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Formation of Reactive Oxygen by N2O Decomposition over Binuclear Cationic Sites of Fe-Ferrierite Zeolite: Periodic DFT + U Study Научная публикация

Журнал Chemical Physics Letters
ISSN: 0009-2614 , E-ISSN: 1873-4448
Вых. Данные Год: 2018, Том: 695, Страницы: 222-227 Страниц : 6 DOI: 10.1016/j.cplett.2018.02.011
Ключевые слова OVER-EXCHANGED FE/ZSM5; NITROUS-OXIDE DECOMPOSITION; DENSITY-FUNCTIONAL THEORY; ELECTRONIC-STRUCTURE; ZSM-5 ZEOLITE; VOX/TIO2 CATALYSTS; XAFS SPECTROSCOPY; DIRECT OXIDATION; ACTIVE OXYGEN; IRON SITES
Авторы Avdeev Vasilii I. 1 , Bedilo Alexander F. 1
Организации
1 Boreskov Institute of Catalysis SB RAS, Novosibirsk 630090, Russia

Информация о финансировании (1)

1 Федеральное агентство научных организаций России 0303-2016-0001

Реферат: The electronic nature of sites over Fe-ferrierite zeolite stabilizing active α-oxygen is analyzed by the periodic DFT + U approach. It is shown that two antiferromagnetically coupled Fe2+ cations with bridging OH-bonds form a stable bi-nuclear site of the [Fe2+<2OH>Fe2+] doped FER complex. Frontier orbitals of this complex populated by two electrons with minority spins are localized in the bandgap. As a result, [Fe2+<2OH>Fe2+] unit acquires the properties of a binuclear Lewis acid dipolarophile for 1,3-dipole N2O. First reaction step of N2O decomposition follows the Huisgen′s concept of the 1,3-dipolar cycloaddition concept followed by the formation of reactive oxygen species FeO.
Библиографическая ссылка: Avdeev V.I. , Bedilo A.F.
Formation of Reactive Oxygen by N2O Decomposition over Binuclear Cationic Sites of Fe-Ferrierite Zeolite: Periodic DFT + U Study
Chemical Physics Letters. 2018. V.695. P.222-227. DOI: 10.1016/j.cplett.2018.02.011 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 18 сент. 2017 г.
Принята к публикации: 6 февр. 2018 г.
Опубликована online: 7 февр. 2018 г.
Опубликована в печати: 1 мар. 2018 г.
Идентификаторы БД:
Web of science: WOS:000427386500035
Scopus: 2-s2.0-85042073635
РИНЦ: 35502436
Chemical Abstracts: 2018:304648
Chemical Abstracts (print): 169:11666
OpenAlex: W2789635997
Цитирование в БД:
БД Цитирований
Web of science 7
Scopus 7
РИНЦ 6
OpenAlex 8
Альметрики: