纳米网
材料科学
纳米孔
析氧
分解水
催化作用
氢氧化物
氧化还原
电化学
纳米技术
化学工程
相(物质)
镍
多孔性
电极
石墨烯
冶金
复合材料
物理化学
光催化
有机化学
化学
工程类
生物化学
作者
Junfeng Xie,Jianping Xin,Ruoxing Wang,Xiaodong Zhang,Fengcai Lei,Haichao Qu,Pin Hao,Guanwei Cui,Bo Tang,Yi Xie
出处
期刊:Nano Energy
[Elsevier]
日期:2018-08-21
卷期号:53: 74-82
被引量:103
标识
DOI:10.1016/j.nanoen.2018.08.045
摘要
Herein, abundant and uniform nanopores with sub-3-nm sizes are introduced to 1.5 nm-thick nickel-iron layered double hydroxide (NiFe LDH) ultrathin nanosheets via an etching-aging process, realizing remarkable enhancement in oxygen evolution reaction (OER) performance. Detailed analyses revealed that the NiFe LDH phase around the nanopores can be preferentially oxidized into electroactive Fe:NiOOH phase. In addition, the buffering space provided by the nanopores can effectively avoid structural deformation during repeated redox cycling, leading to better electrochemical stability, which synergistically make the catalyst a promising candidate for commercial water splitting. This work highlights the positive role of porous structure in accelerating the formation of active phases beyond just increment of surface area, which can provide insight in designing advanced catalysts.
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