Hi,
Over the past few weeks I've been using a standard electrochemical set up consisting of a gold disk (Working electrode) electrode, platinum wire (Counter Electrode) and a Calomel (Reference) electrode to study methylene blue. The work consisted of doing square wave voltammetry scans on methylene blue in Phosphate Buffered Saline (PBS). Typically doing a scan on methylene blue gives rise to an oxidation peak at ~-0.2V in pH7.4 PBS.
Now if I use those same electrodes (after having polished and electrochemically cleaned them) in a buffered saline solution without methylene blue, I still see a peak at -0.2V (albeit its relatively smaller, being no bigger than .5uA in height).
What I've tried:
1. Preparing new solutions
2. Decontaminating every surface and item in contact with the electrode/buffer solution.
3. Sanding the gold electrode with 1200 grit Carbimet paper.
4. Leaving the gold electrode in piranha solution for ~10 minutes prior to electrochemical cleaning.
If any one has an idea as to why I could still be seeing a peak (especially after having sanded a good karat off the electrode), I'd love to hear your thoughts.
Thanks,
Best
Vlad