In situ monitoring redox processes in energy storage using UV-Vis spectroscopy

Understanding energy storage mechanisms in electrochemical energy storage devices lays the foundations for improving their energy and power density. Here we introduce in situ ultraviolet-visible (UV-Vis) spectroscopy method to distinguish battery-type, pseudocapacitive and electrical double-layer charge storage processes. On the basis of Ti3C2Tx MXene in aqueous acidic and neutral electrolytes, and lithium titanium oxide in an organic electrolyte, we found a correlation between the evolution of UV-Vis spectra and the charge storage mechanism. The electron transfer number for Ti3C2Tx in an acidic electrolyte was calculated using quantitative analysis, which was close to previous measurements using X-ray absorption spectroscopy. Further, we tested the methodology to distinguish the non-Faradaic process in Ti3C2Tx MXene in a water-in-salt electrolyte, despite well-defined peaks in cyclic voltammograms. In situ UV-Vis spectroscopy is a fast and cost-effective technique that effectively supplements electrochemical characterization to track changes in oxidation state and materials chemistry and determine the charge storage mechanism. It can be challenging for conventional electrochemical measurements to distinguish different types of charge storage mechanisms in electrochemical systems. Here the authors develop an in situ ultraviolet-visible spectroscopy approach as a powerful and affordable tool for this purpose.

Automated summary

Understanding energy storage mechanisms is crucial for improving the energy and power density of electrochemical energy storage devices. In this study, the authors introduce an in situ UV-Vis spectroscopy method to distinguish different charge storage processes. They found a correlation between the evolution of UV-Vis spectra and the charge storage mechanism, and successfully used this method to differentiate non-Faradaic processes. In situ UV-Vis spectroscopy is a fast and cost-effective technique that can effectively supplement electrochemical characterization and determine the charge storage mechanism.