I have been working on coating my CTAB-capped GNRs with a mesoporous silica coating via a modified Stober method that has been reported many times. however everytime I try, my GNRs continue to aggregate and my final uv-vis spectra is so wide there is no consistency in my sample. Some general questions I have that may help me understand this better are: 1. why is an additional washing step of the as-synthesised GNRs required before starting the coating process if we wash several times after the GNR synthesis process, especially if the protocols state to just resuspend in a 1 mM CTAB solution anyway. 2. when fresh CTAB solution is added, how long does it need to react with the GNRs before moving on to pH adjustment? 3. how do you mix the solution when TEOS is added? I have seen protocols that say "gently mixing" and some that have gone as far as using an ultrasonic bath. 4. Does final resuspension solution matter in terms of agglomeration? I have been resuspending in MeOH, but have seen some that use water, and some with EtOH. Any help on this would be much appreciated!

More Luis Trabucco's questions See All
Similar questions and discussions