Hydrangea flower-like nanostructure of dysprosium-doped Fe-MOF for highly efficient oxygen evolution reaction

被引:27
|
作者
Ma, Yan [1 ]
Mu, Guo-Mei [1 ]
Miao, Yu-Jie [1 ]
Lin, Dun-Min [1 ]
Xu, Cheng-Gang [1 ]
Xie, Feng-Yu [1 ]
Zeng, Wen [2 ]
机构
[1] Sichuan Normal Univ, Coll Chem & Mat Sci, Chengdu 610068, Peoples R China
[2] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 401331, Peoples R China
关键词
METAL-ORGANIC FRAMEWORK; BIFUNCTIONAL ELECTROCATALYST; NANOPARTICLES; HYDROGEN; NETWORK;
D O I
10.1007/s12598-021-01851-9
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Developing catalysts with high intrinsic activity toward oxygen evolution reaction (OER) has paramount importance to meet the ever-increasing quest for sustainability demands for green energy solutions but challenging. Herein, a one-step synthesized hydrangea flower-like metal-organic framework (MOF) by dysprosium (Dy)-doped Fe-MOF is reported (Dy0.05Fe-MOF/NF). Impressively, the obtained electrocatalyst possesses optimal OER intrinsic activity, showing a low overpotential of 258 mV at 100 mA·cm−2, superior to the capability of the noble metal RuO2. In addition, an overpotential of 318 mV is needed for Dy0.05Fe-MOF/NF to drive 500 mA·cm−2. The remarkable performance of Dy0.05Fe-MOF/NF can be explained by the surface-active electron density modulation of Fe sites, because the doping of Dy with a lower electronegativity than doping of Fe could donate electrons to the neighboring Fe atoms, resulting in profoundly improved OER performance. Beyond that, this work not only offers a perspective to understand the OER mechanism of rare earth doping, but also guides us to design more ideal electrocatalyst and beyond. Graphic abstract: [Figure not available: see fulltext.] © 2021, Youke Publishing Co.,Ltd.
引用
收藏
页码:844 / 850
页数:7
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