dc.contributor.author
Kaur, Harmanjot
dc.contributor.author
Thürmer, Stephan
dc.contributor.author
Gholami, Shirin
dc.contributor.author
Credidio, Bruno
dc.contributor.author
Trinter, Florian
dc.contributor.author
Vasconcelos, Debora
dc.contributor.author
Marinho, Ricardo
dc.contributor.author
Pinheiro, Joel
dc.contributor.author
Bluhm, Hendrik
dc.contributor.author
Naves de Brito, Arnaldo
dc.date.accessioned
2025-04-16T12:28:24Z
dc.date.available
2025-04-16T12:28:24Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/47408
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-47126
dc.description.abstract
The effects of atmospheric aerosols are key uncertainties in climate models. One reason is the complex aerosol composition which includes a relatively large fraction of organics. Another reason is the small size of aerosols, which makes surface effects and processes important. These two factors make surface-active organics relevant for atmospheric aerosols, as they can affect crucial processes, such as chemical aging and water accommodation, as well as properties such as the surface tension, which drives droplet formation. Two exemplary types of atmospherically relevant organics are carboxylic acids and alkyl amines, and often both are found together within aerosols. In the most atmospherically significant pH range, these exist as alkyl-carboxylate ions and alkyl-ammonium ions. Using liquid-jet photoelectron spectroscopy, tuned to high surface sensitivity, we measured the alkyl-carboxylate anions and the alkyl-ammonium cations of alkyl chain lengths of 1 to 6 carbon atoms, both as single-component and mixed-component aqueous solutions. This enabled us to systematically study how their surface propensity is affected by the length of the alkyl chains and how cooperative ion–ion interactions result in strongly increased surface propensity. An exponential increase in surface propensity is found for the single-species solutions, with cooperative solute–solute effects in mixed solutions of 1 : 1 molar ratio drastically increasing the number of molecules present at the solutions' surfaces up to a factor of several hundred. This cooperative surface propensity is shown to strongly affect the amounts of organics at the surface. These changes can significantly influence radiative forcing via aerosol growth, cloud condensation nuclei activity, and aerosol chemical aging. Our results demonstrate the principal feasibility of a more advanced input of molecular details for creating parameterized descriptions of aerosol surface composition needed to properly account for their impacts in climate models.
en
dc.format.extent
16 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
atmospheric aerosols
en
dc.subject
climate models
en
dc.subject
aerosol surface effects
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::550 Geowissenschaften, Geologie::550 Geowissenschaften
dc.title
Boosting aerosol surface effects: strongly enhanced cooperative surface propensity of atmospherically relevant organic molecular ions in aqueous solution
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.5194/acp-25-3503-2025
dcterms.bibliographicCitation.journaltitle
Atmospheric Chemistry and Physics
dcterms.bibliographicCitation.number
6
dcterms.bibliographicCitation.pagestart
3503
dcterms.bibliographicCitation.pageend
3518
dcterms.bibliographicCitation.volume
25
dcterms.bibliographicCitation.url
https://doi.org/10.5194/acp-25-3503-2025
refubium.affiliation
Physik
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1680-7324
refubium.resourceType.provider
WoS-Alert