4.7 Article

Cu doping in CeO2 to form multiple oxygen vacancies for dramatically enhanced ambient N2 reduction performance

Journal

CHEMICAL COMMUNICATIONS
Volume 55, Issue 20, Pages 2952-2955

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc00123a

Keywords

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Funding

  1. Natural Science Foundation of China [51672277, 51432009]
  2. CAS Pioneer Hundred Talents Program
  3. CAS/SAFEA International Partnership Program for Creative Research Teams of Chinese Academy of Sciences, China

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Here, we report the synthesis of Cu-doped CeO2 nanorods (denoted as Cu-CeO2-x, x represents the mass content (wt%) of the doped Cu) by a facile hydrothermal method, followed by thermal treatment in an H-2/Ar atmosphere. As the electrocatalyst, Cu-CeO2-3.9 with a large surface area of 95.2 m(2) g(-1) and mesoporous structure exhibits high electrocatalytic activity toward the N-2 reduction reaction (NRR), delivering an NH3 yield rate of 5.3 x 10(-10) mol s(-1) cm(-2) and a faradaic efficiency of 19.1% at -0.45 V (vs. RHE) in a 0.1 M Na2SO4 electrolyte (pH = 6.3), much higher than the NRR performance achieved with pure CeO2 nanorods. The Cu doping can effectively tune the concentration of multiple oxygen vacancies in CeO2, thus resulting in significantly improved NRR activity.

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