成核
二硫化钼
屏障激活
化学物理
外延
结晶学
六方晶系
材料科学
二硫键
化学
纳米技术
统计物理学
物理
计算化学
密度泛函理论
热力学
图层(电子)
冶金
生物化学
作者
Jiajun Chen,Enbo Zhu,Juan Liu,Shuai Zhang,Zhaoyang Lin,Xiangfeng Duan,Hendrik Heinz,Yu Huang,James J. De Yoreo
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2018-12-07
卷期号:362 (6419): 1135-1139
被引量:198
标识
DOI:10.1126/science.aau4146
摘要
Assembly of two-dimensional (2D) molecular arrays on surfaces produces a wide range of architectural motifs exhibiting unique properties, but little attention has been given to the mechanism by which they nucleate. Using peptides selected for their binding affinity to molybdenum disulfide, we investigated nucleation of 2D arrays by molecularly resolved in situ atomic force microscopy and compared our results to molecular dynamics simulations. The arrays assembled one row at a time, and the nuclei were ordered from the earliest stages and formed without a free energy barrier or a critical size. The results verify long-standing but unproven predictions of classical nucleation theory in one dimension while revealing key interactions underlying 2D assembly.
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