4.8 Article

Atomic iridium species anchored on porous carbon network support: An outstanding electrocatalyst for CO2 conversion to CO

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 292, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2021.120173

Keywords

Electrocatalysis; CO2 conversion; Atomic single site; Porous carbon; Iridium

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Science and ICT [NRF-2019R1A2C2088174]
  2. Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Ministry of Trade, Industry & Energy (MOTIE) of the Republic of Korea [20172010106300]
  3. Korea Institute of Energy Technology Evaluation and Planning (KETEP) from the Ministry of Trade, Industry & Energy, Republic of Korea [20204010600100]
  4. National Research Foundation of Korea - Korean Government [NRF2017R1D1A1B04031539]
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [20204010600100, 20172010106300] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

In this study, atomically dispersed Ir species supported on 3D porous carbon networks are proposed as efficient electrocatalysts for CO2 conversion to CO production, showing high Faradaic efficiency and turnover frequency values. This outstanding catalytic performance is attributed to the structural advantages of the 3D carbon network and atomically dispersed Ir species on the carbon support, as revealed by detailed experimental studies and DFT calculations.
Converting CO2 into valuable chemicals using electrocatalysis is an attractive approach for sustainable energy storage and artificial carbon cycle. In this study, atomically dispersed Ir species (Ad-Ir) that are supported on three-dimensional (3D) porous carbon networks are proposed as electrocatalysts for highly efficient CO2 conversion. The resulting catalysts can preferentially and rapidly produce CO with a high Faradaic efficiency of 95.6 % and a very high turnover frequency (TOF) value of 33,365 h(-1). Furthermore, it shows no obvious decay in both FE for CO and current density over 20 h of continuous operation. Based on detailed experimental studies and density functional theory (DFT) calculations, such outstanding catalytic performance for CO2 conversion to CO production can be attributed to the structural advantages of 3D network of porous carbon and atomically dispersed Ir species on the 3D carbon support.

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