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We reveal an iodine vapor-induced degradation mechanism in formamidinium–lead-iodide-based perovskite solar cells stressed under combined heat and light illumination.

The deployment of Li‐garnet Li7La3Zr2O12 (LLZO) solid‐state electrolytes in solid‐state batteries is severely hampered by their poor wettability with metallic Li. In this work, Sb is presented as a compelling interfacial layer allowing superior wetting of Li onto a LLZO surface, resulting in a remarkably low Li/LLZO interfacial resistance of 4.1(1) Ω cm2. An atomistic insight into Sb‐coated LLZO interface using soft and hard X‐ray photoelectron spectroscopy and focused ion beam time‐of‐flight secondary ion mass spectrometry shows the formation of a Li‐Sb alloy as an interlayer. It is determined that the Li/Sb‐coated LLZO/Li symmetrical cells exhibit a high critical current density of up to 0.64 mA cm−2 and low overpotentials of 40–50 mV at a current density of 0.2 mA cm−2 without applying external pressure. The electrochemical performance of Sb coated‐LLZO pellets is also assessed with an intercalation‐type V2O5 cathode. Li/Sb‐coated‐LLZO/V2O5 full cells deliver stable capacities of around 0.45 mAh cm−2, with a peak current density of 0.3 mA cm−2.

The modified three-step sequential extraction procedure proposed by the Community Bureau of Reference (or Bureau Communautaire de Reference, BCR) was used to predict trace element mobility in soils affected by an accidental spill comprising arsenopyrite- and heavy metal-enriched sludge particles and acid waste waters. The procedure was used to obtain the distribution of both the major (Al, Ca, Fe, Mg, and Mn) and trace elements (As, Bi, Cd, Cu, Pb, Tl, and Zn) in 13 soils of contrasting properties with various levels of contamination and in the sludge itself. The distributions of the major elements enabled us to confirm the main soil fractions solubilized in each of the three steps, and, in turn, to detect the presence of pyritic sludge particles by the high Fe extractability obtained in the third step. Cadmium was identified as being the most mobile of the elements, having the highest extractability in the first step, followed by Zn and Cu, Lead, Tl, Bi, and As were shown to be poorly mobile or nonmobile. In the case of some of the trace elements, the residual fractions decreased at higher levels of contamination, which was attributed to the anthropogenic contributions to the polluted samples. Comparison with soil-plant transfer factors, calculated in plants growing in the affected area, indicated that a relative sequence of trace element mobility was well predicted from data of the first step.

Garnet Li7La3Zr2O12 (LLZO) is a promising solid-state electrolyte due to its wide electrochemical stability window and high Li-ion conductivity. This electrolyte has potential to be employed in the form of thin films for solid-state batteries, a promising approach in the quest for safer batteries with higher energy densities at lower fabrication costs. In this study, we use a scalable cosputtering process to fabricate LLZO thin films with subsequent postannealing at a temperature of 700 °C, significantly below the sintering temperatures employed in ceramic pellet processing. We investigate the roles that Li excess and incorporation of Al play in the film’s crystalline phase, microstructure, phase stability, and, ultimately, ionic conductivity. Our results reveal that improving the conductivity of LLZO thin films requires not only the stabilization of the cubic phase but especially the densification of the film and the minimization of the proton exchange degradation mechanism in the presence of moisture and CO2. These issues can be mitigated by effectively controlling the amount of Li and incorporating Al as sintering agent. An ionic conductivity at room temperature of 1.9 × 10–5 S cm–1 was achieved with a 400 nm Al-substituted LLZO thin film. Finally, we prove that these LLZO thin films can be successfully deposited and crystallized on a LiCoO2 cathode.