过电位
析氧
掺杂剂
材料科学
兴奋剂
化学工程
过渡金属
催化作用
价(化学)
纳米晶
密度泛函理论
电化学
化学
纳米技术
物理化学
光电子学
计算化学
有机化学
工程类
生物化学
电极
作者
Byeongyoon Kim,Mrinal Kanti Kabiraz,Jaewan Lee,Changhyeok Choi,Hionsuck Baik,Yousung Jung,Hyung‐Suk Oh,Sang‐Il Choi,Kwangyeol Lee
出处
期刊:Matter
[Elsevier]
日期:2021-11-01
卷期号:4 (11): 3585-3604
被引量:39
标识
DOI:10.1016/j.matt.2021.09.003
摘要
The layered transition metal oxyhydroxides have received increasing interest owing to the efficient energy conversion performance and material stability during the oxygen evolution reaction (OER). In particular, Fe-doped NiOOH has shown record-high OER performance in alkaline media among various catalysts. Theoretically, undercoordinated facets including Ni4+, exposed at the edges of NiOOH, were predicted to perform highly active OER. Therefore, here we suggest a rational catalyst design, a vertical-crystalline β-Fe/NiOOH layer built on faceted Fe/Ni nanocrystals, which exposes Ni4+ sites and could improve the OER performance dramatically. Electrochemical OER tests recorded the overpotential of 210 mV at a current density of 10 mA cm−2GEO and stable operation for 5 days. In situ/operando and density functional theory studies revealed that the Ni valence cycle between +2 and +4 assisted by Fe dopant is the key engine that greatly accelerates OER kinetics and that the vertical-crystalline β-Fe/NiOOH layers on Ni octahedra are stable under harsh OER conditions.
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