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Hierarchical Cross‐Linked Carbon Aerogels with Transition Metal‐Nitrogen Sites for Highly Efficient Industrial‐Level CO2 Electroreduction

Developing highly efficient carbon aerogels (CA) electrocatalysts based on transition metal‐nitrogen sites is critical for the CO2 electroreduction reaction (CO2RR). However, simultaneously achieving a high current density and high Faradaic efficiency (FE) still remains a big challenge. Herein, a se...

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Bibliographic Details
Published in:Advanced functional materials 2021-11, Vol.31 (45), p.n/a
Main Authors: Zhang, Yikai, Wang, Xinyue, Zheng, Sixing, Yang, Bin, Li, Zhongjian, Lu, Jianguo, Zhang, Qinghua, Adli, Nadia Mohd, Lei, Lecheng, Wu, Gang, Hou, Yang
Format: Article
Language:English
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Summary:Developing highly efficient carbon aerogels (CA) electrocatalysts based on transition metal‐nitrogen sites is critical for the CO2 electroreduction reaction (CO2RR). However, simultaneously achieving a high current density and high Faradaic efficiency (FE) still remains a big challenge. Herein, a series of unique 3D hierarchical cross‐linked nanostructured CA with metal‐nitrogen sites (MN, M = Ni, Fe, Co, Mn, Cu) is developed for efficient CO2RR. An optimal CA/N‐Ni aerogel, featured with unique hierarchical porous structure and highly exposed M‐N sites, exhibits an unusual CO2RR activity with a CO FE of 98% at −0.8 V. Notably, an industrial current density of 300 mA cm−2 with a high FE of 91% is achieved on CA/N‐Ni aerogel in a flow‐cell reactor, which outperforms almost all previously reported M‐N/carbon based catalysts. The CO2RR activity of different CA/N‐M aerogels can be arranged as Ni, Fe, Co, Mn, and Cu from high to low. In situ spectroelectrochemistry analyses validate that the rate‐determining step in the CO2RR is the formation of *COOH intermediate. A ZnCO2 battery is further assembled with CA/N‐Ni as the cathode, which shows a maximum power density of 0.5 mW cm−2 and a superior rechargeable stability. A series of hierarchical cross‐linked nanostructured carbon aerogels with transition metal‐nitrogen sites are developed for efficient CO2 electroreduction reaction at industrial current densities.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202104377