4.8 Article

Multimicrometer Noncovalent Monolayer Domains on Layered Materials through Thermally Controlled Langmuir-Schaefer Conversion for Noncovalent 2D Functionalization

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 9, 期 41, 页码 36409-36416

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b11683

关键词

self-assembly; noncovalent functionalization; 2D materials; self-assembled monolayer; Langmuir Schaefer transfer; polymerizable amphiphile

资金

  1. NSF Career award [NSF-CHE 1555173]
  2. NSF MRI grant [NSF-CHE 1531767]

向作者/读者索取更多资源

As functionalized 2D materials are incorporated into hybrid materials, ensuring large-area structural control in noncovalently adsorbed films becomes increasingly important. Noncovalent functionalization avoids disrupting electronic structure in 2D materials; however, relatively weak molecular interactions in such monolayers typically reduce stability toward solution processing and other common material handling conditions. Here; we find that controlling substrate temperature during Langmuir-Schaefer conversion of a standing phase monolayer of diynoic amphiphiles on water a horizontally defiled monolayer on a 2D substrate routinely produces multimicrometer domains, atleast an order of magnitude larger than those typically achieved through drop-casting. Following polymerization, these highly ordered monolayers retain their structures during vigorous washing with solvents including water, ethanol, tetrahydrofuran, and toluene. These findings point to a convenient and broadly applicable strategy for noncovalent functionalization of 2D materials in applications that require large-area structural control, for instance, to minimize desorption at defects during subsequent solution processing.

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