scholarly journals Porous dendritic copper: an electrocatalyst for highly selective CO2 reduction to formate in water/ionic liquid electrolyte

2017 ◽  
Vol 8 (1) ◽  
pp. 742-747 ◽  
Author(s):  
Tran Ngoc Huan ◽  
Philippe Simon ◽  
Gwenaëlle Rousse ◽  
Isabelle Génois ◽  
Vincent Artero ◽  
...  

An ionic liquid/water electrolyte promotes excellent selectivity for CO2 electroreduction to formic acid at a porous dendritic copper electrode material.

2017 ◽  
Vol 10 (10) ◽  
pp. 2090-2094 ◽  
Author(s):  
K. Beltrop ◽  
S. Beuker ◽  
A. Heckmann ◽  
M. Winter ◽  
T. Placke

In this contribution, we report for the first time a novel potassium ion-based dual-graphite battery concept (K-DGB), applying graphite as the electrode material for both the anode and cathode, in combination with an ionic liquid electrolyte.


Author(s):  
S. Selvam ◽  
Jin-Heong Yim

In this study, we prepared ceramic-based hydroxyapatite (HAp)/polyvinylpyrrolidone (PVP)/MnO2@MnCO3 composites for high temperature-operable electrolyte-engraved planar supercapacitors. The electrode material was prepared depositing a composite coating of HAp, PVP, and MnO2@MCO3...


2015 ◽  
Vol 3 (41) ◽  
pp. 20767-20771 ◽  
Author(s):  
Changsheng Ding ◽  
Toshiyuki Nohira ◽  
Rika Hagiwara

Carbon-coated TiO2 (TiO2/C) nanopowders were synthesized as a negative electrode material for sodium secondary batteries. The TiO2/C negative electrode delivers a high reversible discharge capacity of 275 mA h g−1 at 10 mA g−1 at 363 K.


2018 ◽  
Vol 30 (7) ◽  
pp. 2362-2373 ◽  
Author(s):  
Jonnathan Medina-Ramos ◽  
Weiwei Zhang ◽  
Kichul Yoon ◽  
Peng Bai ◽  
Ashwin Chemburkar ◽  
...  

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.


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