4.8 Article

Irreversible synthesis of an ultrastrong two-dimensional polymeric material

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NATURE
卷 602, 期 7895, 页码 91-+

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NATURE PORTFOLIO
DOI: 10.1038/s41586-021-04296-3

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资金

  1. Center for Enhanced Nanofluidic Transport (CENT), an Energy Frontier Research Center - US Department of Energy (DOE), Office of Science, Basic Energy Sciences [DE-SC0019112]
  2. Army Research Laboratory [W911NF-18-2-0055]
  3. Burroughs Wellcome Fund
  4. Center for Nanoscale Systems at Harvard
  5. National Science Foundation under NSF [1541959]
  6. DOE Office of Science by Brookhaven National Laboratory [DE-SC0012704]
  7. Cypher VRS DURIP award [N000142012203]
  8. German Research Foundation (DFG) [KU 3952/1-1]
  9. U.S. Department of Defense (DOD) [N000142012203] Funding Source: U.S. Department of Defense (DOD)

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Polymers that extend covalently in two dimensions have attracted recent attention as a means of combining the mechanical strength and in-plane energy conduction of conventional two-dimensional (2D) materials with the low densities, synthetic processability and organic composition of their one-dimensional counterparts. Here we demonstrate a homogenous 2D irreversible polycondensation that results in a covalently bonded 2D polymeric material that is chemically stable and highly processable. Further processing yields highly oriented, free-standing films that have a 2D elastic modulus and yield strength of 12.7 +/- 3.8 gigapascals and 488 +/- 57 megapascals, respectively. This synthetic route provides opportunities for 2D materials in applications ranging from composite structures to barrier coating materials.
Polymers that extend covalently in two dimensions have attracted recent attention(1,2) as a means of combining the mechanical strength and in-plane energy conduction of conventional two-dimensional (2D) materials(3,4) with the low densities, synthetic processability and organic composition of their one-dimensional counterparts. Efforts so far have proven successful in forms that do not allow full realization of these properties, such as polymerization at flat interfaces(5,6) or fixation of monomers in immobilized lattices(7-9). Another frequently employed synthetic approach is to introduce microscopic reversibility, at the cost of bond stability, to achieve 2D crystals after extensive error correction(10,11). Here we demonstrate a homogenous 2D irreversible polycondensation that results in a covalently bonded 2D polymeric material that is chemically stable and highly processable. Further processing yields highly oriented, free-standing films that have a 2D elastic modulus and yield strength of 12.7 +/- 3.8 gigapascals and 488 +/- 57 megapascals, respectively. This synthetic route provides opportunities for 2D materials in applications ranging from composite structures to barrier coating materials.

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