4.8 Article

One Pot-Synthesized Ag/Ag-Doped CeO2 Nanocomposite with Rich and Stable 3D Interfaces and Ce3+ for Efficient Carbon Dioxide Electroreduction

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 50, 页码 59993-60001

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c19529

关键词

electrochemical CO2 reduction; interfaces; composite catalysts; numerical simulations; local pH effect; faradaic efficiency

资金

  1. Jiangsu Nature Science Foundation for Distinguished Young Scholars [BK20170043]
  2. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  3. National Natural Science Foundation of China [21878158, 21576135]

向作者/读者索取更多资源

A novel silver and silver-doped ceria (Ag/CeO2) nanocomposite catalyst synthesized by a facile one-pot coprecipitation method shows high efficiency and activity in converting CO2 into CO due to its rich 3D interface and high Ce3+ concentration. The strong interfacial interaction between Ag and CeO2 enables improved durability during electrolysis, with accelerated CO formation rate being the main factor contributing to the superior ECR performance of Ag/CeO2.
Electrochemical CO2 reduction (ECR) technology is promising to produce value-added chemicals and alleviate the climate deterioration. Interface engineering is demonstrated to improve the ECR performance for metal and oxide composite catalysts. However, the approach to form a substantial interface is still limited. In this work, we report a facile one-pot coprecipitation method to synthetize novel silver and silver-doped ceria (Ag/CeO2) nanocomposites. This catalyst provides a rich 3D interface and high Ce3+ concentration (33.6%), both of which are beneficial for ECR to CO. As a result, Ag/CeO2 exhibits a 99% faradaic efficiency and 10.5 A g(-1) mass activity to convert CO2 into CO at an overpotential of 0.83 V. The strong interfacial interaction between Ag and CeO2 may enable the presence of surface Ce3+ and guarantee the improved durability during the electrolysis. We also develop numerical simulation to understand the local pH effect on the ECR performance and propose that the superior ECR performance of Ag/CeO2 is mainly due to the accelerated CO formation rate rather than the suppressed hydrogen evolution reaction.

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