Ruben Windey, Nick Goossens, Marion Cardous, Jeroen Soete, Jozef Vleugels, Martine Wevers
{"title":"将Ti3AlC2 MAX剥离成Ti3C2Tz MXene:一种增强PVDF纳米电介质高压介电性能的有效策略","authors":"Ruben Windey, Nick Goossens, Marion Cardous, Jeroen Soete, Jozef Vleugels, Martine Wevers","doi":"10.1002/admi.202400499","DOIUrl":null,"url":null,"abstract":"<p>All-solid-state polymer dielectrics benefit from a superior voltage window and conveniently circumvent fire hazards associated with liquid electrolytes. Nevertheless, their future competitiveness with alternative energy storage technologies requires a significant enhancement in their energy density. The addition of conductive 2D MXene particles is a promising strategy for creating percolation-based nanodielectrics with improved dielectric response. However, a full understanding of the nanodielectric production – microstructure – dielectric performance correlations is crucial. Therefore, this research considered Ti<sub>3</sub>AlC<sub>2</sub> MAX phase and Ti<sub>3</sub>C<sub>2</sub>T<i><sub>z</sub></i> MXene as electrically conductive ceramic fillers in polyvinylidene fluoride (PVDF). Microstructural characterization of both nanodielectrics demonstrated excellent filler dispersion. Additionally, the exfoliation of Ti<sub>3</sub>AlC<sub>2</sub> brought forth extensive alignment and interface accessibility, synergistically activating a pronounced interfacial polarization and nanocapacitor mechanism that enhanced the energy density of PVDF by a factor 100 to 3.1 Wh kg<sup>−1</sup>@0.1 Hz at 22.9 vol% MXene filler. The stellar increase in the PVDF energy density occurred for a broad MXene filler loading range owing to the unique 2D morphology of MXenes, whereas the addition of Ti<sub>3</sub>AlC<sub>2</sub> fillers only caused a detrimental reduction. Hence, this study buttressed the importance to exfoliate the parental MAX phase into multi-layered MXene as a decisive strategy for boosting nanodielectric performance.</p>","PeriodicalId":115,"journal":{"name":"Advanced Materials Interfaces","volume":"11 36","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admi.202400499","citationCount":"0","resultStr":"{\"title\":\"Exfoliating Ti3AlC2 MAX into Ti3C2Tz MXene: A Powerful Strategy to Enhance High-Voltage Dielectric Performance of Percolation-Based PVDF Nanodielectrics\",\"authors\":\"Ruben Windey, Nick Goossens, Marion Cardous, Jeroen Soete, Jozef Vleugels, Martine Wevers\",\"doi\":\"10.1002/admi.202400499\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>All-solid-state polymer dielectrics benefit from a superior voltage window and conveniently circumvent fire hazards associated with liquid electrolytes. Nevertheless, their future competitiveness with alternative energy storage technologies requires a significant enhancement in their energy density. The addition of conductive 2D MXene particles is a promising strategy for creating percolation-based nanodielectrics with improved dielectric response. However, a full understanding of the nanodielectric production – microstructure – dielectric performance correlations is crucial. Therefore, this research considered Ti<sub>3</sub>AlC<sub>2</sub> MAX phase and Ti<sub>3</sub>C<sub>2</sub>T<i><sub>z</sub></i> MXene as electrically conductive ceramic fillers in polyvinylidene fluoride (PVDF). Microstructural characterization of both nanodielectrics demonstrated excellent filler dispersion. Additionally, the exfoliation of Ti<sub>3</sub>AlC<sub>2</sub> brought forth extensive alignment and interface accessibility, synergistically activating a pronounced interfacial polarization and nanocapacitor mechanism that enhanced the energy density of PVDF by a factor 100 to 3.1 Wh kg<sup>−1</sup>@0.1 Hz at 22.9 vol% MXene filler. The stellar increase in the PVDF energy density occurred for a broad MXene filler loading range owing to the unique 2D morphology of MXenes, whereas the addition of Ti<sub>3</sub>AlC<sub>2</sub> fillers only caused a detrimental reduction. 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Exfoliating Ti3AlC2 MAX into Ti3C2Tz MXene: A Powerful Strategy to Enhance High-Voltage Dielectric Performance of Percolation-Based PVDF Nanodielectrics
All-solid-state polymer dielectrics benefit from a superior voltage window and conveniently circumvent fire hazards associated with liquid electrolytes. Nevertheless, their future competitiveness with alternative energy storage technologies requires a significant enhancement in their energy density. The addition of conductive 2D MXene particles is a promising strategy for creating percolation-based nanodielectrics with improved dielectric response. However, a full understanding of the nanodielectric production – microstructure – dielectric performance correlations is crucial. Therefore, this research considered Ti3AlC2 MAX phase and Ti3C2Tz MXene as electrically conductive ceramic fillers in polyvinylidene fluoride (PVDF). Microstructural characterization of both nanodielectrics demonstrated excellent filler dispersion. Additionally, the exfoliation of Ti3AlC2 brought forth extensive alignment and interface accessibility, synergistically activating a pronounced interfacial polarization and nanocapacitor mechanism that enhanced the energy density of PVDF by a factor 100 to 3.1 Wh kg−1@0.1 Hz at 22.9 vol% MXene filler. The stellar increase in the PVDF energy density occurred for a broad MXene filler loading range owing to the unique 2D morphology of MXenes, whereas the addition of Ti3AlC2 fillers only caused a detrimental reduction. Hence, this study buttressed the importance to exfoliate the parental MAX phase into multi-layered MXene as a decisive strategy for boosting nanodielectric performance.
期刊介绍:
Advanced Materials Interfaces publishes top-level research on interface technologies and effects. Considering any interface formed between solids, liquids, and gases, the journal ensures an interdisciplinary blend of physics, chemistry, materials science, and life sciences. Advanced Materials Interfaces was launched in 2014 and received an Impact Factor of 4.834 in 2018.
The scope of Advanced Materials Interfaces is dedicated to interfaces and surfaces that play an essential role in virtually all materials and devices. Physics, chemistry, materials science and life sciences blend to encourage new, cross-pollinating ideas, which will drive forward our understanding of the processes at the interface.
Advanced Materials Interfaces covers all topics in interface-related research:
Oil / water separation,
Applications of nanostructured materials,
2D materials and heterostructures,
Surfaces and interfaces in organic electronic devices,
Catalysis and membranes,
Self-assembly and nanopatterned surfaces,
Composite and coating materials,
Biointerfaces for technical and medical applications.
Advanced Materials Interfaces provides a forum for topics on surface and interface science with a wide choice of formats: Reviews, Full Papers, and Communications, as well as Progress Reports and Research News.