Anion-rich Ir-doped CoOx for boosting oxygen evolution reaction in water electrolysis

Wan Rong, Kang Huang*, Longlong Dong, Yongqing Fu, Jiuyang Xia, Rui Dang, Yunfei Chen, Jianfei Liu, Qigao Cao, Bowei Zhang*, Junsheng Wu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

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.
Original languageEnglish
JournalAdvanced Energy Materials
DOIs
Publication statusAccepted/In press - 23 Apr 2025

Keywords

  • oxygen evolution reaction
  • co-based compounds
  • Ir atoms
  • crystalline/amorphous structures
  • High-valence Co4+

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