Ultrahigh thermal-stability polyimides with low CTE and required flexibility by formation of hydrogen bonds between poly(amic acid)s

The flexibility of organic light-emitting diode (OLED) displays highly depends on the properties of the flexible substrates. In this paper, a series of aromatic polyimides have been fabricated via the copolycondensation of pyromellitic dianhydride (PMDA), the two different rigid heterocyclic diamines, 2,5-bis(4-aminophenyl)pyrimidine (PRM) or 2,5-bis(4-aminophenyl)pyridine (PRD), and another flexible diamine, 4,4' -oxydianiline (ODA). The performance of the polyimide films could be systematically tailored by means of adjusting the main-chain rigidity, as well as the close packing and orientation of polymer chains by the formation of the intermolecular hydrogen bonds between poly(amic acid)s. The optimal results (PIb-4, PIb-5, PIc-2) showed that the polyimides were endowed with ultra-high glass transition temperature (T-g) exceeding 450 degrees C, low coefficient of thermal expansion (CTE) at 0-5 ppm K-1 and excellent thermal stability (T-d5% = 570-590 degrees C). Meanwhile, all of them exhibited sufficient flexibility, the elongation at break at of 40-60%, extremely high tensile strength of 250-380 MPa and modulus of 4.1-6.1 GPa. Hence, the polyimide films should be the promising candidates for application as the polymer substrates for flexible OLED displays.

Automated summary

This paper investigates a series of aromatic polyimides, showing that their performance can be systematically tailored by adjusting the main-chain rigidity and formation of intermolecular hydrogen bonds between polymer chains. The optimal results demonstrate ultra-high glass transition temperature, low coefficient of thermal expansion, excellent thermal stability, along with sufficient flexibility and high tensile strength. These polyimide films are promising candidates for flexible OLED displays as polymer substrates.