Hi all.

Currently, I am synthesizing the gold nanoparticles (AuNPs) using different approaches, but it seems that I never obtain the correct burgundy/red wine color that most AuNPs possess. 

Here are the strategies I used: 

a/ Excess citrate with heating and magnetic stirring (please note that the magnetic stirrer I have does not support heat. Therefore, I add citrate to the HAuCl4 solution then boil it using a hot plate before proceeding to stir)

b/ Excess citrate with magnetic stirring, under the support of a secondary reductant. I chose hydroxylamine at the concentration of 0.22M and even 0.11% NaBH4 in citrate solution. 

All the AuNPs I obtain are in blueish/violet color (you can check the image of (a) case on the left and (b) case on the right), in which I assume they are all in high diameter, so agglomeration occurred minutes after. You can see that the agglomerated AuNPs even stained on my stirrer.

For your information, the HAuCl4 solution I used was from dissolved gold in aqua regia (1000 ppm). There was an impurity of silver in the gold, so I added excess chloride and removed AgCl through centrifugation. The filtrate was then heated to repel residual acid vapor. Before forming AuNPs, all HAuCl4 solutions were adjusted to pH 6 using NaOH.

I hope to see you guys pointing out the defects in my procedure. I need a stable AuNPs solution to measure its plasmon band at 520nm, and I think I have tried out all I could. 

Please do not hesitate to ask me for more detailed description.

Thanks so much in advance.

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