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Engineering Silk Protein to Modulate Polymorphic Transitions for Green Lithography Resists

Authors
Chung, Soon-ChunPark, Joon-SongJha, Rakesh KumarKim, JieunKim, JinhaKim, MuyoungChoi, JuwanKim, HongdeokPark, Da-HyeGogurla, NarendarLee, Tae-YunJeon, HeonsuPark, Ji-YongChoi, JoonmyungKim, GinamKim, Sunghwan
Issue Date
Dec-2022
Publisher
American Chemical Society (ACS)
Keywords
green photoresist; lithography; polymorphic transition; silk protein; synthetic biology
Citation
ACS Applied Materials & Interfaces, v.14, no.51, pp 56623 - 56634
Pages
12
Indexed
SCIE
SCOPUS
Journal Title
ACS Applied Materials & Interfaces
Volume
14
Number
51
Start Page
56623
End Page
56634
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/111210
DOI
10.1021/acsami.2c17843
ISSN
1944-8244
1944-8252
Abstract
Silk protein is being increasingly introduced as a prospective material for biomedical devices. However, a limited locus to intervene in nature-oriented silk protein makes it challenging to implement on-demand functions to silk. Here, we report how polymorphic transitions are related with molecular structures of artificially synthesized silk protein and design principles to construct a green-lithographic and high-performative protein resist. The repetition number and ratio of two major building blocks in synthesized silk protein are essential to determine the size and content of β-sheet crystallites, and radicals resulting from tyrosine cleavages by the 193 nm laser irradiation induce the β-sheet to α-helix transition. Synthesized silk is designed to exclusively comprise homogeneous building blocks and exhibit high crystallization and tyrosine-richness, thus constituting an excellent basis for developing a high-performance deep-UV photoresist. Additionally, our findings can be conjugated to design an electron-beam resist governed by the different irradiation-protein interaction mechanisms. All synthesis and lithography processes are fully water-based, promising green lithography. Using the engineered silk, a nanopatterned planar color filter showing the reduced angle dependence can be obtained. Our study provides insights into the industrial scale production of silk protein with on-demand functions. © 2022 American Chemical Society.
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COLLEGE OF ENGINEERING SCIENCES > DEPARTMENT OF MECHANICAL ENGINEERING > 1. Journal Articles

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