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Daseul Ham

Publications and source records attributed to Daseul Ham.

2 recordsLinked to original sources

Jamming-controlled stochasticity in metal-insulator switching

Understanding and controlling phase transitions is a fundamental part of physics and has been central to many technological revolutions, from steam engines to field-effect transistors. At present, there is strong interest in materials with strongly coupled structural and electronic phase transitions, which hold promise for energy-efficient technologies. Utilizing a structural phase transition and controlling its plasticity naturally leads to built-in memory, a key feature for emulating neurons and synapses in neuromorphic technologies. Here, $\textit{operando}$ Bragg X-ray photon correlation spectroscopy is used to study the evolution of the nano-domain distribution at the micron-scale in neuromorphic devices made from the archetypal Mott insulator vanadium dioxide. It is found that after electrical switching, slow nano-domain reconfiguration occurs on timescales of thousands of seconds and that the domains undergo a jamming transition, offering control over switching stochasticity at the micron scale. More precisely, repetitive above-threshold currents plastically drive the system into a jammed/glassy state where switching becomes deterministic, while sub-threshold currents erase the short-term memory contained in the nano-domain distribution, recovering stochastic switching, thus offering a path for in-device learning. The results illustrate the importance of studying the nanoscale physics associated with phase transitions in strongly correlated materials, even for macroscopic devices, and offer guidance for future device operation schemes.

cond-mat.mes-hall

Dynamic nanoscale spatial heterogeneity in a perovskite to brownmillerite topotactic phase transformation

Phase transitions are omnipresent in modern condensed matter physics and its applications. In solids, first-order phase transformations typically occur by nucleation and growth under non-equilibrium conditions. Under constant external conditions, $\textit{e.g.}$, constant annealing temperature and pressure, the nucleation and growth dynamics are often thought of as spatially and temporally independent. Here, $\textit{in-situ}$ Bragg X-ray photon correlation spectroscopy (XPCS) reveals nanoscale spatial and dynamical heterogeneity in the perovskite-to-brownmillerite topotactic phase transformation in La$_{0.7}$Sr$_{0.3}$CoO$_3$ thin films annealed under constant reducing conditions over a time span of multiple hours. Specifically, a timescale associated with domain growth remains stable, with a corresponding domain wall speed of $v_d = 6 \pm 0.5 \times10^{-4}$~nm/s ($2 \pm 0.2$~nm/h), while a slower timescale, associated with temperature-driven de-pinning of domains, leads to accelerating dynamics with timescales following an aging power law with exponent -2.2$\pm$0.5. This experiment demonstrates that Bragg XPCS is a powerful tool to study nanoscale dynamics in structural phase transformations, with the ability to extract quantitative average values related to nano-domain motion $\textit{in-situ}$. The results are relevant for phase engineering of phase-change devices, as they show that nanoscale dynamics, linked to domain and domain-wall motion, can continuously evolve and speed up with time, even hours after the initiation of the phase transformation, with potential repercussions on electrical performance.

cond-mat.mtrl-sci