The electrochemical reduction of CO 2 to produce carbon-based fuels and chemicals possesses huge potentials to alleviate current environmental problems. However, it is confronted by great challenges in the design of active electrocatalysts with low overpotentials and high product selectivity. Here we report the atomic tuning of a single-Fe-atom catalyst with phosphorus (Fe-N/P-C) on commercial carbon black as a robust electrocatalyst for CO 2 reduction. The Fe-N/P-C catalyst exhibits impressive performance in the electrochemical reduction of CO 2 to CO, with a high Faradaic efficiency of 98% and a high mass-normalized turnover frequency of 508.8 h -1 at a low overpotential of 0.34 V. On the basis of ex-situ X-ray absorption spectroscopy measurements and DFT calculations, we reveal that the tuning of P in single-Fe-atom catalysts reduces the oxidation state of the Fe center and decreases the free-energy barrier of *CO intermediate formation, consequently maintaining the electrocatalytic activity and stability of single-Fe-atom catalysts.
Keyphrases
- metal organic framework
- molecular dynamics
- visible light
- highly efficient
- ionic liquid
- gold nanoparticles
- electron transfer
- high resolution
- aqueous solution
- density functional theory
- molecularly imprinted
- mental health
- nitric oxide
- magnetic resonance
- label free
- gene expression
- transition metal
- reduced graphene oxide
- risk assessment
- computed tomography
- heavy metals
- molecular docking
- human health
- mass spectrometry
- single cell
- dna methylation
- postmenopausal women
- dual energy