Effects of Electron Irradiation and Temperature on Mechanical Properties of Polyimide Film.

Polyimide (PI) is widely deployed in space missions due to its good radiation resistance and durability. The influences from radiation and harsh temperatures should be carefully evaluated during the long-term service life. In the current work, the coupled thermal and radiation effects on the mechanical properties of PI samples were quantitatively investigated via experiments. At first, various PI specimens were prepared, and electron irradiation tests were conducted with different fluences. Then, both uniaxial tensile tests at room temperature and the dynamic mechanical analysis at varied temperatures of PI specimens with and without electron irradiation were performed. After that, uniaxial tensile tests at low and high temperatures were performed. The fracture surface of the PI film was observed using a scanning electron microscope, and its surface topography was measured using atomic force microscopy. In the meantime, the Fourier-transform infrared spectrum tests were conducted to check for chemical changes. In conclusion, the tensile tests showed that electron irradiation has a negligible effect during the linear stretching period but significantly impacts the hardening stage and elongation at break. Moreover, electron irradiation slightly influences the thermal properties of PI according to the differential scanning calorimetry results. However, both high and low temperatures dramatically affect the elastic modulus and elongation at break of PI.

Flexible Hard Coatings with Self-Evolution Behavior in a Low Earth Orbit Environment.

Lightweight, long lifetime, and flexible polymer membrane-based structures, which are tightly folded on the ground and then unfolded in space, suffer from repeated bending before launching and fatal erosion on exposure to atomic oxygen (AO) in a low Earth orbit (LEO). Although various AO-resistant coatings have been developed, a coating that can simultaneously meet the critical requirements for the mechanical robustness and long-term protection of polymer membranes is rare. Here, we fabricated a coating with mechanical robustness and long-term space endurance, starting from an inorganic polymer precursor. A hybrid coating with a nanoscale polymer/silica bicontinuous phase is first prepared on the ground, which exhibits outstanding flexibility and excellent abrasion resistance. Then, the coating shows an in situ self-evolution behavior under AO and ultraviolet (UV) synergism to afford dense and crack-free silica coating with outstanding endurance. Our strategy displays great potential for protecting deployable membrane structures serving in the LEO.

Enhanced vertical carrier mobility in poly(3-alkylthiophene) thin films sandwiched between self-assembled monolayers and surface-segregated layers.

End-functionalized poly(3-butylthiophene) with a thiol group (P3BT-S) was synthesized and used to form a self-assembled monolayer (SAM). It can induce the end-on orientation in the thin film which has the potential to further enhance hole mobility up to 1.1 × 10(-2) cm(2) V(-1) s(-1) in the vertical direction.

End-on orientation of semiconducting polymers in thin films induced by surface segregation of fluoroalkyl chains.

Controlling the orientation of highly anisotropic structures of polymers is important because the majority of their mechanical, electronic, and optical properties depend on the orientation of the polymer backbone. In thin films, the polymer chains tend to adopt an orientation parallel to the substrate; therefore, forcing the chains to stand perpendicular to the substrate is challenging. We have developed a simple way to achieve this end-on orientation. We functionalized one end of a poly(3-butylthiophene) (P3BT) chain with a 1H,1H,2H,2H,3H,3H-perfluoroundecyl group, which caused spontaneous self-segregation of the polymer (P3BT-F17) to the surface of the polymer film. In P3BT-F17/polystyrene (PS) blend films, a highly ordered end-on orientation of the conjugated backbone was observed in the surface-segregated layer of the crystalline P3BT-F17. Furthermore, when the film was spin-coated from a mixture of P3BT-F17 and P3BT, the chain orientation of P3BT-F17 at the surface forced the P3BT in the bulk of the film to adopt the end-on orientation because of the high crystallinity of P3BT. The electronic conductivity measured perpendicular to the film surface also reflected the end-on orientation in the bulk, resulting in a more than 30-fold enhancement of the hole mobility.

Electric field-induced dipole switching at the donor/acceptor interface in organic solar cells.

Order of dipole moment layers at donor and acceptor interfaces in bilayer organic solar cells is manipulated reversibly by applying bias voltages. The energy level shifts at the interfaces induce reversible changes in the open circuit voltage and the diode properties. This finding could lead to a better understanding of the structure-property relationship at the materials interfaces in organic optoelectronic devices.