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Published on: February 11, 2016
IrPd Nanoalloy-Structured Bifunctional Electrocatalyst for Efficient and pH-Universal Water Splitting.
Xing Yang1, Zihe Wu1, Zhenyu Xing1
1College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, 610065, P. R. China.
This study presents an efficient IrPd electrocatalyst for water splitting, enabling green hydrogen production. The catalyst demonstrates high performance in both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) across various pH levels.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Efficient electrocatalysts are crucial for large-scale green hydrogen production via water splitting.
- Current bifunctional electrocatalysts often lack high efficiency and pH universality for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER).
Purpose of the Study:
- To develop a highly efficient and pH-universal bifunctional electrocatalyst for water splitting.
- To investigate the performance of an iridium-palladium (IrPd) electrocatalyst supported on ketjenblack for both HER and OER.
Main Methods:
- Synthesis of an IrPd electrocatalyst supported on ketjenblack.
- Electrochemical characterization of the catalyst for HER and OER performance.
- Testing the catalyst in an anion exchange membrane electrolyzer for water decomposition.
Main Results:
- The optimized IrPd catalyst shows specific activities of 4.46 A mgIr-1 for HER and 3.98 A mgIr-1 for OER at 100 mV and 370 mV overpotential, respectively, in alkaline conditions.
- The Ir44Pd56/KB catalyst demonstrated stability exceeding 20 hours at 250 mA cm-2 in an anion exchange membrane electrolyzer.
- The catalyst exhibits outstanding bifunctional performance across a wide range of pH conditions.
Conclusions:
- The developed IrPd electrocatalyst offers a promising solution for efficient and stable water splitting.
- This work provides insights into designing advanced bifunctional electrocatalysts by tuning metal site microenvironments and electronic structures.
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