- Zhao, Lu;
- Zhang, Yun;
- Huang, Lin-Bo;
- Liu, Xiao-Zhi;
- Zhang, Qing-Hua;
- He, Chao;
- Wu, Ze-Yuan;
- Zhang, Lin-Juan;
- Wu, Jinpeng;
- Yang, Wanli;
- Gu, Lin;
- Hu, Jin-Song;
- Wan, Li-Jun
Although single-atomically dispersed metal-Nx on carbon support (M-NC) has great potential in heterogeneous catalysis, the scalable synthesis of such single-atom catalysts (SACs) with high-loading metal-Nx is greatly challenging since the loading and single-atomic dispersion have to be balanced at high temperature for forming metal-Nx. Herein, we develop a general cascade anchoring strategy for the mass production of a series of M-NC SACs with a metal loading up to 12.1 wt%. Systematic investigation reveals that the chelation of metal ions, physical isolation of chelate complex upon high loading, and the binding with N-species at elevated temperature are essential to achieving high-loading M-NC SACs. As a demonstration, high-loading Fe-NC SAC shows superior electrocatalytic performance for O2 reduction and Ni-NC SAC exhibits high electrocatalytic activity for CO2 reduction. The strategy paves a universal way to produce stable M-NC SAC with high-density metal-Nx sites for diverse high-performance applications.