Ex-situ and In-situ Soft X-Ray Spectro-Microscopy Studies of Manganese Oxide Electrodes for Energy Storage Applications
| Autor: | Eraky, Haytham |
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| Jazyk: | angličtina |
| Rok vydání: | 2024 |
| Předmět: | |
| Druh dokumentu: | Diplomová práce |
| Popis: | Energy storage systems such as batteries and supercapacitors store electrical energy in the form of chemical energy and release it when required. Among the various electrode materials, manganese oxides (MnOx) are promising electrode materials for these devices. Despite its outstanding theoretical capacitance, Mn-based oxide electrodes have several limitations that impede their electrochemical performance. Understanding how the charges are efficiently stored in the electrodes or across the electrode/electrolyte interface is crucial for developing advanced electrode material in the field of energy storage applications. The goal of my thesis is to develop and apply synchrotron-based scanning transmission X-ray microscopy (STXM) to investigate changes in the oxidation state of Mn and their spatial distributions in MnOx electrodes in the context of energy storage and release. To achieve high- precision qualitative and quantitative STXM identification and mapping of different MnOx species, calibrated and high-quality reference Mn 2p and O 1s NEXAFS (near edge X-ray absorption fine structure) spectra were measured. In collaboration with Wenjuan Yang and her PhD supervisor, Prof. Igor Zhitomirsky, I performed ex-situ STXM studies on Mn3O4-based supercapacitor electrode materials to investigate the influence of different synthesis methods and activation protocols on the charging behavior and capacitance performance. In collaboration with Pablo Ingino and his supervisor, Prof. Martin Obst (Bayreuth University), and my colleague, Dr. Chunyang Zhang, I helped develop a three-electrode, microfluidic-based flow electrochemical device for in-situ STXM. This device was used to electrodeposit MnO2 on the working electrode (WE) and track the oxidation state and morphological changes by STXM while scanning the potential of the cell in different electrolyte pH. The in-situ STXM studies showed a spontaneous reduction of the initially deposited MnO2 resulting from the local pH change at the WE. Additionally, a significant change from a quasi-uniform MnO2 film to a dendritic MnO2 structure was observed at oxidative potential. This dendritic growth resulted from dissolution/redeposition of MnO2 during charging/discharging processes, indicating a partial reversibility of dissoluble Mn species. The ex-situ and in-situ STXM studies I performed provide mechanistic insights that will help further improve Mn oxides-based electrodes and their applications as energy storage devices. Thesis Doctor of Philosophy (PhD) |
| Databáze: | Networked Digital Library of Theses & Dissertations |
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