Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 25, Pages 29532-29540Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c04644
Keywords
carbon monoxide; bismuth; gold; heterogeneous catalysis; density functional calculations
Funding
- National Key R&D Program of China [2016YFA0401801]
- Fundamental Research Funds for the Central Universities [WK2060000032]
- National Natural Science Foundation [51772283, 22072140, 21972145]
- Hong Kong Scholars Program [XJ2019022]
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A Au/Bi2O3 interfacial catalyst was designed in this study for preferential oxidation of CO in hydrogen, achieving 100% CO conversion over a wide temperature range and being compatible with the operating temperatures of PEMFCs. The catalyst demonstrated excellent high flow performance and long-term stability. Density functional theory calculations revealed the mechanism behind the enhanced catalytic performance of the catalyst.
Preferential oxidation (PROX) of CO in hydrogen is of great significance for proton exchange membrane fuel cells (PEMFCs) that need a CO-free hydrogen stream as fuel. The key technical problem is developing catalysts that can efficiently remove CO from the H-2-rich stream within the working temperature range of PEMFCs. Herein, we design a Au/Bi2O3 interfacial catalyst for PROX with excellent catalytic performance, which can achieve 100% CO conversion in the PROX reaction over a wide temperature window (70-200 degrees C) and is perfectly compatible with the operating temperature window (80-180 degrees C) of PEMFCs. Moreover, the catalyst also demonstrates excellent high flow performance and long-term stability. Density functional theory (DFT) calculations reveal that the electrons transferring from Bi2O3 to Au and then to adsorbed perimeter CO and O-2 molecules promote the activation of CO and O-2, thus enhancing the catalytic performance of PROX.
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