Enhancing Mechanical Energy Transfer of Piezoelectric Supercapacitors Show others and affiliations
2021 (English) In: Advanced Materials Technologies, E-ISSN 2365-709XArticle in journal (Refereed) Published
Abstract [en]
The expected widespread use of wearable and other low-power healthcare devices has triggered great interest in piezoelectric materials as a promising energy harvester. However, traditional piezoelectric materials suffer from poor interfacial energy transfer when used in self-charging power cells. Herein, piezoelectric supercapacitors (PSCs) are engineered using MXene-incorporated polymeric piezo separator and MXene (Ti3C2Tx) multilayered sheets as electrodes. The MXene-blended polymer film showed considerable improvement with maximum output voltage of 28 V and current of 1.71 µA. The electromechanical properties studied by piezoelectric force microscopy suggest that the integration of MXene in polyvinylidene fluoride (PVDF) matrix induces the degree of dipole moment alignment, thereby improving the piezoelectric properties of PVDF. At the device level, the PSC featured the capacitance of 61 mF cm–2, the energy density of 24.9 mJ cm−2, the maximum power density of 1.3 mW cm−3, and the excellent long-term cycling stability. A way is paved toward green, integrated energy harvesting and storing technology for next-generation self-powered implantable and wearable electronics. © 2021 Wiley-VCH GmbH
Place, publisher, year, edition, pages John Wiley and Sons Inc , 2021.
Keywords [en]
MXene, nanogenerators, piezo-supercapacitor, piezoelectricity, polyvinylidene fluoride, supercapacitors, Capacitance, Crystallography, Energy transfer, Fluorine compounds, Piezoelectric materials, Polymer films, Semiconducting films, Supercapacitor, Wearable technology, Energy Harvester, Energy-transfer, Low Power, Mechanical energies, Piezoelectric, Polyvinylidene fluorides
Identifiers URN: urn:nbn:se:miun:diva-43441 DOI: 10.1002/admt.202100550 ISI: 000698504200001 Scopus ID: 2-s2.0-85115358520 OAI: oai:DiVA.org:miun-43441 DiVA, id: diva2:1604045
2021-10-182021-10-182022-09-15 Bibliographically approved