Related Experiment Video
Updated: Nov 9, 2025

10:22
In Situ SIMS and IR Spectroscopy of Well-defined Surfaces Prepared by Soft Landing of Mass-selected Ions
Published on: June 16, 2014
18.4K
Highly active and stable Ir nanoclusters derived from Ir1/MgAl2O4 single-atom catalysts
Jingyi Yang1, Jingcai Zhang1, Qike Jiang2
1CAS Key Laboratory of Science and Technology on Applied Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
The Journal of Chemical Physics
|April 9, 2021
Summary
Stable single-atom catalysts (SACs) were used as seeds to create highly active iridium nanocluster catalysts. This method significantly enhanced catalytic performance for N2O decomposition, offering industrial applications.
Area of Science:
- Materials Science
- Catalysis
- Nanotechnology
Background:
- Single-atom catalysts (SACs) offer high stability but limited activity due to strong metal-support interactions.
- Developing nanoclusters or nanoparticles from SACs can enhance intrinsic catalytic activity.
Purpose of the Study:
- To prepare stable iridium single-atom catalysts (SACs) on MgAl2O4 using atomic trapping.
- To use these SACs as seeds for fabricating highly active and stable iridium nanocluster catalysts.
Main Methods:
- Atomic trapping method for preparing stable Ir SACs on MgAl2O4.
- High-temperature reduction to convert Ir SACs into Ir nanoclusters.
- Evaluation of catalytic activity for N2O decomposition.
Main Results:
- Extremely stable Ir SACs were successfully synthesized on MgAl2O4.
- Iridium nanocluster catalysts fabricated from Ir SAC seeds showed significantly enhanced activity.
- Catalytic activity for N2O decomposition increased over tenfold compared to parent Ir SACs.
Conclusions:
- Using stable SACs as seeds is an effective strategy to design highly active catalysts.
- The developed Ir nanocluster catalysts demonstrate potential for industrial applications in N2O decomposition.
- This approach offers a new pathway for creating advanced, stable, and active catalysts.

