Author(s):  
Urbi Pal ◽  
Fangfang Chen ◽  
Derick Gyabang ◽  
Thushan Pathirana ◽  
Binayak Roy ◽  
...  

We explore a novel ether aided superconcentrated ionic liquid electrolyte; a combination of ionic liquid, <i>N</i>-propyl-<i>N</i>-methylpyrrolidinium bis(fluorosulfonyl)imide (C<sub>3</sub>mpyrFSI) and ether solvent, <i>1,2</i> dimethoxy ethane (DME) with 3.2 mol/kg LiFSI salt, which offers an alternative ion-transport mechanism and improves the overall fluidity of the electrolyte. The molecular dynamics (MD) study reveals that the coordination environment of lithium in the ether aided ionic liquid system offers a coexistence of both the ether DME and FSI anion simultaneously and the absence of ‘free’, uncoordinated DME solvent. These structures lead to very fast kinetics and improved current density for lithium deposition-dissolution processes. Hence the electrolyte is used in a lithium metal battery against a high mass loading (~12 mg/cm<sup>2</sup>) LFP cathode which was cycled at a relatively high current rate of 1mA/cm<sup>2</sup> for 350 cycles without capacity fading and offered an overall coulombic efficiency of >99.8 %. Additionally, the rate performance demonstrated that this electrolyte is capable of passing current density as high as 7mA/cm<sup>2</sup> without any electrolytic decomposition and offers a superior capacity retention. We have also demonstrated an ‘anode free’ LFP-Cu cell which was cycled over 50 cycles and achieved an average coulombic efficiency of 98.74%. The coordination chemistry and (electro)chemical understanding as well as the excellent cycling stability collectively leads toward a breakthrough in realizing the practical applicability of this ether aided ionic liquid electrolytes in lithium metal battery applications, while delivering high energy density in a prototype cell.


Ionics ◽  
2019 ◽  
Vol 25 (9) ◽  
pp. 4351-4360 ◽  
Author(s):  
Zhongliang Yu ◽  
Jiahe Zhang ◽  
Chunxian Xing ◽  
Lei Hu ◽  
Lili Wang ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (43) ◽  
pp. 33855-33862 ◽  
Author(s):  
Molang Cai ◽  
Xu Pan ◽  
Weiqing Liu ◽  
John Bell ◽  
Songyuan Dai

DMImBS is used as a novel additive in dye-sensitized solar cells to restrain the electron recombination and intercalation of Li+.


2018 ◽  
Vol 5 (10) ◽  
pp. 1340-1344 ◽  
Author(s):  
Shubham Kaushik ◽  
Jinkwang Hwang ◽  
Kazuhiko Matsumoto ◽  
Yuta Sato ◽  
Rika Hagiwara

2006 ◽  
Vol 51 (12) ◽  
pp. 2471-2476 ◽  
Author(s):  
Paul S. Murray ◽  
Stephen F. Ralph ◽  
Chee O. Too ◽  
Gordon G. Wallace

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