Triboelectric nanogenerators with ultrahigh current density enhanced by hydrogen bonding between nylon and graphene oxideShow others and affiliations
2023 (English)In: Nano Energy, ISSN 2211-2855, E-ISSN 2211-3282, Vol. 115, article id 108737Article in journal (Refereed) Published
Abstract [en]
The triboelectric properties of the tribolayers are essential factors affecting the current density of triboelectric nanogenerators (TENGs). To enhance the current density, composites have been developed to tune their triboelectric properties. Previous studies have reported enhanced TENG performance with composite materials, primarily based on their composition, while chemical interactions between the components have been less analyzed. In this study, we report a novel approach to improve the current density of a TENG by introducing dipole-dipole interactions between a nylon filter membrane and graphene oxide (GO) through hydrogen bonds. The Raman spectroscopy confirmed the occurrence of the interactions resulting from hydrogen bonding. The enhancing mechanisms of hydrogen bonds were further analyzed by Kelvin probe force microscope (KPFM) measurement, which demonstrated that hydrogen bonding could influence the surface potential of the coated GO, leading to increased output of the nylon/GO@NFM TENG (NGN-TENG). Our results show that an ultrahigh current density of 1757 mA·m−2 was obtained with a 2 × 2 cm2 NGN-TENG. Additionally, we demonstrated the feasibility of using the NGN-TENG as a motion sensor to sense finger motions. These findings suggest that the introduction of hydrogen bonds in TENG composites can provide a promising route for improving their performance.
Place, publisher, year, edition, pages
2023. Vol. 115, article id 108737
Keywords [en]
Current density, Dipoles, Graphene oxide, KPFM, Nylon (PA66), Triboelectric nanogenerators
National Category
Tribology (Interacting Surfaces including Friction, Lubrication and Wear)
Identifiers
URN: urn:nbn:se:miun:diva-49097DOI: 10.1016/j.nanoen.2023.108737ISI: 001060205900001Scopus ID: 2-s2.0-85166197638OAI: oai:DiVA.org:miun-49097DiVA, id: diva2:1788870
2023-08-172023-08-172024-01-12Bibliographically approved