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Thioglycolic acid (TGA -stabilized CdTGA -stabilizedere prepared by an aqueous method as reported previously [10, 11].
Ag nanoparticles used in this study were prepared by an aqueous method as follows: Ag nanoparticles were synthesized through a chemical reduction reaction of AgNO3 using sodium citrate dehydrate as reducing agent.
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The hierarchical multi-branched Ag1Pt2 nanocorallines (NCs) were prepared in a large scale by a rapid aqueous method, using l-arginine as the eco-friendly shape-directing agent.
Transferable ZnO tetrapods were grown by an aqueous solution method.
ZnO NRs were deposited on AZO substrates by an aqueous solution method.
Vertically aligned ZnO NRAs were synthesized by an aqueous chemical method, and the Al2O3 and ZnO shell layers were prepared by the highly conformal atomic layer deposition technique.
Pyrochlore bismuth titanate (Bi2−xTi0.75x Ti2O7 was prepared by an aqueous sol gel method and annealed at different temperatures.
SnO2 NR arrays were fabricated by an aqueous synthesis method in the presence of hydrochloric acid and using thin compact SnO2 as seeds.
Yttrium iron garnet (Y3Fe5O12; YIG) and terbium iron garnet (Tb3Fe5O12; TbIG) were prepared by an aqueous sol gel method using two different complexing agents (1,2-ethanediol and glycerol).
The pristine Li1.2Ni0.13Co0.13Mn0.54O2 powder was synthesized by an aqueous solution method, followed by calcination at 900 °C in air, and the surface was then modified by coating with samaria doped ceria (SDC).
This size regulation method has great promise for applications that require homogeneous-sized MNPs made by an aqueous solution coprecipitation method.
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