4.8 Article

Millisecond Ordering of Block Copolymer Films via Photothermal Gradients

Journal

ACS NANO
Volume 9, Issue 4, Pages 3896-3906

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn5071827

Keywords

laser zone annealing; block copolymers; directed self-assembly; coarsening kinetics; thermophoresis

Funding

  1. U.S. Department of Energy, Office of Basic Energy Sciences [DE-AC02-98CH10886]

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For the promise of self-assembly to be realized, processing techniques must be developed that simultaneously enable control of the nanoscale morphology, rapid assembly, and, ideally, the ability to pattern the nanostructure. Here, we demonstrate how photothermal gradients can be used to control the ordering of block Copolymer thin films. Highly localized laser heating leads to intense thermal gradients, which induce a thermophoretic force on morphological defects. This increases the ordering kinetics by at least 3 orders of magnitude compared to conventional oven annealing. By simultaneously exploiting the thermal gradients to induce shear fields, we demonstrate uniaxial alignment of a block copolymer film in less than a second. Finally, we provide examples of how control of the incident light field can be used to generate prescribed configurations of block copolymer nanoscale patterns.

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