TIIK CATALYTIC MECHANISM OF CO OXIDATION IN AIAu6 CLUSTERS DETERMINED BY DENSITY FUNCTIONAL THEORY
We present density functional calculations of 02 and CO adsorption on an AlAu6 cluster. It is found that in the AlAu6 cluster the active sites would be first occupied by coming 02 rather than CO due to a more negative binding energy of the former. Furthermore, the catalytic mechanisms of CO oxidation in AlAu6 clusters, which are based on a single CO molecule and double CO molecules, are discussed. This investigation reveals that the reaction of a single CO molecule with the AlAu602 complex has the lowest activation barrier (0.27 eV), which is 0.51 eV lower than that of the pure Au^ cluster. For the AlAu602(C0)2 complex, due to the
structural distortion of the Аu6 cluster, the activation barrier of the determination rate is higher by 0.53 cV than that of the AlAu6O2CO complex, which shows that the cooperation effect of the second CO molecule can go against CO oxidation. For the А1@Аu6О2(СО)2 complex, the activation barrier of the determination rate is lower by 0.07 eV than the path of one CO molecule, which demonstrates that the cooperation effect of the second CO molecule can prompt CO oxidation.
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We present density functional calculations of 02 and CO adsorption on an AlAu6 cluster. <...> It is found that in the AlAu6 cluster the active sites would be first occupied by coming 02 rather than CO due to a more negative binding energy of the former. <...> Furthermore, the catalytic mechanisms of CO oxidation in AlAu6 clusters, which are based on a single CO molecule and double CO molecules, are discussed. <...> This investigation reveals that the reaction of a single CO molecule with the AlAu602 complex has the lowest activation barrier (0.27 eV), which is 0.51 eV lower than that of the pure Au^ cluster. <...> For the AlAu602(C0)2 complex, due to the
structural distortion of the Аu6 cluster, the activation barrier of the determination rate is higher by 0.53 cV than that of the AlAu6O2CO complex, which shows that the cooperation effect of the second CO molecule can go against CO oxidation. <...> For the А1@Аu6О2(СО)2 complex, the activation barrier of the determination rate is lower by 0.07 eV than the path of one CO molecule, which demonstrates that the cooperation effect of the second CO molecule can prompt CO oxidation.
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<...> We present density functional calculations of 02 and CO adsorption on an AlAu6 cluster. <...> It is found that in the AlAu6 cluster the active sites would be first occupied by coming 02 rather than CO due to a more negative binding energy of the former. <...> Furthermore, the catalytic mechanisms of CO oxidation in AlAu6 clusters, which are based on a single CO molecule and double CO molecules, are discussed. <...> This investigation reveals that the reaction of a single CO molecule with the AlAu602 complex has the lowest activation barrier (0.27 eV), which is 0.51 eV lower than that of the pure Au^ cluster. <...> For the AlAu602(C0)2 complex, due to the
structural distortion of the Аu6 cluster, the activation barrier of the determination rate is higher by 0.53 cV than that of the AlAu6O2CO complex, which shows that the cooperation effect of the second CO molecule can go against CO oxidation. <...> For the А1@Аu6О2(СО)2 complex, the activation barrier of the determination rate is lower by 0.07 eV than the path of one CO molecule, which demonstrates that the cooperation <...>
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