TY - JOUR
T1 - A New Pathway for CO2Reduction Relying on the Self-Activation Mechanism of Boron-Doped Diamond Cathode
AU - Du, Jinglun
AU - Fiorani, Andrea
AU - Inagaki, Taichi
AU - Otake, Atsushi
AU - Murata, Michio
AU - Hatanaka, Miho
AU - Einaga, Yasuaki
N1 - Funding Information:
The authors thank Sumitomo Heavy Industries, Ltd. for useful discussions. A.F. acknowledges the Japan Society for the Promotion of Science (fellowship ID no. P19333) and Grant-in-Aid for JSPS Fellows (19F19333). Also, this work was partially supported by Grant-in-Aid for Scientific Research A 19H00832 and New Energy and Industrial Technology Development Organization (NEDO) P16002 (to Y.E.).
Publisher Copyright:
© 2022 The Authors. Published by American Chemical Society.
PY - 2022/6/27
Y1 - 2022/6/27
N2 - By means of an initial electrochemical carbon dioxide reduction reaction (eCO2RR), both the reaction current and Faradaic efficiency of the eCO2RR on boron-doped diamond (BDD) electrodes were significantly improved. Here, this effect is referred to as the self-activation of BDD. Generally, the generation of carbon dioxide radical anions (CO2•-) is the most recognized pathway leading to the formation of hydrocarbons and oxygenated products. However, the self-activation process enabled the eCO2RR to take place at a low potential, that is, a low energy, where CO2•- is hardly produced. In this work, we found that unidentate carbonate and carboxylic groups were identified as intermediates during self-activation. Increasing the amount of these intermediates via the self-activation process enhances the performance of eCO2RR. We further evaluated this effect in long-term experiments using a CO2 electrolyzer for formic acid production and found that the electrical-to-chemical energy conversion efficiency reached 50.2% after the BDD self-activation process.
AB - By means of an initial electrochemical carbon dioxide reduction reaction (eCO2RR), both the reaction current and Faradaic efficiency of the eCO2RR on boron-doped diamond (BDD) electrodes were significantly improved. Here, this effect is referred to as the self-activation of BDD. Generally, the generation of carbon dioxide radical anions (CO2•-) is the most recognized pathway leading to the formation of hydrocarbons and oxygenated products. However, the self-activation process enabled the eCO2RR to take place at a low potential, that is, a low energy, where CO2•- is hardly produced. In this work, we found that unidentate carbonate and carboxylic groups were identified as intermediates during self-activation. Increasing the amount of these intermediates via the self-activation process enhances the performance of eCO2RR. We further evaluated this effect in long-term experiments using a CO2 electrolyzer for formic acid production and found that the electrical-to-chemical energy conversion efficiency reached 50.2% after the BDD self-activation process.
KW - COreduction
KW - boron-doped diamond
KW - energy conversion efficiency
KW - intermediates
KW - self-activation
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U2 - 10.1021/jacsau.2c00081
DO - 10.1021/jacsau.2c00081
M3 - Article
AN - SCOPUS:85141019418
VL - 2
SP - 1375
EP - 1382
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 6
ER -