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Speciation and hydration forces in sodium carbonate/bicarbonate aqueous solutions nanoconfined between mica sheets

Abstract:
The equilibrium between hydrated and hydrolysed forms of CO2 in water is central to a multitude of processes in geology, oceanography and biology. Chemistry of the carbonate system is well understood in bulk solution, however processes such as mineral weathering and biomineralisation frequently occur in nano-confined spaces where carbonate chemistry is less explored. For confined systems, the speciation equilibria are expected to tilt due to surface reactivity, electric fields and reduced configurational entropy. In this discussion paper we provide measurements of interaction force between negatively charged aluminosilicate (mica) sheets across aqueous carbonate/bicarbonate solutions confined to nanoscale films in equilibrium with a reservoir of the solution. By fitting the measurements to a Poisson–Boltzmann equation modified to account for charge regulation at the bounding walls, we discuss features of the bicarbonate speciation in confinement. We find that (i) the presence of bicarbonate in the bulk reservoir causes a repulsive excess pressure in the slit compared to pH-neutral salt solutions at the same concentration, arising from a higher (negative) effective charge on the mica surfaces; (ii) the electrostatic screening length is lower for solutions of Na2CO3 compared to NaHCO3 at the same bulk concentration, due to a shift in the speciation equilibria with pH and in accordance with Debye–Hückel theory; (iii) hydration forces are observed at distances below 2 nm with features of size 0.1 nm and 0.3 nm; this was reproducible across the various bicarbonate electrolytes studied, and contrasts with hydration forces of uniform step size measured in pH-neutral electrolytes.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1039/d5fd00145e

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0009-0004-4279-693X
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0000-0002-1840-3866
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0000-0001-5096-0083
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0000-0002-5875-5217


More from this funder
Funder identifier:
https://ror.org/052gg0110


Publisher:
Royal Society of Chemistry
Journal:
Faraday Discussions More from this journal
Publication date:
2026-01-26
Acceptance date:
2026-01-20
DOI:
EISSN:
1364-5498
ISSN:
1359-6640


Language:
English
Keywords:
Source identifiers:
4002519
Deposit date:
2026-04-30
ARK identifier:
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