image: Schematic of Pt/TiO2-Ov design and characterization. (a) Diagram of preparation process of Pt/TiO2-Ov; (b) XRD spectra of Pt/TiO2-Ov and TiO2-Ov; (c) SEM image and (d) N2 adsorption/ desorption isotherm of TiO2 etched in 0.5% HF; (e, f) TEM of Pt/TiO2-Ov; (g) HR-TEM images of Pt/TiO2-Ov; (h) HAADF-STEM image of Pt/TiO2-Ov; (i–m) elemental mapping images of Ti, Pt, O, Si of Pt/TiO2-Ov.
Credit: HIGHER EDUCATION PRESS
Hydrogen fuel cells, especially proton exchange membrane fuel cells (PEMFCs), are gaining traction as zero-emission power sources for electric vehicles. However, PEMFCs face challenges like the corrosion of carbon supports in platinum (Pt) catalysts and contamination from impurities such as CO and H₂S, which can deactivate the catalysts.
A recent study, "Bifunctional Pt/TiO₂-Ov catalysts for enhanced electron transfer and CO tolerance in acidic HOR and ORR," presents a novel non-carbon supported catalyst, Pt/TiO₂-Ov, enriched with oxygen vacancies (Ov). This catalyst was synthesized using a microwave-assisted method, leveraging the electronic metal-support interaction (EMSI) to enhance electron transfer between Pt and Ti atoms.
The research team, led by authors from Fuzhou University and Shanghai University, optimized the synthesis process of TiO₂-Ov by etching TiO₂/SiO₂ samples with varying HF concentrations and high-temperature hydrogen annealing. Pt nanoparticles were then immobilized onto the TiO₂-Ov support through ethylene glycol reduction and microwave heating.
The Pt/TiO₂-Ov catalyst demonstrated superior performance in both hydrogen oxidation reaction (HOR) and oxygen reduction reaction (ORR). In a 0.1 mol/L HClO₄ electrolyte, its normalized Pt mass activity and specific activity were 1.24 times higher than commercial Pt/C. Notably, it showed remarkable CO tolerance, with a significantly higher relative retention rate than Pt/C under a H₂/(1000×10–6) CO atmosphere.
The catalyst also exhibited excellent durability. After 5000 cycles of accelerated durability tests, it showed an exceptionally low half-wave potential loss of only 7 mV for ORR and a minimal current density decay of 13.44% after a 24-hour HOR test.
This study underscores the importance of the strong metal-support interaction between reducible oxide supports and noble metal Pt in improving long-term performance and CO poisoning resistance. The Pt/TiO₂-Ov catalyst’s exceptional performance and durability offer a promising alternative to conventional carbon-supported catalysts, paving the way for more efficient and practical PEMFC applications.
This work provides valuable insights into the design of noble metal-loaded electrocatalysts with oxygen-rich reducible oxide supports, which can enhance catalytic efficiency in energy conversion reactions and improve resilience against CO poisoning.
Journal
Frontiers in Energy
Method of Research
Experimental study
Subject of Research
Not applicable
Article Title
Bifunctional Pt/TiO2-Ov catalysts for enhanced electron transfer and CO tolerance in acidic HOR and ORR
Article Publication Date
6-May-2025