Highly Durable and Active PtFe Nanocatalyst for Electrochemical Oxygen Reduction Reaction

被引:585
作者
Chung, Dong Young [1 ,2 ]
Jun, Samuel Woojoo [1 ,2 ]
Yoon, Gabin [1 ,3 ]
Kwon, Soon Gu [1 ,2 ]
Shin, Dong Yun [4 ]
Seo, Pilseon [1 ,2 ]
Yoo, Ji Mun [1 ,2 ]
Shin, Heejong [1 ,2 ]
Chung, Young-Hoon [5 ]
Kim, Hyunjoong [1 ,2 ]
Mun, Bongjin Simon [6 ]
Lee, Kug-Seung [7 ]
Lee, Nam-Suk [8 ]
Yoo, Sung Jong [5 ]
Lim, Dong-Hee [4 ]
Kang, Kisuk [1 ,3 ]
Sung, Yung-Eun [1 ,2 ]
Hyeon, Taeghwan [1 ,2 ]
机构
[1] Inst for Basic Sci Korea, Ctr Nanoparticle Res, Seoul 151742, South Korea
[2] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151742, South Korea
[3] Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 151742, South Korea
[4] Chungbuk Natl Univ, Dept Environm Engn, Chungbuk 361763, South Korea
[5] Korea Inst Sci & Technol, Fuel Cell Res Ctr, Seoul 136791, South Korea
[6] Gwangju Inst Sci & Technol, Ertl Ctr Electrochem & Catalyst, Dept Phys & Photon Sci, Gwangju 500712, South Korea
[7] Pohang Univ Sci & Technol POSTECH, PAL, Pohang 790784, South Korea
[8] Pohang Univ Sci & Technol POSTECH, NINT, Pohang 790784, South Korea
关键词
STABLE ELECTROCATALYSTS; FEPT NANOPARTICLES; SHAPE-CONTROL; PLATINUM; ALLOY; CATALYSIS; DESIGN; NANOCRYSTALS; STABILITY; STRATEGY;
D O I
10.1021/jacs.5b09653
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Demand on the practical synthetic approach to the high performance electrocatalyst is rapidly increasing for fuel cell commercialization. Here we present a synthesis of highly durable and active intermetallic ordered face-centered tetragonal (fct)-PtFe nanoparticles (NPs) coated with a "dual purpose" N-doped carbon shell. Ordered fct-PtFe NPs with the size of only a few nanometers are obtained by thermal annealing of polydopamine-coated PtFe NPs, and the N-doped carbon shell that is in situ formed from dopamine coating could effectively prevent the coalescence of NPs. This carbon shell also protects the NPs from detachment and agglomeration as well as dissolution throughout the harsh fuel cell operating conditions. By controlling the thickness of the shell below 1 nm, we achieved excellent protection of the NPs as well as high catalytic activity, as the thin carbon shell is highly permeable for the reactant molecules. Our ordered fct-PtFe/C nanocatalyst coated with an N-doped carbon shell shows 11.4 times-higher mass activity and 10.5 times-higher specific activity than commercial Pt/C catalyst. Moreover, we accomplished the long-term stability in membrane electrode assembly (MEA) for 100 h without significant activity loss. From in situ XANES, EDS, and first-principles calculations, we confirmed that an ordered fct-PtFe structure is critical for the long-term stability of our nanocatalyst. This strategy utilizing an N-doped carbon shell for obtaining a small ordered-fct PtFe nanocatalyst as well as protecting the catalyst during fuel cell cycling is expected to open a new simple and effective route for the commercialization of fuel cells.
引用
收藏
页码:15478 / 15485
页数:8
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