The regulation mechanism of ethephon-mediated delaying of postharvest physiological deterioration in cassava storage roots based on quantitative acetylproteomes analysis.

Ethylene plays diverse roles in post-harvest processes of horticultural crops. However, its impact and regulation mechanism on the postharvest physiological deterioration (PPD) of cassava storage roots is unknown. In this study, a notable delay in PPD of cassava storage roots was observed when ethephon was utilized as an ethylene source. Physiological analyses and quantitative acetylproteomes were employed to investigate the regulation mechanism regulating cassava PPD under ethephon treatment. Ethephon was found to enhance the reactive oxygen species (ROS) scavenging system, resulting in a significant decrease in H2O2 and malondialdehyde (MDA) content. The comprehensive acetylome analysis identified 12,095 acetylation sites on 4403 proteins. Subsequent analysis demonstrated that ethephon can regulate the acetylation levels of antioxidant enzymes and members of the energy metabolism pathways. In summary, ethephon could enhance the antioxidant properties and regulate energy metabolism pathways, leading to the delayed PPD of cassava.

Discovery of superconductivity in technetium borides at moderate pressures.

Advances in theoretical calculations have boosted the search for high-temperature superconductors, such as sulfur hydrides and rare-earth polyhydrides. However, the required extremely high pressures for stabilizing these superconductors has handicapped further implementation. Based upon thorough structural searches, we identified a series of unprecedented superconducting technetium borides at moderate pressures, including TcB (P63/mmc) with a superconducting transition temperature of Tc = 20.2 K at ambient pressure and TcB2 (P6/mmm) with Tc = 23.1 K at 20 GPa. Superconductivity in these technetium borides mainly originates from the coupling between the low-frequency vibrations of technetium atoms and the dominant technetium-4d electrons at the Fermi level. Our work therefore presents a fresh group in the family of superconducting borides, whose diversified crystal structures suggest rich possibilities in the discovery of other superconducting transition-metal borides.

Elevating Charge Transport Layer for Stable Perovskite Light-Emitting Diodes.

Ion migration is a major factor affecting the long term stability of perovskite light-emitting diodes (LEDs), which limits their commercialization potential. The accumulation of excess halide ions at the grain boundaries of perovskite films is a primary cause of ion migration in these devices. Here, it is demonstrated that the channels of ion migrations can be effectively impeded by elevating the hole transport layer between the perovskite grain boundaries, resulting in highly stable perovskite LEDs. The unique structure is achieved by reducing the wettability of the perovskites, which prevents infiltration of the upper hole-transporting layer into the spaces of perovskite grain boundaries. Consequently, nanosized gaps are formed between the excess halide ions and the hole transport layer, effectively suppressing ion migration. With this structure, perovskite LEDs with operational half-lifetimes of 256 and 1774 h under current densities of 100 and 20 mA cm-2 respectively are achieved. These lifetimes surpass those of organic LEDs at high brightness. It is further found that this approach can be extended to various perovskite LEDs, showing great promise for promoting perovskite LEDs toward commercial applications.

Leading components and pressure-induced color changes in N-doped lutetium hydride.

Recent experimental study by Dasenbrock-Gammon et al. (Nature 2023;615:244) claims to have discovered room-temperature superconductivity in lutetium-nitrogen-hydrogen system at 1 GPa, which sheds light on the long-held dream of ambient superconductivity. However, all follow-up experiments found no evidence of superconductivity. The compositions and the crystal structures of the lutetium-nitrogen-hydrogen system remain unknown. By employing the density functional theory based structure prediction algorithm, we suggest that in lutetium-nitrogen-hydrogen the major component is LuH2 (Fm3¯m), together with minor LuN (Fm3¯m). The blue LuH2 at ambient pressure will turn into purple and red color at higher pressures, possibly accompanied by the formation of vacancies at hydrogen-sites. In LuH2 and LuN, the density of states at the Fermi level is dominated by the Lu-5d orbitals, while those from hydrogen and nitrogen are very small, leading to the absence of superconductivity in these two compounds. Nitrogen-doping to LuH2 fails to enhance the superconductivity as well. In this work, we identify the leading components in N-doped lutetium hydride, explain its intriguing color changes under pressure, and elucidate why superconductivity is absent in the follow-up experiments.