Synergistic Two‐Color Photochemical Polymer Network Formation and Lithography

J Jan Hobich (Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany) X Xingyu Wu (Department of Clinical Laboratory, Peking University People’s Hospital) F Florian Feist (Institute of Functional Interfaces (IFG) Karlsruhe Institute of Technology (KIT) Eggenstein‐Leopoldshafen Germany) W Willie Scheibel (Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany) N Natalia Herdt (Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany) P Paul Somers (Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany) E Eva Blasco (Institute for Molecular Systems Engineering and Advanced Materials Heidelberg University Heidelberg Germany) H Hatice Mutlu C Christopher Barner‐Kowollik (Soft Matter Materials Laboratory School of Chemistry and Physics Queensland University of Technology (QUT) Brisbane Queensland Australia)

Abstract

Abstract We introduce synergistic two‐color lithography as an advanced wavelength‐gated strategy for spatially and temporally controlling polymer network formation. Our photoresist entails two photoswitches, i.e., diarylindenone epoxide (DIO) and strained azobenzene (SA), each activated at a judiciously selected wavelength, i.e., 375 or 430 nm. Under specific conditions of photon flux, simultaneous irradiation at both wavelengths induces a (3 + 2) cycloaddition between the photoactivated DIO′ and SA′ species, generating covalently crosslinked networks, whereas under these specifically determined conditions, single‐wavelength exposure does not induce solidification. Kinetic analysis highlights the potential of synergistic activation to enable advanced additive manufacturing. We implemented the two‐color activated covalent bond forming system in a dual‐laser lithographic platform enabling the fabrication of well‐defined structures, including segmented ring and butterfly architectures by simply activating and deactivating one of the colors of light.

Article Details

Volume / Issue Vol. 64, Issue 48
Published November 24, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

J

Jan Hobich

Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany

X

Xingyu Wu

Department of Clinical Laboratory, Peking University People’s Hospital

F

Florian Feist

Institute of Functional Interfaces (IFG) Karlsruhe Institute of Technology (KIT) Eggenstein‐Leopoldshafen Germany

W

Willie Scheibel

Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany

N

Natalia Herdt

Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany

P

Paul Somers

Institute of Nanotechnology (INT) Karlsruhe Institute of Technology (KIT) Kaiserstraße 12 76131 Karlsruhe Germany

E

Eva Blasco

Institute for Molecular Systems Engineering and Advanced Materials Heidelberg University Heidelberg Germany

H

Hatice Mutlu

C

Christopher Barner‐Kowollik

Soft Matter Materials Laboratory School of Chemistry and Physics Queensland University of Technology (QUT) Brisbane Queensland Australia