The electrochemical reduction reaction of carbon dioxide (CO2RR) is an effective way towards carbon neutralization. Single-atom catalysts (SACs) are expected to be efficient for CO2RR due to maximum atom utilization and excellent catalytic performance. Here, nitrogen-doped carbon supported Ni SACs (Ni-SAC@NCs) were prepared through effective fast pyrolysis. CO2 can convert into CO efficiently with Ni-SAC@NCs as electrocatalysts for CO2RR. The faradaic efficiency kept well above 80% in the applied potential window of -0.6 to -0.9 V (vs. reversible hydrogen electrode (RHE)), with a highest FECO of 95% at -0.6 V (vs. RHE). Ni-SAC@NCs can achieve the best CO selectivity under a small overpotential, surpassing most other state-of-the-art catalysts. Computations also indicate that the unique defect-Ni-N-3 structure is the active site. This work not only provides a simple and promising new route for the preparation of SACs, but also proves the key role of the coordination environment in electrocatalysis.
NSTL
Elsevier