Elucidation of the Oxygen Reduction Volcano in Alkaline Media using a Copper-Platinum(111) Alloy

被引:77
作者
Jensen, Kim D. [1 ,2 ]
Tymoczko, Jakub [3 ]
Rossmeisl, Jan [2 ]
Bandarenka, Aliaksandr S. [4 ]
Chorkendorff, Ib [1 ]
Escudero-Escribano, Maria [1 ,2 ]
Stephens, Ifan E. L. [1 ,5 ]
机构
[1] Tech Univ Denmark DTU, Dept Phys, DK-2800 Lyngby, Denmark
[2] Univ Copenhagen KU, Nanosci Ctr, Dept Chem, Univ Pk 5, DK-2100 Kbh O, Denmark
[3] Ruhr Univ Bochum, Analyt Chem, CES, Univ Str 150, D-44780 Bochum, Germany
[4] Tech Univ Munich, Phys Dept, ECS, James Franck Str 1, D-85748 Garching, Germany
[5] Imperial Coll London, Royal Sch Mines, Dept Mat, Prince Consort Rd, London SW7 2AZ, England
关键词
electrocatalysis; oxygen reduction; platinum; Sabatier principle; surface chemistry; STEPPED PLATINUM SURFACES; ELECTROLYTE FUEL-CELLS; NONCOVALENT INTERACTIONS; OXIDE CATALYSTS; ACIDIC MEDIA; WATER; ELECTROCATALYSIS; ADSORPTION; BATTERIES; EVOLUTION;
D O I
10.1002/anie.201711858
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The relationship between the binding of the reaction intermediates and oxygen reduction activity in alkaline media was experimentally explored. By introducing Cu into the 2nd surface layer of a Pt(111) single crystal, the surface reactivity was tuned. In both 0.1(M) NaOH and 0.1(M) KOH, the optimal catalyst should exhibit OH binding circa 0.1 eV weaker than Pt(111), via a Sabatier volcano; this observation suggests that the reaction is mediated via the same surface bound intermediates as in acid, in contrast to previous reports. In 0.1(M) KOH, the alloy catalyst at the peak of the volcano exhibits a maximum activity of 101 +/- 8 mAcm(-2) at 0.9 V vs. a reversible hydrogen electrode (RHE). This activity constitutes a circa 60-fold increase over Pt(111) in 0.1(M) HClO4.
引用
收藏
页码:2800 / 2805
页数:6
相关论文
共 50 条
[1]  
[Anonymous], 2014, ANGEW CHEM, V126, P3749
[2]  
[Anonymous], 2012, ANGEW CHEM, V124, P13171
[3]  
[Anonymous], 2017, ANGEW CHEM, V129, P15221
[4]   Elucidating the activity of stepped Pt single crystals for oxygen reduction [J].
Bandarenka, Aliaksandr S. ;
Hansen, Heine A. ;
Rossmeisl, Jan ;
Stephens, Ifan E. L. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (27) :13625-13629
[5]   Anion adsorption, CO oxidation, and oxygen reduction reaction on a Au(100) surface: The pH effect [J].
Blizanac, BB ;
Lucas, CA ;
Gallagher, ME ;
Arenz, M ;
Ross, PN ;
Markovic, NM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (02) :625-634
[6]   A cell for the controllable thermal treatment and electrochemical characterisation of single crystal alloy electrodes [J].
Bondarenko, Alexander S. ;
Stephens, Ifan E. L. ;
Chorkendorff, Ib .
ELECTROCHEMISTRY COMMUNICATIONS, 2012, 23 :33-36
[7]   Why conclusions from platinum model surfaces do not necessarily lead to enhanced nanoparticle catalysts for the oxygen reduction reaction [J].
Calle-Vallejo, Federico ;
Pohl, Marcus D. ;
Reinisch, David ;
Loffreda, David ;
Sautet, Philippe ;
Bandarenka, Aliaksandr S. .
CHEMICAL SCIENCE, 2017, 8 (03) :2283-2289
[8]   Tailoring the catalytic activity of electrodes with monolayer amounts of foreign metals [J].
Calle-Vallejo, Federico ;
Koper, Marc T. M. ;
Bandarenka, Aliaksandr S. .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (12) :5210-5230
[9]   Co-adsorption of Cations as the Cause of the Apparent pH Dependence of Hydrogen Adsorption on a Stepped Platinum Single-Crystal Electrode [J].
Chen, Xiaoting ;
McCrum, Ian T. ;
Schwarz, Kathleen A. ;
Janik, Michael J. ;
Koper, Marc T. M. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2017, 56 (47) :15025-15029
[10]   Electrocatalyst approaches and challenges for automotive fuel cells [J].
Debe, Mark K. .
NATURE, 2012, 486 (7401) :43-51