Takashi Yamamoto, Taiga Ozawa, Mai Tomisaki, Yasuaki Einaga
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引用次数: 0
Abstract
The electrochemical carbon dioxide reduction reaction (eCO2RR) on boron-doped diamond (BDD) electrodes predominantly yields formic acid (HCOOH) as the primary product. Redirecting the reaction pathway toward highly valuable carbon monoxide (CO) remains a significant challenge due to the chemical inertness of the BDD surface. Herein, we present an interfacial engineering strategy to tune the product selectivity from HCOOH to CO on BDD electrodes. First, functionalisation of the BDD surface with nitrogen-containing molecules such as aniline and pyrazole effectively captured CO2, successfully directing the reaction pathway toward CO, and established molecular modification as a proof of concept for redirecting selectivity. Second, utilising an aqueous KClO4 electrolyte dynamically facilitated CO production by minimising specific anion adsorption, providing a considerably more facile and practical route to the same selectivity switch. Through systematic optimisation of the eCO2RR conditions in 0.1 M KClO4, we achieved a maximum faradaic efficiency for CO production (FECO) of 72% at an applied potential of -1.9 V (vs. Ag/AgCl; -1.46 V vs. RHE), an electrolyte flow rate of 500 mL min-1, and an operating temperature of 5 °C. Electrochemical analyses revealed that increasing the flow rate enhanced the CO2 supply by significantly reducing the diffusion layer thickness. Moreover, decreasing the temperature not only increased CO2 solubility but also selectively suppressed the competing hydrogen evolution reaction (HER). Temperature-dependent linear sweep voltammetry experiments further revealed that this suppression is driven primarily by a negative shift of the HER onset potential rather than by any appreciable shift of the CO2 reduction onset. These findings provide fundamental insights into the reaction mechanisms on inert sp3-carbon surfaces and demonstrate that interfacial engineering is an effective strategy for developing selective CO2 conversion systems on BDD, although practical implementation will require further advances in electrode fabrication, operating conditions, and energy efficiency.
在掺硼金刚石(BDD)电极上进行的电化学二氧化碳还原反应(eCO2RR)主要生成甲酸(HCOOH)作为初级产物。由于BDD表面的化学惰性,将反应路径重定向到高价值的一氧化碳(CO)仍然是一个重大挑战。在此,我们提出了一种界面工程策略来调整BDD电极上从HCOOH到CO的产物选择性。首先,用苯胺和吡唑等含氮分子对BDD表面进行功能化,有效地捕获了二氧化碳,成功地将反应途径导向CO,并建立了分子修饰作为重定向选择性概念的证明。其次,通过减少特定阴离子的吸附,利用KClO4水溶液动态地促进CO的产生,为相同的选择性开关提供了一种相当简单和实用的途径。通过在0.1 M KClO4条件下对eCO2RR条件进行系统优化,我们在-1.9 V(相对于Ag/AgCl; -1.46 V相对于RHE)、电解液流速为500 mL min-1、工作温度为5°C的条件下,实现了CO生产(FECO)的最大法拉第效率为72%。电化学分析表明,增加流速可以通过显著降低扩散层厚度来增加CO2供应量。降低温度不仅可以提高CO2的溶解度,还可以选择性地抑制竞争性析氢反应(HER)。温度相关的线性扫描伏安法实验进一步揭示,这种抑制主要是由HER起始电位的负移驱动的,而不是由CO2还原起始电位的任何明显的移动驱动的。这些发现为惰性sp3-碳表面上的反应机制提供了基本的见解,并表明界面工程是在BDD上开发选择性CO2转化系统的有效策略,尽管实际实施需要在电极制造、操作条件和能源效率方面取得进一步进展。