Dual-frequency resonance tracking in switching spectroscopy piezoresponse force microscopy for ferroelectric thin
Hugo Valloire1, Nicolas Vaxelaire1, Thomas Jalabert1
1Univ. Grenoble Alpes, CEA, Leti, F-38000 Grenoble, France.
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Switching spectroscopy piezoresponse force microscopy (SSPFM) is widely used to probe local polarization reversal in ferroelectric thin films, but resonance-enhanced implementations remain difficult to apply to large datasets because they typically rely on repeated frequency sweeps, leading to longer acquisition times, higher noise levels, and fitting-related instability. Here, we introduce an approach that combines SSPFM with real-time dual-frequency resonance tracking (DFRT), allowing the excitation frequency to remain locked to the instantaneous contact-resonance frequency throughout the spectroscopy sequence. This strategy extends the benefits of real-time resonance tracking, commonly exploited in continuous measurements, to pulsed switching spectroscopy, while avoiding repeated reconstruction of the full resonance peak at each voltage step. The method is evaluated on a Pb()thin film and compared with two conventional SSPFM approaches: sweep-based and fixed-frequency measurements. At short segment durations, sweep-based SSPFM becomes increasingly affected by phase noise, phase-inversion artifacts, and fitting errors, whereas SSPFM-DFRT preserves low noise and measurement stability. In addition, the conversion of raw data into hysteresis loops is substantially faster because no repeated resonance fitting is required. Compared with fixed-frequency SSPFM, it also compensates resonance shifts, which become critical during prolonged measurements such as point matrix acquisitions and would otherwise reduce measurement repeatability and robustness. Finally, SSPFM-DFRT is demonstrated in mapping mode on apoint matrix, where it enables robust extraction of switching parameters with high fit quality across the dataset. Overall, this approach provides a practical route to faster, more stable, and more robust resonance-enhanced SSPFM for spectroscopy and mapping, particularly when short measurement times and reliable large-scale measurements are required.

