NPSNPs were prepared by adding 3.16 g cetyltrimethylammonium bromide (CTAB) and 0.23 g diethanolamine (DEA) to a solution of 75 mL ultrapure water and 13.4 mL absolute ethanol. The mixture was heated to 40°C and stirred. After 30 min, 8.56 mL tetraethoxysilane (TEOS) were added and the reaction mixture was stirred for additional 2 h. The product was centrifuged (30 min at 18000 g) and washed twice with water and once with ethanol. Afterwards, the particles were dried overnight at 60°C. To remove the structure-directing agent, a calcination for 5 h at 550°C (heating rate: 1 K min-1) followed [58 ].
The amino modification of the silica surface was performed via post-grafting by dispersing 500 mg of NPSNPs in 20 mL toluene. To this dispersion 75 μL 1,8-diaza-bicyclo[5.4.0]undec-7-ene (DBU) and 95 μL 3-aminopropyltrimethoxysilane (APTMS) were added. Afterwards, the solution was stirred for 2 h at 80°C. The modified nanoparticles were collected by centrifugation, washed three times with ethanol and dried at 60°C [52 ].