Hello everyone, currently I am working with square wave voltammetry for detection with screen printed electrodes that are conformed by a carbon working electrode, a carbon counter electrode and Ag as reference (or pseudoreference according to bibliography). Whithout chlorides I am able to detect my analyte very well without problem, but when I introduce Chlorides in the mix, my peak is moved to another potencial (I assum that is due to the fact of a higher conductivity in the mix) and it becomes wider, so much, that is not possible to detect it. My question is: Does this occur because Chlorides are affecting the migration of my molecule to the working electrode? or maybe Does this occur because Chlorides are affecting to my working electrode? In whatever of both cases, how can I fix this situation?

I have been trying to find an answer to this issue in bibliography, but I failed several times in this... I would be very grateful if someone is able to help me!

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