AVS 66th International Symposium & Exhibition | |
Chemical Analysis and Imaging Interfaces Focus Topic | Wednesday Sessions |
Session CA+NS+SS+VT-WeA |
Session: | Chemical Analysis and Imaging of Liquid/Vapor/Solid Interfaces I |
Presenter: | Henrik Bergersen, Scienta Omicron |
Authors: | S. Eriksson, Scienta Omicron H. Bergersen, Scienta Omicron |
Correspondent: | Click to Email |
Hard X-ray photoelectron spectroscopy (HAXPES) has traditionally found its application in the core topics of condensed matter physics, but the slowly growing number of beamlines worldwide has widened its appeal to other interest groups. HAXPES uses X-rays in the 2-10 keV range to excite photoelectrons, which are used to non-destructively study the chemical environment and electronic structure of materials.
In contrast to the very surface-sensitive XPS, HAXPES is much more bulk sensitive. This makes it applicable to bulk materials and structured samples, e.g. layered samples and heterostructures. In addition, its bulk sensitivity means that realistic samples can be investigated without the need of prior surface preparation. However, the number of existing HAXPES systems is very small and they are predominantly located at synchrotrons (approx. 20 beamlines worldwide) due to low photoionization cross sections necessitating high X-ray intensities, limiting their availability to users and applications.
This work presents a new laboratory-based instrument capable of delivering monochromated hard X-rays with an energy of 9.25 keV and a focused 30x45 μm2 X-ray spot, giving excellent energy resolution of <0.5 eV. Systematic reference measurements are presented outlining the systems capability as well as the latest results from various application fields including energy related materials such as batteries.
Ultimately, this spectrometer presents an alternative to synchrotron-based endstations and will help to expand the number and range of HAXPES experiments performed in the future. HAXPES is a cutting edge characterisation method and the advancement of this technique will tremendously increase the potential to study an ever increasing range of inorganic materials and beyond.