This review explores the integration of polymer materials into piezoelectric composite structures, focusing on their application in sensor technologies, and wearable electronics. Piezoelectric composites combining ceramic phases like BaTiO₃, KNN, or PZT with polymers such as PVDF exhibit significant potential due to their enhanced flexibility, processability, and electrical performance. The synergy between the high piezoelectric sensitivity of ceramics and the mechanical flexibility of polymers enables the development of advanced materials for biomedical devices, energy conversion, and smart infrastructure applications. This review discusses the evolution of lead-free ceramics, the challenges in improving polymer–ceramic interfaces, and innovations like 3D printing and surface functionalization, which enhance charge transfer and material durability. It also covers the effects of radiation on these materials, particularly in nuclear applications, and strategies to enhance radiation resistance. The review concludes that polymer materials play a critical role in advancing piezoelectric composite technologies by addressing environmental and functional challenges, paving the way for future innovations.

The paper presents a comparative experimental study of heat-transfer behavior in three alloys considered candidate materials for nuclear reactors: the austenitic stainless steel 316L, Zircaloy-4 (currently used in CANDU reactors), and an ODS alloy with a ferritic matrix. The investigation was conducted across five temperature intervals, each sample being subjected to a thermal shock through short-term overheating to the upper limit of its respective interval. The variation of thermal diffusivity in the three alloys was determined as a function of both measurement temperature and applied thermal shock, and trends in heat-transfer behavior were compared across the five temperature ranges. The experimental results show that up to 400 °C, Zircaloy-4 exhibits the highest thermal diffusivity, followed by the ODS alloy, with the lowest values measured for 316L steel. At approximately 450 °C, the ratio between 316L and the ODS alloy reverses. Beyond this point, increasing the temperature up to 900 °C is accompanied by a continuous rise in thermal diffusivity for both 316L stainless steel and Zircaloy-4. In contrast, for the ODS steel, increasing temperature leads to a continuous decrease in thermal diffusivity, reaching a minimum near the Curie point. The novelty of the study lies in the comparative assessment of the influence of temperature on the heat-transfer process in three alloys relevant to nuclear energy, covering the operating temperature ranges of CANDU and ALFRED reactors, as well as potential accidental overheating up to 900 °C. A particular feature of the work is the prior application of a short-duration overheating step produced using solar energy. The results are relevant not only for nuclear reactors but also for other high-temperature applications in corrosive environments.

This study presents an experimental investigation of the influence of dopant type and calcination temperature on BaTiO₃-based piezoceramics synthesized by a solid-state calcination process. The effects of Mn, Nb, La, and Ce dopants on the structural, morphological, and piezoelectric characteristics of powders calcined at 1000 °C and 1100 °C were systematically evaluated. In addition, two co-doped BaTiO₃ compositions, namely Mn–Nb and La–Nb, calcined at 1000 °C, were investigated in order to assess the combined effect of acceptor–donor and donor–donor doping strategies on microstructural evolution and structural stability. The synthesized powders were characterized by scanning electron microscopy (SEM), particle size analysis, energy-dispersive X-ray spectroscopy (EDS), elemental mapping, and X-ray diffraction (XRD), in comparison with a commercial BaTiO₃ reference powder. The piezoelectric response was assessed by correlating the structural modifications induced by doping with the estimated piezoelectric coefficient d₃₃, calculated as a function of the tetragonality ratio (c/a) and further correlated with the crystallite size. The results reveal significant variations in grain growth, dopant distribution, and crystallographic stability, highlighting the critical role of dopant chemistry and calcination temperature in tailoring the functional properties of BaTiO₃ for piezoelectric applications.