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Oxygen Storage by Tin Oxide Monolayers on Pt3Sn(111)
被引:3
|作者:
Merte, Lindsay R.
[2
,3
]
Braud, Nicolas
[1
]
Buss, Lars
[4
]
Bisbo, Malthe Kjaer
[5
]
Wallander, Harald J.
[2
,3
]
Krisponeit, Jon -Olaf
[1
,6
]
Flege, Jan Ingo
[7
]
Hammer, Bjork
[5
]
Falta, Jens
[1
,6
]
Lundgren, Edvin
[3
,8
]
机构:
[1] Univ Bremen, Inst Solid State Phys, D-28359 Bremen, Germany
[2] Malmo Univ, Mat Sci & Appl Math, S-20506 Malmo, Sweden
[3] Lund Univ, NanoLund, S-22100 Lund, Sweden
[4] Brandenburg Univ Technol Cottbus Senftenberg, Appl Phys & Semicond Spect, D-03046 Cottbus, Germany
[5] Aarhus Univ, Ctr Interstellar Catalysis, Dept Phys & Astron, DK-8000 Aarhus, Denmark
[6] Univ Bremen, MAPEX Ctr Mat & Proc, D-28359 Bremen, Germany
[7] Brandenburg Univ Technol Cottbus Senftenberg, Appl Phys & Semicond Spect, D-03046 Cottbus, Germany
[8] Lund Univ, Div Synchrotron Radiat Res, S-22100 Lund, Sweden
基金:
瑞典研究理事会;
新加坡国家研究基金会;
关键词:
PT-SN ELECTROCATALYSTS;
CARBON-MONOXIDE;
CO OXIDATION;
ELECTROOXIDATION;
INTERFACE;
METAL;
ADSORPTION;
CATALYSTS;
SURFACE;
D O I:
10.1021/acs.jpcc.2c09041
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The high performance of platinum-tin catalysts for oxidation reactions has been linked to the formation of tin oxides at the metal surface, but little is known about the structure of these oxides or the chemical behavior that determines their catalytic properties. We show here how surface oxides on Pt3Sn(111) incorporate oxygen at the metal interface, which may be subsequently removed by reaction with CO. The storage mechanism, where oxygen uptake occurs without loss of interfacial Pt-Sn bonds, is enabled by the peculiar asymmetrical coordination state of Sn2+. O atoms are bound at pocket sites in the 2D oxide sheet between these outward-buckled Sn atoms and metallic Sn in the alloy surface below.
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页码:2988 / 2994
页数:7
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