TY - JOUR
T1 - Anion-rich Ir-doped CoOx for boosting oxygen evolution reaction in water electrolysis
AU - Rong, Wan
AU - Huang, Kang
AU - Dong, Longlong
AU - Fu, Yongqing
AU - Xia, Jiuyang
AU - Dang, Rui
AU - Chen, Yunfei
AU - Liu, Jianfei
AU - Cao, Qigao
AU - Zhang, Bowei
AU - Wu, Junsheng
PY - 2025/4/23
Y1 - 2025/4/23
N2 - Owing to the sluggish kinetics of oxygen evolution reaction (OER) in electrochemical water electrolysis process, efficient and durable OER electrocatalysts are crucially needed. However, it is a great challenge to improve the comprehensive performance of OER electrocatalysts by utilizing various synergistic methodologies. To solve these issues, herein, Ir-doped Co-based compounds with regulated anions were synthesized using a coprecipitation method as the electrodes for boosting the OERs. Doping with Ir atoms modified the coordination environments and electronic structures of the CoOx-CO3 2- lattice, and the generated Co3+ species promoted the generation of active species for the OER. It is worthwhile noting that a hybrid crystalline/amorphous IrCoOx-CO3 2- compound was obtained with an Ir content of 10.09 wt.% and a large amount of Co3+, and demonstrated excellent electrocatalytic OER performance. The overpotential required for the developed IrCoOx-CO3 2- to achieve 10 mA cm-2 was as low as 207 mV with a very low Tafel slope of 61.7 mV dec-1, which is better than the commercial IrO2. Furthermore, anions created in the IrCoOx significantly promoted the OER, and their effects were decreased in the order of CO3 2- > PO4 3- > OH-. This work clarifies the synergistic mechanism of cations and anions on the electrocatalytic OER performance of Co-based compounds, providing new insights for designs of high-performance OER electrocatalysts for water electrolysis.
AB - Owing to the sluggish kinetics of oxygen evolution reaction (OER) in electrochemical water electrolysis process, efficient and durable OER electrocatalysts are crucially needed. However, it is a great challenge to improve the comprehensive performance of OER electrocatalysts by utilizing various synergistic methodologies. To solve these issues, herein, Ir-doped Co-based compounds with regulated anions were synthesized using a coprecipitation method as the electrodes for boosting the OERs. Doping with Ir atoms modified the coordination environments and electronic structures of the CoOx-CO3 2- lattice, and the generated Co3+ species promoted the generation of active species for the OER. It is worthwhile noting that a hybrid crystalline/amorphous IrCoOx-CO3 2- compound was obtained with an Ir content of 10.09 wt.% and a large amount of Co3+, and demonstrated excellent electrocatalytic OER performance. The overpotential required for the developed IrCoOx-CO3 2- to achieve 10 mA cm-2 was as low as 207 mV with a very low Tafel slope of 61.7 mV dec-1, which is better than the commercial IrO2. Furthermore, anions created in the IrCoOx significantly promoted the OER, and their effects were decreased in the order of CO3 2- > PO4 3- > OH-. This work clarifies the synergistic mechanism of cations and anions on the electrocatalytic OER performance of Co-based compounds, providing new insights for designs of high-performance OER electrocatalysts for water electrolysis.
KW - oxygen evolution reaction
KW - co-based compounds
KW - Ir atoms
KW - crystalline/amorphous structures
KW - High-valence Co4+
U2 - 10.20517/energymater.2025.21
DO - 10.20517/energymater.2025.21
M3 - Article
SN - 1614-6832
JO - Advanced Energy Materials
JF - Advanced Energy Materials
ER -