4.7 Article

Block Copolymer Self Assembly during Rapid Solvent Evaporation: Insights into Cylinder Growth and Stability

期刊

ACS MACRO LETTERS
卷 3, 期 1, 页码 16-20

出版社

AMER CHEMICAL SOC
DOI: 10.1021/mz400572r

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资金

  1. SOLAR Program of the National Science Foundation [DMR 1035292, DMR 1035480]
  2. Center for Scientific Computing from the CNSI
  3. MRL: an NSF MRSEC [DMR-1121053]
  4. Hewlett-Packard
  5. NSF [CNS-0960316]
  6. National Science Foundation [OCI-1053575]
  7. NSF Grant DMS [1016310, 0645766]
  8. Direct For Mathematical & Physical Scien [0645766, 1016310, 1035480, 1035292] Funding Source: National Science Foundation
  9. Division Of Chemistry [1035292] Funding Source: National Science Foundation
  10. Division Of Materials Research [1035480] Funding Source: National Science Foundation
  11. Division Of Mathematical Sciences [0645766, 1016310] Funding Source: National Science Foundation

向作者/读者索取更多资源

Solvent evaporation has proven, to be a remarkably successful tool for directing self-assembly in block copolymers, yet the microscopic mechanisms, processing history dependence and macroscopic control parameters influencing pattern Selection remain poorly understood. Here, we leverage dynamical field theory simulations to clarify how copolymer self-assembly proceeds during evaporation. We find that cylinders in the vertical orientation tend to form under modest evaporation rates and relatively weak segregation strengths, and link this behavior to nontrivial, morphology-dependent density correlations present at the ordering front.

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