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High-order elastic multipoles as colloidal atoms

机译:高阶弹性多极作为胶体原子

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Achieving and exceeding diversity of colloidal analogs of chemical elements and molecules as building blocks of matter has been the central goal and challenge of colloidal science ever since Einstein introduced the colloidal atom paradigm. Recent advances in colloids assembly have been achieved by exploiting the machinery of DNA hybridization but robust physical means of defining colloidal elements remain limited. Here we introduce physical design principles allowing?us to define high-order elastic multipoles emerging when colloids with controlled shapes and surface alignment are introduced into a nematic host fluid. Combination of experiments and numerical modeling of equilibrium field configurations using a spherical harmonic expansion allow?us to probe elastic multipole moments, bringing analogies with electromagnetism and a structure of atomic orbitals. We show that, at least in view of the symmetry of the "director wiggle wave functions," diversity of elastic colloidal atoms can far exceed that of known chemical elements.
机译:自从爱因斯坦提出胶体原子范式以来,实现和超越作为元素的化学元素和分子的胶体类似物的多样性一直是胶体科学的中心目标和挑战。胶体组装的最新进展是通过利用DNA杂交机制而实现的,但定义胶体元素的有效物理手段仍然有限。在这里,我们介绍物理设计原理,使我们能够定义将形状和表面排列受控的胶体引入向列型主流体时出现的高阶弹性多极子。使用球形谐波展开的实验和平衡场配置的数值模型相结合,使我们能够探测弹性多极矩,从而产生与电磁学和原子轨道结构相似的东西。我们表明,至少鉴于“导演摆动波函数”的对称性,弹性胶体原子的多样性可以远远超过已知化学元素的多样性。

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