Synthesis of Ni SiO2/C Supported Platinum Catalysts for Improved Electrochemical Activity Towards Ethanol Oxidation

被引:7
作者
Ferreira, Hadla S. [1 ]
Ferreira, Hadma S. [2 ]
Gliech, Manuel [3 ]
Bergmann, Arno [3 ]
Beermann, Vera [3 ]
Rangel, Maria do C. [2 ]
Eguiluz, Katlin I. B. [1 ,4 ]
Salazar-Banda, Giancarlo R. [1 ,4 ]
机构
[1] Inst Tecnol & Pesquisa, Lab Eletroquim & Nanotecnol, Av Murilo Dantas 300, BR-49032490 Aracaju, SE, Brazil
[2] Univ Fed Bahia, Inst Quim, Campus Univ Mina, BR-40290170 Salvador, BA, Brazil
[3] Tech Univ Berlin, Dept Chem, Str 17, D-10623 Berlin, Germany
[4] Univ Tiradentes, Programa Posgrad Engn Proc, Av Murilo Dantas 300, BR-49032490 Aracaju, SE, Brazil
关键词
Electrocatalyst Support; Fuel Cells; Nanotechnology; Catalyst Stability; METHANOL ELECTROOXIDATION; CARBON NANOTUBES; ENHANCED ACTIVITY; SILICA SPHERES; ANODE CATALYST; NANOPARTICLES; ELECTROCATALYSTS; PERFORMANCE; INTERFACE; STABILITY;
D O I
10.1166/jnn.2019.16915
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of Pt/Ni-SiO2/C catalysts with different mass proportions of Ni-SiO2/C (0:100, 30:70, 50:50, 70:30 and 100:0) were prepared and studied towards ethanol electrochemical oxidation in acid medium. The support silica particles were initially synthesized via sol-gel and then modified with NiCl2. The Ni deposited on the silica surface plays a role promoting nucleation sites for the reduction of platinum. Pt was further chemically reduced onto Ni-SiO2 using formic acid and loaded onto carbon Vulcan XC-72 R. The PUNT-SiO2/C catalysts were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, temperature-programmed reduction, X-ray photoelectron spectroscopy, transmission electron microscopy and inductively coupled plasma-optical emission spectroscopy. The physical characterizations reveal the formation of oxide-metal composite and strong interaction between Pt and the Ni-S1O(2) composite. The Pt/Ni-SiO2/C catalyst with meso/macroporous structure exhibits higher electrocatalytic activity towards ethanol oxidation and better stability, after 48 h of electrolysis, than a commercial Pt/C catalyst. These improved features could be due to presence of Ni-SiO2 composite that promotes corrosion resistance of the support and prevents the aggregation of Pt nanoparticles and their detachment from the support. The low poisoning of the Pt/Ni-SiO2/C catalyst is probably due to the enhanced oxygen content on the composite surface. The high electrocatalytic activity and enhanced electrochemical stability of the Pt/Ni-SiO2/C catalyst make it promising for further fuel cell applications.
引用
收藏
页码:4590 / 4598
页数:9
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