Emergent properties of van der Waals bilayers revealed by computational stacking

Abstract

Stacking of two-dimensional (2D) materials has emerged as a facile strategy for realising exotic quantum states of matter and engineering electronic properties. Yet, developments beyond the proof-of-principle level are impeded by the vast size of the configuration space defined by layer combinations and stacking orders. Here we employ a density functional theory (DFT) workflow to calculate interlayer binding energies of 8451 homobilayers created by stacking 1052 different monolayers in various configurations. Analysis of the stacking orders in 247 experimentally known van der Waals crystals is used to validate the workflow and determine the criteria for realizable bilayers. For the 2586 most stable bilayer systems, we calculate a range of electronic, magnetic, and vibrational properties, and explore general trends and anomalies. We identify an abundance of bistable bilayers with stacking order-dependent magnetic or electrical polarisation states making them candidates for slidetronics applications.

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• Auto-resolving the atomic structure at van der Waals interfaces using a generative model
• High-purity and stable single-photon emission in bilayer WSe${}_2$ via phonon-assisted excitation
• Large-scale Integration of Experimental and Computational Data for 2D Materials
• Non-van der Waals Heterostructures
• Stabilization of sliding ferroelectricity through exciton condensation