The formation of nanoscale vanadium carbide (VC) precipitates is reported in steels subjected to two different thermal treatments. The thermal treatments lead to either interphase precipitation (IP) or random precipitation (RP). Small-angle neutron scattering measurements coupled with transmission electron microscopy analysis are performed to determine the VC precipitate volume fraction and size distribution. It is seen that the samples exhibiting IP show a higher number density of VC precipitates compared to those undergoing RP. Moreover, a broader size distribution of the precipitate radii is observed in the samples with RP, where lens-shaped nanoscale VC precipitates are found predominantly at grain boundaries (GBs) and sub-grain boundaries (SGBs), with smaller precipitates dispersed within the matrix. It is seen that the addition of carbon and vanadium does not increase the VC precipitate number density when the mechanism of precipitation is IP, whereas an increase in the VC precipitate number density with carbon and vanadium addition is seen in case of RP.

Titanium dioxide (TiO₂) has been widely used as a photocatalyst in CO₂ reduction reaction (CO₂RR) due to its low cost, high stability, and strong absorption in the close-to-visible ultra-violet (UV) range. However, TiO₂ films suffer from poor selectivity in CO₂ reduction due to their unfavorable electronic properties. In this work, we address this challenge by fabricating ultra-thin (14 nm) defective TiO₂ films (TiO₂-DTF) to enhance the selectivity of CO₂RR towards formate. TiO₂ sol was prepared using a facile and reproducible sol-gel method and directly deposited onto the surface of the electrode, forming a uniform, ultra-thin TiO₂ layers with a high number of defects. The activity of the TiO₂-DTF catalyst was studied in both photochemical and photoelectrochemical CO₂RR, indicating that the applied potential increases both the yield and selectivity of CO₂RR to formate. The TiO₂-DTF photocathode exhibited remarkable formate production during CO₂ reduction, achieving exceptional Faradaic efficiencies of up to 45 %. To elucidate the mechanism of photoelectrochemical CO₂RR on TiO₂-DTF, an in-situ attenuated total reflection Fourier-transform infrared spectroscopy (in-situ ATR-FTIR) was used and experimental results were supported by density functional theory (DFT) calculations. This study demonstrates that ultra-thin highly defective TiO₂ film, prepared using the cost-effective and environmentally friendly sol-gel method, can be used as photoelectrocatalyst for CO₂ reduction.

Terahertz heterodyne spectrometer instruments have been traditionally limited to a single pixel or a handful of pixels due to integration and assembly constraints and a limited availability of local oscillator (LO) power. As a solution we propose a novel silicon-micromachined planar and modular packaging strategy, that will allow for a dense integration of a large number of pixels. Moreover, the RF- and LO signals will be quasi-optically coupled via two identical but opposite lens arrays, such that a single LO-source can efficiently pump all HEB-mixers of the 2x2 pixel demonstrator array simultaneously. This work reports on an intermediate step, where we validate the lens array performance and LO power coupling efficiency, by slightly modifying the silicon package into a transmit array configuration. In this way, the LO power coupled into the stack is directly reradiated on the other side, which is then measured using a liquid helium cooled bolometer.

The authors regret that the original graphical abstract contained an error by accident. In particular, the values of the OH density for the calcined SBA-15 and solvent-&-Fenton-treated SBA-15 were swapped. These values contradict the main message of the study. The values contained in the paper are however correct. In summary, the paper's data are correct but the graphical abstract contained swapped data leading to a contradiction. Below, an amended graphical abstract can be found, as well as in the online journal website. The authors would like to apologise for any inconvenience caused. [Figure presented]

Hafnia-based thin films exhibit unconventional ferroelectricity. These materials also show rich polymorphism, and thus temperature and field-driven phase transitions, as well as oxygen migration. In a bigger context of exploring the synergy between ferroelectricity and diffusion-based structural phenomena, here we study temperature-dependent phase transitions in epitaxial Hf0.5Zr0.5O2(HZO)/La0.67Sr0.33MnO3 (LSMO, bottom electrode) heterostructures. We report topotactic phase transitions and their clear pathways in both LSMO and HZO layers upon heating under vacuum, using in situ scanning transmission electron microscopy (STEM). Specifically, we directly image oxygen and cationic columns using integrated differential phase contrast STEM and follow their evolution with temperature. We also perform in situ high temperature X-ray diffraction in air and show that the LSMO layer undergoes reversible thermal expansion and contraction when heated up to 850 °C, whereas HZO undergoes strain relaxation beyond 750 °C without any reversible phase transition. Our results provide a comprehensive and direct understanding of temperature-dependent structure, defect, and property correlations in these systems.

A cold-rolled Ti-V high strength low alloy (HSLA) steel was isothermally annealed at 650 °C and 700 °C for different times. A unique combination of techniques including visible light microscopy (VLM), transmission electron microscopy (TEM), matrix dissolution, small angle neutron scattering (SANS) and hardness measurement has been employed to investigate the evolution of microstructure, hardness and precipitate composition, size and volume fraction. Results show that recrystallization is completed after annealing 8 h at 650 °C and 30 min at 700 °C. Three types of precipitates were identified: large Ti(C,N), medium-size (Ti,V)(C,N) and small (Ti,V)C. The Ti/(Ti+V) atomic ratio in the (Ti,V)C precipitates decreases with increasing radius in the 1–15 nm range, which can be explained by the initial nucleation of a TiC-rich core. The average size of the (Ti,V)C precipitates increases, whereas the number density decreases during annealing. The volume fractions of the three types of precipitates were separately determined by the matrix dissolution method. The volume fractions of (Ti,V)C precipitates obtained by matrix dissolution are comparable even slightly more accurate than those obtained by SANS. The hardness first increases and then decreases when annealing at both temperatures, which can be correlated well with the observed microstructural and precipitate evolution.

Magnesium thin films covered with a layer of Pd absorb hydrogen at much higher pressures than bulk Mg. Such an effect was originally explained as a consequence of elastic clamping on Mg by the capping Pd layer. An alternative interpretation later suggested that the pressure increase could originate from simple alloying between Mg and Pd. Here we resolve this controversy by measuring the hydrogenation and dehydrogenation isotherms of Mg-Pd thin film alloys over a wide range of compositions. Our results disentangle the effects of elastic clamping and alloying and highlight the role of plastic deformations.

The alloys (GeTe)_x(AgSbTe₂)_100-x, commonly known as TAGS-x, are among the best performing p-type thermoelectric materials for the composition range 80 ≤ x ≤ 90 and in the temperature range 200-500 °C. They adopt a rhombohedrally distorted rocksalt structure at room temperature and are reported to undergo a reversible phase transition to a cubic structure at ∼250 °C. However, we show that, for the optimal x = 85 composition (TAGS-85), both the structural and thermoelectric properties are highly sensitive to the initial synthesis method employed. Single-phase rhombohedral samples exhibit the best thermoelectric properties but can only be obtained after an annealing step at 600 °C during initial cooling from the melt. Under faster cooling conditions, the samples obtained are inhomogeneous, containing multiple rhombohedral phases with a range of lattice parameters and exhibiting inferior thermoelectric properties. We also find that when the room-temperature rhombohedral phase is heated, an intermediate trigonal structure containing ordered cation vacancy layers is formed at ∼200 °C, driven by the spontaneous precipitation of argyrodite-type Ag₈GeTe₆ which alters the stoichiometry of the TAGS-85 matrix. The rhombohedral and trigonal phases of TAGS-85 coexist up to 380 °C, above which a single cubic phase is obtained and the Ag₈GeTe₆ precipitates redissolve into the matrix. On subsequent cooling a mixture of rhombohedral, trigonal, and Ag₈GeTe₆ phases is again obtained. Initially single-phase samples exhibit thermoelectric power factors of up to 0.0035 W m^-1 K^-2 at 500 °C, a value that is maintained on subsequent thermal cycling and which represents the highest power factor yet reported for undoped TAGS-85. Therefore, control over the structural homogeneity of TAGS-85 as demonstrated here is essential in order to optimize the thermoelectric performance.