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Orthorhombic (Ru, Mn)2O3: A superior electrocatalyst for acidic oxygen evolution reaction

  • Yin Qin
  • , Bin Cao
  • , Xiao Ye Zhou*
  • , Zhuorui Xiao
  • , Hanxiang Zhou
  • , Zhenyi Zhao
  • , Yibo Weng
  • , Jianshuai Lv
  • , Yang Liu
  • , Yan Bing He
  • , Feiyu Kang
  • , Kaikai Li
  • , Tong Yi Zhang
  • *Corresponding author for this work
  • Harbin Institute of Technology
  • Shanghai University
  • Shenzhen MSU-BIT University
  • Tsinghua University
  • The Hong Kong University of Science and Technology (Guangzhou)

Research output: Contribution to journalArticlepeer-review

Abstract

The development of efficient oxygen evolution reaction (OER) electrocatalysts is of vital importance for acidic water decomposition. Currently, the rutile structured RuO2 is considered to be the best candidate and has been studied widely. However, the state-of-the-art rutile RuO2 still suffers from unsatisfactory activity and stability, while other crystalline structures of Ru-based oxides are seldom reported as OER electrocatalysts. The present work, for the first time, successfully synthesizes orthorhombic (Ru, Mn)2O3 electrocatalyst through cation exchange. The orthorhombic (Ru, Mn)2O3 particles exhibit the outstanding electrocatalysis performance as OER electrocatalyst, showing an ultralow overpotential of 168 mV at 10 mA cm−2 in acidic water and good stability in 40 h of OER. The outstanding electrocatalysis performance is attributed to the distinct Ru d-band structure together with the larger surface density of Ru active site, which reduces the free energy of the rate-limiting step during OER.

Original languageEnglish
Article number108727
JournalNano Energy
Volume115
DOIs
StatePublished - Oct 2023
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Keywords

  • Cation exchange
  • OER electrocatalyst
  • Orthorhombic (Ru, Mn)O
  • Oxygen evolution reaction
  • Ultralow overpotential

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