Unveiling the distinctive mechanical and thermal properties of γ-GeSe.

γ-GeSe is a newly identified polymorph among group-IV monochalcogenides, characterized by a distinctive interatomic bonding configuration. Despite its promising applications in electrical and thermal domains, the experimental verification of its mechanical and thermal properties remains unreported. Here, we experimentally characterize the in-plane Young's modulus (E) and thermal conductivity ([Formula: see text]) of γ-GeSe. The mechanical vibrational modes of freestanding γ-GeSe flakes are measured using optical interferometry. Nano-indentation via atomic force microscopy is also conducted to induce mechanical deformation and to extract the E. Comparison with finite-element simulations reveals that the E is 97.3[Formula: see text]7.5 GPa as determined by optical interferometry and 109.4[Formula: see text]13.5 GPa as established through the nano-indentation method. Additionally, optothermal Raman spectroscopy reveals that γ-GeSe has a lattice thermal conductivity of 2.3 [Formula: see text] 0.4 Wm-1K-1 and a total thermal conductivity of 7.5 [Formula: see text] 0.4 Wm-1K-1 in the in-plane direction at room temperature. The notably high [Formula: see text] ratio in γ-GeSe, compared to other layered materials, underscores its distinctive structural and dynamic characteristics.

Precise Determination of Offset between Optical Axis and Re-Chain Direction in Rhenium Disulfide.

ReS2 is a group-VII chalcogenide with a crystal structure that has inversion symmetry only. Due to the low symmetry, it has in-plane anisotropy, and the two vertical orientations are not equivalent. The in-plane anisotropy leads to optical birefringence that can be observed by using polarized optical microscopy. We found ReS2 crystals with domains of inequivalent vertical orientations but with the same Re-chain directions. Polarized Raman spectroscopy was used to determine the vertical orientations and the b-axis (Re-chain) directions of the domains, and high-resolution scanning transmission electron microscopy measurements confirmed that the Re-chain directions of the two types of the neighboring domains are exactly parallel. From polarized optical reflectivity measurements of the two types of domains, we found that the optical slow axis is not along the b-axis as previously believed but is tilted by ∼2.4° from the b-axis of the crystal. This offset makes the two neighboring domains with parallel Re-chains optically inequivalent and enables one to observe optical contrast between the two types of domains in polarized optical microscopy. We propose a quick and easy method to determine the crystallographic orientations of such domains by using polarized optical microscopy only.

γ-GeSe: A New Hexagonal Polymorph from Group IV-VI Monochalcogenides.

The family of group IV-VI monochalcogenides has an atomically puckered layered structure, and their atomic bond configuration suggests the possibility for the realization of various polymorphs. Here, we report the synthesis of the first hexagonal polymorph from the family of group IV-VI monochalcogenides, which is conventionally orthorhombic. Recently predicted four-atomic-thick hexagonal GeSe, so-called γ-GeSe, is synthesized and clearly identified by complementary structural characterizations, including elemental analysis, electron diffraction, high-resolution transmission electron microscopy imaging, and polarized Raman spectroscopy. The electrical and optical measurements indicate that synthesized γ-GeSe exhibits high electrical conductivity of 3 × 105 S/m, which is comparable to those of other two-dimensional layered semimetallic crystals. Moreover, γ-GeSe can be directly grown on h-BN substrates, demonstrating a bottom-up approach for constructing vertical van der Waals heterostructures incorporating γ-GeSe. The newly identified crystal symmetry of γ-GeSe warrants further studies on various physical properties of γ-GeSe.