Operational message
There are currently operational disruptions. Troubleshooting is in progress.
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Hydration- and Temperature-Dependent Rotational Dynamics and Water Diffusion in Nanocellulose
Stockholm University, Faculty of Science, Department of Chemistry.ORCID iD: 0009-0006-3703-3238
Stockholm University, Faculty of Science, Department of Chemistry.ORCID iD: 0000-0002-7156-559x
Stockholm University, Faculty of Science, Department of Chemistry. Paul Scherrer Institute, Switzerland.ORCID iD: 0000-0003-4441-8882
Stockholm University, Faculty of Science, Department of Chemistry.ORCID iD: 0009-0007-2207-398X
Show others and affiliations
2025 (English)In: Small Structures, E-ISSN 2688-4062, Vol. 6, no 10, article id 2500229Article in journal (Refereed) Published
Abstract [en]

Nanocellulose is a promising alternative to fossil-derived materials, but its development is hindered by a limited understanding of cellulose–water interactions. Herein, quasielastic neutron scattering (QENS) is used to investigate how hydration and temperature affect the localized rotations in cellulose nanocrystals (CNC) and the diffusion of mobile water. QENS reveals that the C6 hydrogens and the C6 OH in the surface regions of CNC exhibit an isotropic rotation. The extracted mean square displacement shows that hydration enhances the overall hydrogen mobility in the cellulose chains. The mobile water diffusion at 270 K is unaffected by cellulose and consistent with diffusion of supercooled bulk water. At 310 K, the diffusion slows compared to bulk water, consistent with water diffusing on the CNC surface. Decoupling of the translational and rotational motion provides insight into the local cellulose–water motions. The localized motions of the nondiffusing water are found to be coupled with cellulose at 310 K, indicating a more complex dynamics at higher temperature. These findings provide new insights into how hydration modulates hydrogen mobility in cellulose, highlighting the interplay between water diffusion and molecular motion.

Place, publisher, year, edition, pages
2025. Vol. 6, no 10, article id 2500229
Keywords [en]
cellulose–water interactions, nanocellulose, quasielastic neutron scattering, water diffusion
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:su:diva-241181DOI: 10.1002/sstr.202500229ISI: 001531499700001Scopus ID: 2-s2.0-105010968535OAI: oai:DiVA.org:su-241181DiVA, id: diva2:1947010
Funder
Swedish Foundation for Strategic Research, GSn15-008Swedish Foundation for Strategic Research, SNP21-004Swedish Research Council Formas, 2021-01952Knut and Alice Wallenberg FoundationAvailable from: 2025-03-24 Created: 2025-03-24 Last updated: 2025-11-20Bibliographically approved
In thesis
1. Cellulose Iß -Water Interactions: Exploring Moisture-Driven Vibrational Dynamics and Structural Transformations
Open this publication in new window or tab >>Cellulose Iß -Water Interactions: Exploring Moisture-Driven Vibrational Dynamics and Structural Transformations
2025 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Nanocellulose is an excellent candidate to replace traditionally fossil-derived materials. Although several cellulose nanomaterials (CNM) have reached the commercial market, the full potential of nanocellulose has yet to be realized. For the continued development of CNM for realistic applications, a deeper understanding on the influence of moisture on the structure and dynamics of these hygroscopic materials is needed. In this thesis, a combination of neutron and X-ray scattering has been deployed to evaluate the moisture-induced structural and dynamical alterations of CNM.

Inelastic neutron scattering (INS) was used to access the full vibrational spectra of nanocellulose with three different crystallinities, revealing that moisture primarily interacts with the disordered regions of the cellulose chains. A combination of INS, small angle neutron scattering, and wide angle X-ray scattering (WAXS) was used to link moisture-induced structural modifications in anisotropic cellulose nanocrystals (CNC) foams to the population change in the phonon density of states; an increasing separation distance between nanoparticles was suggested to suppress the effect of higher crystallinity index and larger coherence length.

The hydration-dependent dynamics and temperature-dependent water diffusion in nanocellulose were investigated using quasielastic neutron scattering. A localized rotational motion of the C6 hydrogens could be detected, and hydration was found to result in an increased cellulose chain mobility. At 270 K, water was found to diffuse independently of cellulose, with the extracted diffusion coefficient matching that of bulk water. At 310 K, the diffusion coefficient was lower than that of bulk water. This could be attributed to water diffusing on the surface of CNC, where the water-cellulose interactions may slow the diffusion.

Anisotropic cellulose nanofibril (CNF) foams obtained from upcycled cotton waste textiles (upCNF) and softwood (wCNF) were subjected to a relative humidity range of 10 and 90% and their structural humidity-response evaluated using in-situ small angle X-ray scattering (SAXS), WAXS, and X-ray microtomography. Across the investigated length scales, the upCNF foams exhibited a superior integrity compared to the wCNF foams, highlighting the potential of cotton waste textiles as a source of nanocellulose.

Multidirectional neutron dark-field tomography (MD-NDFT) has been demonstrated as a non-destructive and non-invasive method for advanced characterization of hierarchical materials. This was achieved by using the simple hierarchical structure of anisotropic CNC and CNF foams as model systems, where the alignment of nanoparticles in the full foams was revealed by MD-NDFT and cross-validated with SAXS on the nanometer scale. The dactyl club of the mantis shrimp was also measured, highlighting the potential of MD-NDFT for nature’s more complex hierarchical constructs.

Place, publisher, year, edition, pages
Stockholm: Department of Chemistry, Stockholm University, 2025. p. 54
Keywords
nanocellulose, cellulose-water interactions, neutron scattering, X-ray scattering, phonon transport, vibrational dynamics
National Category
Materials Chemistry
Research subject
Materials Chemistry
Identifiers
urn:nbn:se:su:diva-241224 (URN)978-91-8107-178-8 (ISBN)978-91-8107-179-5 (ISBN)
Public defence
2025-05-09, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16B, Stockholm, 14:00 (English)
Opponent
Supervisors
Funder
Swedish Foundation for Strategic Research, GSn15-008
Available from: 2025-04-14 Created: 2025-03-24 Last updated: 2025-04-11Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textScopus

Authority records

Åhl, AgnesJaworski, AleksanderNocerino, ElisabettaAndersson, MatildaSipponen, Mika H.Bergström, Lennart

Search in DiVA

By author/editor
Åhl, AgnesJaworski, AleksanderNocerino, ElisabettaAndersson, MatildaSipponen, Mika H.Bergström, Lennart
By organisation
Department of Chemistry
In the same journal
Small Structures
Materials Chemistry

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 127 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf