拉曼光谱
碳纳米管
共价键
DNA
材料科学
格子(音乐)
光致发光
鸟嘌呤
结晶学
纳米技术
化学
化学物理
物理
光电子学
有机化学
光学
核苷酸
基因
生物化学
声学
作者
Zhiwei Lin,L.C. Beltran,Zeus A. De los Santos,Yinong Li,Tehseen Adel,Jeffrey Fagan,Angela R. Hight Walker,Edward H. Egelman,Ming Zheng
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-07-29
卷期号:377 (6605): 535-539
被引量:21
标识
DOI:10.1126/science.abo4628
摘要
Covalent modification of carbon nanotubes is a promising strategy for engineering their electronic structures. However, keeping modification sites in registration with a nanotube lattice is challenging. We report a solution using DNA-directed, guanine (G)-specific cross-linking chemistry. Through DNA screening we identify a sequence, C 3 GC 7 GC 3 , whose reaction with an (8,3) enantiomer yields minimum disorder-induced Raman mode intensities and photoluminescence Stokes shift, suggesting ordered defect array formation. Single-particle cryo–electron microscopy shows that the C 3 GC 7 GC 3 functionalized (8,3) has an ordered helical structure with a 6.5 angstroms periodicity. Reaction mechanism analysis suggests that the helical periodicity arises from an array of G-modified carbon-carbon bonds separated by a fixed distance along an armchair helical line. Our findings may be used to remodel nanotube lattices for novel electronic properties.
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