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Citation
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HERO ID
4272330
Reference Type
Journal Article
Title
Mechanochemical Synthesis of Carbon Nanothread Single Crystals
Author(s)
Li, X; Baldini, M; Wang, T; Chen, B; Xu, ES; Vermilyea, B; Crespi, VH; Hoffmann, R; Molaison, JJ; Tulk, CA; Guthrie, M; Sinogeikin, S; Badding, JV
Year
2017
Is Peer Reviewed?
Yes
Journal
Journal of the American Chemical Society
ISSN:
0002-7863
EISSN:
1520-5126
Volume
139
Issue
45
Page Numbers
16343-16349
Language
English
PMID
29040804
DOI
10.1021/jacs.7b09311
Web of Science Id
WOS:000415785900050
URL
https://www.proquest.com/docview/2116893724?accountid=171501&bdid=64576&_bd=VNQwlAMo4tSNQLumoeHXR%2BcjbJc%3D
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Abstract
Synthesis of well-ordered reduced dimensional carbon solids with extended bonding remains a challenge. For example, few single-crystal organic monomers react under topochemical control to produce single-crystal extended solids. We report a mechanochemical synthesis in which slow compression at room temperature under uniaxial stress can convert polycrystalline or single-crystal benzene monomer into single-crystalline packings of carbon nanothreads, a one-dimensional sp3carbon nanomaterial. The long-range order over hundreds of microns of these crystals allows them to readily exfoliate into fibers. The mechanochemical reaction produces macroscopic single crystals despite large dimensional changes caused by the formation of multiple strong, covalent C-C bonds to each monomer and a lack of reactant single-crystal order. Therefore, it appears not to follow a topochemical pathway, but rather one guided by uniaxial stress, to which the nanothreads consistently align. Slow-compression room-temperature synthesis may allow diverse molecular monomers to form single-crystalline packings of polymers, threads, and higher dimensional carbon networks.
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