Component-dependent electrocatalytic activity of PdCu bimetallic nanoparticles for hydrogen evolution reaction

被引:58
作者
Zhang, Xing [1 ]
Wu, Dengfeng [1 ]
Cheng, Daojian [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing Key Lab Energy Environm Catalysis, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
PdCu bimetallic nanoparticles; hydrogen evolution reaction; Pt-free electrocatalysts; CATALYTIC-ACTIVITY; CARBON NANOTUBES; GRAPHENE; PALLADIUM; ELECTRODE; ENERGY; FABRICATION; COMPOSITES; MOLYBDENUM; COPPER;
D O I
10.1016/j.electacta.2017.06.076
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The development of high efficient electrocatalysts in water electrolysis is of great importance for sustainable hydrogen production. Herein, monodispersed bimetallic PdxCu100-x nanoparticles with average size about 4.7 nm are prepared by a one-pot method in oleylamine medium. Electrochemical measurements toward hydrogen evolution reaction (HER) indicate that both the activity and stability of carbon black loaded PdxCu(100-x) nanoparticles (PdxCu100-x/C) are highly dependent on the Pd/Cu atomic ratios. Among these electrocatalysts, Pd71Cu29/C exhibits the best electrocatalytic activity in terms of onset potential (75 mV vs. RHE), exchange current density (0.38 mA cm(-2)) and Tafel slope (48 mV dec(-1)) in 0.1 M H2SO4 among these nanoparticles. It is found that the activity toward HER of Pd71Cu29/C is better than that of commercial Pd/C and most of Pd-based electrocatalysts ever reported before. Moreover, Pd71Cu29/C shows superior catalytic stability to the commercial Pt/C. The superior HER activities and high durability (after 1000 CV cycles) of Pd71Cu29/C should be attributed to small size, the synergy effect between Cu and Pd. This work provides a facile strategy to develop the effective and stable Pt-free electrocatalyst for hydrogen generation. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:572 / 579
页数:8
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