9,098 research outputs found

    Piezoelectric effect and electroactive phase nucleation in self-standing films of unpoled PVDF nanocomposite films

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    Novel polymer-based piezoelectric nanocomposites with enhanced electromechanical properties open new opportunities for the development of wearable energy harvesters and sensors. This paper investigates how the dissolution of different types of hexahydrate metal salts affects β-phase content and piezoelectric response (d33) at nano-and macroscales of polyvinylidene fluoride (PVDF) nanocomposite films. The strongest enhancement of the piezoresponse is observed in PVDF nanocomposites processed with Mg(NO3)2·6H2O. The increased piezoresponse is attributed to the synergistic effect of the dipole moment associated with the nucleation of the electroactive phase and with the electrostatic interaction between the CF2group of PVDF and the dissolved salt through hydrogen bonding. The combination of nanofillers like graphene nanoplatelets or zinc oxide nanorods with the hexahydrate salt dissolution in PVDF results in a dramatic reduction of d33, because the nanofiller assumes a competitive role with respect to H-bond formation between PVDF and the dissolved metal salt. The measured peak value of d33reaches the local value of 13.49 pm/V, with an average of 8.88 pm/V over an area of 1 cm2. The proposed selection of metal salt enables low-cost production of piezoelectric PVDF nanocomposite films, without electrical poling or mechanical stretching, offering new opportunities for the development of devices for energy harvesting and wearable sensors

    An Effective Method to Estimate Composition Amplitude of Spinodal Decomposition for Atom Probe Tomography Validated by Phase Field Simulations

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    Reasonable evaluation of composition amplitude in spinodal decomposition is a challenge to microanalysis of atom probe tomography, especially at early stages when phase separation is not prominent. This impedes quantitative analysis of spinodal structure in atom probe tomography as well as comparison with simulated results from phase field simulations. We hereby report an effective method to estimate the composition amplitude by constructing an amplitude density spectrum. This method can sensitively determine the composition amplitude at early stages. In particular, it substantially bridges experimental and simulation techniques comprising both discrete and continuum data in the study of spinodal decomposition. Moreover, it was found that the commonly adopted Langer-Bar-on-Miller method for atom probe analysis underestimates the composition amplitude of spinodal decomposition. Case studies have been performed on the Fe-Cr binary alloys.Comment: 5 pages, 4 figure

    High density array of epitaxial BiFeO3 nanodots with robust and reversibly switchable topological domain states

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    The exotic topological domains in ferroelectrics and multiferroics have attracted extensive interest in recent years due to their novel functionalities and potential applications in nanoelectronic devices. One of the key challenges for such applications is a realization of robust yet reversibly switchable nanoscale topological domain states with high density, wherein spontaneous topological structures can be individually addressed and controlled. This has been accomplished in our work using high density arrays of epitaxial BiFeO3 (BFO) nanodots with lateral size as small as ~60 nm. We demonstrate various types of spontaneous topological domain structures, including center-convergent domains, center-divergent domains, and double-center domains, which are stable over sufficiently long time yet can be manipulated and reversibly switched by electric field. The formation mechanisms of these topological domain states, assisted by the accumulation of compensating charges on the surface, have also been revealed. These result demonstrated that these reversibly switchable topological domain arrays are promising for applications in high density nanoferroelectric devices such as nonvolatile memoriesComment: 5 figures, 18 pages, plus supplementary material
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