Interaction and kinetics of H2, CO2, and H2O on Ti3C2Tx MXene probed by X-ray photoelectron spectroscopy
Lars-{\AA}ke N\"aslund, Esko Kokkonen, and Martin Magnuson

TL;DR
This study uses X-ray photoelectron spectroscopy to analyze how H2, CO2, and H2O interact with Ti3C2Tx MXene surfaces, revealing surface terminations and their effects on adsorption and reactivity relevant to energy and environmental applications.
Contribution
It provides detailed insights into the adsorption behavior and surface chemistry of Ti3C2Tx MXene with key gases, informing better preparation and application strategies.
Findings
H2O strongly bonds to Ti-Ti bridge sites, acting as a termination species.
O and H2O terminations restrict CO2 adsorption to Ti on-top sites.
O and H2O terminations enable water splitting on the surface.
Abstract
One of the most explored MXenes is Ti3C2Tx, where Tx is designated to inherently form termination species. Among many applications, Ti3C2Tx is a promising material for energy storage, energy conversion, and CO2-capturing devices. However, active sites for adsorption and surface reactions on the Ti3C2Tx-surface are still open questions to explore, which have implications for preparation methods when to obtain correct and optimized surface requirements. Here we use X-ray photoelectron spectroscopy (XPS) to study the adsorption of common gas molecules such as H2, CO2, and H2O, which all may be present in energy storage, energy converting, and CO2-capturing devices based on Ti3C2Tx. The study shows that H2O, with a strong bonding to the Ti-Ti bridge-sites, can be considered as a termination species. An O and H2O terminated Ti3C2Tx-surface restricts the CO2 adsorption to the Ti on-top sites…
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Taxonomy
TopicsMXene and MAX Phase Materials · 2D Materials and Applications · Inorganic Chemistry and Materials
