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Role of the Zn atomic arrangements in enhancing the activity and stability of the kinked Cu(211) site in CH3OH production by CO2 hydrogenation and dissociation: First-principles microkinetic modeling study

Authors
Jo, Deok YeonLee, Min WooHam, Hyung ChulLee, Kwan-Young
Issue Date
5월-2019
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Density functional theory; Methanol synthesis; CO2 hydrogenation; Reaction mechanism; Formate route; Carboxylate route; Cu/Zn catalyst; (211) surface; Zn ensembles; Microkinetic modeling; Role of Zn
Citation
JOURNAL OF CATALYSIS, v.373, pp.336 - 350
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CATALYSIS
Volume
373
Start Page
336
End Page
350
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/65952
DOI
10.1016/j.jcat.2019.04.009
ISSN
0021-9517
Abstract
In this work, we unravel the beneficial role of the Zn ensemble (in particular, an a single Zn atom) in the sixfold-coordinated kinked (Cu-vacant) site of the stepped Cu(2 1 1) surface for enhancing the reactivity and durability of catalyst in the CH3OH production from CO2 and H-2. For such purpose, by using the density functional theory (DFT) and microkinetic modeling methods, we systematically calculate the catalytic properties (activation energy barrier, turn of frequency (TOF), and rate constant), physical properties (cohesive and formation energy) and electronic structures (local density of state, and local charge distribution) of the different defective Cu sites [such as the stepped, kinked, Zn-substituted stepped Cu(2 1 1) surfaces] and the different Zn ensembles [dimer, and linear ensemble]. First, our DFT calculations exhibit that the Zn atoms at the sevenfold-coordinated site of the Cu(2 1 1) surface tend to be isolated and acts as the modifier to suppress the loss of Cu atoms from the stepped Cu (2 1 1) surface. Second, we find that the catalysis of CH3OH synthesis strongly depends on the type of defects at the Cu(2 1 1) surface. In particular, the single Zn atom-substituted (sevenfold-coordinated) stepped site in the Cu(2 1 1) surface is found to have the superior catalytic activity (TOF = 3.07 x 10(-5) s(-1) @ P = 75 bar and T = 523 K) toward the CH3OH formation compared to the traditionally-known active Cu(2 1 1) surface (TOF = 2.73 x 10(-7) s(-1)). In contrast, the sixfoldcoordinated kinked site is determined to largely slow down the rate of CH3OH production (TOF = 3.34 x 10(-15) s(-1) ). The increased catalysis in the Zn-associated stepped site is related to the significant enhancement of the surface affinity toward the adsorbate having the oxygen moiety (especially, HCOO), which leads to the large reduction of the activation energy barrier in the initial energydemanding CO2 hydrogenation reaction and in turn the improved catalysis of CH3OH synthesis. Our DFT calculation also elucidates that the stronger covalent-like overlap between O 2p-Zn 3d electrons (which is caused by the electronic charge loss of the Zn atom to the near-neighboring Cu sites) than the O 2p-Cu 3d case is responsible for such enhanced affinity of oxygen-containing adsorbates. In addition, we found that the single Zn atom exhibit the highest activity of CH3OH production (TOFCH3OH = 3.07 x 10(-5) s(-1)) over the dimer (1.62 x 10(-7) s(-11)) and linear ensemble (5.53 x 10(-7) s(-1)), which is related to the weaker affinity of Zn with H than the Cu-H case, which leads to the low coverage of surface H atom and in turn retard the CH3OH production via CH3O hydrogenation. Our study highlights the novel strategy of engineering the activity and stability of the defective under-coordinated kinked site for the enhanced CH3OH synthesis from CO2 and H-2 by controlling the arrangement of surface Zn atom at the stepped Cu(2 1 1) surface. (C) 2019 Elsevier Inc. All rights reserved.
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Lee, Kwan Young
공과대학 (화공생명공학과)
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