Colloidal Syntheses of Shape- and Size-Controlled Pt Nanoparticles for Electrocatalysis

被引:54
作者
Coutanceau, Christophe [1 ]
Urchaga, Patrick [1 ]
Brimaud, Sylvain [1 ]
Baranton, Steve [1 ]
机构
[1] Univ Poitiers, IC2MP, F-86022 Poitiers, France
关键词
Colloidal synthesis; Electrochemistry; Nanoparticles; Platinum; Shape controlled; Size controlled; FORMIC-ACID ELECTROOXIDATION; CO MONOLAYER OXIDATION; PLATINUM NANOPARTICLES; CONTROLLED GROWTH; PARTICLE-SIZE; ELECTROCHEMICAL CHARACTERIZATION; DEPENDENT ELECTROCATALYSIS; SURFACE CHARACTERIZATION; METAL NANOPARTICLES; NANOCRYSTALS;
D O I
10.1007/s12678-012-0079-0
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
Different colloidal synthesis methods of platinum nanoparticles with controlled sizes and shapes that are relevant for electrocatalysis studies are reviewed. Four main methods, i.e., water in oil microemulsion (w/o) method, polyacrylate (PA) method, tetradecyltrimethylammonium bromide (TTAB) method, and ethylene glycol method, are used to synthesize platinum nanoparticles. The PA method allowed us to synthesize reproducibly nanocubes, nanooctahedrons, or nanocuboctahedrons/truncated nanooctahedrons with size between 8 and 10 nm, the TTAB method led to the synthesis of nanocubes of about 10 nm, and the w/o method allowed the synthesis of spherical particles of about 3 nm. All these samples could be cleaned for further electrochemical characterization of their surface structure by hydrogen underpotential deposition and by spontaneous deposition and oxidation of bismuth and germanium, leading to a quantitative determination of the (100) and (111) surface domains. The samples prepared by the ethylene glycol method, in the presence or not of polyvinylpyrrolydone as surfactant, were size or shape controlled, but did not allow the electrochemical characterization of their surface due to remaining of strongly adsorbed organic species even after cleaning steps.
引用
收藏
页码:75 / 87
页数:13
相关论文
共 101 条
[71]   Recent Advances in the Liquid-Phase Synthesis of Metal Nanostructures with Controlled Shape and Size for Catalysis [J].
Semagina, Natalia ;
Kiwi-Minsker, Lioubov .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 2009, 51 (02) :147-217
[72]  
Sergeev GB, 2006, NANOCHEMISTRY, P1, DOI 10.1016/B978-044451956-6/50003-1
[73]   Hydrogenation of α, β unsaturated aldehydes over polycrystalline, (111) and (100) preferentially oriented Pt nanoparticles supported on carbon [J].
Serrano-Ruiz, J. C. ;
Lopez-Cudero, A. ;
Solla-Gullon, J. ;
Sepulveda-Escribano, A. ;
Aldaz, A. ;
Rodriguez-Reinoso, F. .
JOURNAL OF CATALYSIS, 2008, 253 (01) :159-166
[74]   Shape-dependent electrocatalysis:: methanol and formic acid electrooxidation on preferentially oriented Pt nanoparticles [J].
Solla-Gullon, J. ;
Vidal-Iglesias, F. J. ;
Lopez-Cudero, A. ;
Garnier, E. ;
Feliu, J. M. ;
Aldaza, A. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (25) :3689-3698
[75]   CO monolayer oxidation on semi-spherical and preferentially oriented (100) and (111) platinum nanoparticles [J].
Solla-Gullón, J ;
Vidal-Iglesias, FJ ;
Herrero, E ;
Feliu, JM ;
Aldaz, A .
ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (01) :189-194
[76]   In situ surface characterization of preferentially oriented platinum nanoparticles by using electrochemical structure sensitive adsorption reactions [J].
Solla-Gullón, J ;
Vidal-Iglesias, FJ ;
Rodríguez, P ;
Herrero, E ;
Feliu, JM ;
Clavilier, J ;
Aldaz, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (36) :13573-13575
[77]   Surface characterization of platinum electrodes [J].
Solla-Gullon, Jose ;
Rodriguez, Paramaconi ;
Herrero, Enrique ;
Aldaz, Antonio ;
Feliu, Juan M. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (10) :1359-1373
[78]  
SOLLIARD C, 1983, THESIS ECOLE POLYTEC
[79]   Research in nanosciences - Great opportunity for catalysis science [J].
Somorjai, GA ;
Borodko, YG .
CATALYSIS LETTERS, 2001, 76 (1-2) :1-5
[80]   Pt nanocrystals: Shape control and Langmuir-Blodgett monolayer formation [J].
Song, H ;
Kim, F ;
Connor, S ;
Somorjai, GA ;
Yang, PD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (01) :188-193