Electrocatalytic Stability Over Ruthenium‐Based Catalysts for Proton Exchange Membrane Water Electrolysis

Abstract Achieving large‐scale, low‐cost hydrogen production through proton exchange membrane water electrolysis (PEMWE) is a key strategic direction in the energy revolution. However, the high potential of oxygen evolution reaction (OER) and the acidic environment seriously limit the hydrogen production efficiency. RuO 2 ‐based catalysts have garnered significant attention due to their unique electronic structure and exceptional activity in the OER. Nevertheless, their durability remains insufficient for long‐term PEMWE and hydrogen generation. This paper explores the fundamental causes of catalyst degradation and strategies to enhance the catalyst stability under different reaction pathways. Additionally, the importance of PEMWE components, including bipolar plates and membrane electrode assemblies, in improving system stability and efficiency is emphasized, highlighting their role in large‐scale applications of PEMWE. Looking forward, research efforts should prioritize the optimization of both catalysts and system components to achieve a balance between the performance, cost, and long‐term durability. By addressing these factors, we can unlock the full potential of PEMWE technology and make hydrogen a viable, large‐scale solution for clean energy production.

Authors

Institutions

Publication Details

Journal
ChemCatChem
Published
2024-12-06
DOI
https://doi.org/10.1002/cctc.202401707
Citations
2
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.20
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Electrocatalytic Stability Over Ruthenium‐Based Catalysts for Proton Exchange Membrane Water Electrolysis

Yu Zhang, Hehe Wei, Wenwen Huang
2 citations
ChemCatChem
Electrocatalysts for Energy Conversion
0.20
article

Electrocatalytic Stability Over Ruthenium‐Based Catalysts for Proton Exchange Membrane Water Electrolysis

Yu Zhang, Hehe Wei, Wenwen Huang
article en
2 citations

Abstract

Abstract Achieving large‐scale, low‐cost hydrogen production through proton exchange membrane water electrolysis (PEMWE) is a key strategic direction in the energy revolution. However, the high potential of oxygen evolution reaction (OER) and the acidic environment seriously limit the hydrogen production efficiency. RuO 2 ‐based catalysts have garnered significant attention due to their unique electronic structure and exceptional activity in the OER. Nevertheless, their durability remains insufficient for long‐term PEMWE and hydrogen generation. This paper explores the fundamental causes of catalyst degradation and strategies to enhance the catalyst stability under different reaction pathways. Additionally, the importance of PEMWE components, including bipolar plates and membrane electrode assemblies, in improving system stability and efficiency is emphasized, highlighting their role in large‐scale applications of PEMWE. Looking forward, research efforts should prioritize the optimization of both catalysts and system components to achieve a balance between the performance, cost, and long‐term durability. By addressing these factors, we can unlock the full potential of PEMWE technology and make hydrogen a viable, large‐scale solution for clean energy production.

ChemCatChemVol. 17(5)
East China University of Science and Technology (CN), State Key Laboratory of New Ceramics and Fine Processing
Industry, innovation and infrastructure
Openalex Percentile: Top 56%
Electrocatalysts for Energy Conversion
0.20
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.