Polar nanoregions (PNRs) are central to understanding the exceptional dielectric and piezoelectric properties of relaxor ferroelectrics and are key to advancing dielectrics for high-energy storage. However, direct real-space imaging of their formation and evolution remains a major challenge in condensed matter physics. Here, we report the real-space mappings of both PNRs and chemically ordered regions (CORs) in the prototypical relaxor Pb(Mg1/3Nb2/3)O3 and their temperature dependence using convergent-beam electron diffraction combined with four-dimensional scanning transmission electron microscopy. The results reveal that CORs, with sizes of 2–5 nm, remain static with temperature and act to suppress PNR growth. In contrast, PNRs evolve from isolated 2–5 nm regions at room temperature to interconnected structures ∼10 nm in size at low temperatures, indicative of a percolation transition. These observations support the random-field model, in which PNRs emerge from a paraelectric matrix and their growth and collective interactions are constrained by random local fields associated with CORs.
Hino et al. (Sun,) studied this question.
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