期刊
ACS MACRO LETTERS
卷 3, 期 1, 页码 16-20出版社
AMER CHEMICAL SOC
DOI: 10.1021/mz400572r
关键词
-
资金
- SOLAR Program of the National Science Foundation [DMR 1035292, DMR 1035480]
- Center for Scientific Computing from the CNSI
- MRL: an NSF MRSEC [DMR-1121053]
- Hewlett-Packard
- NSF [CNS-0960316]
- National Science Foundation [OCI-1053575]
- NSF Grant DMS [1016310, 0645766]
- Direct For Mathematical & Physical Scien [0645766, 1016310, 1035480, 1035292] Funding Source: National Science Foundation
- Division Of Chemistry [1035292] Funding Source: National Science Foundation
- Division Of Materials Research [1035480] Funding Source: National Science Foundation
- Division Of Mathematical Sciences [0645766, 1016310] Funding Source: National Science Foundation
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.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据