Biodegradable Single-Electrode Triboelectric Nanogenerator for Self-Powered Robotic Texture Sensing

Abstract

Human tactile acuity relies on the microstructured morphology of the fingertips, which enables sensitive detection of fine surface features during object manipulation. While triboelectricbased self-powered object, recognition has gained much attention, conventional triboelectric materials are typically non-biodegradable, contributing to persistent electronic waste. This work focuses on fabricating biodegradable triboelectric interfaces for intelligent robotic texture perception and sustainable energy harvesting. Three biodegradable polymers, polylactide (PLA), poly(ε-caprolactone) (PCL), and poly(lactide-co-trimethylene carbonate) (PTMC), were evaluated as negative triboelectric layers against an aluminum electrode to form a singleelectrode triboelectric nanogenerator (TENG). The PCL/Al TENG achieved a superior electrical output of 118 V and 772 nA, with a peak power of 24.5 µW at 200 MΩ, primarily due to its higher surface roughness enhancing charge transfer. The powering of the low-power electronics and charging of the capacitors using the TENG was demonstrated. In addition, the platform was integrated into a robotic gripper for real-time texture recognition. Combined with a convolutional neural network (CNN), the system achieved 96.9% classification accuracy across eight distinct textures. This sustainable platform reduces environmental impact through the use of degradable materials while maintaining the mechanical robustness required for advanced robotic sensing.

Supplementary files

Article information

Article type
Research Article
Submitted
17 Mar 2026
Accepted
11 May 2026
First published
14 May 2026
This article is Open Access
Creative Commons BY license

Mater. Chem. Front., 2026, Accepted Manuscript

Biodegradable Single-Electrode Triboelectric Nanogenerator for Self-Powered Robotic Texture Sensing

S. Hajra, S. Pal, K. R. Kaja, Y. Choi, S. Panda, B. K. Panigrahi, H. J. Kim and A. Finne Wistrand, Mater. Chem. Front., 2026, Accepted Manuscript , DOI: 10.1039/D6QM00202A

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