New Pt(0) Nanoparticles as Highly Active and Reusable Catalysts in the C1-C3 Alcohol Oxidation and the Room Temperature Dehydrocoupling of Dimethylamine-Borane (DMAB)

被引:63
作者
Erken, Esma [1 ]
Pamuk, Handan [1 ]
Karatepe, Ozlem [1 ]
Baskaya, Gaye [1 ]
Sert, Hakan [2 ]
Kalfa, Orhan Murat [3 ]
Sen, Fatih [1 ]
机构
[1] Dumlupinar Univ, Dept Biochem, TR-43100 Kutahya, Turkey
[2] Usak Univ, Dept Chem Engn, TR-64100 Usak, Turkey
[3] Dumlupinar Univ, Dept Chem, TR-43100 Kutahya, Turkey
关键词
Energy storage; Alcohol oxidation; Nanostructure; X-ray diffraction; METHANOL FUEL-CELLS; PT-RU/C CATALYSTS; ELECTROCATALYTIC OXIDATION; PLATINUM NANOPARTICLES; ETHANOL; CARBON; SURFACTANTS; 2-PROPANOL; DEHYDROGENATION; ELECTRODES;
D O I
10.1007/s10876-015-0892-8
中图分类号
O61 [无机化学];
学科分类号
070301 [无机化学];
摘要
New Pt(0) nanoparticles were easily and reproducibly prepared by the simultaneous reduction method using 1-butylamine (BA) and tributylamine (TBA) for the first time as capturing ligands at room temperature. X-ray diffraction, X-ray photoelectron microscopy and transmission electron microscopy measurements verify the formation of well-dispersed Pt(0) nanoparticles [similar to 3.63 and similar to 3.98 nm for catalysts prepared using BA (catalyst I) and TBA (catalyst II), respectively] on an activated carbon surface. The catalytic performances of these nanoparticles in terms of activity, isolability and reusability were investigated for both alcohol oxidation and the dehydrocoupling of dimethylamine-borane (DMAB). These nanoparticles were shown to be as active and reusable heterogeneous catalysts even at room temperature. The prepared catalysts can catalyze the dehydrogenation of DMAB with one of the highest known activities at room temperature and also C1-C3 alcohol oxidation with very high electrochemical activities.
引用
收藏
页码:9 / 23
页数:15
相关论文
共 51 条
[1]
MECHANISM OF ELECTRO-OXIDATION OF METHANOL ON PLATINUM ELECTRODE [J].
BAGOTZKY, VS ;
VASSILYEW, YB .
ELECTROCHIMICA ACTA, 1967, 12 (09) :1323-+
[2]
A direct 2-propanol polymer electrolyte fuel cell [J].
Cao, DX ;
Bergens, SH .
JOURNAL OF POWER SOURCES, 2003, 124 (01) :12-17
[3]
Quaternary Pt-based electrocatalyst for methanol oxidation by combinatorial electrochemistry [J].
Choi, WC ;
Kim, JD ;
Woo, SI .
CATALYSIS TODAY, 2002, 74 (3-4) :235-240
[4]
Homogeneous, titanocene-catalyzed dehydrocoupling of amine-borane adducts [J].
Clark, Timothy J. ;
Russell, Christopher A. ;
Manners, Ian .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (30) :9582-9583
[5]
A comprehensive study on the effect of Ru addition to Pt electrodes for direct ethanol fuel cell [J].
Datta, J. ;
Singh, S. ;
Das, S. ;
Bandyopadhyay, N. R. .
BULLETIN OF MATERIALS SCIENCE, 2009, 32 (06) :643-652
[6]
Preparation of PtNi nanoparticles for the electrocatalytic oxidation of methanol [J].
Deivaraj, TC ;
Chen, WX ;
Lee, JY .
JOURNAL OF MATERIALS CHEMISTRY, 2003, 13 (10) :2555-2560
[7]
Platinum nanocatalysts prepared with different surfactants for C1-C3 alcohol oxidations and their surface morphologies by AFM [J].
Ertan, Salih ;
Sen, Fatih ;
Sen, Selda ;
Gokagac, Gulsun .
JOURNAL OF NANOPARTICLE RESEARCH, 2012, 14 (06)
[8]
The activated complex in chemical reactions [J].
Eyring, H .
JOURNAL OF CHEMICAL PHYSICS, 1935, 3 (02) :107-115
[9]
Ruthenium-Catalyzed Dimethylamineborane Dehydrogenation: Stepwise Metal-Centered Dehydrocyclization [J].
Friedrich, Anja ;
Drees, Markus ;
Schneider, Sven .
CHEMISTRY-A EUROPEAN JOURNAL, 2009, 15 (40) :10339-10342
[10]
Ethanol oxidation on PtRu electrodes studied by differential electrochemical mass spectrometry [J].
Fujiwara, N ;
Friedrich, KA ;
Stimming, U .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 472 (02) :120-125