“…The formation mechanism of the β-crystal of iPP induced by DCHT/DCHN is well explained by epitaxial crystallization, which defines a favorable dimensional match with a mismatch less than ±15% on the contact plane between the deposit and substrate. − A two-dimensional match between the β-crystal and DCHT/DCHN crystal, including the chain axis and interchain directions, has been proposed to be a premise to readily induce the formation of β - nuclei. ,− Importantly, the β-nucleation efficiency of aromatic amide β-NAs is determined by the epitaxial match between the growth planes of β-crystal and the specific surfaces of β-NA crystal, which is profoundly influenced by the chemical structure and crystal structure of NAs . Several studies demonstrated that the K β value in iPP is remarkably affected by the chemical structure of aromatic/aliphatic amide-based β-NAs, including the symmetry of the molecules, type and length of the central alkyl group, and type and size of the peripheral substitution. − The dominant role of the crystal structure of NAs was reported by Zhou et al, who found that 2,6-naphthalenedicarboxamide and 1,4-naphthalenedicarboxamide show different crystal structures, and the former selectively induces the formation of β - crystals, while the latter exhibits a very weak α-nucleation effect . Interestingly, aromatic bisamide-based β-NAs can be dissolved to different extents in the iPP melt, depending on the final heating temperature ( T f ) and their content, and can subsequently crystallize to form different morphologies, including dotlike, needle-like, and dendritic morphologies, in the following cooling process. ,− Accordingly, the K β value is indispensably influenced by the recrystallized morphology of β-NAs in the iPP melt.…”