The interaction of carbon disulfide, CS2, with polycrystalline MgO was investigated by means of infrared and UV-visible spectroscopies and ab initio electronic structure calculations. The aim was to understand the modi cations of the surface properties of MgO microcrystals induced by the substitution of O2- with S2- anions. The interaction of CS2 with MgO shows the formation of thiocarbonates followed by O-S exchange reactions and formation of Mg2+-S2- clusters in a MgO matrix. The O-S exchange reaction involves mainly the low-coordinated O2- anions at the steps and corner sites, and only at high temperature are a small number of O2- anions at the (100) terrace sites involved. The replacement of the O with the S atoms at the low-coordinated sites of the MgO surface transforms the reactive polycrystalline material into a chemically inert system
Scarano, D., Bertarione, S., Zecchina, A., Soave, R., Pacchioni, G. (2002). Adsorption of CS2 on MgO microcrystals: Formation of a S-doped MgO surface. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 4(2), 366-374 [10.1039/B104566K].
Adsorption of CS2 on MgO microcrystals: Formation of a S-doped MgO surface
PACCHIONI, GIANFRANCO
2002
Abstract
The interaction of carbon disulfide, CS2, with polycrystalline MgO was investigated by means of infrared and UV-visible spectroscopies and ab initio electronic structure calculations. The aim was to understand the modi cations of the surface properties of MgO microcrystals induced by the substitution of O2- with S2- anions. The interaction of CS2 with MgO shows the formation of thiocarbonates followed by O-S exchange reactions and formation of Mg2+-S2- clusters in a MgO matrix. The O-S exchange reaction involves mainly the low-coordinated O2- anions at the steps and corner sites, and only at high temperature are a small number of O2- anions at the (100) terrace sites involved. The replacement of the O with the S atoms at the low-coordinated sites of the MgO surface transforms the reactive polycrystalline material into a chemically inert systemI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.