Acute lung injury (ALI) is a severe clinical disease marked by dysregulated inflammation response and has a high rate of morbidity and mortality. Macrophages, which play diverse roles in the inflammatory response, are becoming therapeutic targets in ALI. In this study we investigated the effects of dehydrocostus lactone (DHL), a natural sesquiterpene, on macrophage activation and LPS-induced ALI. The macrophage cell line RAW264.7 and primary lung macrophages were incubated with DHL (0, 3, 5, 10 and 30 μmol/L) for 0.5 h and then challenged with LPS (100 ng/mL) for up to 8 hours. C57BL/6 mice were intratracheally injected with LPS (5 mg/kg) to induce acute lung injury (ALI) and then treated with a range of DHL doses intraperitoneally (5 to 20 mg/kg). The results showed that DHL inhibited LPS-induced production of proinflammatory mediators such as iNOS, NO, and cytokines including TNF-α, IL-6, IL-1β, and IL-12 p35 by suppressing the activity of NF-κB via p38 MAPK/MK2 and Akt signaling pathway in macrophages. The in vivo results revealed that DHL significantly attenuated LPS-induced pathological injury and reduced cytokines expression in the lung. NF-κB, p38 MAPK/MK2 and Akt signaling molecules were also involved in the anti-inflammatory effect. Collectively, our findings suggested that DHL is a promising agent for alleviating LPS-induced ALI.

Suppressing the recombination of photogenerated charges is one of the most important routes for enhancing the catalytic performance of semiconductor photocatalysts. In addition to the built‐in field produced by semiconductor heterostructures and the photo‐electrocatalysis realized by applying an external electrical potential to photocatalysts assembled on electrodes, other strategies are waiting to be scientifically explored and understood. In this work, a Lorentz force–assisted charge carrier separation enhancement strategy is reported to improve the photocatalytic efficiency by applying a magnetic field to a photocatalytic system. The photocatalytic efficiency can be improved by 26% just by placing a permanent magnet beneath the normal photocatalytic system without any additional power supply. The mechanism by which the Lorentz force acts oppositely on the photogenerated electrons and holes is introduced, resulting in the suppression of the photoinduced charge recombination. This work provides insights into the specific role of the Lorentz force in suppressing the recombination of electron–hole pairs in their initial photogenerated states. This suppression would increase the population of charge carriers that would subsequently be transported in the semiconductor. It is believed that this strategy based on magnetic effects will initiate a new way of thinking about photoinduced charge separation.

Magnetoelectric coupling is of high current interest because of its potential applications in multiferroic memory devices. Although magnetoelectric coupling has been widely investigated in inorganic materials, such observations in organic materials are extremely rare. Here, we report our discovery that organic charge-transfer (CT) complex pyrene-2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (pyrene–F4TCNQ) can display anisotropic magnetoelectric coupling. Investigation of the crystal structure of pyrene–F4TCNQ complex demonstrates that the magnetoelectric coupling coefficient along the π–π interaction direction is much larger than the value along other directions. Furthermore, magnetoelectric coupling and magnetization can be tuned by changing the fluorine content in complexes. Besides, the Cotton–Mouton effect in pyrene–F4TCNQ is observed, enabling the control of optomagnetic devices. These results can pave the way for a new method for the future development of organic CT complexes and their applications in perpendicular memory devices and energy-transfer-related multiferroics.

In this work, through designing organic helix donor–acceptor complexes, one type of room-temperature chiral magnet was reported. Within these chiral charge transfer magnets, circularly polarized light could induce a larger saturation magnetization compared to linearly polarized light illumination with identical intensity. Moreover, the transmission light polarization from chiral magnets could be tuned via applying the magnetic field. Overall, room-temperature organic chiral magnets with optomagnetic effects will enhance the function of organic magnetochiral materials.

In this work, we designed a type of organic chiral polymeric nanowire with strong orbital angular momentum to fabricate circularly polarized light detectors. In chiral polymeric nanowires, chirality induced orbital angular momentum could lead to the splitting of spin up and spin down energy levels, which determines the performance of circularly polarized light detection. In addition, chiral polymeric nanowire based circularly polarized light detectors exhibit excellent reversibility and stability after several hundred switching operations, which provides a solid footstone for potential applications.