TY - JOUR
T1 - Ultrafast Encapsulation of Metal Nanoclusters into MFI Zeolite in the Course of Its Crystallization
T2 - Catalytic Application for Propane Dehydrogenation
AU - Zhu, Jie
AU - Osuga, Ryota
AU - Ishikawa, Ryo
AU - Shibata, Naoya
AU - Ikuhara, Yuichi
AU - Kondo, Junko N.
AU - Ogura, Masaru
AU - Yu, Jihong
AU - Wakihara, Toru
AU - Liu, Zhendong
AU - Okubo, Tatsuya
N1 - Publisher Copyright:
© 2020 Wiley-VCH GmbH
PY - 2020/10/26
Y1 - 2020/10/26
N2 - Encapsulating metal nanoclusters into zeolites combines the superior catalytic activity of the nanoclusters with high stability and unique shape selectivity of the crystalline microporous materials. The preparation of such bifunctional catalysts, however, is often restricted by the mismatching in time scale between the fast formation of nanoclusters and the slow crystallization of zeolites. We herein demonstrate a novel strategy to overcome the mismatching issue, in which the crystallization of zeolites is expedited so as to synchronize it with the rapid formation of nanoclusters. The concept was demonstrated by confining Pt and Sn nanoclusters into a ZSM-5 (MFI) zeolite in the course of its crystallization, leading to an ultrafast, in situ encapsulation within just 5 min. The Pt/Sn-ZSM-5 exhibited exceptional activity and selectivity with stability in the dehydrogenation of propane to propene. This method of ultrafast encapsulation opens up a new avenue for designing and synthesizing composite zeolitic materials with structural and compositional complexity.
AB - Encapsulating metal nanoclusters into zeolites combines the superior catalytic activity of the nanoclusters with high stability and unique shape selectivity of the crystalline microporous materials. The preparation of such bifunctional catalysts, however, is often restricted by the mismatching in time scale between the fast formation of nanoclusters and the slow crystallization of zeolites. We herein demonstrate a novel strategy to overcome the mismatching issue, in which the crystallization of zeolites is expedited so as to synchronize it with the rapid formation of nanoclusters. The concept was demonstrated by confining Pt and Sn nanoclusters into a ZSM-5 (MFI) zeolite in the course of its crystallization, leading to an ultrafast, in situ encapsulation within just 5 min. The Pt/Sn-ZSM-5 exhibited exceptional activity and selectivity with stability in the dehydrogenation of propane to propene. This method of ultrafast encapsulation opens up a new avenue for designing and synthesizing composite zeolitic materials with structural and compositional complexity.
KW - bifunctional catalyst
KW - heterogeneous catalysis
KW - nanoclusters
KW - propane dehydrogenation
KW - zeolites
UR - http://www.scopus.com/inward/record.url?scp=85089393621&partnerID=8YFLogxK
U2 - 10.1002/anie.202007044
DO - 10.1002/anie.202007044
M3 - Article
C2 - 32602591
AN - SCOPUS:85089393621
SN - 1433-7851
VL - 59
SP - 19669
EP - 19674
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 44
ER -