posted on 2022-04-26, 16:05authored byYizhen Chen, Rachita Rana, Zhennan Huang, Fernando D. Vila, Tyler Sours, Jorge E. Perez-Aguilar, Xiao Zhao, Jiyun Hong, Adam S. Hoffman, Xu Li, Chunyan Shang, Thomas Blum, Jie Zeng, Miaofang Chi, Miquel Salmeron, Coleman X. Kronawitter, Simon R. Bare, Ambarish R. Kulkarni, Bruce C. Gates
Atomically
dispersed metals on metal oxide supports are a rapidly
growing class of catalysts. Developing an understanding of where and
how the metals are bonded to the supports is challenging because support
surfaces are heterogeneous, and most reports lack a detailed consideration
of these points. Herein, we report two atomically dispersed CO oxidation
catalysts having markedly different metal–support interactions:
platinum in the first layer of crystalline MgO powder and platinum
in the second layer of this support. Structural models have been determined
on the basis of data and computations, including those determined
by extended X-ray absorption fine structure and X-ray absorption near
edge structure spectroscopies, infrared spectroscopy of adsorbed CO,
and scanning transmission electron microscopy. The data demonstrate
the transformation of surface to subsurface platinum as the temperature
of sample calcination increased. Catalyst performance data demonstrate
the lower activity but greater stability of the subsurface platinum
than of the surface platinum.