Evolution of the crystal structure of ceramics BiFeO₃–BaTiO₃ across the morphotropic phase boundary was analyzed using the results of macroscopic measuring techniques such as X-ray diffraction, differential scanning calorimetry, and differential thermal analysis, as well as the data obtained by local scale methods of scanning probe microscopy. The obtained results allowed to specify the concentration and temperature regions of the single phase and phase coexistent regions as well as to clarify a modification of the structural parameters across the rhombohedral–cubic phase boundary. The structural data show unexpected strengthening of structural distortion specific for the rhombohedral phase, which occurs upon dopant concentration and temperature-driven phase transitions to the cubic phase. The obtained results point to the non-monotonous character of the phase evolution, which is specific for metastable phases. The compounds with metastable structural state are characterized by enhanced sensitivity to external stimuli, which significantly expands the perspectives of their particular use.

Direct hydrogenation of CO₂ to methanol is an interesting method to recycle CO₂ emitted e.g., during combustion of fossil fuels. However, it is a challenging process because both the selectivity to methanol and its production are low. The metal-organic frameworks are relatively new class of materials with a potential to be used as catalysts or catalysts supports, also in the reaction of MeOH production. Among many interesting structures, the UiO-66 draws significant attention owing to its chemical and thermal stability, developed surface area, and the possibility of tuning its properties e.g., by exchanging the zirconium in the nodes to other metal cations. In this work we discuss—for the first time—the performance of Cu supported on UiO-66(Ce/Zr) in CO₂ hydrogenation to MeOH. We show the impact of the composition of UiO-66-based catalysts, and the character of Cu-Zr and Cu-Ce interactions on MeOH production and MeOH selectivity during test carried out for 25 h at T = 200 °C and p = 1.8 MPa. Significant increase of selectivity to MeOH was noticed after exchanging half of Zr⁴⁺ cations with Ce⁴⁺; however, no change in MeOH production occurred. It was found that the Cu-Ce coexistence in the UiO-66-based catalytic system reduced the selectivity to MeOH when compared to Cu/UiO-66(Zr), which was ascribed to lower concentration of Cu⁰ active sites in Cu/UiO-66(Ce/Zr), and this was caused by oxygen spill-over between Cu⁰ and Ce⁴⁺, and thus, the oxidation of the former. The impact of reaction conditions on the structure stability of tested catalyst was also determined.

A series of TiO₂ photocatalysts loaded with various metals (Pt, Pd, Ni, and Cu) were prepared by using the wet impregnation method. Their physicochemical properties were studied by using XRD, BET, TPR-H₂, FTIR and TPD-NH₃/CO₂ techniques. The photocatalytic activity of samples was investigated in the gas-phase reduction of carbon dioxide under continuous flow operation mode. Among all investigated catalysts, the Pt and Ni were the most active in terms of the formation rate of methanol. In general, the photocatalytic activity of modified TiO₂ decreased with increasing metal loading and reaction time. The reversible deactivation of photocatalysts was associated with the covering of TiO₂ surface by the reaction products.