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Engineering entropy for the inverse design of colloidal crystals from hard shapes

机译:从硬形状逆设计胶体晶体的工程熵

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摘要

Throughout the physical sciences, entropy stands out as a pivotal but enigmatic concept that, in materials design, typically takes a backseat to energy. Here, we demonstrate how to precisely engineer entropy to achieve desired colloidal crystals via particle shapes that, importantly, can be made in the laboratory. We demonstrate the inverse design of symmetric hard particles that assemble six different target colloidal crystals due solely to entropy maximization. Our approach efficiently samples 108 particle shapes from 92- and 188-dimensional design spaces to discover thermodynamically optimal shapes. We design particle shapes that self-assemble into known crystals with optimized symmetry and thermodynamic stability, as well as new crystal structures with no known atomic or other equivalent.
机译:在整个物理科学中,熵是一个至关重要但神秘的概念,它在材料设计中通常会落后于能源。在这里,我们演示了如何通过重要地可以在实验室中制成的颗粒形状精确地改造熵以实现所需的胶体晶体。我们演示了对称的硬粒子的逆设计,该硬粒子仅由于熵最大化而组装了六个不同的目标胶体晶体。我们的方法从92维和188维设计空间中有效采样了10 8 个粒子形状,以发现热力学最佳形状。我们设计的粒子形状可以自组装成具有最佳对称性和热力学稳定性的已知晶体,以及不具有已知原子或其他等效物的新晶体结构。

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