Printing nanomaterials in shrinking gels

Photopatterning of reactive sites in gels enables arbitrary patterning of nanoparticles The creation of nanoscale electronics, photonics, plasmonics, and mechanically robust metamaterials will benefit from nanofabrication processes that allow a designer full control in manipulating nanomaterial prec...

Full description

Saved in:
Bibliographic Details
Published inScience (American Association for the Advancement of Science) Vol. 362; no. 6420; pp. 1244 - 1245
Main Authors Long, Timothy E, Williams, Christopher B
Format Journal Article
LanguageEnglish
Published United States The American Association for the Advancement of Science 14.12.2018
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Photopatterning of reactive sites in gels enables arbitrary patterning of nanoparticles The creation of nanoscale electronics, photonics, plasmonics, and mechanically robust metamaterials will benefit from nanofabrication processes that allow a designer full control in manipulating nanomaterial precursors in a programmable and volumetric manner. Despite decades of research, it remains challenging to design nanofabrication processes that can produce complex free-form three-dimensional (3D) objects at the scale of tens of nanometers. On page 1281 of this issue, Oran et al. ( 1 ) report on the photopatterning of reactive sites into water-swollen, chemically cross-linked acrylic gels for the subsequent site-specific deposition of nanomaterials and nanoparticles. After chemical and thermal dehydration, the gel scaffold holds the nanomaterials in a distinct 3D arrangement. This process, termed implosion fabrication (ImpFab) because the scaffold of the gel effectively “implodes” upon solvent removal, provides an opportunity to fabricate centimeter-scale assemblies of nanomaterials that possess multiple functionalities.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Commentary-1
ISSN:0036-8075
1095-9203
DOI:10.1126/science.aav5712