In Spite of the Chemist’s Belief: Metastable Hydrates of CsCl

In this work, we focus on the low-temperature behavior of concentrated aqueous solutions of cesium chloride and discover two hydrates of CsCl. We employ four different methods, namely, (i) simple cooling at rates between 0.5 and 80 K s<sup>-1</sup>, (ii) simple cooling followed by pressurization, (iii) hyperquenching at 10<sup>6</sup> to 10<sup>7</sup> K s<sup>-1</sup>, and (iv) hyperquenching followed by pressurization. Depending on the method, different types of phase behaviors are observed, which encompass crystallization involving freeze-concentration, pressure-induced amorphization, full vitrification, and polyamorphic transformation. The CsCl hydrates discovered in our work cold-crystallize above 150 K upon heating after ultrafast vitrification (routes iii and iv) and show melting temperatures <i>below</i> the eutectic temperature of 251 K. We determine the composition of these hydrates to be CsCl·5H<sub>2</sub>O and CsCl·6H<sub>2</sub>O and find evidence for their existence in ESEM, calorimetry, and X-ray diffraction. The dominant and less metastable hydrate is the hexahydrate, where the pentahydrate appears as a minority species. We also reveal the birthplace for the CsCl hydrates, namely, the freeze-concentrated solution (FCS) formed upon cold-crystallization of the fully glassy solution (from iii and iv). The spongy FCS produced upon <i>cooling</i> of the liquid (from i and ii) is incapable of crystallizing CsCl-hydrates. By contrast, the FCS produced upon <i>heating</i> the glassy solution (from iii and iv) shows tiny, fine features that are capable of crystallizing CsCl-hydrates. Our findings contradict the current knowledge that alkali chlorides only have hydrates for the smaller cations Li<sup>+</sup> and Na<sup>+</sup>, but not for the larger cations K<sup>+</sup>, Rb<sup>+</sup>, and Cs<sup>+</sup> and pave the way for future determination of CsCl-hydrate crystal structures. The pathway to metastable crystalline materials outlined here might be more generally applicable and found in nature, e.g., in comets or on interstellar dust grains, when glassy aqueous solutions crystallize upon heating.

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Journal
ACS Physical Chemistry Au
Published
2025-02-06
DOI
https://doi.org/10.1021/acsphyschemau.4c00093
Primary Topic
Material Dynamics and Properties
Type
article
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0.00

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article

In Spite of the Chemist’s Belief: Metastable Hydrates of CsCl

Ľubica Vetráková, Kamila Závacká, Johannes Bachler, Vilém Neděla et al.
ACS Physical Chemistry Au
Material Dynamics and Properties
article

In Spite of the Chemist’s Belief: Metastable Hydrates of CsCl

Ľubica Vetráková, Kamila Závacká, Johannes Bachler, Vilém Neděla, Thomas Loerting
article en

Abstract

In this work, we focus on the low-temperature behavior of concentrated aqueous solutions of cesium chloride and discover two hydrates of CsCl. We employ four different methods, namely, (i) simple cooling at rates between 0.5 and 80 K s<sup>-1</sup>, (ii) simple cooling followed by pressurization, (iii) hyperquenching at 10<sup>6</sup> to 10<sup>7</sup> K s<sup>-1</sup>, and (iv) hyperquenching followed by pressurization. Depending on the method, different types of phase behaviors are observed, which encompass crystallization involving freeze-concentration, pressure-induced amorphization, full vitrification, and polyamorphic transformation. The CsCl hydrates discovered in our work cold-crystallize above 150 K upon heating after ultrafast vitrification (routes iii and iv) and show melting temperatures <i>below</i> the eutectic temperature of 251 K. We determine the composition of these hydrates to be CsCl·5H<sub>2</sub>O and CsCl·6H<sub>2</sub>O and find evidence for their existence in ESEM, calorimetry, and X-ray diffraction. The dominant and less metastable hydrate is the hexahydrate, where the pentahydrate appears as a minority species. We also reveal the birthplace for the CsCl hydrates, namely, the freeze-concentrated solution (FCS) formed upon cold-crystallization of the fully glassy solution (from iii and iv). The spongy FCS produced upon <i>cooling</i> of the liquid (from i and ii) is incapable of crystallizing CsCl-hydrates. By contrast, the FCS produced upon <i>heating</i> the glassy solution (from iii and iv) shows tiny, fine features that are capable of crystallizing CsCl-hydrates. Our findings contradict the current knowledge that alkali chlorides only have hydrates for the smaller cations Li<sup>+</sup> and Na<sup>+</sup>, but not for the larger cations K<sup>+</sup>, Rb<sup>+</sup>, and Cs<sup>+</sup> and pave the way for future determination of CsCl-hydrate crystal structures. The pathway to metastable crystalline materials outlined here might be more generally applicable and found in nature, e.g., in comets or on interstellar dust grains, when glassy aqueous solutions crystallize upon heating.

ACS Physical Chemistry AuVol. 5(2)
Universität Innsbruck (AT), Czech Academy of Sciences, Institute of Scientific Instruments (CZ)
Österreichischen Akademie der Wissenschaften, Grantová Agentura České Republiky, Austrian Science Fund, Universität Innsbruck
Life below water
Openalex Percentile: Top 99%
Material Dynamics and Properties
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