Tonglin Yang , Fangqi Yang , Fangqiang Yang , Yang Ding , Fa Cao , Quan Zhang
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引用次数: 0
摘要
电化学将二氧化碳还原为有价值的燃料或原料,在零排放碳回收和可再生能源储存方面具有很大的前景。然而,制备用于电还原CO2的高性能稀土单原子催化剂(SACs)仍然是一个巨大的挑战。在这项工作中,我们报道了用g-C3N4作为载体(Nd1/NC),方便地合成了具有原子分散的Nd- n6活性位点的Nd SACs,以有效地电还原CO2为CO。Nd1/NC的最大FE为83 %,CO分电流密度为7.0 mA cm−2,在h -电池中,在−0.8 V下稳定性为50 h。值得注意的是,在流动电池中获得了50.6 mA cm−2的CO分电流密度,FECO高达93 %。DFT计算表明,Nd- n6位点促进了电子从g-C3N4向Nd的转移,增强了对*COOH中间体的吸附,从而提高了催化活性。
Rare-earth neodymium single atom catalyst for efficient electrochemical CO2 reduction
Electrochemical reduction of carbon dioxide (CO2) to valuable fuels or feedstocks holds great promise for zero-emission carbon recycling and renewable energy storage. However, it remains a great challenge to prepare high-performance rare earth single-atom catalysts (SACs) for electroreduction of CO2. In this work, we reported the facile synthesis of Nd SACs with atomically dispersed Nd-N6 active sites by using g-C3N4 as support (Nd1/NC) for efficient electroreduction of CO2 to CO. Nd1/NC exhibited a maximum FE of 83 % and a CO partial current density of 7.0 mA cm−2, and a stability of 50 h at −0.8 V in an H-cell. Notably, a dramatically improved CO partial current density of 50.6 mA cm−2 with FECO of up to 93 % was obtained in the flow cell. DFT calculations revealed that the Nd-N6 sites facilitate the transfer of electrons from g-C3N4 to Nd, which strengthens the adsorption of the *COOH intermediate, contributing to the enhanced catalytic activity.
期刊介绍:
Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues.
Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.