Local Environment Sensitivity of the Cu K-Edge XANES Features in Cu-SSZ-13: Analysis from First-Principles

Renqin Zhang; Jean-Sabin McEwen

doi:10.1021/acs.jpclett.8b00675

Local Environment Sensitivity of the Cu K-Edge XANES Features in Cu-SSZ-13: Analysis from First-Principles

J Phys Chem Lett. 2018 Jun 7;9(11):3035-3042. doi: 10.1021/acs.jpclett.8b00675. Epub 2018 May 22.

Authors

Renqin Zhang¹, Jean-Sabin McEwen^{1

2

3

4

5}

Affiliations

¹ The Gene and Linda Voiland School of Chemical Engineering and Bioengineering , Washington State University , Pullman , Washington 99164 , United States.
² Department of Physics and Astronomy , Washington State University , Pullman , Washington 99164 , United States.
³ Department of Chemistry , Washington State University , Pullman , Washington 99164 , United States.
⁴ Department of Biological Systems Engineering , Washington State University , Pullman , Washington 99164 , United States.
⁵ Institute for Integrated Catalysis , Pacific Northwest National Laboratory , Richland , Washington 99352 , United States.

PMID: 29665684
DOI: 10.1021/acs.jpclett.8b00675

Abstract

Cu K-edge X-ray absorption near-edge spectra (XANES) have been widely used to study the properties of Cu-SSZ-13. In this Letter, the sensitivity of the XANES features to the local environment for a Cu⁺ cation with a linear configuration and a Cu²⁺ cation with a square-linear configuration in Cu-SSZ-13 is reported. When a Cu⁺ cation is bonded to H₂O or NH₃ in a linear configuration, the XANES has a strong peak at around 8983 eV. The intensity of this peak decreases as the linear configuration is broken. As for the Cu²⁺ cations in a square-planar configuration with a coordination number of 4, two peaks at around 8986 and 8993 eV are found. An intensity decrease for both peaks at around 8986 and 8993 eV is found in an NH₃_4_Z₂Cu model as the N-Cu-N angle changes from 180 to 100°. We correlate these features to the variation of the 4p state by PDOS analysis. In addition, the feature peaks for both the Cu⁺ cation and Cu²⁺ cation do not show a dependence on the Cu-N bond length. We further show that the feature peaks also change when the coordination number of the Cu cation is varied, while these feature peaks are independent of the zeolite topology. These findings help elucidate the experimental XANES features at an atomic and an electronic level.