Optimization of the sensing performance of BaTiO3/P(VDF-TrFE) via proton irradiation
Abstract
A pyroelectric–piezoelectric dual-mode sensor simultaneously decodes temperature and strain, serving as a core component for health monitoring, human–machine interfaces, and bionic skin applications. To achieve high fidelity, self-powering, and long-term endurance, the sensing materials must balance sensitivity, stability, and multi-physics field coordination across multiple scales. This study employs a synergistic strategy combining a barium titanate (BaTiO3) composite with proton irradiation to regulate a polyvinylidene fluoride-trifluoroethylene (P(VDF-TrFE)) copolymer. By enhancing the crystallinity and the β-phase content of P(VDF-TrFE) while introducing oxygen vacancies and lattice distortions within the BaTiO3 lattice, the strategy significantly strengthens interfacial polarization coupling and charge transport efficiency. As a result, a composite with 2 wt% BaTiO3 shows an increased pyroelectric coefficient (p) of 66.1 µC m−2 K−1. Although the piezoelectric coefficient (d33) slightly decreases from 22.0 pC N−1 to 20.1 pC N−1, its variation range (standard deviation) narrows from 3.9 to 3.1. Subsequent proton irradiation at 1 × 1010 p cm−2 further increases p to 86.6 µC m−2 K−1, accompanied by a slight decrease in d33. At 5 × 1010 p cm−2 fluence, p maintains a 6.8% increase compared to pre-irradiation levels, and d33 recovers to 20.0 pC N−1 with a standard deviation reduced to 2.4, effectively balancing piezoelectric uniformity and stability with high pyroelectric sensitivity. The composite film exhibits a linear sensitivity of 1.2 V K−1 over the temperature range of 0.1–12.2 K, with no degradation observed after 103 thermal cycles. It conformally adheres to the human body and enables real-time analysis of respiration, pulse, and touch signals, offering a novel approach for high-sensitivity, high-reliability dual-mode sensing in wearable electronics and bionic skin applications.
- This article is part of the themed collection: Journal of Materials Chemistry C HOT Papers

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