TY - JOUR
T1 - Pretreatment of diamond electrodes toward CO2 electroreduction at high current density
AU - Iwai, Goki
AU - Yamamoto, Takashi
AU - Einaga, Yasuaki
N1 - Publisher Copyright:
© 2026 Elsevier Ltd.
PY - 2026/8/1
Y1 - 2026/8/1
N2 - Boron-doped diamond (BDD) electrodes are promising candidates for long-term and scalable CO2 electroreduction, a key technology to realize a sustainable society. BDD electrodes have been shown to maintain a high Faradaic efficiency in CO2 electroreduction for over 1,000 h of continuous operation. Furthermore, a preliminary CO2 electroreduction step at low current density performed prior to main electrolysis (hereafter referred to as pre-electrolysis treatment) has been proposed as an effective surface treatment unique to BDD electrodes. However, it remains unclear whether this pre-electrolysis treatment is still effective for CO2 electroreduction at high current density. In this work, we optimized a pre-electrolysis treatment protocol for BDD electrodes to achieve an efficient CO2 electroreduction even at high current density. X-ray photoelectron spectroscopy studies revealed that the proportion of C–O/C=O and COOH bonding states at the BDD surface were increased after the pre-electrolysis treatment. Consequently, linear sweep voltammetry studies in a CO2-saturated electrolyte solution showed that the BDD electrode after the pre-electrolysis treatment exhibited a significant increase in current compared to the BDD electrode without the pre-electrolysis treatment. We propose that interactions between CO2 molecules in the electrolyte solution and the oxygen-containing functional groups introduced at the BDD surface by the pre‑electrolysis treatment enhances the local CO2 concentration, thereby promoting the CO2 electroreduction. With the optimized pre-electrolysis treatment protocol, the Faradaic efficiency for formic acid production was enhanced from 19% to 71%, representing a 3.7-fold increase.
AB - Boron-doped diamond (BDD) electrodes are promising candidates for long-term and scalable CO2 electroreduction, a key technology to realize a sustainable society. BDD electrodes have been shown to maintain a high Faradaic efficiency in CO2 electroreduction for over 1,000 h of continuous operation. Furthermore, a preliminary CO2 electroreduction step at low current density performed prior to main electrolysis (hereafter referred to as pre-electrolysis treatment) has been proposed as an effective surface treatment unique to BDD electrodes. However, it remains unclear whether this pre-electrolysis treatment is still effective for CO2 electroreduction at high current density. In this work, we optimized a pre-electrolysis treatment protocol for BDD electrodes to achieve an efficient CO2 electroreduction even at high current density. X-ray photoelectron spectroscopy studies revealed that the proportion of C–O/C=O and COOH bonding states at the BDD surface were increased after the pre-electrolysis treatment. Consequently, linear sweep voltammetry studies in a CO2-saturated electrolyte solution showed that the BDD electrode after the pre-electrolysis treatment exhibited a significant increase in current compared to the BDD electrode without the pre-electrolysis treatment. We propose that interactions between CO2 molecules in the electrolyte solution and the oxygen-containing functional groups introduced at the BDD surface by the pre‑electrolysis treatment enhances the local CO2 concentration, thereby promoting the CO2 electroreduction. With the optimized pre-electrolysis treatment protocol, the Faradaic efficiency for formic acid production was enhanced from 19% to 71%, representing a 3.7-fold increase.
KW - CO electroreduction
KW - Diamond electrode
KW - Formic acid
KW - High current density operation
KW - Surface pretreatment
UR - https://www.scopus.com/pages/publications/105035159120
UR - https://www.scopus.com/pages/publications/105035159120#tab=citedBy
U2 - 10.1016/j.electacta.2026.148807
DO - 10.1016/j.electacta.2026.148807
M3 - Article
AN - SCOPUS:105035159120
SN - 0013-4686
VL - 566
JO - Electrochimica Acta
JF - Electrochimica Acta
M1 - 148807
ER -