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Strong Electronic Pt‐Carbide Interaction Boosted CO2 Hydrogenation to CO Научная публикация

Журнал ChemCatChem
ISSN: 1867-3880 , E-ISSN: 1867-3899
Вых. Данные Год: 2025, Номер статьи : e202500076, Страниц : DOI: 10.1002/cctc.202500076
Ключевые слова Electronic interaction; Carbides; CO2 hydrogenation
Авторы Dong Hongsen 1 , Lin Xiao 1 , Zhao Yan 4 , Kolokolov Daniil I. 5 , Chen Xi 3 , Ding Shipeng 1,2
Организации
1 Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, School of Energy and Environment, Southeast University, Nanjing, 210096, Jiangsu, China
2 College of Environmental Science and Engineering, Beijing Forestry University, Beijing, 100083, China
3 China-UK Low Carbon College, Shanghai Jiao Tong University, 201306, Shanghai, China
4 Zhejiang Key Laboratory of Petrochemical Environmental Pollution Control, Zhejiang Ocean University, Zhoushan 316004, China
5 Boreskov Institute of Catalysis Novosibirsk, Ac. Lavrentiev av. 5, Novosibirsk 630090, Russia

Реферат: Tunning the metal-support interaction is a common strategy to regulate the electro and geometric structure of supported metal; However, most of supports were limited to oxides, and how the carbides tune the activity of supported metal in CO2 hydrogenation is still elusive. Herein, Pt nanoparticles dispersed on carbides were fabricated and examined in CO2 hydrogenation to CO. Among the carbides (ZrC, SiC, WC and TiC), Pt nanoparticles supported on ZrC showed the best catalytic activity, with the CO2 conversion of up to around 37% and 99% selectivity towards CO; it also displayed decent stability in the time-on-stream for 60 hours. The mechanistic study indicated the strong metal-carbide electronic interaction enabled the electron transfer from the Pt nanoparticle to ZrC in the Pt/ZrC catalysts. The modulation of Pt electronic structure tunned the adsorption configuration of CO2 and H2, thus enhancing the catalytic performance of Pt nanoparticles in CO2 hydrogenation to CO. This work demonstrates the importance of carbides in modulating the electronic structure of supported metals.
Библиографическая ссылка: Dong H. , Lin X. , Zhao Y. , Kolokolov D.I. , Chen X. , Ding S.
Strong Electronic Pt‐Carbide Interaction Boosted CO2 Hydrogenation to CO
ChemCatChem. 2025. e202500076 . DOI: 10.1002/cctc.202500076 WOS Scopus OpenAlex
Даты:
Опубликована online: 13 мар. 2025 г.
Идентификаторы БД:
Web of science: WOS:001477502100001
Scopus: 2-s2.0-105004190869
OpenAlex: W4408465930
Цитирование в БД: Пока нет цитирований
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