Polystyrene Brush Evolution by Grafting to Reaction on Deglazed and Not‐Deglazed Silicon Substrates

Two model substrates for the grafting to reaction are considered: not‐deglazed silicon, whose surface is coated by a thin oxide layer with reactive silanol groups on its surface; and deglazed silicon, where the oxide layer is removed by treatment with hydrofluoric acid. The reactive polymers are hydroxy‐terminated polystyrenes with molecular weights ranging from 3.9 to 13.9 kg mol⁻1. The grafting to reaction is carried out at different temperatures and for different periods of time on the two different substrates. The thickness and the thermal stability of the resulting brushes are evaluated. Furthermore, the grafting of a highly dispersed system is simulated by blending two polymers with different molecular weights. Although the brush thickness growth is found to be faster on deglazed silicon, the preferential grafting of short chains occurs with equal chain selection propensity on both substrates. Hydroxy‐terminated polystyrenes are reacted by grafting to reaction in melt on deglazed and not‐deglazed silicon substrates. The characteristics of the resulting brushes are evaluated by ellipsometry and thermogravimetry‐gas chromatography‐mass spectrometry analysis.