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A zeolitic vanadotungstate family with structural diversity and ultrahigh porosity for catalysis

Design of the structure and composition of crystalline microporous inorganic oxides is of great importance in catalysis. Developing new zeolites is one approach towards this design because of the tunable pore system and high thermal stability. Zeolites are limited to main group elements, which limit...

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Detalles Bibliográficos
Autores principales: Zhang, Zhenxin, Zhu, Qianqian, Sadakane, Masahiro, Murayama, Toru, Hiyoshi, Norihito, Yamamoto, Akira, Hata, Shinichi, Yoshida, Hisao, Ishikawa, Satoshi, Hara, Michikazu, Ueda, Wataru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141569/
https://www.ncbi.nlm.nih.gov/pubmed/30224654
http://dx.doi.org/10.1038/s41467-018-06274-2
Descripción
Sumario:Design of the structure and composition of crystalline microporous inorganic oxides is of great importance in catalysis. Developing new zeolites is one approach towards this design because of the tunable pore system and high thermal stability. Zeolites are limited to main group elements, which limits their applications in redox catalysis. Another promising choice is zeolitic transition metal oxides providing both porosity and redox activity, thereby further expanding the diversity of porous materials. However, the examples of zeolitic transition metal oxides are rare. Here, we report a new class of zeolitic vanadotungstates with tunable frameworks exhibiting a large porosity and redox activity. The assembly of [W(4)O(16)](8−) units with VO(2+) forms two isomeric porous frameworks. Owing to the complex redox properties and open porosity, the vanadotungstates efficiently catalyse the selective reduction of NO by NH(3). This finding provides an opportunity for design and synthesis of inorganic multifunctional materials for future catalytic applications.