journal article·2022-07Open access

Surface Structure Dependent Circular Dichroism in Single and Double Gyroid Metamaterials

Bryan M. Cote, William R. Lenart, Christopher J. Ellison, Vivian E. Ferry

Advanced Optical Materials· Volume 10· Issue 13

Abstract

Abstract Gyroid optical metamaterials consist of triply periodic chiral networks that are attractive photonic structures due to the combination of intriguing optical properties and spontaneous self‐assembly‐based fabrication routes using materials such as block copolymers. A previous experimental investigation found that gyroid metamaterials support strong circular dichroism, beyond what simulations only considering bulk interactions predict. In this work, simulations are used to unravel the contributions of bulk and surface interactions on the circular dichroism spectra of silver‐infilled gyroid metamaterial films. It is found that surface interactions have a significant, often dominating, contribution to circular dichroism. The relative strength of bulk and surface contributions can be tuned by controlling the crystallographic orientation, termination plane of the film, thickness, metal volume fraction, and defect density. Importantly, the dominance of surface interactions allows double gyroids, which are achiral in the bulk, to support strong circular dichroism responses with g‐factor magnitudes as large as 0.25.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Metamaterials and Metasurfaces Applications · Liquid Crystal Research Advancements · Photonic Crystals and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical Engineering and Materials Science University of Minnesota 421 Washington Ave SE Minneapolis MN 55455 USA

Funding

National Science Foundation

References (31)

Show source-provided references
1. 10.1002/adom.20140033310.1002/adom.201400333 ↗
2. 10.1002/adom.20180048510.1002/adom.201800485 ↗
3. 10.1021/acsmacrolett.0c0038010.1021/acsmacrolett.0c00380 ↗
4. 10.1038/nphoton.2013.4210.1038/nphoton.2013.42 ↗
5. 10.1098/rsif.2007.106510.1098/rsif.2007.1065 ↗
6. 10.1073/pnas.090961610710.1073/pnas.0909616107 ↗
7. 10.1016/j.jsb.2011.01.00410.1016/j.jsb.2011.01.004 ↗
8. 10.1073/pnas.210135711810.1073/pnas.2101357118 ↗
9. 10.1098/rsfs.2011.012010.1098/rsfs.2011.0120 ↗
10. 10.1146/annurev.pc.09.100158.00222110.1146/annurev.pc.09.100158.002221 ↗
11. 10.1126/science.117703110.1126/science.1177031 ↗
12. 10.1364/OL.35.00159310.1364/OL.35.001593 ↗
13. 10.1002/adom.20210017510.1002/adom.202100175 ↗
14. 10.1039/C4CS00517A10.1039/C4CS00517A ↗
15. 10.1021/acs.macromol.7b0152810.1021/acs.macromol.7b01528 ↗
16. 10.1002/admi.20200122710.1002/admi.202001227 ↗
17. 10.1002/anie.20110488810.1002/anie.201104888 ↗
18. 10.1002/adma.20120278810.1002/adma.201202788 ↗
19. 10.1002/adom.20190213110.1002/adom.201902131 ↗
20. 10.1002/adma.20180347810.1002/adma.201803478 ↗
21. 10.1016/j.matpr.2014.09.02310.1016/j.matpr.2014.09.023 ↗
22. 10.1021/acsphotonics.8b0136510.1021/acsphotonics.8b01365 ↗
23. 10.1088/0957-4484/27/41/41200110.1088/0957-4484/27/41/412001 ↗
24. 10.1002/anie.20201638410.1002/anie.202016384 ↗
25. 10.1021/la903443p10.1021/la903443p ↗
26. 10.1021/cm062136n10.1021/cm062136n ↗
27. 10.1021/acs.macromol.6b0239910.1021/acs.macromol.6b02399 ↗
28. 10.1021/acsami.6b1588510.1021/acsami.6b15885 ↗
29. 10.1016/j.polymer.2019.01.08510.1016/j.polymer.2019.01.085 ↗
30. 10.1103/PhysRevB.68.11510710.1103/PhysRevB.68.115107 ↗
31. Palik E. D. · 1998 · 350