“…A variety of experimental techniques including small-angle X-ray scattering (SAXS), transmission electron microscopy (TEM), , and nuclear magnetic resonance (NMR) were utilized to investigate the thickness and composition of the interphase of multiphase polymers. Solid-state NMR (SSNMR) spectroscopy has been proven to be a nondestructive and powerful multiscale technique to study the interphase property of polymers, including related interfacial intermolecular interactions on the length scale from the atomic level to several tens of nanometers. , Usually, high-resolution 1 H or 13 C NMR experiments provide useful information on the intermolecular interaction because of their sensitivity to local chemical environments. , Furthermore, by measuring the time scale of proton spin diffusion, the length scales in nanoscopic heterogeneities from a few angstroms up to 100 nm and the interphase between different microdomains in polymers can be well-determined. , On the basis of the differences in molecular mobility of different phases, 1 H dipolar filter spin-diffusion NMR experiments have been extensively applied to investigate the microphase structure in multiphase solid polymers, such as polymer blends, block copolymers, core–shell polymers, and so on.…”