Abstract: Ferroelectricity on the nanoscale has remained a subject of
much fascination in condensed matter physics for the last several
decades. It is well-recognized that stability of the ferroelectric state
necessitates effective polarization screening, and hence screening
mechanism and screening charge dynamics become strongly coupled to
ferroelectric phase stability and domain behavior. Previously, the role
of the screening charge in macroscopic ferroelectrics was observed in
phenomena such as potential retention above Curie temperature, back
switching of ferroelectric domains, and chaos and intermittency during
domain switching. In the last several years, multiple reports claiming
ferroelectricity in ultrathin ferroelectrics based on formation of
remanent polarization states, local hysteresis loops, and pressure
induced switching were made. However, similar phenomena were reported
for traditionally non-ferroelectric materials, creating significant
level of uncertainty in the field. We pose that in the nanoscale
systems, the ferroelectric state is fundamentally inseparable from
electrochemical state of the surface, leading to emergence of coupled
electrochemical-ferroelectric states. I will present the results of
experimental and theoretical work exploring the basic mechanisms of
emergence of these coupled states including the basic theory and
phase-field formulation for domain evolution. I further discuss the
thermodynamics and thickness evolution of this state using analytical
theory and phase-field modelling. These considerations further stimulate
the development of the novel SPM modalities addressing time-dependent
dynamics and chemical changes during SPM imaging. I will introduce the
general data acquisition mode (GMode) of SPM, based on full data capture
and subsequent information theory and physics based analysis of the data
stream. I will further delineate the applications of in-situ SPM – time
of flight secondary ion mass spectrometry (ToF SIMS) to map the changes
in surface chemistry during tribological and local electrochemical
experiments, including ferroelectric polarization switching and
pressure-induced resistance changes in oxides. These analyses reconcile
multiple prior studies, and set forward the predictive pathways for new
generations of ferroelectric devices and applications.