Exceptional Oxygen Reduction Reaction Activity and Durability of Platinum-Nickel Nanowires through Synthesis and Post-Treatment Optimization

被引:56
作者
Alia, Shaun M. [1 ]
Ngo, Chilan [2 ]
Shulda, Sarah [2 ]
Ha, Mai-Anh [1 ]
Dameron, Arrelaine A. [1 ,4 ]
Weker, Johanna Nelson [3 ]
Neyerlin, Kenneth C. [1 ]
Kocha, Shyam S. [1 ]
Pylypenko, Svitlana [2 ]
Pivovar, Bryan S. [1 ]
机构
[1] Chem & Nanoscience Ctr, Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA
[2] Colorado Sch Mines, Dept Chem, 1012 14th St, Golden, CO 80401 USA
[3] Stanford Synchrotron Radiat Lightsource, SLAC Natl Accelerator Lab, 257S Sand Hill Rd, Menlo Pk, CA 94025 USA
[4] Forge Nano, 1172 West Century Dr 240, Louisville, CO 80027 USA
关键词
INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; AUGMENTED-WAVE METHOD; MEMBRANE FUEL-CELLS; ALLOY SURFACES; REDUCING ELECTROCATALYSTS; BASIS-SET; IN-SITU; CATALYSTS; NANOPARTICLES;
D O I
10.1021/acsomega.7b00054
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For the first time, extended nanostructured catalysts are demonstrated with both high specific activity (> 6000 mu A cm(Pt)(-2) at 0.9 V) and high surface areas (> 90 m2 g(Pt)(-1)). Platinum-nickel (Pt. Ni) nanowires, synthesized by galvanic displacement, have previously produced surface areas in excess of 90 m(2) gPt -1, a significant breakthrough in and of itself for extended surface catalysts. Unfortunately, these materials were limited in terms of their specific activity and durability upon exposure to relevant electrochemical test conditions. Through a series of optimized postsynthesis steps, significant improvements were made to the activity (3-fold increase in specific activity), durability (21% mass activity loss reduced to 3%), and Ni leaching (reduced from 7 to 0.3%) of the Pt. Ni nanowires. These materials show more than a 10-fold improvement in mass activity compared to that of traditional carbon-supported Pt nanoparticle catalysts and offer significant promise as a new class of electrocatalysts in fuel cell applications.
引用
收藏
页码:1408 / 1418
页数:11
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