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Non-Noble-Metal-Based Electrocatalysts for Acidic Oxygen Evolution Reaction: Recent Progress, Challenges, and
Tingting Liu1, Chen Chen1, Zonghua Pu1,2
1Fujian Key Laboratory of Polymer Materials, Fujian Provincial Key Laboratory of Advanced Materials Oriented Chemical Engineering, College of Chemistry and Materials Science, Fujian Normal University, Fuzhou, 350007, P. R. China.
Developing cost-effective, non-noble metal catalysts is crucial for advancing proton exchange membrane water electrolysis (PEMWE). This review explores acidic oxygen evolution reaction (OER) mechanisms and highlights promising metal-free catalysts for efficient hydrogen production.
Area of Science:
- Electrochemistry
- Materials Science
- Renewable Energy
Background:
- The oxygen evolution reaction (OER) is vital for renewable energy technologies like water electrolysis.
- Proton exchange membrane (PEM) water electrolysis offers high efficiency but is hindered by expensive Ir/Ru catalysts.
- Developing affordable, high-performance OER catalysts is essential for widespread PEM water splitting adoption.
Purpose of the Study:
- To review the mechanisms of acidic OER, including AEM, LOM, and OPM.
- To systematically summarize recent advancements in noble-metal-free OER catalysts.
- To discuss challenges and future directions for precious-metal-free acidic OER.
Main Methods:
- Comprehensive analysis of acidic OER mechanisms.
- Systematic review of noble-metal-free catalyst research.
- Compilation of in situ/operando characterization techniques.
Main Results:
- Detailed examination of adsorbate evolution mechanism (AEM), lattice oxygen mechanism (LOM), and oxide path mechanism (OPM).
- Summary of transition metal-based, carbon-based, and other non-noble metal catalysts for OER.
- Overview of characterization techniques for mechanistic studies.
Conclusions:
- Non-noble metal catalysts are critical for cost-effective PEM water electrolysis.
- Further research into acidic OER mechanisms and catalyst development is needed.
- In situ/operando techniques are key to understanding and advancing OER catalysis.
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