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Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
Published on: August 23, 2018
TiO-supported RuIr alloy as an efficient and CO-resistant catalyst for hydrogen oxidation
Lingfei Li1, Haishan Liu1, Chenhui Xu1
1Institute for New Energy Materials & Engineering, School of Materials Science & Engineering, Fuzhou University, Fuzhou City, Fujian Province 350108, PR China; Fujian Engineering Research Center of High Energy Batteries and New Energy Equipment & Systems, Fuzhou University, Fuzhou City, Fujian Province 350108, PR China.
Ruthenium-Iridium alloy catalysts on titanium oxide show enhanced alkaline hydrogen oxidation reaction (HOR) activity and CO tolerance. This RuIr/TiO catalyst offers a promising alternative to platinum for fuel cell applications.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Ruthenium (Ru) is a promising catalyst for hydrogen oxidation reaction (HOR) due to its favorable hydrogen binding energy and oxygen affinity.
- Challenges for Ru catalysts include limited intrinsic activity and poor tolerance to carbon monoxide (CO) poisoning.
- Developing efficient and durable HOR catalysts is crucial for advancing fuel cell technology.
Purpose of the Study:
- To design and synthesize an efficient and durable catalyst for alkaline HOR using a RuIr alloy supported on titanium oxide (RuIr/TiO).
- To investigate the catalytic performance and CO tolerance of the RuIr/TiO catalyst compared to commercial platinum catalysts.
- To elucidate the underlying mechanisms responsible for the enhanced catalytic activity and durability.
Main Methods:
- Synthesis of RuIr alloy nanoparticles supported on titanium oxide (TiO).
- Electrochemical characterization including cyclic voltammetry and chronoamperometry to evaluate HOR activity and durability.
- Experimental characterizations (e.g., X-ray diffraction, X-ray photoelectron spectroscopy) and density functional theory (DFT) calculations to analyze catalyst structure and electronic properties.
Main Results:
- The RuIr/TiO catalyst exhibited a mass activity of 10.36 A mg-1PGM at 50 mV overpotential, significantly outperforming commercial Pt/C (4.84 times higher).
- RuIr/TiO demonstrated excellent CO tolerance, with only a 6.85% drop in current density after prolonged electrolysis under 1000 ppm CO/H2, compared to 27.84% for Pt/C.
- DFT calculations and characterizations revealed that alloying and strong metal-support interactions modulate the electronic structure of Ru sites, optimizing H adsorption and OH binding, and promoting CO oxidation.
Conclusions:
- The RuIr/TiO alloy catalyst is highly efficient and durable for alkaline HOR.
- Alloying Ru with Ir and strong metal-support interaction with TiO are key strategies to enhance catalytic activity and CO tolerance.
- This work provides a promising pathway for developing advanced electrocatalysts for fuel cells and other electrochemical energy conversion systems.
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