dorsal/arxiv
View SchemaDynamic nanoscale spatial heterogeneity in a perovskite to brownmillerite topotactic phase transformation
| Authors | Nicolò D'Anna, Erik S. Lamb, Robin Glefke, Daseul Ham, Ishmam Nihal, Su Yong Lee, Yayoi Takamura, Oleg Shpyrko |
|---|---|
| Categories | |
| ArXiv ID | 2601.06365vv1 |
| URL | https://arxiv.org/abs/2601.06365 |
| License | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
Abstract
Phase transitions are omnipresent in modern condensed matter physics and its applications. In solids, phase transformations typically occur by nucleation and growth under non-equilibrium conditions. Under constant external conditions, $\textit{e.g.}$, constant heating 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$_3$ (LSCO) thin films 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 $-2.2 \pm 0.5$. The experiment demonstrates that Bragg XPCS is a powerful tool to study nanoscale dynamics in phase transformations. 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.
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"abstract": "Phase transitions are omnipresent in modern condensed matter physics and its applications. In solids, phase transformations typically occur by nucleation and growth under non-equilibrium conditions. Under constant external conditions, $\\textit{e.g.}$, constant heating 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$_3$ (LSCO) thin films 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 $-2.2 \\pm 0.5$. The experiment demonstrates that Bragg XPCS is a powerful tool to study nanoscale dynamics in phase transformations. 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.",
"arxiv_id": "2601.06365",
"authors": [
"Nicol\u00f2 D\u0027Anna",
"Erik S. Lamb",
"Robin Glefke",
"Daseul Ham",
"Ishmam Nihal",
"Su Yong Lee",
"Yayoi Takamura",
"Oleg Shpyrko"
],
"categories": [
"cond-mat.mtrl-sci",
"cond-mat.mes-hall"
],
"license": "http://creativecommons.org/licenses/by-nc-nd/4.0/",
"title": "Dynamic nanoscale spatial heterogeneity in a perovskite to brownmillerite topotactic phase transformation",
"url": "https://arxiv.org/abs/2601.06365",
"version": "v1"
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