Issue 1, 2018

Direct monitoring of trace water in Li-ion batteries using operando fluorescence spectroscopy

Abstract

The direct monitoring of trace water in real time during electrochemical cycles is of vital importance because water impurities are one of the causes of reduced lifetimes and capacity fading in Li-ion batteries. However, the most common Karl-Fischer titration lacks the ability to perform real-time monitoring of trace water while the battery is operating. Here, we demonstrate the use of nanosized coordination polymers as a sensing platform for the rapid and highly sensitive detection of water molecules, which gives a distinguishable turn-on fluorescence (FL) response toward water with a quantifiable detection range from 0 to 1.2% v/v, offering a novel opportunity to monitor trace water during electrochemical cycles. To demonstrate the practical value of our platform, we designed an in situ measurement system using nanosized coordination polymers as an electrolyte additive. Within the platform, the findings indicate that trace water is indeed generated during the first discharge process, in which the FL intensity shows a linear increase over time along with the gradual formation of water. We believe that this strategy provides new insights into the in situ monitoring of complex electrochemical processes, and it may help to pave the way for the development of new operando analytical techniques for lithium-ion batteries.

Graphical abstract: Direct monitoring of trace water in Li-ion batteries using operando fluorescence spectroscopy

Supplementary files

Article information

Article type
Edge Article
Submitted
21 Jul 2017
Accepted
20 Oct 2017
First published
23 Oct 2017
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2018,9, 231-237

Direct monitoring of trace water in Li-ion batteries using operando fluorescence spectroscopy

X. Ren, J. Wang, Z. Peng and L. Lu, Chem. Sci., 2018, 9, 231 DOI: 10.1039/C7SC03191B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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