TUHH Open Research
Help
  • Log In
    New user? Click here to register.Have you forgotten your password?
  • English
  • Deutsch
  • Communities & Collections
  • Publications
  • Research Data
  • People
  • Institutions
  • Projects
  • Statistics
  1. Home
  2. TUHH
  3. Publications
  4. Decoupling geometry and surface chemistry in 3D-printed ALD-functionalized porous ceramic channels
 
Options

Decoupling geometry and surface chemistry in 3D-printed ALD-functionalized porous ceramic channels

Citation Link: https://doi.org/10.15480/882.17437
Publikationstyp
Journal Article
Date Issued
2026-06-29
Sprache
English
Author(s)
Jimenez, Antoine E.
Gomes, Diego R.  orcid-logo
Hedrich, Carina  
Betriebseinheit Elektronenmikroskopie BEEM  
Brinker, Manuel  orcid-logo
Material- und Röntgenphysik M-2  
Minna, Fortune
Huber, Patrick  orcid-logo
Material- und Röntgenphysik M-2  
Pagnan Furlan, Kaline  orcid-logo
TORE-DOI
10.15480/882.17437
TORE-URI
https://hdl.handle.net/11420/63817
Journal
ACS omega  
Citation
ACS Omega (in Press): (2026)
Publisher DOI
10.1021/acsomega.6c02566
Publisher
American Chemical Society (ACS)
Capillary-driven transport is traditionally attributed to the static pore geometry and wettability. However, the time-dependent surface energy of metal oxides, amplified by the high surface area of porous media, remains a key yet underexplored aspect. This study introduces a novel manufacturing route capable of decoupling macroscopic geometry from surface chemistry by integrating additive manufacturing combined with colloidal assembly (AMCA) and functionalization by atomic layer deposition (ALD). This approach enables the fabrication of highly porous aluminum(III) oxide (Al2O3) and titanium dioxide (TiO2) ceramic channels after thermal burn-out. Within these structures, the structural and chemical properties are tuned and investigated. Spontaneous imbibition experiments at 0, 6, and 24 h after burn-out reveal a transition from a classical Lucas−Washburn rise to a resistance-limited regime dominated by evaporation and viscous drag. Time-resolved contact-angle measurements revealed that both oxides become superhydrophilic after burn-out and undergo subsequent hydrophobic recovery. Despite TiO2 being intrinsically more hydrophilic, Al2O3 channels consistently exhibited faster imbibition rates and a higher liquid rise. This behavior is attributed to the rapid surface relaxation of Al2O3, which reduces contact-line friction and minimizes pinning at high-energy adsorption sites, thereby enhancing fluid uptake. Macroscopic geometrical variations in printed channels did not affect the imbibition height but scaled linearly with imbibed volume, confirming the successful decoupling of geometric and chemical transport factors. The excellent structural reproducibility of the AMCA-ALD method establishes it as a robust manufacturing platform for programmable capillary transport. This approach provides a general pathway to design porous ceramics with independently engineered geometries and surface chemistries for applications in microfluidics, diagnostics, and catalysis.
DDC Class
620.11: Engineering Materials
Funding(s)
533771286
Lizenz
https://creativecommons.org/licenses/by/4.0/
Publication version
publishedVersion
Loading...
Thumbnail Image
Name

decoupling-geometry-and-surface-chemistry-in-3d-printed-ald-functionalized-porous-ceramic-channels.pdf

Type

Main Article

Size

6.03 MB

Format

Adobe PDF

TUHH
Weiterführende Links
  • Contact
  • Send Feedback
  • Cookie settings
  • Privacy policy
  • Impress
DSpace Software

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science
Design by effective webwork GmbH

  • Deutsche NationalbibliothekDeutsche Nationalbibliothek
  • ORCiD Member OrganizationORCiD Member Organization
  • DataCiteDataCite
  • Re3DataRe3Data
  • OpenDOAROpenDOAR
  • OpenAireOpenAire
  • BASE Bielefeld Academic Search EngineBASE Bielefeld Academic Search Engine
Feedback