4.8 Article

Efficient and stable noble-metal-free catalyst for acidic water oxidation

Journal

NATURE COMMUNICATIONS
Volume 13, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-022-30064-6

Keywords

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Funding

  1. International Cooperation Project of the Ministry of Science and Technology [2014DFE60170]
  2. National Natural Science Foundation of China [61674084]
  3. Overseas Expertise Introduction Project for Discipline Innovation of Higher Education of China [B16027]
  4. Tianjin Science and Technology Project [18ZXJMTG00220]
  5. Haihe Laboratory of Sustainable Chemical Transformations
  6. Fundamental Research Funds for the Central Universities, Nankai University [63211108]
  7. Natural Science Basic Research Program of Shaanxi [2020JQ-136]
  8. Fundamental Research Funds for the Central Universities [G2020KY0519]
  9. European Union [838686]
  10. NSFC [21875042]
  11. STCSM [21DZ1207102, 21DZ1207103]
  12. Marie Curie Actions (MSCA) [838686] Funding Source: Marie Curie Actions (MSCA)

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This study reports a cost-effective and stable manganese oxybromide catalyst with excellent oxygen evolution reaction (OER) activity in acidic electrolytes. The catalyst exhibits low overpotential and good stability, making it suitable for hydrogen production from water, and provides crucial insights for the design of non-noble metal electrocatalysts.
Developing non-noble catalysts with superior activity and durability for oxygen evolution reaction (OER) in acidic media is paramount for hydrogen production from water. Still, challenges remain due to the inadequate activity and stability of the OER catalyst. Here, we report a cost-effective and stable manganese oxybromide (Mn7.5O10Br3) catalyst exhibiting an excellent OER activity in acidic electrolytes, with an overpotential of as low as 295 +/- 5 mV at a current density of 10 mA cm(-2). Mn7.5O10Br3 maintains good stability under operating conditions for at least 500 h. In situ Raman spectroscopy, X ray absorption near edge spectroscopy, and density functional theory calculations confirm that a self-oxidized surface with enhanced electronic transmission capacity forms on Mn7.5O10Br3 and is responsible for both the high catalytic activity and long-term stability during catalysis. The development of Mn7.5O10Br3 as an OER catalyst provides crucial insights into the design of non-noble metal electrocatalysts for water oxidation. While acidic water splitting offers a renewable means to obtain renewable hydrogen fuel, the catalysts needed to oxidize water often require expensive noble metals. Here, authors show manganese oxyhalides as acidic oxygen evolution electrocatalysts.

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