Active-Phase Formation and Stability of Gd/Pt(111) Electrocatalysts for Oxygen Reduction: An In Situ Grazing Incidence X-Ray Diffraction Study

被引:18
作者
Escudero-Escribano, Maria [1 ,2 ,3 ]
Pedersen, Anders F. [2 ]
Ulrikkeholm, Elisabeth T. [2 ]
Jensen, Kim D. [1 ,2 ]
Hansen, Martin H. [3 ]
Rossmeisl, Jan [1 ]
Stephens, Ifan E. L. [2 ,4 ]
Chorkendorff, Ib [2 ]
机构
[1] Univ Copenhagen, Dept Chem, Nanosci Ctr, Univ Pk 5, DK-2100 Copenhagen O, Denmark
[2] Tech Univ Denmark, Dept Phys Surface Phys & Catalysis, Fys Vej,Bldg 312, DK-2800 Lyngby, Denmark
[3] Stanford Univ, SUNCAT Ctr Interface Sci & Catalysis, Dept Chem Engn, 443 Via Ortega, Stanford, CA 94305 USA
[4] Imperial Coll London, Dept Mat, Royal Sch Mines, 2-03b,Prince Consort Rd, London SW7 2AZ, England
关键词
active phase; electrocatalysis; oxygen reduction reaction; platinum; X-ray diffraction; AUTOMOTIVE FUEL-CELLS; TRANSITION-METALS; ALLOY CATALYSTS; SURFACE; PLATINUM; PT(111); ELECTROREDUCTION; STRAIN; BENCHMARKING; ELUCIDATION;
D O I
10.1002/chem.201801587
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alloys of platinum and gadolinium present significant activity enhancement over pure Pt for the oxygen reduction reaction (ORR), both in the form of extended electrode surfaces and nanoparticulate catalysts. The active phase consists of a compressed Pt overlayer formed on Pt5Gd electrodes upon exposure to the electrolyte by acid leaching. Here, we investigate the formation, strain and correlation lengths of the active Pt overlayer by using in situ synchrotron grazing incidence X-ray diffraction on Gd/Pt(111) single-crystalline electrodes. The overlayer forms upon exposure to electrolyte under open circuit conditions; the compressive strain relaxes slightly upon repeated electrochemical cycling in the potential range 0.6 to 1.0 V versus the reversible hydrogen electrode (RHE). In addition, the strain relaxes strongly when exposing the electrode to 1.2 V versus RHE, and the thickness of the crystalline portion of the overlayer increases with potential above 1.3 V versus RHE.
引用
收藏
页码:12280 / 12290
页数:11
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