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Ionic‐Liquid‐Gating‐Induced Hydrogenation in Epitaxial Strontium Ferrite

Abstract Incorporating hydrogen into complex oxides holds promise for discovering exotic phenomena and novel functionalities by promoting couplings between ion and lattice/charge/spin/orbital degrees of freedom. Here, electrolyte gating‐driven hydrogenation is investigated in epitaxial brownmillerite SrFeO 2.5 thin films in which the hydrogenation‐induced lattice distortion is qualitatively different from its counterpart SrCoO 2.5 . The achievable lattice expansion in hydrogenated SrFeO 2.5 is weaker than in SrCoO 2.5 and primarily occurs along the normal of the stacked octahedral FeO 6 and tetrahedral FeO 4 layers. Upon the substitution of Fe with Co, the lattice expansion monotonically increases with increase of Co/Fe ratio, implying an intrinsic difference in accommodating hydrogen between Fe‐ and Co‐based brownmillerites. Moreover, a net magnetic moment in hydrogenated SrFeO 2.5 films is observed above room temperature, which gradually weakens with the increase of Co substitution, suggesting a stronger canted magnetism in Fe‐based hydrogenated brownmillerites. This work clarifies the electrolyte gating‐driven hydrogenation mechanisms in brownmillerite SrFeO 2.5 epitaxial thin films and those with Co substitution, particularly the deterministic role of Co/Fe ratio in the evolution of structure and properties upon hydrogenation.

Chemistry↗

X-Ray Photoelectron Spectroscopy of Chlorometallate Ionic Liquids: Speciation and Anion Basicity

X-ray photoelectron spectroscopy is used to detect the formation of different chlorometallate anions and to differentiate the electronic environment of each element present in chlorometallate anions. The impact of the degree of the charge delocalization of chlorometallate anions on the Cl 2p binding energy is demonstrated in detail. The basicity of chlorostannate and chloroferrate anions is estimated based upon the measured N 1s binding energy. It is found that chlorostannate and chloroferrate anions can be considered as the least basic anions.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

A Chemical Separation Procedure Using Ionic Liquid Extraction for Fe-59 and Fe-55 Quantification

Quantitating iron (Fe) isotopes, Fe-55 and Fe-59, radiometrically can be difficult due to emission interferences or high spectral backgrounds due to the presence of other activation products or fission product contaminants. The purpose of this work was to demonstrate a separation procedure for Fe activation products from complex samples that contain either activated soil components or freshly produced fission products generated from highly enriched uranium. The developed procedure succesfully allowed for quantitative analysis of both the Fe-59 (by gamma spectroscopy) and Fe-55 (by low energy photon spectrsocopy) with > 90% elemental recovery.

Morrison, Samuel S.↗