Triboelectric polymer with high charge density is the foundation to promote the wide range of applications of triboelectric nanogenerators. This work develops a method to produce triboelectric polymer based on repeated rheological forging. The fluorinated ethylene propylene film fabricated by repeated forging method not only has excellent mechanical properties and good transmittance, but also can maintain an ultrahigh tribo-charge density. Based on the film with a thickness of 30 μm, the output charge density from contact-separation nanogenerator reaches 352 μC·m−2. Then, the same film is applied for the nanogenerator with air-breakdown mode and a charge density of 510 μC·m−2 is further achieved. The repeated forging method can effectively regulate the composition of surface functional groups, the crystallinity, and the dielectric constants of the fluorinated ethylene propylene, leading to the superior capability of triboelectrification. Finally, we summarize the key parameters for elevating the electrification performance on the basis of molecular structure and related fabrication crafts, which can guide the further development of triboelectric polymers.
Although
electrostriction is ubiquitous for dielectric polymers,
giant electrostriction has not been observed until relaxor ferroelectric
(RFE) poly(vinylidene fluoride) (PVDF)-based polymers are achieved.
However, the exact origin for giant electrostriction in these polymers
has not been fully understood. By studying the electrostriction in
the uniaxially stretched films of a ferroelectric poly(VDF-co-trifluoroethylene) [P(VDF-TrFE)] random copolymer and
an RFE poly(VDF-co-TrFE-co-chlorotrifluoroethylene)
[P(VDF-TrFE-CTFE)] random terpolymer in this work, we confirmed that
ferroelectric switching with large hysteresis, such as in the case
of P(VDF-TrFE), was not genuine electrostriction. By decreasing large
ferroelectric domains to the nanometer scale (i.e., 2–3 nm),
such as in the case of the P(VDF-TrFE-CTFE) terpolymer, electrostriction
with low hysteresis could be achieved. Two origins of the large electrostriction
in these polymers were identified. The first was the mechano-electrostriction
due to the poling field-induced conformation transformation of oriented
polymer chains. The second was the electric repulsion of electrically
aligned nanodomains. These effects could occur in both crystals and
the oriented amorphous fraction, which links between the nanocrystals
and the isotropic amorphous fraction. When the poling field was relatively
low (e.g., <40 MV/m), the mechano-electrostriction was the major
contribution and the electric repulsion effect was a minor contribution
to electrostriction. Meanwhile, a strong temperature dependence of
the low-field electrostriction coefficient was observed. Finally,
we found an empirical inverse relationship between the electrostriction
coefficient and the product of Young’s modulus and dielectric
constant. The knowledge obtained from this study provides an insightful
understanding of the electrostriction mechanism in PVDF-based electroactive
polymers, which will find potential applications in sensors and actuators
for wearable electronics and soft robotics.
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