Polymorphic Control of CsGaE <sub>2</sub> (E = S, Se) Using Diorganyl Dichalcogenide Precursors

Diorganyl dichalcogenides (R-E-E-R, where R = organyl and E = S, Se, Te) are employed for the polymorphic control of diamond-like crystal structures, due to their tunable C-E bond reactivity. In this work, we extend their application to non-close-packed alkali-metal-based chalcogenides by demonstrating the selective synthesis of CsGaE<sub>2</sub> (E = S, Se) polymorphs. Weaker C-E bonds or higher temperatures promote the formation of the thermodynamically stable <i>mC</i>64 phases, while stronger C-E bonds or lower temperatures allow for the isolation of the metastable <i>mC</i>16 phases. Heat-treatment studies reveal the pronounced metastability of CsGaSe<sub>2</sub>-<i>mC</i>16 particles and the irreversible phase transition of CsGaS<sub>2</sub> analogous to its bulk counterpart.

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Publication Details

Journal
Inorganic Chemistry
Published
2025-10-24
DOI
https://doi.org/10.1021/acs.inorgchem.5c04153
Citations
2
Primary Topic
Chalcogenide Semiconductor Thin Films
Type
article
Field-Weighted Citation Impact
1.46
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article

Polymorphic Control of CsGaE 2 (E = S, Se) Using Diorganyl Dichalcogenide Precursors

Richard L. Brutchey, Shaama Mallikarjun Sharada, Zhaohong Sun, Eitan I. Feldman et al.
2 citations
Inorganic Chemistry
Chalcogenide Semiconductor Thin Films
1.46
article

Polymorphic Control of CsGaE 2 (E = S, Se) Using Diorganyl Dichalcogenide Precursors

Richard L. Brutchey, Shaama Mallikarjun Sharada, Zhaohong Sun, Eitan I. Feldman, U. Saleem, Christopher P. Pakhanyan
article en
2 citations

Abstract

Diorganyl dichalcogenides (R-E-E-R, where R = organyl and E = S, Se, Te) are employed for the polymorphic control of diamond-like crystal structures, due to their tunable C-E bond reactivity. In this work, we extend their application to non-close-packed alkali-metal-based chalcogenides by demonstrating the selective synthesis of CsGaE<sub>2</sub> (E = S, Se) polymorphs. Weaker C-E bonds or higher temperatures promote the formation of the thermodynamically stable <i>mC</i>64 phases, while stronger C-E bonds or lower temperatures allow for the isolation of the metastable <i>mC</i>16 phases. Heat-treatment studies reveal the pronounced metastability of CsGaSe<sub>2</sub>-<i>mC</i>16 particles and the irreversible phase transition of CsGaS<sub>2</sub> analogous to its bulk counterpart.

Inorganic ChemistryVol. 64(44)
University of Southern California (US), California Southern University (US), Department of Physics, Mathematics and Informatics (BY), Applied Natural Sciences (US), Rice University (US)
Openalex Percentile: Top 15%
Chalcogenide Semiconductor Thin Films
1.46
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