Increasing CO Binding Energy and Defects by Preserving Cu Oxidation State via O2‑Plasma-Assisted N Doping on CuO Enables High C2+ Selectivity and Long-Term Stability in Electrochemical CO2 Reduction

• Published in: ACS catalysis Vol. 13; no. 13; pp. 9222 - 9233
• Main Authors: Park, Dong Gyu, Choi, Jae Won, Chun, Hoje, Jang, Hae Sung, Lee, Heebin, Choi, Won Ho, Moon, Byeong Cheul, Kim, Keon-Han, Kim, Min Gyu, Choi, Kyung Min, Han, Byungchan, Kang, Jeung Ku
• Format: Journal Article
• Language: English
• Published: American Chemical Society 07.07.2023
• Subjects: in situ X-ray absorption spectroscopy; electrochemical CO2 reduction to C2+ product; O2-plasma-assisted N doping; increasing CO binding energy and defect sites; preserving Cu oxidation state
• ISSN: 2155-5435; 2155-5435
• DOI: 10.1021/acscatal.3c01441

Cu is considered as the most promising catalyst for the electrochemical carbon dioxide reduction reaction (CO2RR) to produce C2+ hydrocarbons, but achieving high C2+ product selectivity and efficiency with long-term stability remains one of great challenges. Herein, we report a strategy to realize the CO2RR catalyst allowing high C2+ product selectivity and stable catalytic properties by utilizing the benefits of oxygen-plasma-assisted nitrogen doping on CuO. It is exhibited that the defects such as oxygen vacancies and grain boundaries suitable for CO2RR are generated by N2 plasma radicals on CuO. Also, the oxidation state of Cu is maintained without Cu reduction by O2 plasma. Indeed, ON–CuO synthesized through oxygen-plasma-assisted nitrogen doping is demonstrated to enable a high C2+ product selectivity of 77% (including a high C2H4 selectivity of 56%) with a high current density of −34.6 mA/cm2 at −1.1 V vs RHE, as well as a long-term stability for 22 h without performance degradation. High CO2RR performances are ascribed to the increased CO binding energy and catalytic sites in N-doped CuO. Furthermore, an in situ X-ray absorption near-edge structure analysis reveals that the defects in ON–CuO are favorable for C–C coupling leading to C2+ products.