Du Jinglun, Fiorani Andrea, Inagaki Taichi, Otake Atsushi, Murata Michio, Hatanaka Miho, Einaga Yasuaki
Department of Chemistry, Keio University, 3-14-1 Hiyoshi, Yokohama 223-8522, Japan.
JACS Au. 2022 May 23;2(6):1375-1382. doi: 10.1021/jacsau.2c00081. eCollection 2022 Jun 27.
By means of an initial electrochemical carbon dioxide reduction reaction (eCORR), both the reaction current and Faradaic efficiency of the eCORR 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 (CO ) is the most recognized pathway leading to the formation of hydrocarbons and oxygenated products. However, the self-activation process enabled the eCORR to take place at a low potential, that is, a low energy, where CO 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 eCORR. We further evaluated this effect in long-term experiments using a CO electrolyzer for formic acid production and found that the electrical-to-chemical energy conversion efficiency reached 50.2% after the BDD self-activation process.
通过初始电化学二氧化碳还原反应(eCORR),硼掺杂金刚石(BDD)电极上eCORR的反应电流和法拉第效率均得到显著提高。在此,这种效应被称为BDD的自激活。一般来说,二氧化碳自由基阴离子(CO )的生成是导致碳氢化合物和含氧化合物形成的最公认途径。然而,自激活过程使eCORR能够在低电位下发生,即低能量下发生,此时几乎不产生CO 。在这项工作中,我们发现单齿碳酸盐和羧基在自激活过程中被确定为中间体。通过自激活过程增加这些中间体的数量可提高eCORR的性能。我们使用用于生产甲酸的CO电解槽在长期实验中进一步评估了这种效应,发现在BDD自激活过程后,电-化学能量转换效率达到了50.2%。