Faculty of Science, Ningbo University, Ningbo, PR China.
Phys Chem Chem Phys. 2013 Aug 21;15(31):12846-51. doi: 10.1039/c3cp44712j.
Using density functional theory, we have investigated the catalytic properties of bimetallic complex catalysts PtlAum(CO)n (l + m = 2, n = 1-3) in the reduction of SO2 by CO. Due to the strong coupling between the C-2p and metal 5d orbitals, pre-adsorption of CO molecules on the PtlAum is found to be very effective in not only reducing the activation energy, but also preventing poisoning by sulfur. As result of the coupling, the metal 5d band is broadened and down-shifted, and charge is transferred from the CO molecules to the PtlAum. As SO2 is adsorbed on the catalyst, partial charge moves to the anti-σ bonding orbitals between S and O in SO2, weakening the S-O bond strength. This effect is enhanced by pre-adsorbing up to three CO molecules, therefore the S-O bonds become vulnerable. Our results revealed the mechanism of the excellent catalytic properties of the bimetallic complex catalysts.
我们使用密度泛函理论研究了 PtlAum(CO)n(l + m = 2,n = 1-3)双金属配合物催化剂在 CO 还原 SO2 反应中的催化性能。由于 C-2p 和金属 5d 轨道之间的强耦合作用,预吸附的 CO 分子在降低反应的活化能方面非常有效,同时还能防止硫中毒。由于这种耦合作用,金属 5d 带被展宽和向下移动,电荷从 CO 分子转移到 PtlAum。当 SO2 被吸附在催化剂上时,部分电荷转移到 SO2 中 S 和 O 之间的反 σ 键轨道上,从而削弱了 S-O 键的强度。预吸附多达三个 CO 分子后,这种效果会增强,因此 S-O 键变得脆弱。我们的结果揭示了双金属配合物催化剂具有优异催化性能的机制。