Sol-Gel Synthesis of Ruthenium Oxide Nanowires To Enhance Methanol Oxidation in Supported Platinum Nanoparticle Catalysts

被引:11
|
作者
Sztaberek, Lukasz [1 ,3 ]
Mabey, Hannah [2 ]
Beatrez, William [1 ]
Lore, Christopher [2 ]
Santulli, Alexander C. [2 ]
Koenigsmann, Christopher [1 ]
机构
[1] Fordham Univ, Dept Chem, 441 East Fordham Rd, Bronx, NY 10458 USA
[2] Manhattan Coll, Dept Chem & Biochem, 4513 Manhattan Coll Pkwy, Riverdale, NY 10471 USA
[3] New York City Coll Technol, Dept Environm Control Technol, 300 Jay St, Brooklyn, NY 11201 USA
来源
ACS OMEGA | 2019年 / 4卷 / 10期
基金
美国国家科学基金会;
关键词
CARBON-MONOXIDE; CO OXIDATION; FORMIC-ACID; RU; ELECTROCATALYSTS; PTRU; ELECTROOXIDATION; DURABILITY; PT/RU;
D O I
10.1021/acsomega.9b01489
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A template-directed, sol-gel synthesis is utilized to produce crystalline RuO2 nanowires. Crystalline nanowires with a diameter of 128 +/- 15 nm were synthesized after treating the nanowires at 600 degrees C in air. Analysis of these nanowires by X-ray powder diffraction revealed the major crystalline phase to be tetragonal RuO2 with a small quantity of metallic ruthenium present. Further analysis of the nanowire structures by high-resolution transmission electron microscopy reveals that they are polycrystalline and are composed of interconnected, highly crystalline, nanoparticles having an average size of similar to 25 nm. Uniform 3 nm Pt nanoparticles were dispersed on the surface of RuO2 nanowires using an ambient, solution-based technique yielding a hybrid catalyst for methanol oxidation. Linear sweep voltammograms (LSVs) and chronoam-perometry performed in the presence of methanol in an acidic electrolyte revealed a significant enhancement in the onset potential, mass activity, and long-term stability compared with analogous Pt nanoparticles supported on commercially available Vulcan XC-72R carbon nanoparticles. Formic acid oxidation LSVs and CO stripping voltammetry revealed that the RuO2-supported Pt nanoparticles exhibit significantly higher CO tolerance, which leads to higher catalytic stability over a period of several hours. X-ray photoelectron spectroscopy results suggest that crystalline RuO2 leads to less-significant oxidation of the Pt surface relative to more widely studied hydrous RuO2 supports, thereby increasing catalytic performance.
引用
收藏
页码:14226 / 14233
页数:8
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