The development of polyimide (PI) films with excellent
mechanical
properties and low dielectric constants is crucial for flexible optoelectronic
devices and printed circuit boards. Here, a method to improve the
mechanical properties and decrease the dielectric constant of PI films
is reported by introducing a synergistic effect between hydrogen bonding
(H-bonding) and microbranched cross-linking structures. A triamine
monomer (4,4′,4″-(1H-imidazole-2,4,5-triyl)
trianiline, DTI) acting as a hydrogen bond donor was designed and
synthesized. It was then in situ polymerized with commercial 3,3′,4,4′-biphenyl
tetracarboxylic dianhydride (BPDA), 4,4′-(hexafluoroisopropylidene)
diphthalic anhydride (6FDA), 4,4′-oxidianiline (ODA), and 1,4-phenylenediamine
(PDA) to obtain four different PI films, BPDA/ODA/DTI, BPDA/PDA/DTI,
6FDA/ODA/DTI, and 6FDA/PDA/DTI. With the introduction of DTI, the
corresponding PI films exhibited high modulus and low dielectric constant
and coefficient of thermal expansion (CTE). When the DTI content was
optimized, several high-performance PI films suitable for electronic
applications were achieved. At 10 MHz, the dielectric constant of
the 6FDA/PDA series films decreased from 3.39 to 2.89, while the modulus
increased from 3.41 to 4.60 GPa. The CTE of the BPDA/PDA series films
was reduced from 8.61 to 0.27, a reduction of approximately 97%. Structural
characterization, density functional theory (DFT), and molecular dynamics
(MD) simulations revealed the synergistic and competitive relationships
between hydrogen bonds and branched cross-links within the PI molecular
chains. This approach offers a strategy to overcome the performance
trade-off in polyimide films.