Orientation-Adjustable Metal-Organic Framework Nanorods for Efficient Oxygen Evolution Reaction

被引:25
|
作者
Xu, Zichen [1 ]
Yeh, Chia-Lin [2 ]
Jiang, Yuanjuan [1 ]
Yun, Xinru [1 ]
Li, Chun-Ting [3 ]
Ho, Kuo-Chuan [2 ,4 ]
Lin, Jiann T. [5 ]
Lin, Ryan Yeh-Yung [1 ]
机构
[1] Dalian Univ Technol, Zhang Dayu Sch Chem, State Key Lab Fine Chem, Dalian 116024, Liaoning, Peoples R China
[2] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
[3] Natl Taiwan Normal Univ, Dept Chem, Taipei 11677, Taiwan
[4] Natl Taiwan Univ, Adv Res Ctr Green Mat Sci & Technol, Inst Polymer Sci & Engn, Taipei 10617, Taiwan
[5] Acad Sinica, Inst Chem, Taipei 11529, Taiwan
基金
中国国家自然科学基金;
关键词
metal-organic framework; 1D nanorods; oxygen evolution reaction; orientation; solvent compositions; ALPHA-FEOOH; ARRAYS; ELECTROCATALYSTS; PERFORMANCE; NANOSHEETS; GAS; CO; REDUCTION; CATALYST; STORAGE;
D O I
10.1021/acsami.1c05944
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A series of orientation-adjustable metal-organic framework (MOF) nanorods, CoFe(dobpdc)-I to CoFe(dobpdc)-III (dobpdc = 4,4'-dihydroxybiphenyl-3,3'-dicarboxylate), is developed on a 3D nickel foam (NF) template. By modulating the solvent composition for synthesis, the feature of MOF nanorods on the template can be varied from disorganized to a unidirectional orientation perpendicular to the NF. Well-aligned, vertically oriented CoFe(dobpdc)-III nanorods are hydrophilic and have more exposed active sites and interfacial charge transfer ability. Consequently, they exhibit a superior activity for oxygen evolution reaction (OER) with ultralow overpotentials of 176 and 240 mV at 10 and 300 mA cm(-2) in 1.0 M KOH (aq), respectively. CoFe(dobpdc)-III also shows a record low overpotential of 204 mV at J(10) mA cm(-2) among the electrocatalysts based on CoFe MOF and an excellent overpotential at a high current density (100 mA cm(-2)) of 312 mV in 0.1 M KOH (aq). This is the first report of a convenient method to straighten up MOF nanorods on a template for highly efficient OER.
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页码:28242 / 28251
页数:10
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