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Zwitterions Layer at but Do Not Screen Electrified Interfaces

[Image: see text] The role of ionic electrostatics in colloidal processes is well-understood in natural and applied contexts; however, the electrostatic contribution of zwitterions, known to be present in copious amounts in extremophiles, has not been extensively explored. In response, we studied th...

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Detalles Bibliográficos
Autores principales: Ridwan, Muhammad Ghifari, Shrestha, Buddha Ratna, Maharjan, Nischal, Mishra, Himanshu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900129/
https://www.ncbi.nlm.nih.gov/pubmed/35194995
http://dx.doi.org/10.1021/acs.jpcb.1c10388
Descripción
Sumario:[Image: see text] The role of ionic electrostatics in colloidal processes is well-understood in natural and applied contexts; however, the electrostatic contribution of zwitterions, known to be present in copious amounts in extremophiles, has not been extensively explored. In response, we studied the effects of glycine as a surrogate zwitterion, ion, and osmolyte on the electrostatic forces between negatively charged mica–mica and silica–silica interfaces. Our results reveal that while zwitterions layer at electrified interfaces and contribute to solutions’ osmolality, they do not affect at all the surface potentials, the electrostatic surface forces (magnitude and range), and solutions’ ionic conductivity across 0.3–30 mM glycine concentration. We infer that the zwitterionic structure imposes an inseparability among positive and negative charges and that this inseparability prevents the buildup of a counter-charge at interfaces. These elemental experimental results pinpoint how zwitterions enable extremophiles to cope with the osmotic stress without affecting finely tuned electrostatic force balance.