Palladium Nanoparticles/Defective Graphene Composites as Oxygen Reduction Electrocatalysts: A First-Principles Study

被引:92
|
作者
Liu, Xin [1 ,2 ]
Li, Lin [2 ]
Meng, Changgong [2 ]
Han, Yu [1 ]
机构
[1] King Abdullah Univ Sci & Technol, Adv Membranes & Porous Mat Ctr, Thuwal 239556900, Saudi Arabia
[2] Dalian Univ Technol, Sch Chem, Dalian 116024, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2012年 / 116卷 / 04期
关键词
CATALYST SUPPORT STRUCTURES; CATALYTICALLY ACTIVE GOLD; INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; NITROGEN-DOPED GRAPHENE; GRAPHITE OXIDE; SURFACE SCIENCE; FORMIC-ACID; PD; DESIGN;
D O I
10.1021/jp2096983
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The impact of graphene substrate-Pd nanoparticle interaction on the O, OH, and OOH adsorption that is directly related to the electrocatalytic performance of these composites in oxygen reduction reaction (ORR) has been investigated by first-principles-based calculations. The calculated binding energy of a Pd-13 nanoparticle on a single vacancy graphene is as high as -6.10 eV, owing to the hybridization between the dsp states of the Pd particles with the sp(2) dangling bonds at the defect sites. The strong interaction results in the averaged d-band center of the deposited Pd nanoparticles shifted away from the Fermi level from -1.02 to -1.45 eV. Doping the single vacancy graphene with B or N will further tune the average d-band center and also the activity of the composite toward O, OH, and OOH adsorption. The adsorption energies of O, OH, and OOH are reduced from -4.78, -4.38, and -1.56 eV on the freestanding Pd-13 nanopartide to -4.57, -2.66, and -1.39 eV on Pd-13/single vacancy graphene composites, showing that the defective graphene substrate will not only stabilize the Pd nanoparticles but also reduce the adsorption energies of the O-containing species to the Pd particle, and so as the poisoning of the ORR active sites.
引用
收藏
页码:2710 / 2719
页数:10
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