4.7 Article

Preferential Adsorption of Hydroxide Ions onto Partially Crystalline NiFe-Layered Double Hydroxides Leads to Efficient and Selective OER in Alkaline Seawater

Journal

ACS APPLIED ENERGY MATERIALS
Volume 4, Issue 5, Pages 4630-4637

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.1c00262

Keywords

seawater electrocatalysis; alkaline water splitting; oxygen evolution reaction; chloride adsorption; NiFe-layered double hydroxide

Funding

  1. Natural Science Foundation of Shandong Province of China [ZR2019QB007]
  2. Nature Science Foundation of China [21802051, 21906065]
  3. Shandong Provincial Program of Talent-Leading Teams

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A NiFe-LDH catalyst with partially crystalline characteristics was synthesized, showing high catalytic activity and stability during seawater electrolysis. The presence of more boundaries in the partially crystalline NiFe-LDH contributes to its higher catalytic efficiency and stability in alkalized seawater.
A variety of compounds, including Ni-, Fe-, and Co-containing layered double hydroxides (LDHs), have been explored as catalysts for the oxygen evolution reaction (OER). However, few can meet the industrially mandated overpotential of 0.30 V at 500 mA/cm(2) and cell voltage of 1.60 V, let alone be applied to electrolysis of seawater. We synthesized a nickel foam (NF)-supported NiFe-LDH whose OER overpotential is only 0.257 V at 500 mA/cm(2) in an alkaline saline solution and requires a cell voltage of 1.54 V for the same current density when coupled with a MoNi4/MoO2/NF cathode for electrolyzing alkalized seawater. The NiFe-LDH catalyst comprises numerous nanometer-sized crystalline facets surrounded by an amorphous phase, in contrast to its highly crystalline counterpart. X-ray photoelectron spectroscopy reveals that the boundaries separating crystalline facets and amorphous phase contain more Ni3+ than other areas. Anion chromatographic analysis indicates that OH- adsorbs preferentially over Cl- onto the sites of Ni3+ of both partially and highly crystalline NiFe-LDHs, whereas Cl- adsorbs more extensively onto the crystalline planes or facets. These adsorption behaviors and the resultant different catalytic activities at high current densities can be readily rationalized by the Pearson's hard-soft acid-base principle. Because more boundaries exist in the partially crystalline NiFe-LDH, the partially crystalline NiFe-LDH catalyst is not only more catalytically efficient than its highly crystalline counterpart and other catalysts reported up to the present, but it is also stable in alkalized seawater and unaffected by Cl- adsorption.

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