Affiliation:
1. State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing 100029 P. R. China
2. Institute of High Energy Physics The Chinese Academy of Sciences Beijing 100049 P. R. China
Abstract
AbstractElectrocatalytic reduction of CO2 to high‐value‐added chemicals provides a feasible path for global carbon balance. Herein, the fabrication of NiNPx@NiSAy‐NG (x,y = 1, 2, 3; NG = nitrogen‐doped graphite) is reported, in which Ni single atom sites (NiSA) and Ni nanoparticles (NiNP) coexist. These NiNPx@NiSAy‐NG presented a volcano‐like trend for maximum CO Faradaic efficiency (FECO) with the highest point at NiNP2@NiSA2‐NG in CO2RR. NiNP2@NiSA2‐NG exhibited ≈98% of maximum FECO and a large current density of −264 mA cm−2 at −0.98 V (vs. RHE) in the flow cell. In situ experiment and density functional theory (DFT) calculations confirmed that the proper content of NiSA and NiNP balanced kinetic between proton‐feeding and CO2 hydrogenation. The NiNP in NiNP2@NiSA2‐NG promoted the formation of H* and reduced the energy barrier of *CO2 hydrogenation to *COOH, and CO desorption can be efficiently facilitated by NiSA sites, thereby resulting in enhanced CO2RR performance.
Funder
Fundamental Research Funds for the Central Universities
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
11 articles.
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