共 34 条
Pd/WO3/C nanocomposite with APTMS-functionalized tungsten oxide nanosheet for formic acid electrooxidation enhancement
被引:10
|作者:
Yang, Yang
[1
]
Li, Yun-Hua
[1
]
Zhao, Ya-Fei
[1
]
Li, Peng-Wei
[1
]
Li, Qiao-Xia
[1
]
机构:
[1] Shanghai Univ Elect Power, Coll Environm & Chem Engn, Shanghai Key Lab Mat Protect & Adv Mat Elect Powe, 2588 Changyang Rd, Shanghai 200090, Peoples R China
基金:
美国国家科学基金会;
关键词:
Pd/WO3/C nanocomposite;
APTMS-functionalized tungsten oxide nanosheets;
Electrocatalyst;
Formic acid oxidation reaction;
Hydrogen storage;
CARBON-SUPPORTED PD;
ETHANOL ELECTROOXIDATION;
ALKALINE MEDIA;
FUEL-CELL;
ELECTROCHEMICAL OXIDATION;
EFFICIENT CATALYST;
DOPED CARBON;
NANOPARTICLES;
PALLADIUM;
ELECTROCATALYSTS;
D O I:
10.1007/s11051-017-4116-z
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A Pd/WO3/C nanocomposite with 3-aminopropyltrimethoxysilane (APTMS)-functionalized tungsten oxide nanosheets (Pd/WO3/C-APTMS) was synthesized and applied as the efficient anode catalyst for direct formic acid fuel cells (DFAFCs). The mechanism for synthesizing the nanocomposite is as follows: initially, [PdCl4](2-) was assembled onto the tungsten oxide nanosheets modified with APTMS. Following this, Pd nanoparticles were reduced via traditional impregnation reduction of [PdCl4](2-) with NaBH4. The transmission electron microscope (TEM) images revealed that the Pd nanoparticles were uniformly dispersed on WO3 nanosheets and were approximately 2.7 nm in size. The electrochemical test results showed that enhanced electrocatalytic activity for the formic acid oxidation reaction (FAOR) was obtained on the Pd/WO3/C catalyst compared with Pd/C. The higher electrocatalytic activity might be attributed to the uniform distribution of Pd with smaller particles. Furthermore, it is likely that the improvement in catalytic stability for the Pd/WO3/C catalyst is due to the hydrogen spillover effect of WO3 particles. These results indicate that this novel Pd/WO3/C-APTMS nanocomposite exhibits promising potential for use as an anode electrocatalyst in DFAFCs.
引用
收藏
页数:8
相关论文