Abstract
Recent advancements in self-charging power devices highlight the potential of dielectric nanofillers in polymer matrixes to improve the performance of microsupercapacitor-triboelectric nanogenerator (TENG) integrated devices. However, achieving homogeneous dispersion of nanofillers into polymer matrixes remains a key bottleneck, often leading to inconsistent performance, reduced stability, and lower energy efficiency. This work presents an innovative chemical functionalization strategy covalently knitting MXene/graphene oxide (GO)/siloxene and MXene/reduced GO/siloxene networks into textile substrates, resulting in a consistent output performance and the development of a durable device. The single-electrode TENG delivered an output voltage of 380 V, a current density of 6.3 μA/cm2, a power density of 627 μW/cm2, and the transfer of 0.55 ± 0.03 μC of charge. The integrated device charged a voltage of 2.4 V after 110 s of continuous hand tapping, powering smart electronics. These results showcase the potential of chemically engineered heterostructures to address longstanding challenges in self-charging devices.
| Original language | English |
|---|---|
| Pages (from-to) | 6942-6949 |
| Number of pages | 8 |
| Journal | Nano Letters |
| Volume | 25 |
| Issue number | 17 |
| DOIs | |
| State | Published - 30 Apr 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- chemically modified textiles
- citric acid-induced stabilization
- covalently bonded frameworks
- integrated energy devices
- sustainable power systems
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