Su Ya-Qiong, Filot Ivo A W, Liu Jin-Xun, Hensen Emiel J M
Laboratory of Inorganic Materials Chemistry, Schuit Institute of Catalysis, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
ACS Catal. 2018 Jan 5;8(1):75-80. doi: 10.1021/acscatal.7b03295. Epub 2017 Nov 20.
Doping CeO with Pd atoms has been associated with catalytic CO oxidation, but current surface models do not allow CO adsorption. Here, we report a new structure of Pd-doped CeO(111), in which Pd adopts a square planar configuration instead of the previously assumed octahedral configuration. Oxygen removal from this doped structure is favorable. The resulting defective Pd-doped CeO surface is active for CO oxidation and is also able to cleave the first C-H bond in methane. We show how the moderate CO adsorption energy and dynamic features of the Pd atom upon CO adsorption and CO oxidation contribute to a low-barrier catalytic cycle for CO oxidation. These structures, which are also observed for Ni and Pt, can lead to a more open coordination environment around the doped-transition-metal center. These thermally stable structures are relevant to the development of single-atom catalysts.
用钯原子掺杂二氧化铈已与催化一氧化碳氧化相关联,但目前的表面模型不允许一氧化碳吸附。在此,我们报告了一种钯掺杂二氧化铈(111)的新结构,其中钯采用平面正方形构型而非先前假定的八面体构型。从这种掺杂结构中去除氧是有利的。由此产生的有缺陷的钯掺杂二氧化铈表面对一氧化碳氧化具有活性,并且还能够裂解甲烷中的第一个碳氢键。我们展示了一氧化碳吸附能量适中以及钯原子在一氧化碳吸附和一氧化碳氧化时的动态特征如何促成一氧化碳氧化的低势垒催化循环。这些结构在镍和铂中也有观察到,可导致掺杂过渡金属中心周围形成更开放的配位环境。这些热稳定结构与单原子催化剂的开发相关。