Phosphorus-modified cobalt single-atom catalysts loaded on crosslinked carbon nanosheets for efficient alkaline hydrogen evolution reaction

Efficient and low-cost transition metal single-atom catalysts (TMSACs) for hydrogen evolution reaction (HER) have been recognized as research hotspots recently with advances in delivering good catalytic activity without noble metals. However, the high-cost complex preparation of TMSACs and insufficient stability limited their practical applications. Herein, a simple top-down pyrolysis approach to obtain P-modified Co SACs loaded on the crosslinked defect-rich carbon nanosheets was introduced for alkaline hydrogen evolution, where Co atoms are locally confined before pyrolysis to prevent aggregation. Thereby, the abundant defects and the unsaturated coordination formed during the pyrolysis significantly improved the stability of the monatomic structure and reduced the reaction barrier. Furthermore, the synergy between cobalt atoms and phosphorus atoms was established to optimize the decomposition process of water molecules, which delivers the key to promoting the slow reaction kinetics of alkaline HER. As the result, the cobalt SAC exhibited excellent catalytic activity and stability for alkaline HER, with overpotentials of 70 mV and 192 mV at current densities of -10 mA cm(-2) and -100 mA cm(-2), respectively.

Automated summary

Efficient and low-cost transition metal single-atom catalysts (TMSACs) have gained significant attention for hydrogen evolution reaction (HER) due to their good catalytic activity without noble metals. However, the complex preparation process and insufficient stability have limited their practical applications. In this study, a simple top-down pyrolysis approach was introduced to obtain P-modified Co SACs loaded on the crosslinked defect-rich carbon nanosheets, which exhibited excellent catalytic activity and stability for alkaline HER.