TY - JOUR
T1 - Multi-Atom Catalysts
T2 - Structural Design, Electronic Modulation, and Synergistic Catalysis
AU - Yang, Gege
AU - Cai, Hairui
AU - Yang, Zhimao
AU - Wang, Bin
AU - Liang, Chao
AU - Yang, Shengchun
N1 - Publisher Copyright:
© 2026 Wiley-VCH GmbH.
PY - 2026/2/23
Y1 - 2026/2/23
N2 - Multi-Atom catalysts (MACs) have emerged as a pioneering domain in heterogeneous catalysis, distinguished by their exceptional intrinsic characteristics. These catalysts not only preserve the atomic dispersion and superior atomic utilization efficiency characteristic of single-atom catalysts, but also address their inherent limitations through enhanced metal loading capacity. Crucially, the interatomic synergy within the cluster facilitates the formation of more intricate and adaptable active sites, thereby potentially elevating catalytic performance and expanding reaction scope to more complex chemical processes. This comprehensive review systematically examines three fundamental aspects: (1) The architectural diversity of atom cluster catalysts; (2) Advanced strategies for electronic structure modulation, encompassing atomic interface engineering, coordination environment optimization, and substrate-mediated regulation; (3) Synergistic mechanisms that transcend conventional linear scaling relationships and enable precise control over critical catalytic parameters. We further consolidate contemporary synthesis methodologies and cutting-edge characterization techniques specifically tailored for these catalytic systems. Particular emphasis is placed on their transformative applications across electrocatalytic, photocatalytic, and thermocatalytic domains. The work concludes by outlining persistent challenges and future research directions in catalyst design principles, mechanistic elucidation through advanced characterizations, and practical implementation strategies. This systematic analysis provides theoretical guidance and methodological references for developing next-generation high-performance catalysts.
AB - Multi-Atom catalysts (MACs) have emerged as a pioneering domain in heterogeneous catalysis, distinguished by their exceptional intrinsic characteristics. These catalysts not only preserve the atomic dispersion and superior atomic utilization efficiency characteristic of single-atom catalysts, but also address their inherent limitations through enhanced metal loading capacity. Crucially, the interatomic synergy within the cluster facilitates the formation of more intricate and adaptable active sites, thereby potentially elevating catalytic performance and expanding reaction scope to more complex chemical processes. This comprehensive review systematically examines three fundamental aspects: (1) The architectural diversity of atom cluster catalysts; (2) Advanced strategies for electronic structure modulation, encompassing atomic interface engineering, coordination environment optimization, and substrate-mediated regulation; (3) Synergistic mechanisms that transcend conventional linear scaling relationships and enable precise control over critical catalytic parameters. We further consolidate contemporary synthesis methodologies and cutting-edge characterization techniques specifically tailored for these catalytic systems. Particular emphasis is placed on their transformative applications across electrocatalytic, photocatalytic, and thermocatalytic domains. The work concludes by outlining persistent challenges and future research directions in catalyst design principles, mechanistic elucidation through advanced characterizations, and practical implementation strategies. This systematic analysis provides theoretical guidance and methodological references for developing next-generation high-performance catalysts.
KW - electronic modulation
KW - geometric structural
KW - multi-atom catalysts
KW - multifaceted reactivity
KW - synergistic effects
UR - https://www.scopus.com/pages/publications/105029630495
U2 - 10.1002/smtd.202502368
DO - 10.1002/smtd.202502368
M3 - 文献综述
C2 - 41656600
AN - SCOPUS:105029630495
SN - 2366-9608
VL - 10
JO - Small Methods
JF - Small Methods
IS - 4
M1 - e02368
ER -