I am working on synthesis of silver nanoparticles (AgNPs) using the condition below. I would like to use this AgNPs for further application; however, the leftover silver nitrate (AgNO3) in the solution is not ideal for the application. When I measured the silver ion concentration the next day from the reaction using a silver ion probe after calibration (99% linearity based on the calibration), the remaining AgNO3 concentration was 30 - 40 uM, which seemed to be quite high. I've re-worked on the synthesis using higher concentration of sodium borohydride (37.5 and 50 uM), but this resulted in fading of bright yellow color to almost colorless after 1-2 hrs. It seems like excess borohydride promoted dissolution of AgNPs.

Is there anyway to modify the scheme so the AgNO3 will be consumed more ? Does the rate of dropwise addition of sodium borohydride have effect on consumption of AgNO3 ?

(1) DI water (volume needed to make up 15 mL was added)

(2) 100 uM Trisodium citrate

(3) 100 uM Silver Nitrate

(4) 25 uM Sodium borohydride (always freshly prepared)

*These reagents were added in the order of 1 to 4.

**These concentrations are final concentrations after all the reagents are added.

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