Polarity from the Bottom Up: A Computational Framework for Predicting Spontaneous Polar Order

Abstract

So-called polar liquid crystals possess spontaneous long-range mutual orientation of their electric dipole moments, conferring bulk polarity to fluid phases of matter. The combination of polarity and fluidity leads to complex phase behaviour, and rich new physics, yet the limited understanding around how specific molecular features generate long-range polar ordering in a fluid is a hindrance to development of new materials. In this work, we introduce a computational framework that probes the bimolecular potential energy landscape of candidate molecules, enabling us to dissect the role of directional intermolecular interactions in establishing polar order. In closely related families of materials we find conflicting preferences for (anti)parallel ordering which can be accounted for by specific interactions between molecules. Thus, our results allow us to argue that the presence (or absence) of polar order is a product of specific molecular features and strong directional intermolecular interactions rather than being simply a product of dipole-dipole forces. The design principles established can be leveraged to developing new polar liquid crystalline materials.

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