Low-Coordination Sites in Oxygen-Reduction Electrocatalysis: Their Roles and Methods for Removal

被引:67
作者
Cai, Yun [1 ]
Ma, Chao [2 ]
Zhu, Yimei [2 ]
Wang, Jia X. [1 ]
Adzic, Radoslav R. [1 ]
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Brookhaven Natl Lab, Condensed Matter Phys & Mat Sci Dept, Upton, NY 11973 USA
关键词
SINGLE-CRYSTAL ELECTRODES; TRANSITION-METAL SURFACES; PARTICLE-SIZE; ACIDIC MEDIA; CATALYTIC-ACTIVITY; ALKALINE-SOLUTIONS; PLATINUM; PALLADIUM; PT(111); CHEMISORPTION;
D O I
10.1021/la200753z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Low-coordination sites, including edges, kinks, and defects, play an important role in oxygen-reduction electrocatalysis. Their role was studied experimentally and theoretically for various Pt surfaces. However, the roughness effect on similar-sized nanoparticles that could elucidate the role of low-coordination sites has attracted much less attention, with no studies on Pd nanoparticles. Here, using Br- adsorption/desorption, we introduce an effective approach to reduce surface roughness, yielding Pd nanoparticles with smoother surfaces and an increased number of (111)-oriented facets. The resulting nanoparticles have a slightly contracted structure and narrow size distribution. Pt monolayer catalysts that contain such nanoparticles as the cores showed a 1.5-fold enhancement in specific and Pt mass activities for the oxygen reduction reaction compared with untreated ones. Furthermore, a dramatic increase in durability was observed with bromide-treated Pd(3)Co cores. These results demonstrate a simple approach to preparing nanoparticles with smooth surfaces and confirm the adverse effect of low-coordination sites on the kinetics of the oxygen-reduction reaction.
引用
收藏
页码:8540 / 8547
页数:8
相关论文
共 40 条
[1]   Platinum monolayer fuel cell electrocatalysts [J].
Adzic, R. R. ;
Zhang, J. ;
Sasaki, K. ;
Vukmirovic, M. B. ;
Shao, M. ;
Wang, J. X. ;
Nilekar, A. U. ;
Mavrikakis, M. ;
Valerio, J. A. ;
Uribe, F. .
TOPICS IN CATALYSIS, 2007, 46 (3-4) :249-262
[2]   Adsorption-Driven Surface Segregation of the Less Reactive Alloy Component [J].
Andersson, Klas J. ;
Calle-Vallejo, Federico ;
Rossmeisl, Jan ;
Chorkendorff, Lb .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (06) :2404-2407
[3]  
[Anonymous], 2006, ANGEW CHEM-GER EDIT, DOI DOI 10.1002/ANGE.200504386
[4]   PHENOMENOLOGICAL ASPECTS RELATED TO THE ELECTROCHEMICAL-BEHAVIOR OF SMOOTH PALLADIUM ELECTRODES IN ALKALINE-SOLUTIONS [J].
BOLZAN, AE .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 380 (1-2) :127-138
[5]  
Budevski E., 1996, ELECT PHASE FORMATIO
[6]   Electrode-surface coordination chemistry: Ligand substitution and competitive coordination of halides at well-defined Pd(100) and Pd(111) single crystals [J].
Carrasquillo, A ;
Jeng, JJ ;
Barriga, RJ ;
Temesghen, WF ;
Soriaga, MP .
INORGANICA CHIMICA ACTA, 1997, 255 (02) :249-254
[7]   A method to prepare single crystal electrodes of reactive metals:: application to Pd(hkl) [J].
Cuesta, A ;
Kibler, LA ;
Kolb, DM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 466 (02) :165-168
[8]   Mesoporous palladium - the surface electrochemistry of palladium in aqueous sodium hydroxide and the cathodic reduction of nitrite [J].
Denuault, G ;
Milhano, C ;
Pletcher, D .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2005, 7 (20) :3545-3551
[9]   Expansion of interatomic distances in platinum catalyst nanoparticles [J].
Du, K. ;
Emst, F. ;
Pelsozy, M. C. ;
Barthel, J. ;
Tillmann, K. .
ACTA MATERIALIA, 2010, 58 (03) :836-845
[10]   CORRELATION BETWEEN CATALYTIC ACTIVITY AND BONDING AND COORDINATION-NUMBER OF ATOMS AND MOLECULES ON TRANSITION-METAL SURFACES - THEORY AND EXPERIMENTAL-EVIDENCE [J].
FALICOV, LM ;
SOMORJAI, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (08) :2207-2211