I synthesized nanoparticles but I am getting aggregation of nanoparticles. I tried different variables such as solvent media, time, pH, temperature but could not get rid of it.
Our experience shows that minimal number of chemicals should be used:
1) simple salt as precursor,
2) good selection of reducing agent,
3) optimization of solvent type and conditions,
4) no additives,
5) no stabilizers,
6) simple conditions.
A variety of different particles can be obtained.
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Efficient General Procedure To Access a Diversity of Gold(0) Particles and Gold(I) Phosphine Complexes from a Simple HAuCl4 Source. Localization of Homogeneous/Heterogeneous System's Interface and Field-Emission Scanning Electron Microscopy Study,
I would suggest using some stabilizing agent. Somewhere in the RG there is a huge topic about creating nanoparticles in room temperature. Check there if you can find some interesting information.
I don't konw in which condition the aggregation occur, but a method to reducing this aggregation in the dry state is dispersing the glod particles in water and then lyophilizing them.
Dear researchers The crux of getting nano is encourage nucleation and not growth - please my book " Nano science and technology " CRC press( 2004) with prof A.Subramania and many good papers
It will be easier to figure out the cause for aggregation of nanoparticle if you have mentioned the reaction details. In general, all the nanoparticles tend to get aggregated unless they are in suitable condition. The aggregation can be minimized or avoided with the choice of suitable surfactant/stabilizer (CTAB, PVP, Sodium Citrate, thiols, polymers... etc) and also reaction medium (pH), temperature etc. Storage of nanoparticles in solution form rather than powder form will also help to reduce aggregation in some cases.
I am not generalizing the storage for all cases. Of course, CTAB stabilized nanoparticles will grow in solution form. But there are some examples (even from our own experience) that solution in proper environment (pH, solvent etc) will be stable (in some cases).
In some case we will not be able to use any surfactant due to experimental limitation. In that case if we want to use the nanoparticles we have to be adjust the pH with surface charge ~ +/- 30 mV. I think it will work. In case of metalic nanoparticle we can use the bimetalic procedure such as Au/Ni combination.
What kind of NP's u want to synthesize...?....one can also stabilize the NP's by using stabilizer/capping groups to attached with the surface of NP's...like citrate stabilized AuNP's...
Often, the stabilisation (mechanism) of nanoparticles is simply electrostatic. This stabilisation type is overcome by salt = high ionic strength. (In many cases, a buffer salt is enough to aggregate the nanoparticles.) Today, polymer colloid synthesis experts tend to change the stabilisation mechanism (by synthesis) from electrostatic to electrosteric. The result are so-called 'hairy' polymeric nanoparticles. They even do not aggregate or flocculate at pH 0 - 1.
Our experience shows that minimal number of chemicals should be used:
1) simple salt as precursor,
2) good selection of reducing agent,
3) optimization of solvent type and conditions,
4) no additives,
5) no stabilizers,
6) simple conditions.
A variety of different particles can be obtained.
--
Efficient General Procedure To Access a Diversity of Gold(0) Particles and Gold(I) Phosphine Complexes from a Simple HAuCl4 Source. Localization of Homogeneous/Heterogeneous System's Interface and Field-Emission Scanning Electron Microscopy Study,
Increasing the temperature will enhance the aggregation of nanoparticles.
Keeping them dispersed in a solvent rather than powder form, low concentration of dispersion, suitable stabilizer based on the type of nanoparticles (for example oleic acid, oleyl amine stabilized magnetic nanopartilces), mild reducing agent and the use of simple salt are some of the common ways to avoid nanoparticles aggregation.
Nanoparticle Aggregation: Principles and Modeling gives a brief overview in this area
amino acids can be used as reducing ( aspartic acid or tryptophan) and capping/stabilizing ( lysine) agents. Oleylamide and decanethiol could be used as stabilizing agends as well.