Thermal shock resistance of various two-dimensional materials: a comparative analysis
Understanding the ultrafast thermomechanical response of two-dimensional (2D) materials is crucial for their integration into next-generation nanoelectronic and thermal management technologies. In this study, molecular dynamics simulations are used to systematically evaluate the thermal shock resistance of graphene, C<sub>3</sub>N, BC<sub>3</sub>, three BC<sub>6</sub>N configurations, biphenylene, borophene, and hexagonal boron nitride (h-BN). A localised, rapid temperature increase is applied to generate stress waves, enabling direct assessment of wave-propagation velocity, decay rate, energy dissipation, atomic displacement, and temperature changes in both armchair and zigzag orientations. The findings reveal strong correlations between lattice topology and non-equilibrium thermomechanical behaviour. Graphene and C<sub>3</sub>N show exceptional shock tolerance, with high wave speeds and minimal attenuation; C<sub>3</sub>N demonstrates nearly undamped propagation. Borophene exhibits notable anisotropy, with wave transmission and dissipation depending on direction, whereas biphenylene and BC<sub>3</sub> exhibit significant damping and stress irregularities due to their structures. The trends highlight how thermal shock resistance depends on bonding structure, coordination, and lattice symmetry. This work provides a unified benchmark for transient thermal-mechanical performance in 2D materials and offers valuable guidance for selecting and designing atomically thin systems for high-thermal-demand applications.
Authors
- Nader Malih
- Sadegh Sadeghzadeh (ORCID: https://orcid.org/0000-0002-5710-2556)
- Ali Ghavipanjeh (ORCID: https://orcid.org/0009-0008-0020-2768)
Institutions
- University of Kurdistan (IR)
- Iran University of Science and Technology (IR)
Publication Details
- Journal
- RSC Advances
- Published
- 2026-01-01
- DOI
- https://doi.org/10.1039/d5ra09164k
- Primary Topic
- Thermal properties of materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00