Enhancing the reactivity of Si(100)-Cl toward PBr3 by charging Si dangling bonds

TL;DR

This study demonstrates that charging silicon dangling bonds on Si(100)-Cl surfaces significantly enhances their reactivity with PBr3, leading to dissociation and bond formation, with implications for surface chemistry and molecular adsorption.

Contribution

It reveals that positively charging silicon dangling bonds increases their reactivity with PBr3 and influences molecule adsorption, a novel insight into surface reactivity control.

Findings

Positively charged DBs react with PBr3, causing dissociation.

Charged DBs facilitate PH3 adsorption due to their electronic state.

Charging modifies surface reactivity towards molecules with lone pairs.

Abstract

The interaction of the PBr3 molecule with Si dangling bonds (DBs) on a chlorinated Si(100) surface was studied. The DBs were charged in a scanning tunneling microscope (STM) and then exposed to PBr3 directly in the STM chamber. Uncharged DBs rarely react with molecules. On the contrary, almost all positively charged DBs were filled with molecule fragments. As a result of the PBr3 interaction with the positively charged DB, the molecule dissociated into PBr2 and Br with the formation of a Si-Br bond and PBr2 desorption. These findings show that charged DBs significantly modify the reactivity of the surface towards PBr3. Additionally, we calculated PH3 adsorption on a Si(100)-2x1-H surface with DBs and found that the DB charge also has a significant impact. As a result, we demonstrated that the positively charged DB with a doubly unoccupied state enhances the adsorption of molecules with a lone pair of electrons.