Electrochemical Reduction of 1,3-Propane Sultone on Graphite Electrodes and Its Application in Li-Ion Batteries

2006 ◽  
Vol 9 (4) ◽  
pp. A196 ◽  
Author(s):  
Xiaoxi Zuo ◽  
Mengqing Xu ◽  
Weishan Li ◽  
Dagen Su ◽  
Jiansheng Liu
Keyword(s):  
Electrochemical Reduction ◽  
Li Ion Batteries ◽  
Graphite Electrodes ◽  
Li Ion

scholarly journals Azo Compounds Derived from Electrochemical Reduction of Nitro Compounds for High Performance Li-Ion Batteries

2018 ◽  
Vol 30 (23) ◽  
pp. 1706498 ◽  
Author(s):  
Chao Luo ◽  
Xiao Ji ◽  
Singyuk Hou ◽  
Nico Eidson ◽  
Xiulin Fan ◽  
...  
Keyword(s):  
Electrochemical Reduction ◽  
High Performance ◽  
Nitro Compounds ◽  
Azo Compounds ◽  
Li Ion Batteries ◽  
Li Ion

In situ scanning tunneling microscopy studies of the SEI formation on graphite electrodes for Li+-ion batteries

Nanoscale ◽  
2016 ◽  
Vol 8 (29) ◽  
pp. 14004-14014 ◽  
Author(s):  
Lukas Seidl ◽  
Slađana Martens ◽  
Jiwei Ma ◽  
Ulrich Stimming ◽  
Oliver Schneider
Keyword(s):  
Scanning Tunneling Microscopy ◽  
Scanning Tunneling ◽  
Li Ion Batteries ◽  
Tunneling Microscopy ◽  
Graphite Electrodes ◽  
Li Ion

scholarly journals Capacitive Performance of Water-in-Salt Electrolyte in Supercapacitors: a Simulation Study

2018 ◽  
Author(s):  
Zhujie Li ◽  
Guillaume Jeanmairet ◽  
Trinidad Mendez-Morales ◽  
Benjamin Rotenberg ◽  
Mathieu Salanne
Keyword(s):  
Molecular Dynamics ◽  
Differential Capacitance ◽  
Li Ion Batteries ◽  
Applied Potential ◽  
Graphite Electrodes ◽  
New Family ◽  
Negative Electrodes ◽  
Large Asymmetry ◽  
Li Ion ◽  
Energy Storage Applications

<div>Water-in-salts is a new family of electrolytes with very promising electrochemical properties for energy storage applications. Despite several studies involving them inside Li-ion batteries and supercapacitors, their interfacial properties remain largely unknown. Here we simulate the interface between electrified graphite electrodes and a highly concentrated waterin- salt (where the salt is Bis(trifluoromethane)sulfonimide lithium, LiTFSI) using constant applied potential molecular dynamics. We show that the capacitance differs markedly between the positive and the negative electrodes, which is due to the large asymmetry in size (and</div><div>shape) between the ions. By using importance sampling, we further investigate the changes in the structure of the salt at the interface and we observe that large variations occur, that are at</div><div>the origin of a series of peaks in the differential capacitance.</div>

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