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Oxygen-Evolution Catalysts Based on Iron-Mediated Nickel Metal-Organic Frameworks
被引:55
|作者:
Wan, Zixia
[1
]
Yang, Dandan
[1
]
Chen, Judan
[1
]
Tian, Jianniao
[1
]
Isimjan, Tayirjan Taylor
[2
]
Yang, Xiulin
[1
]
机构:
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, Guangxi Key Lab Low Carbon Energy Mat, Guilin 541004, Peoples R China
[2] KAUST, SABIC, Thuwal 239556900, Saudi Arabia
基金:
中国国家自然科学基金;
关键词:
oxygen-evolution reaction;
Fe-mediated Ni-organic framework;
hierarchical structure;
hydrolysis;
coupling effect;
NANOSHEET ARRAYS;
CARBON NANOTUBES;
WATER;
OXIDE;
ELECTROCATALYST;
EFFICIENCY;
STATES;
D O I:
10.1021/acsanm.9b01330
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Metal-organic frameworks (MOFs) based oxygen-evolution reaction (OER) catalyst is an emerging class of highly porous materials that have become increasingly attractive to develop a highly active and stable OER catalyst for overall water splitting. However, it suffers from poor conductivity and inadequate active sites. Herein, we have developed a series of hierarchical Fe-mediated Ni-based metal-organic frameworks (FexNi1-x-MOF) by an adjustable hydrolysis strategy, where the Ni-MOF is used as a template that is decorated with NiOOH active sites. Although Ni-MOF is dissociated during the ion exchange process, the structural integrity is kept for FexNi1-x-MOF as confirmed by the electron micrographs. Moreover, the optimized Fe0.38Ni0.62-MOF catalyst not only exhibits a remarkable OER catalytic performance with a low overpotential of 190 mV at 10 mA cm(-2) but also shows a small Tafel slope of 58.3 mV dec(-1) and stability. The excellent OER electrocatalytic activity can be attributed to the unique 3D flower-like structure decorated with NiOOH active sites induced by Fe3+ species. This novel methodology expands a new way for the construction of highly efficient alkaline catalytic materials.
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页码:6334 / +
页数:17
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