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Vacuum-Compatible Electrode-Free Poling of PVDF Films Using Glow-Discharge Plasma
Bogdan A Basov1, Evgeniya L Buryanskaya1,2, Kamila T Makarova1
1Laboratory of Ferroelectric Polymers, Bauman Moscow State Technical University, 105005 Moscow, Russia.
Glow-discharge plasma (GDP) poling activates piezoelectricity in poly(vinylidene fluoride) (PVDF) films without electrodes. Optimal poling occurs within 1-5 minutes, enhancing piezoelectric response and surface wettability for flexible electronic devices.
Area of Science:
- Materials Science
- Polymer Science
- Surface Science
Background:
- Glow-discharge plasma (GDP) poling is an electrode-free method for activating piezoelectricity in poly(vinylidene fluoride) (PVDF) films.
- The effects of GDP on PVDF properties have been poorly understood despite its proposal decades ago.
Purpose of the Study:
- To demonstrate efficient electrode-free poling of oriented PVDF films using GDP.
- To investigate the relationship between plasma treatment time, structural evolution, and piezoelectric response in PVDF films.
Main Methods:
- Oriented PVDF films were treated using DC glow discharge for durations ranging from 15 seconds to 15 minutes.
- Characterization involved FTIR, DSC, piezoresponse force microscopy, UV-Vis-NIR spectrophotometry, quasi-static d33 measurements, and water contact-angle measurements.
Main Results:
- GDP poling achieved a piezoelectric coefficient (d33) up to ~25 pC/N within 1-5 minutes, with maxima at 1, 2.5, and 5 minutes.
- Plasma treatment increased ferroelectric domain size and surface wettability (water contact angle reduced to 42° within 3 minutes).
- Longer treatment times (>5 min) led to decreased piezoelectric response and optical transparency due to surface degradation.
Conclusions:
- GDP poling offers an effective processing window of 1-5 minutes for PVDF films.
- This electrode-free, vacuum-compatible method enhances surface wettability for applications in flexible piezoelectric sensors and wearable electronics.
- The process allows for subsequent electrode deposition on the activated polymer surface within a single vacuum cycle.
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