Interface Behavior of Electrolyte/Quinone Organic Active Material in Battery Operation by Operando Surface-Enhanced Raman Spectroscopy was written by Morino, Yusuke;Fukui, Ken-Ichi. And the article was included in Langmuir in 2022.Application of 112-49-2 This article mentions the following:
To elucidate the microscopic charge/discharge (delithiation/lithiation) mechanism at the interface of the electrolyte and organic cathode active material in the lithium-ion battery, we prepared a self-assembled monolayer (SAM) electrode of 1,4-benzoquinone terminated dihexyl disulfide (BQ-C6) on Au(111). An electrochem. setup with the BQ-C6 SAM as a working electrode and 1 M lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI)/triethyleneglycol dimethylether (G3) as the electrolyte was used. We adopted the shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS) method to obtain sufficient Raman signal of SAM for operando Raman spectroscopy measurements by the enhancement with ~100 nm diameter Au particles coated with SiO2 shell (average thickness = 2 nm). By this method, we succeeded in acquiring the Raman signal of the mol. monolayer on the model electrode simulating the interface between the electrolyte and the organic active material. In the cyclic voltammogram, two peaks were observed during the reduction reaction (lithiation), whereas only one peak was detected in the course of the oxidation process (delithiation). Simultaneous operando SHINERS showed a two-step spectral shape change in lithiation and coinciding (or simultaneous) one-step recovery during delithiation to match cyclic voltammetry behavior. The results indicate an asym. lithiation/delithiation mechanism. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Application of 112-49-2).
2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Application of 112-49-2
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem