Solvothermal Synthesis of Platinum Alloy Nanoparticles for Oxygen Reduction Electrocatalysis

被引:378
|
作者
Carpenter, Michael K. [1 ]
Moylan, Thomas E. [1 ]
Kukreja, Ratandeep Singh [2 ]
Atwan, Mohammed H. [2 ]
Tessema, Misle M. [3 ]
机构
[1] Gen Motors R&D Ctr, Electrochem Energy Res Lab, Warren, MI 48090 USA
[2] Trison Business Solut Inc, LeRoy, NY 14482 USA
[3] Optimal Comp Aided Engn Inc, Plymouth, MI 48170 USA
关键词
O-2; REDUCTION; NI; MONOLAYER; SHAPE; FE;
D O I
10.1021/ja300756y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Platinum alloy nanoparticles show great promise as electrocatalysts for the oxygen reduction reaction (ORR) in fuel cell cathodes. We report here on the use of N,N-dimethylformamide (DMF) as both solvent and reductant in the solvothermal synthesis of Pt alloy nanoparticles (NPs), with a particular focus on Pt-Ni alloys. Well-faceted alloy nanocrystals were generated with this method, including predominantly cubic and cuboctahedral nanocrystals of Pt3Ni, and octahedral and truncated octahedral nanocrystals of PtNi. X-ray diffraction (XRD) and high angle annular dark field scanning transmission electron microscopy (HAADF-STEM), coupled with energy dispersive spectroscopy (EDS), were used to characterize crystallite morphology and composition. ORR activities of the alloy nanoparticles were measured with a rotating disk electrode (RDE) technique. While some Pt3Ni alloy nanoparticle catalysts showed specific activities greater than 1000 mu A/cm(P nu)(2) alloy catalysts prepared with a nominal composition of PtNi displayed activities close to 3000 mu A/cm(P nu)(2) or almost 15 times that of a state-of-the-art Pt/carbon catalyst. XRD and EDS confirmed the presence of two NP compositions in this catalyst. HAADF-STEM examination of the PtNi nanoparticle catalyst after RDE testing revealed the development of hollows in a number of the nanoparticles due to nickel dissolution. Continued voltage cycling caused further nickel dissolution and void formation, but significant activity remained even after 20 000 cycles.
引用
收藏
页码:8535 / 8542
页数:8
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