Efficient Alkaline Seawater Oxidation by a Three-dimensional Core-shell Dendritic NiCo@NiFe Layered Double Hydroxide Electrode
Efficient Alkaline Seawater Oxidation by a Three-dimensional Core-shell Dendritic NiCo@NiFe Layered Double Hydroxide Electrode
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DOI:
10.1016/j.mtphys.2022.100841
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发表时间:
2022-09
影响因子:
11.5
通讯作者:
Fanghao Zhang;Yifei Liu;Libo Wu;Minghui Ning;Shaowei Song;X. Xiao;V. Hadjiev;D. Fan;Dezhi Wang;Luo Yu;Shuo Chen;Z. Ren
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文献类型:
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作者:
Fanghao Zhang;Yifei Liu;Libo Wu;Minghui Ning;Shaowei Song;X. Xiao;V. Hadjiev;D. Fan;Dezhi Wang;Luo Yu;Shuo Chen;Z. Ren
Seawater electrolysis for hydrogen generation has received increasing attention recently due to the scarcity of freshwater and the additional prospect of seawater desalination. The development of non-noble-metal-based oxygen evolution reaction (OER) electrocatalysts with high catalytic activity, long-term durability, and high OER selectivity is crucial for large-scale seawater electrolysis but remains a significant challenge. Here we develop a three-dimensional core-shell dendritic catalyst by vertically growing NiFe layered double hydroxide (LDH) nanosheets on dendritic NiCo branches (denoted as NiCo@NiFe LDH). The dendritic NiCo@NiFe LDH is highly active and stable in alkaline seawater due to its large surface area, fast charge transfer and effective mass transfer, and excellent corrosion resistance. It requires only a small overpotential of 222 mV to achieve current densities of 100 mA cm−2in 1 M KOH seawater. To deliver a large current density of 500 mA cm−2, the NiCo@NiFe LDH catalyst requires a record-low overpotential of 266 mV. The nearly 100% OER Faradaic efficiency and the absence of ClO−in the electrolyte following seawater electrolysis indicate the high OER selectivity of our catalyst. The stability of NiCo@NiFe LDH in seawater is proven by its small overpotential fluctuation at a constant current density of 500 mA cm−2over 100 h.