Quantification of ferric iron content in minerals via the STEM-EELS-mapping method†
Abstract
The oxidation state of iron (Fe) in minerals is crucial for Earth and planetary sciences. Accurate determination of the oxidation state of Fe aids in the estimation of redox conditions during mineral formation and thus the reconstruction of the evolutionary history of Earth and other solid celestial bodies. Compared to conventional methods that provide the average bulk Fe3+/ΣFe ratio in minerals, the recently developed scanning transmission electron microscopy electron energy loss spectroscopy (STEM-EELS) technique enables the accurate determination of Fe oxidation states at sub-micrometer scales. However, the focused electron beam in STEM mode can induce the generation of Fe3+ and consequently introduces uncertainty in the quantification of Fe3+ in minerals. In this study, a calibration relationship was established between the relative ratios of the Fe-L3 and Fe-L2 peak areas in the EELS spectra and the Fe3+/ΣFe ratio based on the characterization of a series of pyroxene reference materials with varying Fe3+ contents. The EELS spectra were collected in the STEM-EELS-mapping mode using focused ion beam (FIB)-derived sections. The impacts of sample preparation, data acquisition, and data processing procedures on the determination of the Fe3+ contents in minerals were examined and discussed to gain insights into the constraints of parameters for accurate quantification of Fe3+ in minerals. The obtained calibration relationship was further validated for the accurate determination of Fe3+ content in other Fe-bearing minerals, suggesting its promising applicability in the quantification of Fe3+ in precious nanoscale terrestrial and extraterrestrial materials.