氢氧化物
析氧
碱性水电解
催化作用
分解水
层状双氢氧化物
电解
镍
电解质
电解水
化学工程
材料科学
化学
无机化学
电化学
冶金
电极
物理化学
工程类
生物化学
光催化
作者
Kyoung Ryeol Park,Jaeeun Jeon,Heechae Choi,Junho Lee,Dong‐Ha Lim,Nuri Oh,HyukSu Han,Cheol Hyoun Ahn,Bae-Jung Kim,Sungwook Mhin
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2022-07-08
卷期号:5 (7): 8592-8600
被引量:30
标识
DOI:10.1021/acsaem.2c01115
摘要
Alkaline electrolysis is one of the most promising among gas-to-power technologies to produce hydrogen energy where the oxygen evolution reaction (OER) plays an important role. It has recently been demonstrated that the OER activity of layered double hydroxide (LDH) could be enhanced by accommodating more abundant active sites that offer optimal binding energies between intermediates. Here, we report a study of nickel iron layered double hydroxides by varying the Ni:Fe atomic ratio of the Ni1–xFex-LDH to induce changes to their physiochemical properties through which the optimum OER performance is determined. Optimized NiFe-LDH-38 (Ni0.62Fe0.38LDH) shows an excellent OER performance in alkaline electrolyte, demonstrating a potential of 1.45 V (vs RHE) at 100 mA cm–2, which outperforms the commercial RuO2 catalyst. Also, computational simulations support the OER performance of the single NiFe-LDH phase (NF-LDH-38). This work provides not only a fundamental understanding of the effect of the Ni:Fe atomic ratio of the Ni1–xFex-LDHs on OER performance but also the design strategy of low-cost, earth abundant, and active electrocatalysts toward water oxidation.
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