Agnieszka Witkowska

In this work, an A-site deficient perovskite, (La_0.3Sr_0.6Ce_0.1)_0.9Co_0.1Ti_0.9O_3−δ (LSCCoT) was applied as an additional catalytic layer on Ni–YSZ anode for biogas-fuelled SOFC. Under reducing conditions, the formation of well-dispersed, socketed Co nanoparticles was observed due to the cobalt exsolution from the perovskite lattice. The structural and microstructural characterization confirmed phase stability of the perovskite after high-temperature reduction in hydrogen and the presence of exsolved nanoparticles on the grains’ surface. Electrical conductivity measurements showed thermally activated semiconducting behavior in air (E_a = 0.582 ± 0.121 eV) and a strongly enhanced conductivity with weak temperature dependence in hydrogen (E_a = 0.057 ± 0.001 eV). Single-cell tests performed under a CH₄/CO₂ (60/40 vol%) biogas mixture revealed a 30% increase in maximum power density at 800 °C compared to the reference cell. During 100 h of operation, the modified cell exhibited reduced performance degradation, improved internal reforming activity, and a more stable outlet gas composition.

This study concerns energetics of formation and the stability in high water partial pressure of BaLnCo₂O_6−δ, (Ln = La, Pr, Nd, and Gd) (BLnC) and BaGd_1−xLa_xCo₂O_6−δ, where x = 0.2, 0.5, and 0.7 (BGLC) double perovskite cobaltites.

Due to the development of new photovoltaic technologies, there is a need to research new recycling methods for these new materials. The recovery of metals from photovoltaic (PV) modules would reduce the consumption of raw materials. Therefore, the development of recycling technologies for used and damaged modules of newer generations is important for environmental reasons. The aim of the research is to shed light on the nature of the chemical reactions that occur in recycling technology for second-generation photovoltaic modules. This work is focused mainly on cells made of Cadmium Telluride (CdTe). It was proven that prior thermal delamination was necessary. Moreover, an improvement in understanding of the recovery process depending on used leaching solution was achieved.

The application of double perovskite cobaltites BaLnCo₂O_6−δ (Ln = lanthanide element) in electrochemical devices for energy conversion requires control of their properties at operating conditions. This work presents a study of a series of BaLnCo₂O_6−δ (Ln = La, Pr, Nd) with a focus on the evolution of structural and electrical properties with temperature. Symmetry, oxygen non-stoichiometry, and cobalt valence state have been examined by means of Synchrotron Radiation Powder X-ray Diffraction (SR-PXD), thermogravimetry (TG), and X-ray Absorption Spectroscopy (XAS). The results indicate that all three compositions maintain mainly orthorhombic structure from RT to 1000 °C. Chemical expansion from Co reduction and formation of oxygen vacancies is observed and characterized above 350 °C. Following XAS experiments, the high spin of Co was ascertained in the whole range of temperatures for BLC, BPC, and BNC.

X‐ray and neutron diffraction have been utilized to analyze the crystalline and electronic structure of lanthanum orthoniobate substituted by antimony. Using X‐ray absorption spectroscopy and photoelectron spectroscopy, changes in the electronic structure of the material upon substitution have been analyzed. The structural transition temperature between fergusonite and scheelite phases for 30 mol% antimony substitution was found to be 15°C. Based on the neutron data, the oxygen nonstoichiometry was found to be relatively low. Moreover no influence on the position of the valence band maximum was observed. The influence of the protonation on the electronic structure of constituent oxides has been studied. Absorption data show that the incorporation of protonic defects into the lanthanum orthoniobate structure leads to changes in lanthanum electronic structure and a decrease in the density of unoccupied electronic states.

Advanced metal oxide electrodes in Li-ion batteries usually show reversible capacities exceeding the theoretically expected ones. Despite many studies and tentative interpretations, the origin of this extra-capacity is not assessed yet. Lithium storage can be increased through different chemical processes developing in the electrodes during charging cycles. The solid electrolyte interface (SEI), formed already during the first lithium uptake, is usually considered to be a passivation layer preventing the oxidation of the electrodes while not participating in the lithium storage process. In this work, we combine high resolution soft X-ray absorption spectroscopy with tunable probing depth and photoemission spectroscopy to obtain profiles of the surface evolution of a well-known prototype conversion-alloying type mixed metal oxide (carbon coated ZnFe₂O₄) electrode. We show that a partially reversible layer of alkyl lithium carbonates is formed (∼5–7 nm) at the SEI surface when reaching higher Li storage levels. This layer acts as a Li reservoir and seems to give a significant contribution to the extra-capacity of the electrodes. This result further extends the role of the SEI layer in the functionality of Li-ion batteries.