Block Copolymer-Directed Single-Diamond Hybrid Structures Derived from X-ray Nanotomography

Block copolymers are recognized as a valuable platform for creating nanostructured materials. Morphologies formed by block copolymer self-assembly can be transferred into a wide range of inorganic materials, enabling applications including energy storage and metamaterials. However, imaging of the underlying, often complex, nanostructures in large volumes has remained a challenge, limiting progress in materials development. Taking advantage of recent advances in X-ray nanotomography, we noninvasively imaged exceptionally large volumes of nanostructured hybrid materials at high resolution, revealing a single-diamond morphology in a triblock terpolymer-gold composite network. This morphology, which is ubiquitous in nature, has so far remained elusive in block copolymer-derived materials, despite its potential to create materials with large photonic bandgaps. The discovery was made possible by the precise analysis of distortions in a large volume of the self-assembled diamond network, which are difficult to unambiguously assess using traditional characterization tools. We anticipate that high-resolution X-ray nanotomography, which allows imaging of much larger sample volumes than electron-based tomography, will become a powerful tool for the quantitative analysis of complex nanostructures and that structures such as the triblock terpolymer-directed single diamond will enable the generation of advanced multicomponent composites with hitherto unknown property profiles.

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Publication Details

Journal
ACS Nano
Published
2024-09-16
DOI
https://doi.org/10.1021/acsnano.3c10669
Citations
3
Primary Topic
Block Copolymer Self-Assembly
Type
article
Field-Weighted Citation Impact
0.35

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Block Copolymer-Directed Single-Diamond Hybrid Structures Derived from X-ray Nanotomography

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ACS Nano
Block Copolymer Self-Assembly
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article

Block Copolymer-Directed Single-Diamond Hybrid Structures Derived from X-ray Nanotomography

Ana Díaz, René Iseli, Karolina Godlewska, S. Narjes Abdollahi, Justin Llandro, Claire Donnelly, Mirko Holler, Hiroaki Sai, Ullrich Steiner, Shunsuke Fukami, Dmitry Karpov, Hideo Ohno, Ulrich Wiesner, Ilja Gunkel, Bodo D. Wilts, Michimasa Musya, Kenza Djeghdi, Takeshi Yuasa
article en
3 citations

Abstract

Block copolymers are recognized as a valuable platform for creating nanostructured materials. Morphologies formed by block copolymer self-assembly can be transferred into a wide range of inorganic materials, enabling applications including energy storage and metamaterials. However, imaging of the underlying, often complex, nanostructures in large volumes has remained a challenge, limiting progress in materials development. Taking advantage of recent advances in X-ray nanotomography, we noninvasively imaged exceptionally large volumes of nanostructured hybrid materials at high resolution, revealing a single-diamond morphology in a triblock terpolymer-gold composite network. This morphology, which is ubiquitous in nature, has so far remained elusive in block copolymer-derived materials, despite its potential to create materials with large photonic bandgaps. The discovery was made possible by the precise analysis of distortions in a large volume of the self-assembled diamond network, which are difficult to unambiguously assess using traditional characterization tools. We anticipate that high-resolution X-ray nanotomography, which allows imaging of much larger sample volumes than electron-based tomography, will become a powerful tool for the quantitative analysis of complex nanostructures and that structures such as the triblock terpolymer-directed single diamond will enable the generation of advanced multicomponent composites with hitherto unknown property profiles.

ACS NanoVol. 18(39)
University of Fribourg (CH), University of Salzburg (AT), Tohoku University (JP), Cornell University (US), European Synchrotron Radiation Facility (FR), Paul Scherrer Institute (CH), Max Planck Institute for Chemical Physics of Solids (DE), Adolphe Merkle Institute (CH), Spintronics Research Network of Japan (JP)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Adolphe Merkle Foundation, Max-Planck-Gesellschaft, Tohoku University, Japan Society for the Promotion of Science, National Center of Competence in Research Bio-Inspired Materials, University of Fribourg, Division of Materials Research, HORIZON EUROPE Marie Sklodowska-Curie Actions
Openalex Percentile: Top 44%
Block Copolymer Self-Assembly
0.35
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