纳米尺度
纳米技术
自组装
纳米线
材料科学
三聚氰胺
超分子化学
化学
结晶学
晶体结构
复合材料
作者
Terefe G. Habteyes,Eric Westphal,Kenneth M. Plackowski,Paul G. Kotula,Melissa Meyerson,Stephanie L. White,William C. Corbin,Koushik Ghosh,John K. Grey
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-10-13
卷期号:23 (20): 9474-9481
被引量:7
标识
DOI:10.1021/acs.nanolett.3c02977
摘要
We report a spontaneous and hierarchical self-assembly mechanism of carbon dots prepared from citric acid and urea into nanowire structures with large aspect ratios (>50). Scattering-type scanning near-field optical microscopy (s-SNOM) with broadly tunable mid-IR excitation was used to interrogate details of the self-assembly process by generating nanoscopic chemical maps of local wire morphology and composition. s-SNOM images capture the evolution of wire formation and the complex interplay between different chemical constituents directing assembly over the nano- to microscopic length scales. We propose that residual citrate promotes tautomerization of melamine surface functionalities to produce supramolecular shape synthons comprised of melamine-cyanurate adducts capable of forming long-range and highly directional hydrogen-bonding networks. This intrinsic, heterogeneity-driven self-assembly mechanism reflects synergistic combinations of high chemical specificity and long-range cooperativity that may be harnessed to reproducibly fabricate functional structures on arbitrary surfaces.
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