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ArticleKAUST Department
Environmental Science and Engineering (EnSE) Program, Biological and Environmental Science and Engineering (BESE) Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi ArabiaInterfacial Lab (iLab), Water Desalination and Reuse Center (WDRC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia
Environmental Science and Engineering Program
Water Desalination and Reuse Research Center (WDRC)
Biological and Environmental Science and Engineering (BESE) Division
KAUST Grant Number
BAS/1/1070-01-01Date
2022-02-23Permanent link to this record
http://hdl.handle.net/10754/673269
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Show full item recordAbstract
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.Citation
Ridwan, M. G., Shrestha, B. R., Maharjan, N., & Mishra, H. (2022). Zwitterions Layer at but Do Not Screen Electrified Interfaces. The Journal of Physical Chemistry B. https://doi.org/10.1021/acs.jpcb.1c10388Sponsors
H.M. thanks Changzi Wang, a student from his course on Aquatic Chemistry (EnSE 202) at KAUST, for bringing this problem to his attention. The authors are indebted to Masha Belyi (Research Scientist, Amazon’s Team Alexa) for creating a Python script for analyzing hundreds of AFM force–distance curves generated in this work to pinpoint the trends in Debye lengths and surface potentials. M.G.R. thanks Mohammad Abbas (KAUST) for discussions on cell physiology; B.R.S. thanks Dr. Bruno Torres (KAUST) for providing colloidal probes for AFM experiments. The co-authors thank Ana Rouseva (KAUST) and Paulus Buijs (KAUST) for assisting with osmotic pressure measurements presented in C; Dr. Farizal Hakiki (KAUST) and Prof. Carlos Santamarina (KAUST) for characterizing dielectric responses of solutions presented in D; and Heno Hwang, KAUST Illustrator, for preparing and and TOC. H.M. acknowledges KAUST for funding (grant no. BAS/1/1070-01-01).Publisher
American Chemical Society (ACS)PubMed ID
35194995PubMed Central ID
PMC8900129arXiv
2111.01833Additional Links
https://pubs.acs.org/doi/10.1021/acs.jpcb.1c10388ae974a485f413a2113503eed53cd6c53
10.1021/acs.jpcb.1c10388
Scopus Count
Except where otherwise noted, this item's license is described as Archived with thanks to The Journal of Physical Chemistry B under a Creative Commons license, details at: https://creativecommons.org/licenses/by/4.0/
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