Polymer-based capacitors are very promising for high-power systems due to their high power density and ultrafast charge–discharge speed, yet reaching high dielectric constant and high breakdown strength simultaneously in dielectric polymers required by high-performance capacitors still remains a huge challenge. Herein, poly(vinylidene fluoride- co-trifluoroethylene) (PVDF-TrFE) and poly(vinylidene fluoride- co-hexafluoropropylene) (PVDF-HFP) were coaxial electrospun in core–shell structured fibers to create locally inhomogeneous microstructures deliberately. Through adjusting the functional group HFP/TrFE monomer ratio, P(VDF-HFP)/P(VDF-TrFE) hybrid polymer films with topological composition distribution have been elaborately designed, enabling gradient polarization distribution from core to shell. Compared with homogeneous hybrid films of the same composition, the core–shell structure significantly boosts breakdown strength, thus resulting in a significantly improved energy storage capacity. At an HFP/TrFE monomer ratio of 10:1, an optimal comprehensive energy storage performance has been achieved with Ue ∼ 20.7 J/cm3 and efficiency 67.8%; moreover, the film could maintain its energy storage performance after 106 charge/discharge cycles without reduction. Molecular dynamic simulation and finite element analysis have been employed in combination to reveal the dipole moments distribution at the molecular level and polarization distribution at the microscale, which further demonstrates that elaborate polarization distribution adjustment is an effective strategy toward high-performance electrostatic energy storage capacitors.

Thermoelectrics is the simplest technology applicable for direct energy conversion between heat and electricity. After over 60 years of fruitful research efforts, recent boom in flexible electronics has promoted the rapid development of flexible thermoelectrics with rising performances, discovery of new materials and concepts, unconventional device configuration, and emerging applications not possible for traditional thermoelectric (TE) semiconductors. In this Perspective, we first overview representative flexible TE materials, then discuss recent breakthroughs for flexible TE devices assembled from various types of TE materials employing different technical routes. They exhibit promising power generation and sensing performances, and aim for applications in wearable electronics, such as the power supply harvesting heat from body for low-power electronics, temperature sensors for tactile e-skin, and newly emerged application as a thermo-haptic device in an extended reality system.

High power density capacitors have been highly demanded in modern electronics and pulsed power systems. Yet the long-standing challenge that restricts achieving high power in capacitors lies in the inverse relationship between the breakdown strength and permittivity of dielectric materials. Here, we introduce poly(vinylidene fluoride-co-trifluoroethylene) (PVDF-TrFE) into the host poly(vinylidene fluoride-co-hexafluoro­propylene) (PVDF-HFP) to produce PVDF-based copolymer blends, resulting in composition-driven 0–3 type microstructures, featuring nanospheres of P(VDF-TrFE) lamellar crystals dispersed homogeneously in a P(VDF-HFP) matrix together with crystalline phase evolution from the γ-phase to the α-phase. At the critical composition, the TrFE/HFP mole ratio is equal to 1, and the blend film achieves maximum energy storage performance with discharged energy density (U dis) ∼ 24.3 J/cm3 at 607 MV/m. Finite element analyses reveal the relationship between microstructures, compositions, and the distribution of local electric field and polarization, which provide an in-depth understanding of the microscopic mechanism of the enhancement in energy storage capability of the blend films. More importantly, in a practical charge/discharge circuit, the blend film could deliver an ultrahigh energy density of 20.4 J/cm3, i.e., 88.3% of the total stored energy to 20 kΩ load in 2.8 μs (τ0.9), resulting a high power density of 7.29 MW/cm3, outperforming the reported dielectric polymer-based composites and copolymer films in both energy and power densities. The study thus demonstrates a promising strategy to develop high-performance dielectrics for high power capacitors.