Thermal conductivity (κ) plays an essential role in functional devices. It is advantageous to design materials where one can tune κ in a wide range according to its function: single-crystals and nanowires of anatase polymorph of titanium dioxide, broadly used in applications ranging from photovoltaics, reflective coatings to memristors, have been synthesized in large quantities. Here we identify a new, strong diffusion mechanism of heat by polaronic structures due to oxygen vacancies, which considerably influences both the absolute value and the temperature dependence of κ. The additional decrease of κ is achieved in anatase nanowires organized into foam, where porosity and the quasi-one-dimensional size-effect dramatically hinder the propagation of heat, resulting in an extremely low κ = 0.014 W/Km at room-temperature. Doping this anatase foam could herald promising applications, in particular in thermoelectricity.

Owing to their exceptional mechanical, electronic, and phononic transport properties, compositionally complex alloys, including high-entropy alloys, represent an important class of materials. However, the interplay between chemical disorder and electronic correlations, and its influence on electronic structure-derived properties, remains largely unexplored. This is addressed for the archetypal CrMnFeCoNi alloy using resonant and valence band photoemission spectroscopy, electrical resistivity, and optical conductivity measurements, complemented by linear response calculations based on density functional theory. Utilizing dynamical mean-field theory, correlation signatures and damping in the spectra are identified, highlighting the significance of many-body effects, particularly in states distant from the Fermi edge. Electronic transport remains dominated by disorder and potentially short-range order, especially at low temperatures, while visible-spectrum optical conductivity and high-temperature transport are influenced by short quasiparticle lifetimes. These findings improve our understanding of element-specific electronic correlations in compositionally complex alloys and facilitate the development of advanced materials with tailored electronic properties.

The measurement and description of the charge-carrier lifetime (${\tau }_{\mathrm{c}}$) is crucial for the wide-ranging applications of lead-halide perovskites. We present time-resolved microwave-detected photoconductivity decay (TRMCD) measurements and a detailed analysis of the possible recombination mechanisms including trap-assisted, radiative, and Auger recombination. We prove that performing injection-dependent measurement is crucial in identifying the recombination mechanism. We present temperature and injection level dependent measurements in CsPbBr₃, which is the most common inorganic lead-halide perovskite. In this material, we observe the dominance of charge-carrier trapping, which results in ultra-long charge-carrier lifetimes. Although charge trapping can limit the effectiveness of materials in photovoltaic applications, it also offers significant advantages for various alternative uses, including delayed and persistent photodetection, charge-trap memory, afterglow light-emitting diodes, quantum information storage, and photocatalytic activity.