Superatomic Layer of Cubic Mo<sub>4</sub>S<sub>4</sub> Clusters Connected by Cl Cross-Linking.
basic_science · Level V
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- Record sourced from PubMed, PMID 39054657.
- Also identified by DOI 10.1002/adma.202404249.
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Abstract
Superatomic clusters - assemblies of atoms with various sizes, shapes, and compositions - can form hierarchical architectures that exhibit emergent electronic properties not found in their individual units. In particular, cubic M<sub>4</sub>X<sub>4</sub> clusters of chalcogenides (M = transition metal; X = chalcogen) are recognized as versatile building blocks for 3D structures with tunable morphologies and electronic properties. However, tetrahedral M<sub>4</sub>X<sub>4</sub> clusters rarely assemble into 2D architectures, which could offer a distinct class of functional materials from their 3D analogues. Here, this work reports the preparation of 2D Mo<sub>8</sub>S<sub>8</sub>Cl<sub>11</sub>, a superatomic layer with a sandwich structure consisting of Mo<sub>4</sub>S<sub>4</sub> clusters interconnected through Cl cross-linking. The vapor-phase reaction inside nanotubes promotes the selective growth of Mo<sub>8</sub>S<sub>8</sub>Cl<sub>11</sub> nanoribbons, allowing detailed characterization via transmission electron microscopy. This methodology can be applied to the growth of layered structures containing Mo<sub>8</sub>S<sub>8</sub>Cl<sub>11</sub> at the micrometer scale. This work has demonstrated that mono- and few-layer Mo<sub>8</sub>S<sub>8</sub>Cl<sub>11</sub> can be prepared by exfoliation of parent solids. Electronic structure calculations indicate that the 2D monolayer has quasi-flat bands, giving rise to an indirect-to-direct bandgap transition under mechanical strain. Furthermore, scanning electrochemical microscopy reveals the potential of the layered structures as highly efficient catalysts for the hydrogen-evolution reaction.