Related Experiment Video
Updated: Nov 4, 2025

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Reversible Cycling of Graphite Electrodes in Propylene Carbonate Electrolytes Enabled by Ethyl Isothiocyanate
Xiaolong Li1,2, Limin Guo1, Jing Li1
1State Key Laboratory of Electroanalytical Chemistry, Chinese Academy of Sciences, Changchun Institute of Applied Chemistry, Changchun 130022, China.
Abstract:
As one of the greatest inventions in the history of electrochemistry, the lithium-ion battery (LIB) has radically transformed human beings' daily life by powering portable electronics and electric vehicles. When we look back upon the long and arduous effort devoted to the development of the LIB technology, it is found that the birth of LIBs could have been even earlier if reversible cycling of the graphite electrode had been realized in the propylene carbonate (PC) electrolyte, one of the few dominating electrolytes extensively used in nonaqueous electrochemistry long before the concept of LIBs. In this work, a functional electrolyte additive, that is, ethyl isothiocyanate, has been identified to enable the reversible Li+ ion intercalation/de-intercalation into/out of the graphite electrode in PC electrolyte by forming a high-quality solid electrolyte interphase (SEI) on the graphite electrode. A wide range of advanced in situ and ex situ spectroscopic characterization techniques coupled with theoretical calculations have been employed to understand the SEI formation mechanism. The results reported here rejuvenate the promise of PC as the primary electrolyte solvent for LIBs by artificially rectifying the interfacial electrochemical processes.
More Related Videos
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...

