Synergistically boosting the oxygen evolution reaction activity of NiOOH nanosheets by Fe doping

被引:3
|
作者
Ahmad, Fawad [1 ]
Ali, Asad [2 ,3 ,4 ]
Qin, Jiaqian [2 ,4 ]
机构
[1] Univ Wah, Dept Chem, Quaid Ave, Wah Cantt 47010, Punjab, Pakistan
[2] MOE Key Lab New Proc Technol Nonferrous Met & Mat, Collaborat Innovat Ctr Sustainable Energy Mat, State Key Lab Proc Nonferrous Met & Featured Mat, Nanning 530004, Guangxi, Peoples R China
[3] Guangxi Univ, Nanning 530004, Peoples R China
[4] Chulalongkorn Univ, Met & Mat Sci Res Inst, Bangkok 10330, Thailand
关键词
OER; Doping; Nanotechnology; Electrocatalyst; 2-DNixFexOOH; ELECTROCATALYSIS; XPS;
D O I
10.1016/j.rechem.2023.100808
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical water splitting to generate oxygen and hydrogen is a key process for several energy storage and conversion devices. Developing low-cost, robust, efficient, and earth-abundant electrochemical catalysts for the oxygen evolution reaction (OER) is therefore holding a paramount position. Herein, we report the doping process to prepare two-dimensional Fe-doped NiOOH nanosheets with the tuneable molar ratio of Fe ranging from 0 to 0.4 by using a single-pot synthetic approach. Among the obtained nanomaterials, the Ni0.7Fe0.3OOH nanosheets/ C exhibited greatly enhanced electrocatalytic performance toward OER in alkaline media (1.0 M KOH), with an overpotential of 265 mV to afford 10 mA cm-2 current density. The current density produced at fixed over -potential (300 mV) for Ni0.7Fe0.3OOH was 56.5 mA cm-2 which was 22.6, 6.27, 4.18 and 5.13 times higher than those of NiOOH, Ni0.9Fe0.1OOH, Ni0.8Fe0.2OOH and Ni0.6Fe0.4OOH nanosheets /C, respectively. Moreover, the nanosheets were able to retain excellent performance for over 15 h without obvious degradation. The Tafel slope for Ni0.7Fe0.3OOH was 44.8 mV/decade. Therefore, this approach has opened a new possibility for designing highly efficient catalyst-based active sites.
引用
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页数:6
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