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Superconductivity in high-temperature superconductors such as cuprates or iron pnictides is typically achieved by hole or electron doping and it is of great interest to understand how doping affects their properties leading to superconductivity. To study it we conducted Fe and As K edge x-ray absorption spectroscopy measurements on several electron doped compounds from the 112 and 122 family of Eu-based iron pnictides. XANES and EXAFS results confirm that dopants are located at expected sites. For both families we found an electron charge redistribution between As and Fe occurring with doping. The changes it caused are stronger in the 112 family and they are bigger at As sites, which indicates that doped charges are predominantly localized on the dopant site. However, the results obtained do not provide clues why Ni doping in 122 family does not lead to occurrence of superconductivity. [ABSTRACT FROM AUTHOR]

The incorporation of transition metals (TMs) such as Co, Fe, and Mn into SnO2 substantially improves the reversibility of the conversion and the alloying reaction when used as a negative electrode active material in lithium-ion batteries. Moreover, it was shown that the specific benefits of different TM dopants can be combined when introducing more than one dopant into the SnO2 lattice. Herein, a careful characterization of Co and Mn co-doped SnO2 via transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy and X-ray diffraction including Rietveld refinement is reported. Based on this in-depth investigation of the crystal structure and the distribution of the two TM dopants within the lattice, an ex situ X-ray photoelectron spectroscopy and ex situ X-ray absorption spectroscopy were performed to better understand the de-/lithiation mechanism and the synergistic impact of the Co and Mn co-doping. The results specifically suggest that the antithetical redox behaviour of the two dopants might play a decisive role for the enhanced reversibility of the de-/lithiation reaction. [ABSTRACT FROM AUTHOR]

In this study, operando X-ray absorption spectroscopy (XAS) measurements were carried out on a newly developed O2 bi-functional gas diffusion electrode (GDE) for rechargeable Zn-air batteries, consisting of a mixture of α-MnO2 and carbon black. The architecture and composition of the GDE, as well as the electrochemical cell, were designed to achieve optimum edge-jumps and signal-to-noise ratio in the absorption spectra for the Mn K-edge at current densities that are relevant for practical conditions. Herein, we reported the chemical changes that occur on the MnO2 component when the GDE is tested under normal operating conditions, during both battery discharge (ORR) and charge (OER), on the background of more critical conditions that simulate oxygen starvation in a flooded electrode. [ABSTRACT FROM AUTHOR]