Pt deposited Pt-Pd/C electrocatalysts with the enhanced oxygen reduction activity

被引:19
作者
Park, Jin Hoo [1 ]
Sohn, Yeonsun [1 ]
Jung, Do Hwa [1 ]
Kim, Pil [1 ]
Joo, Ji Bong [2 ]
机构
[1] Chonbuk Natl Univ, Nanomat Proc Res Ctr, Sch Semicond & Chem Engn, Jeonju 561756, Jeonbuk, South Korea
[2] Konkuk Univ, Dept Chem Engn, Seoul 05029, South Korea
关键词
Pt-Pd catalysts; Pt-rich surface; Pt deposition; Core-shell; Oxygen reduction; CORE-SHELL NANOPARTICLES; ELECTROLYTE FUEL-CELLS; PLATINUM MONOLAYER; CATALYTIC-ACTIVITY; CARBON SUPPORT; METHANOL ELECTROOXIDATION; O-2; REDUCTION; ALLOY; PEMFC; CU;
D O I
10.1016/j.jiec.2016.01.039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reducing the cost of state-of-the-art Pt electrocatalysts while maintaining their oxygen reduction performance is always a hotspot in fuel cell research owing to their significant economic benefit for the commercialization of polymer electrolyte membrane fuel cells. Herein, we report a simple and cost-effective synthesis of Pt-Pd catalysts and a systematic study of their characteristics and catalytic performances for the oxygen reduction reaction (ORR). Pt-Pd bimetallic catalysts were prepared by a simple chemical deposition of Pt on the surface of Pd particles using a commercial Pd/C catalyst. During the synthesis, Pt precursor was reduced, and Pt layers were preferentially overgrown on the surface of the preexisting Pd particles resulting in Pd@Pt core-shell particles, which are favorable for ORR. By varying Pt precursors and the amount of Pt deposited, the physicochemical and electrochemical properties of the Pt-Pd catalysts were optimized. The formation of a thin Pt layer on Pd surface is more favorable, when using Pt(NH3)(4)Cl-2 center dot xH(2)O rather than H2PtCl6 center dot xH(2)O. As the amount of Pt increased from 0 to 10%, the surface properties of metal particles changed to similar to that of Pt, and the resulting catalysts mainly consist of a Pt-rich layer with a Pd core such as the Pd@Pt core-shell configuration. Pt(10%)Pd/C catalyst prepared by using Pt(NH3)(4)Cl-2 center dot xH(2)O exhibited a significant improvement in the ORR with the mass activities of 221 and 53 mA/mgpGm at 0.85 and 0.9 V, respectively, which are beatable values compared to those (219 and 59 mA/mg(Pt) at 0.85 and 0.9 V) of commercial Pt/C catalysts. The performance improvement of our bimetallic Pt-Pd/C catalysts mainly originate from the formation of an active Pt surface on the Pd core. In addition, considering that Pd is generally less expensive than Pt, these catalysts should have much better ORR performance and more feasibility of decreasing the total cost of fuel cells. In this study, the characteristics, electrochemical behaviors, and ORR performance improvements of the simply prepared Pt(x)-Pd/C core-shell catalysts were systemically investigated and are discussed. (C) 2016 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 115
页数:7
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