Hierarchical Self-Assembly of Carbon Dots into High-Aspect-Ratio Nanowires

被引:3
|
作者
Habteyes, Terefe G. [2 ]
Westphal, Eric R. [1 ]
Plackowski, Kenneth M. [1 ,2 ]
Kotula, Paul G. [1 ]
Meyerson, Melissa L. [1 ]
White, Stephanie L. [1 ]
Corbin, W. Cody [1 ]
Ghosh, Koushik [1 ]
Grey, John K. [1 ]
机构
[1] Sandia Natl Labs, Albuquerque, NM 87123 USA
[2] Univ New Mexico, Dept Chem, Albuquerque, NM 87131 USA
基金
美国国家科学基金会;
关键词
carbon dots; hierarchical self-assembly; nanowires; scanning near-field spectroscopic imaging; tautomerization; NANOPARTICLES; MELAMINE; LIGHT; ACID;
D O I
10.1021/acs.nanolett.3c02977
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:9474 / 9481
页数:8
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