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Structure of Vanadia-Titania Catalysts Doped with Alkali Metals According to Solid-State NMR, ESR Spectroscopies and DFT Научная публикация

Журнал Catalysis Today
ISSN: 0920-5861 , E-ISSN: 1873-4308
Вых. Данные Год: 2024, Том: 442, Номер статьи : 114909, Страниц : 14 DOI: 10.1016/j.cattod.2024.114909
Ключевые слова Supported vanadia doped with alkali metals; 1H MAS NMR; 51V static and MAS NMR; 7Li, 23Na, 133Cs MAS NMR; ESR; DFT
Авторы Lapina Olga B. 1 , Papulovskiy Evgeniy S. 1 , Khabibulin Dzhalil F. 1 , Lewandowska Anna E. 2 , Bañares Miguel A. 2
Организации
1 Boreskov Institute of Catalysis SB RAS, 5 pr. Lavrentieva, Novosibirsk 630090, Russia
2 Instituto de Catalisis y Petroleoquimica,(ICP) CSIC, Marie Curie 2, Madrid E-28049, Spain

Информация о финансировании (1)

1 Министерство науки и высшего образования Российской Федерации (с 15 мая 2018) FWUR-2024-0034

Реферат: In this work, V/M/TiO₂ catalysts (M = Li, Na, K, Rb and Cs) were investigated with Solid-state nuclear magnetic resonance (SSNMR), electron paramagnetic resonance (ESR) and first-principles calculations. The total vanadium content corresponds to half monolayer (4 V atoms⋅nm⁻² of TiO₂ support surface), with V/M atomic ratio being 4/0.6. Static ⁵¹V and MAS ¹H, ⁷Li, ⁵¹V, ²³Na, ¹³³Cs NMR spectra were acquired. Surface moieties of vanadium oxide on (001) anatase surface were modeled using density functional theory (DFT); their ⁵¹V NMR parameters were calculated with the Gauge-Including Projected Augmented Wave (GIPAW) method and compared to experimental data obtained with ⁵¹V SSNMR spectroscopy. It was found that mainly strongly bound vanadium sites (V₃) are formed on anatase samples, located on TiO₂ terminal oxygen atoms. Weakly bound vanadium sites (V₁, V₂) are formed on bridged anatase oxygen atoms. Supported alkali metals (Li, Na, K, Rb and Cs) on TiO₂ were found to interact with protons located on the terminal and bridged TiO₂ oxygen atoms. The relative ratio of weakly bound vanadium sites (V₁, V₂) increased on alkali-containing samples. Calculations performed showed lithium cation to prefer V-O-Ti or V-O-V bonds over V=O, unsystematically deshielding vanadium nuclei. The presence of V³⁺ is likely to cause a loss of intensity in ⁵¹V NMR spectra.
Библиографическая ссылка: Lapina O.B. , Papulovskiy E.S. , Khabibulin D.F. , Lewandowska A.E. , Bañares M.A.
Structure of Vanadia-Titania Catalysts Doped with Alkali Metals According to Solid-State NMR, ESR Spectroscopies and DFT
Catalysis Today. 2024. V.442. 114909 :1-14. DOI: 10.1016/j.cattod.2024.114909 WOS Scopus РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 10 апр. 2024 г.
Принята к публикации: 24 июн. 2024 г.
Опубликована online: 1 июл. 2024 г.
Опубликована в печати: 1 дек. 2024 г.
Идентификаторы БД:
Web of science: WOS:001265714300001
Scopus: 2-s2.0-85197303382
РИНЦ: 71312753
Chemical Abstracts: 2024:1493542
OpenAlex: W4400216747
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Web of science 1
Scopus 1
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