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The electrophilicity of surface carbon species in the redox of CuO‐CeO2 catalysts
Authors:
Liqun
Kang
(University College London)
,
Bolun
Wang
(University College London)
,
Andreas T.
Güntner
(ETH Zurich)
,
Siyuan
Xu
(Wuhan University)
,
Xuhao
Wan
(Wuhan University)
,
Yiyun
Liu
(University College London)
,
Sushila
Marlow
(University College London)
,
Yifei
Ren
(University College London)
,
Diego
Gianolio
(Diamond Light Source)
,
Chiu C.
Tang
(Diamond Light Source)
,
Vadim
Murzin
(DESY: Deutsches Elektronen-Synchrotron)
,
Hiroyuki
Asakura
(Kyoto University)
,
Qian
He
(National University of Singapore)
,
Shaoliang
Guan
(Cardiff University)
,
Juan J.
Velasco-Vélez
(Fritz-Haber-Institut der MPG Berlin)
,
Sotiris E.
Pratsinis
(ETH Zurich)
,
Yuzheng
Guo
(Wuhan University)
,
Feng Ryan
Wang
(University College London)
Co-authored by industrial partner:
No
Type:
Journal Paper
Journal:
Angewandte Chemie International Edition
State:
Published (Approved)
Published:
March 2021
Abstract: Electronic metal‐support interaction (EMSI) describes the electron flow between metal sites and a metal oxide support. It is generally used to follow the mechanism of redox reactions. In the study of CuO‐CeO2 redox, an additional flow of electron from metallic Cu to surface carbon species is observed via a combination of operando X‐ray absorption spectroscopy, synchrotron X‐ray powder diffraction, near ambient pressure‐near edge X‐ray absorption fine structure, and diffuse reflectance infrared Fourier transform spectroscopy. An electronic metal‐support‐carbon interaction (EMSCI) is proposed to explain the reaction pathway of CO oxidation. The EMSCI provides a complete picture of the mass and electron flow, which will help predict and improve the catalytic performance in the selective activation of CO2 , carbonate or carbonyl species in C1 chemistry.
Journal Keywords: CO oxidation; copper-ceria; EMSI; surface carbon; electrophilicity
Subject Areas:
Chemistry
Facility: BESSY II; SPring-8; DESY
Added On:
28/03/2021 20:15
Documents:
anie.202102570.pdf
Discipline Tags:
Physical Chemistry
Catalysis
Chemistry
Technical Tags: