High-Performance Electrochemical CO2 Reduction Cells Based on Non-noble Metal Catalysts AITranslate
Abstract AITranslate
The promise and challenge of electrochemical mitigation of CO2 calls for innovations on both catalyst and reactor levels. In this work, enabled by our high-performance and earth-abundant CO2 electroreduction catalyst materials, we developed alkaline microflow electrolytic cells for energy-efficient, selective, fast, and durable CO2 conversion to CO and HCOO–. With a cobalt phthalocyanine-based cathode catalyst, the CO-selective cell starts to operate at a 0.26 V overpotential and reaches a Faradaic efficiency of 94% and a partial current density of 31 mA/cm2 at a 0.56 V overpotential. With a SnO2-based cathode catalyst, the HCOO–-selective cell starts to operate at a 0.76 V overpotential and reaches a Faradaic efficiency of 82% and a partial current density of 113 mA/cm2 at a 1.36 V overpotential. In contrast to previous studies, we found that the overpotential reduction from using the alkaline electrolyte is mostly contributed by a pH gradient near the cathode surface.
KeyWords AITranslate
Basic Information:
DOI:https://doi.org/10.1021/acsenergylett.8b01681
Chinese Library Classification Number:
Citation Information:
The promise and challenge of electrochemical mitigation of CO2 calls for innovations on both catalyst and reactor levels. In this work, enabled by our high-performance and earth-abundant CO2 electroreduction catalyst materials, we developed alkaline microflow electrolytic cells for energy-efficient, selective, fast, and durable CO2 conversion to CO and HCOO–. With a cobalt phthalocyanine-based cathode catalyst, the CO-selective cell starts to operate at a 0.26 V overpotential and reaches a Faradaic efficiency of 94% and a partial current density of 31 mA/cm2 at a 0.56 V overpotential. With a SnO2-based cathode catalyst, the HCOO–-selective cell starts to operate at a 0.76 V overpotential and reaches a Faradaic efficiency of 82% and a partial current density of 113 mA/cm2 at a 1.36 V overpotential. In contrast to previous studies, we found that the overpotential reduction from using the alkaline electrolyte is mostly contributed by a pH gradient near the cathode surface.
quote
| GB/T 7714-2015 | [1] Xu Lu, Yueshen Wu, Xiaolei Yuan, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.8b01681. |
| MLA | [1] Xu Lu, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.8b01681. |
| APA | [1] Xu Lu, Yueshen Wu, Xiaolei Yuan, Ling Huang, Zishan Wu, Jin Xuan, Yifei Wang, & Hailiang Wang. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.8b01681 |
| IEEE | [1] Xu Lu, Yueshen Wu, Xiaolei Yuan, Ling Huang, Zishan Wu, Jin Xuan, Yifei Wang, and Hailiang Wang, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.8b01681. |
