Abstract
We report a high-performance flexible piezoelectric generator (PEG) that was based on organic-inorganic lead halide perovskite materials and is operated by controlling the dielectric constant via the partial substitution of Pb2+ with Fe2+ in MAPbI3. The partial replacement of Pb2+ with Fe2+ improved both the morphology and crystallinity of MAPb1-xFexI3 (0.01 ≤ x ≤ 0.50) films that undergo a tetragonal-cubic phase transition above an incorporated concentration of Fe2+ (x > 0.07). In addition, the phase transition temperatures of MAPb1-xFexI3 (0.01 ≤ x ≤ 0.07) films linearly decreased as a function of incorporated concentration, which resulted in a transition temperature for MAPb1-xFexI3 (x = 0.07) of ~ 45.5 ± 1.5 °C. The dielectric properties as a function of incorporated concentration at room temperature suggested that MAPb1-xFexI3 (x = 0.07) exhibited a dielectric constant of ~107 and a dissipation factor of 0.02 at 100 kHz. The MAPb1-xFexI3 (x = 0.07) films exhibited a low leakage current density of ~ 10−6 at a high applied electric field of 40 kV/cm, and the resultant remanent polarization from saturated ferroelectric P-E hysteresis loops was ~ 1.6 µC/cm2. The MAPb1-xFexI3 (x = 0.07) flexible PEG improved output performance by ~ 7.29 V and current density by ~ 0.88 µA/cm2 after poling at 30 kV/cm. This was sufficient to instantly light a commercial light-emitting diode (LED) without a storage device. This approach provides a framework that enhances the output performance of organic-inorganic metal halide perovskite materials-based piezoelectric energy harvesters, which could help pave the road to viable, self-powered, wearable electronics.
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