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In this perspective, we discuss the fundamental mechanisms and the length scales responsible for the formation of micro- and nanoplastics (MNPLs), MNPL size, shape, and morphologies, their metrology, and open questions in the field. 

Coacervate films with varying interaction strengths were exposed to dielectric spectroscopy and it was finally established thatT_gand fragility have opposing trends when interaction strength increases. 

Dielectric capacitors are critical components in electronics and energy storage devices. The polymer-based dielectric capacitors have the advantages of device flexibility, fast charge–discharge rates, low loss, and graceful failure. Elevating the use of polymeric dielectric capacitors for advanced energy applications such as electric vehicles (EVs), however, requires significant enhancement of their energy densities. Here, we report a polymer thin film heterostructure-based capacitor of poly(vinylidene fluoride)/poly(methyl methacrylate) with stratified 2D nanofillers (Mica or h-BN nanosheets) (PVDF/PMMA-2D fillers/PVDF), that shows enhanced permittivity, high dielectric strength, and an ultrahigh energy density of ≈75 J/cm3 with efficiency over 79%. Density functional theory calculations verify the observed permittivity enhancement. This approach of using oriented 2D nanofillers-based polymer heterostructure composites is expected to be versatile for designing high energy density thin film polymeric dielectric capacitors for myriads of applications. 

The block copolymer (BCP) phase separation is an intriguing phenomenon, the dynamics of which can be expected to differ significantly from that of the polymer blends due to the chain connectivity constraints. The BCP phase separation dynamics has been studied theoretically, but there has been little experimental evidence to confirm the BCP domain growth scaling laws put forward by theoretical studies. Here, we demonstrate the dynamics of late-stage lamellar BCP domain coarsening and show that the scaling exponent for domain growth is ≈1/6 (0.17) irrespective of the annealing temperature, which is close to the scaling exponent of 0.2 shown by theoretical studies. Furthermore, we show that the pre-factors in the domain coarsening equation show Arrhenius dependence on temperature indicating that the BCP domain growth dynamics is Arrhenius.