Research output: Contribution to journal › Article › peer-review
Nature of the Surface Intermediates Formed from Methane on Cu-ZSM-5 Zeolite : A Combined Solid-State Nuclear Magnetic Resonance and Density Functional Theory Study. / Kolganov, Alexander A.; Gabrienko, Anton A.; Yashnik, Svetlana A. et al.
In: ACS Applied Materials and Interfaces, Vol. 124, No. 11, 19.03.2020, p. 6242-6252.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Nature of the Surface Intermediates Formed from Methane on Cu-ZSM-5 Zeolite
T2 - A Combined Solid-State Nuclear Magnetic Resonance and Density Functional Theory Study
AU - Kolganov, Alexander A.
AU - Gabrienko, Anton A.
AU - Yashnik, Svetlana A.
AU - Pidko, Evgeny A.
AU - Stepanov, Alexander G.
PY - 2020/3/19
Y1 - 2020/3/19
N2 - The intermediates formed upon the interaction of methane with Cu-modified ZSM-5 zeolites (Cu/H-ZSM-5) have been analyzed with solid-state NMR spectroscopy and DFT methods. Methane activation by Cu/H-ZSM-5 zeolites gives rise to three distinct surface methoxy-like species (-O-CH3) detected by 13C MAS NMR spectroscopy with specific chemical shifts in the range of 53-63 ppm. DFT calculations on representative cluster models of different sites potentially present in Cu/H-ZSM-5 have been used to assign these signals to (i) methanol adsorbed on two neighboring Cu sites (Cu-(HOCH3)-Cu, 62.6 ppm), (ii) methanol adsorbed on zeolite Brønsted acid sites (52.9 ppm), and (iii) lattice-bound methoxy groups (Si-O(CH3)-Al, 58.6). The formation of these methoxy-like intermediates depends on the Cu loading and, accordingly, the type of Cu species in the Cu/H-ZSM-5 zeolite. For the sample with low (0.1 wt %) Cu loading containing exclusively mononuclear isolated Cu species, only the intermediates ii and iii have been detected. The Cu-bound intermediate (i) is formed upon methane activation by multinuclear Cu sites featuring Cu-O-Cu bridging moieties present in the materials with relatively higher Cu loading (1.38 wt %). The presented results indicate that methane activation by Cu/H-ZSM-5 can be promoted by both mono- and multinuclear Cu species confined in the zeolite matrix.
AB - The intermediates formed upon the interaction of methane with Cu-modified ZSM-5 zeolites (Cu/H-ZSM-5) have been analyzed with solid-state NMR spectroscopy and DFT methods. Methane activation by Cu/H-ZSM-5 zeolites gives rise to three distinct surface methoxy-like species (-O-CH3) detected by 13C MAS NMR spectroscopy with specific chemical shifts in the range of 53-63 ppm. DFT calculations on representative cluster models of different sites potentially present in Cu/H-ZSM-5 have been used to assign these signals to (i) methanol adsorbed on two neighboring Cu sites (Cu-(HOCH3)-Cu, 62.6 ppm), (ii) methanol adsorbed on zeolite Brønsted acid sites (52.9 ppm), and (iii) lattice-bound methoxy groups (Si-O(CH3)-Al, 58.6). The formation of these methoxy-like intermediates depends on the Cu loading and, accordingly, the type of Cu species in the Cu/H-ZSM-5 zeolite. For the sample with low (0.1 wt %) Cu loading containing exclusively mononuclear isolated Cu species, only the intermediates ii and iii have been detected. The Cu-bound intermediate (i) is formed upon methane activation by multinuclear Cu sites featuring Cu-O-Cu bridging moieties present in the materials with relatively higher Cu loading (1.38 wt %). The presented results indicate that methane activation by Cu/H-ZSM-5 can be promoted by both mono- and multinuclear Cu species confined in the zeolite matrix.
KW - MOLECULAR-ORBITAL METHODS
KW - ZSM-5 ZEOLITE
KW - DIRECT CONVERSION
KW - COPPER IONS
KW - MECHANISTIC INSIGHTS
KW - CARBON-MONOXIDE
KW - METHOXY GROUPS
KW - OXO-CLUSTERS
KW - ACTIVE-SITE
KW - MFI ZEOLITE
UR - http://www.scopus.com/inward/record.url?scp=85081694425&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.0c00311
DO - 10.1021/acs.jpcc.0c00311
M3 - Article
AN - SCOPUS:85081694425
VL - 124
SP - 6242
EP - 6252
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
SN - 1944-8244
IS - 11
ER -
ID: 23825834