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Mo-Mediated Sub-Nanometer Amorphous Shell Engineering on PtMo Alloy for Enhanced CO Tolerance in Hydrogen Oxidation Reaction
DOI:10.1002/smll.74142.png)
Abstract
En 中文
The growing global demand for clean and sustainable energy has driven rapid advancements in fuel cell technology. However, trace impurities in hydrogen fuel, such as carbon monoxide (CO), can significantly deactivate the anode by blocking its active sites, leading to performance degradation. Consequently, developing CO-tolerant electrocatalysts has become a critical priority. To address this, PtMo/C nanoalloy particles were synthesized by incorporating Mo atoms into Pt nanoparticles, demonstrating exceptional hydrogen oxidation reaction (HOR) performance in proton exchange membrane fuel cells (PEMFCs). Furthermore, MoOx-PtMo/C, with a MoOx-modified surface, exhibited superior CO tolerance. In situ CO adsorption surface-enhanced infrared absorption spectroscopy (SEIRAS) and density functional theory (DFT) calculations revealed that the synergistic effect of dual-stage electronic modulation from MoOx and Mo atoms adjusts the electronic structure of Pt, substantially weakening CO adsorption energy and enhancing CO tolerance. Remarkably, the optimized MoOx-PtMo-5 h/C achieved mass and specific activities of 2.86 A mgPt−1 and 2.80 mA cmECSA−2 at 50 mV, 3.8-fold and 3.0-fold higher than commercial Pt/C, respectively. Additionally, MoOx-PtMo-5 h/C demonstrated exceptional CO resistance in both three-electrode and PEMFC tests.
Keywords:
amorphous shell
CO tolerance
hydrogen oxidation reaction
proton exchange membrane fuel cells
Journal
IF:
12.1
Papers:
3.0W
Citations:
16.4W

