Department of Physics, National University of Singapore, 2 Science Drive 3, Singapore, 117542.
Phys Chem Chem Phys. 2012 Jul 21;14(27):9660-5. doi: 10.1039/c2cp40939a. Epub 2012 Jun 13.
Doping induced metal-insulator transition (MIT) in transition-metal (TM) oxides has been the topic of continued interest outside the field of catalysis chemistry. In this paper, via ab initio (GGA+U) calculations, we show that Nb-doping induced MIT in SrTiO(3) causes a dimensionality crossover of supported Au clusters, and at the same time, greatly enhances the stability and catalytic activity of these clusters. Underlying the predicted high catalytic activity of Au clusters towards the CO oxidation is the MIT induced interaction between the O(2) antibonding 2π* orbital and Au conduction bands, leading to a shift in the population of electrons from Au to the antibonding orbital and the activation of the O(2) molecule. We expect these results to provide a new methodology for the control of catalytic performance of TM-oxide supported Au nanoclusters.
在催化化学领域之外,过渡金属(TM)氧化物中的掺杂诱导金属-绝缘体转变(MIT)一直是人们持续关注的话题。在本文中,通过第一性原理(GGA+U)计算,我们表明,Nb 掺杂诱导 SrTiO3 中的 MIT 导致了负载 Au 团簇的维度交叉,同时极大地提高了这些团簇的稳定性和催化活性。Au 团簇对 CO 氧化具有高催化活性的原因是 MIT 诱导的 O(2)反键 2π*轨道与 Au 导带之间的相互作用,导致电子从 Au 转移到反键轨道,从而激活 O(2)分子。我们预计这些结果将为控制 TM 氧化物负载 Au 纳米团簇的催化性能提供一种新方法。