Single crystal and high area titania supported rhodium: the interaction ofsupported Rh(CO)(2) with NO

Model Rh/TiO2 catalysts have been prepared by metal organic chemical vapour deposition (MOCVD) of [Rh(CO)(2)Cl](2) to TiO2(1 1 0) and high area (Degus sa P25) powder TiO2 samples. The rhodium geminal dicarbonyl species (Rh(CO) (2)) is produced on each surface, and the reaction of the supported Rh(CO) with NO has been studied using FT-RAIRS, transmission FT-IR and XPS. TiO2(1 1 0)-Rh(CO)(2) is converted by exposure to NO at 300 K solely to a h ighly dispersed Rh(NO)(+) species with v(N-O) observed as a transmission ba nd in FT-RAIRS at 1920 cm(-1). This species is thermally more stable than t he geminal dicarbonyl species, and XPS measurements indicate that the NO is removed without the formation of adsorbed nitrogen residues by 600 K. Re-e xposure to CO results in the complete regeneration of TiO2(1 1 0)-Rh(CO)(2) from TiO2(1 1 0)-Rh(NO)(+) TiO2(P25)-Rh(CO)(2) is present in a variety of surface environments, with broad bands observed at the same frequencies as for TiO2(1 1 0)-Rh(CO)(2) (v(sym)(C-O) = 2110 cm(-1) and v(asym)(C-O) = 203 0 cm(-1)). Exposure of TiO2(P25)-Rh(CO)(2) to NO at 300 K results in the fo rmation of TiO2(P25)-Rh(NO)(+) with v(N-O) at 1920 cm(-1), and TiO2(P25)-Rh (CO(NO) with v(N-O) at 1750 cm(-1) and v(C-O) at 2110 cm(-1). TiO2(P25)-Rh-0 clusters, formed through the thermal decomposition of TiO2(P 25)-Rh(CO)(2) at various temperatures, react with NO to produce additional surface nitrosyl species. On a surface heated to 380 K where TiO2(P25)-Rh(C O)(2) decarbonylation has only just taken place, reaction with NO at 300 K results in the formation of the same species as those produced through the reaction of TiO2(P25)-Rh(CO)(2) directly NO, i.e. (TiO2(P25)-Rh(NO)(+)) and TiO(2)P25)-Rh(CO)(NO). Re-exposure of this surface to CO results in the co mplete reconversion of the dispersed nitrosyl to TiO2(P25)-Rh(CO)(2), When larger clusters are formed on a surface by heating to 650 K, reaction with NO leads initially to the adsorption of linear and bridged bound NO on TiO2 (P25)-Rh-0 with respective v(N-O) bands observed in the IR at 1818 and 1680 cm-l Further exposure of NO, however, results in the complete disruption o f the TiO2(P25)-Rh-0 clusters. This is evidenced by the disappearance of th e bridging and linear bands and the appearance of a strong band associated with v(N-O) of TiO2(P25)-Rh(NO)(+) at 1920 cm(-1), and bands at 1745 and 15 50 cm(-1) assigned to dispersed TiO2(P25)-Rh(NO)- and TiO2(P25)-Rh(NO2)(-)/ (NO3)(-). The latter species we suggest are stabilised by surface defects s uch as oxygen vacancies which may have been formed during the clustering of the Rh-0. After thermal treatment to temperatures of 800 K, where encapsul ation of the TiO2(P25)-Rh-0 clusters should occur, we see a strong suppress ion of NO adsorption on the clusters. Nevertheless disruption of clusters s till takes place with the formation of TiO2(P25)-Rh(NO)(-) even under these (SMSI) conditions. (C) 2001 Elsevier Science B.V. All rights reserved.