No abstract

The ever-increasing space exploration enterprise calls for novel and high-quality radiation-resistant materials, among which nonlinear optical materials and devices are particularly scarce. Two-dimensional (2D) materials have shown promising potential, but the radiation effects on their nonlinear optical properties remain largely elusive. We previously fabricated 2D bismuthene for mode-locking sub-ns laser; herein, their space adaption was evaluated under a simulated space radiation environment. The as-synthesized thin layers of bismuthene exhibited strong third-order nonlinear optical responses extending into the near-infrared region. Remarkably, when exposed to 60Co γ-rays and electron irradiation, the bismuthene showed only slight degradation in saturable absorption behaviors that were critical for mode-locking in space. Ultrafast spectroscopy was applied to address the radiation effects and damage mechanisms that are difficult to understand by routine techniques. This work offers a new bottom-up approach for preparing 2D bismuthene, and the elucidation of its fundamental excited-state dynamics after radiation also provides a guideline to optimize the material for eventual space applications.

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Artificial photosynthesis converting carbon dioxide into chemical fuels with a high added value is a promising solution to both fossil fuel shortage/pollution and global climate change; however, the development of highly efficient photocatalysts toward this goal is still largely bereft of fresh ideas. Herein, we propose a “cascade electron transfer” strategy through spurring both interfacial and inner electron transfer rates for a 0D/2D photocatalyst of CsPbBr3/CuTCPP metal organic framework (MOF). Upon photoexcitation, the heterojunction structure with an appropriate band alignment facilitates an ultrafast interfacial electron transfer rate of 1.4 ps from CsPbBr3 segment to CuTCPP MOF and subsequent ultrafast internal electron transfer of 21 ps from CuTCPP ligand to the Cu node within the enlarged 2D framework. The efficient electron transfer ensures efficient charge separation favorable for photocatalytic reactions: The photocatalyst exhibits an outstanding yield of 47.2 μmol g−1 h−1 (CO and CH4 combined) superior to previous reports. Rational design of hierarchical heterojunctions with matching electronic bandgap not only expedites cascade charge transfer but also prevents holes from recombining with electrons or oxidizing the photocatalysts without the necessity of sacrificial reagents. This work thus provides useful insight for boosting photocatalytic efficacy from a dynamic perspective.

Cell morphology and nucleus deformation are important when circulating tumor cells break away from the primary tumor and migrate to a distant organ. Cells are sensitive to the microenvironment and respond to the cell-material interfaces. We fabricated TiO nanorod arrays with mesoscopic micro-nano interfaces through a two-step hydrothermal reaction method to induce severe changes in cell morphology and nucleus deformation. The average size of the microscale voids was increased from 5.1 to 10.5 μm when the hydrothermal etching time was increased from 3 to 10 h, whereas the average distances between voids were decreased from 0.88 to 0.40 μm. The nucleus of the MCF-7 cells on the TiO nanorod substrate that was etched for 10 h exhibited a significant deformation, because of the large size of the voids and the small distance between voids. Nucleus defromation was reversible during the cells proliferate process when the cells were cultured on the mesoscopic micro-nano interface.This reversible process was regulated by combining of the uniform pressure applied by the actin cap and the localized pressure applied by the actin underneath the nucleus. Cell morphology and nucleus shape interacted with each other to adapt to the microenvironment. This mesoscopic micro-nano interface provided a new insight into the cell-biomaterial interface to investigate cell behaviors.