Engineering the Metal/Oxide Interface of Pd Nanowire@CuOx Electrocatalysts for Efficient Alcohol Oxidation Reaction

被引:76
作者
Chen, Zelin [1 ]
Liu, Yunwei [1 ]
Liu, Chang [1 ]
Zhang, Jinfeng [1 ]
Chen, Yanan [1 ]
Hu, Wenbin [2 ]
Deng, Yida [1 ]
机构
[1] Tianjin Univ, Tianjin Key Lab Composite & Funct Mat, Key Lab Adv Ceram & Machining Technol, Minist Educ,Sch Mat Sci & Engn, Tianjin 300372, Peoples R China
[2] Tianjin Univ, Joint Sch Natl Univ Singapore & Tianjin Univ, Int Campus, Fuzhou 350207, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
direct alcohol fuel cells; ethanol oxidation; heterogeneous nanostructures; methanol oxidation; PdCu; CO OXIDATION; MESOPOROUS NANOSPHERES; SELECTIVE OXIDATION; ETHANOL OXIDATION; STACK DESIGN; PALLADIUM; METAL; CATALYST; NANOPARTICLES; NANOSTRUCTURES;
D O I
10.1002/smll.201904964
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of new type electrocatalysts with promising activity and antipoisoning ability is of great importance for electrocatalysis on alcohol oxidation. In this work, Pd nanowire (PdNW)/CuOx heterogeneous catalysts with different types of Pd-O-Cu interfaces (Pd/amorphous or crystalline CuOx) are prepared via a two-step hydrothermal strategy followed by an air plasma treatment. Their interface-dependent performance on methanol and ethanol oxidation reaction (MOR and EOR) is clearly observed. The as-prepared PdNW/crystalline CuOx catalyst with 17.2 at% of Cu on the PdNW surface exhibits better MOR and EOR activity and stability, compared with that of PdNW/amorphous CuOx and pristine PdNW catalysts. Significantly, both the cycling tests and the chronoamperometric measurements reveal that the PdNW/crystalline CuOx catalyst yields excellent tolerance toward the possible intermediates including formaldehyde, formic acid, potassium carbonate, and carbon monoxide generated during the MOR process. The detailed analysis of their chemical state reveals that the enhanced activity and antipoison ability of the PdNW/crystalline CuOx catalyst originates from the electron-deficient Pd delta+ active sites which gradually turn into Pd5O4 species during the MOR catalysis. The Pd5O4 species can likely be stabilized by moderate crystalline CuOx decorated on the surface of PdNW due to the strong Pd-O-Cu interaction.
引用
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页数:9
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