TY - JOUR
T1 - Catalytic Performance of Nanoporous Metal Skeleton Catalysts for Molecular Transformations
AU - Jin, Tienan
AU - Terada, Masahiro
AU - Bao, Ming
AU - Yamamoto, Yoshinori
N1 - Funding Information:
The authors are grateful to the Scientific Research (A) from Japan Society for Promotion of Science (JSPS) (No.23245020 and JSPS KAKENHI Grant No.JP16H01000 in Precisely Designed Catalysts with Customized Scaffolding, and National Natural Science Foundation of China (21373041, 21372035, 21573032, and 21773021) and NSFC-IUPAC Program 21361140375 for their financial support.
Publisher Copyright:
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/7/5
Y1 - 2019/7/5
N2 - Nanoporous metal (MNPore) skeleton catalysts have attracted increasing attention in the field of green and sustainable heterogeneous catalysis owing to their unique three-dimensional nanopore structural features. In general, MNPores are fabricated through chemical or electrochemical corrosive dealloying of monolithic alloys. The dealloying process produces various MNPores with an open nanoporous network structure by formation of concave and convex hyperboloid-like ligaments. The large surface-to-volume ratio compared to bulk metals and high density of steps and kinks on ligaments of the unsupported MNPores make them promising heterogeneous catalyst candidates for highly active and selective molecular transformations. In this context, a variety of heterogeneous catalytic reactions using MNPores as nanocatalysts under gas- and liquid-phase conditions were developed over the last decade. In addition, the bulk metallic shape and mechanistic rigidity of the MNPore catalysts make the processes of catalyst recovery and reuse more facile and greener. This Minireview mainly focuses on the catalytic performance of nanoporous Au, Pd, Cu, and AuPd with respect to the achievements on catalytic applications in various molecular transformations.
AB - Nanoporous metal (MNPore) skeleton catalysts have attracted increasing attention in the field of green and sustainable heterogeneous catalysis owing to their unique three-dimensional nanopore structural features. In general, MNPores are fabricated through chemical or electrochemical corrosive dealloying of monolithic alloys. The dealloying process produces various MNPores with an open nanoporous network structure by formation of concave and convex hyperboloid-like ligaments. The large surface-to-volume ratio compared to bulk metals and high density of steps and kinks on ligaments of the unsupported MNPores make them promising heterogeneous catalyst candidates for highly active and selective molecular transformations. In this context, a variety of heterogeneous catalytic reactions using MNPores as nanocatalysts under gas- and liquid-phase conditions were developed over the last decade. In addition, the bulk metallic shape and mechanistic rigidity of the MNPore catalysts make the processes of catalyst recovery and reuse more facile and greener. This Minireview mainly focuses on the catalytic performance of nanoporous Au, Pd, Cu, and AuPd with respect to the achievements on catalytic applications in various molecular transformations.
KW - bond activation
KW - catalytic performance
KW - heterogeneous catalysis
KW - molecular transformations
KW - nanoporous metal
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U2 - 10.1002/cssc.201900318
DO - 10.1002/cssc.201900318
M3 - Review article
C2 - 30811897
AN - SCOPUS:85065176354
SN - 1864-5631
VL - 12
SP - 2936
EP - 2954
JO - ChemSusChem
JF - ChemSusChem
IS - 13
ER -