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原子力显微镜下电化学诱导的分子晶体成核与生长。

Atomic force microscopy of the electrochemical nucleation and growth of molecular crystals.

出版信息

Science. 1994 Mar 4;263(5151):1261-4. doi: 10.1126/science.263.5151.1261.

Abstract

In situ atomic force microscopy reveals the morphology, surface topography, and growth and dissolution characteristics of microscopic single crystals of the low-dimensional organic conductor (tetrathiafulvalene)Br(0.76)' which are grown by electrocrystallization on a highly oriented pyrolytic graphite electrode in an atomic force microscope liquid cell. The growth modes and the distribution and orientation of topographic features on specific crystal faces, whose identity was determined by "atomic force microscope goniometry," can be correlated with the strength and direction of anisotropic solid-state intermolecular bonding. Growth on the (011) face of (tetrathiafulvalene)Br(0.76) crystals involves the formation of oriented self-similar triangular islands ranging in size from 200 to 5000 angstroms along a side. These nuclei eventually transform into rectangular rafts at larger length scales, where bulk intermolecular bonding interactions and surface energies dominate over nuclei-substrate interactions.

摘要

原位原子力显微镜揭示了在原子力显微镜液室中通过电结晶在高度取向的热解石墨电极上生长的低维有机导体(tetrathiafulvalene)Br(0.76)的微观单晶的形态、表面形貌以及生长和溶解特性。生长模式以及在特定晶面的形貌特征的分布和取向,其特征通过“原子力显微镜测角法”确定,可以与各向异性固态分子间键的强度和方向相关联。(tetrathiafulvalene)Br(0.76)晶体在(011)面上的生长涉及到沿着一侧形成尺寸从 200 到 5000 埃的定向自相似三角形岛的形成。这些核最终在较大的长度尺度上转变为矩形筏,其中体分子间键合相互作用和表面能占主导地位,而核-衬底相互作用则处于次要地位。

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