Affiliation:
1. Materials and Production Engineering The Sirindhorn International Thai-German Graduate School of Engineering King Mongkut's University of Technology North Bangkok Bangkok 10800 Thailand
2. Department of Physics and Astrophysics Central University of Haryana Mahendergarh Haryana 123031 India
3. Department of Optical Science Tokushima University Tokushima 770-8501 Japan
4. Department of Physics University of Allahabad Uttar Pradesh Prayagraj 211002 India
Abstract
AbstractCarbon monoxide (CO) oxidation is crucial in fuel cell anodes. Recent research has focused on electrocatalysts that synergistically enhance CO oxidation alongside alcohol/hydrogen oxidation. High sensitivity and selectivity for CO oxidation at lower onset potentials are the key objectives. Molybdenum (Mo) has emerged as a promising non‐noble transition metal co‐catalyst for CO oxidation. Mo versatility arises from its ability to alloy with Pt and mix with other non‐noble transition metals in various forms (MoOx, MoS2, MoC). Carbon‐supported Mo nanoparticles have shown potential in reducing Pt loading and improving CO tolerance due to Mo oxyphilic properties, effectively oxidizing weakly adsorbed CO and lowering onset and peak potentials. However, challenges persist, such as a limited potential window for CO oxidation and decreased CO adsorption affinity at higher potentials. Addressing these issues requires understanding factors affecting Mo‐based electrocatalysts (Mo‐ECs) activity, including PtMo alloy composition, Mo′s chemical state, cell temperature, and the role of carbon support. This article provides a comprehensive review of Mo‐ECs role in CO electrooxidation in direct alcohol fuel cells (DAFCs) over the past two decades.
Funder
King Mongkut's University of Technology North Bangkok
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis