Oxygen-Evolution Catalysts Based on Iron-Mediated Nickel Metal-Organic Frameworks

被引:58
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.
引用
收藏
页码:6334 / +
页数:17
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