Hello,

I am conducting experiments in which I electrodeposit nickel onto pure Fe substrates and then polymerize polyaniline, followed by observation with optical microscopy (OM). The attached images show my sample and the corresponding OM photographs.

I would like to ask two questions:

  • In most papers, samples after polyaniline polymerization are dried using N₂ gas. However, due to experimental constraints, I dried my samples using a hair dryer or compressed air (air gun). During this drying process, many crack-like marks—similar to shattered glass—appeared in the OM images. Could you please advise me on an appropriate drying method when N₂ gas is not available?
  • After polymerization, the OM observation revealed numerous small particles where the OM light transmitted through(I don't know), appearing on a uniform blue background. What could be the cause of this phenomenon? For reference, I electrodeposited nickel for 180 seconds, and then performed polyaniline polymerization at a constant current density of 3 mA/cm² for 200 seconds. Should I adjust the nickel electrodeposition time, or could there be an issue with my polymerization conditions?
  • Thank you very much for your guidance.

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