کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5148432 | 1497369 | 2017 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Bifunctional Ni1âxFex layered double hydroxides/Ni foam electrodes for high-efficient overall water splitting: A study on compositional tuning and valence state evolution
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موضوعات مرتبط
مهندسی و علوم پایه
شیمی
الکتروشیمی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Toward both hydrogen (HER) and oxygen evolution reaction (OER) in alkaline electrolyte, bifunctional Ni1âxFex layered double hydroxides (LDHs) on Ni foam (NF) have been systematically developed for high-efficient water splitting by changing Fe content. The interlaced NiFe LDHs nanosheets consist of ultra-small γ-NiOOH-like nanoparticles with size of 2-5 nm interconnected by amorphous domains. By tuning Fe content from 15% to 25% and 36%, optimized μ10 values (μ10 is the overpotential required to reach a current density of 10 mA/cm2) of 169 mV (HER) and 140 mV (OER), and Tafel slope of 31 mV/dec have been achieved at x = 0.25. A hydrogen generation rate of 170 μmol/h/cm2 with H2/O2 ratio nearly to 2:1 and Faradic efficiency of 93% have been realized at 1.7 V by using two Ni0.75Fe0.25 LDHs/NF as respective anode and cathode in a 2-electrode system. Based on the valence state evolution of the electrodes, undergoing respectively H2 and O2 generation, tremendous transformation of NiFe(OH)2 to NiFeOOH is deduced, which reaches a Ni3+/Ni2+ ratio of â¼2.35 for the Fe content of 25%. Further or less Fe incorporation will depress the electrocatalytic property. The effective Ni3+ active sites on the NiFe-based nanosheets endow the Ni0.75Fe0.25 LDHs/NF with high bifunctional catalytic property.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Hydrogen Energy - Volume 42, Issue 8, 23 February 2017, Pages 5560-5568
Journal: International Journal of Hydrogen Energy - Volume 42, Issue 8, 23 February 2017, Pages 5560-5568
نویسندگان
Qingyun Liu, Hao Wang, Xina Wang, Rui Tong, Xiaolong Zhou, Xiaoniu Peng, Hanbin Wang, Hualong Tao, Zhihua Zhang,