析氧
氧化物
电催化剂
材料科学
无定形固体
催化作用
分解水
电解水
结晶度
化学工程
碱性水电解
非晶态金属
电解
无机化学
合金
化学
电化学
冶金
物理化学
光催化
结晶学
电极
复合材料
有机化学
电解质
工程类
作者
Guoyu Shi,Chisato Arata,Donald A. Tryk,Tetsuro Tano,Miho Yamaguchi,Akihiro Iiyama,Makoto Uchida,Kazuo Iida,Sumitaka Watanabe,Katsuyoshi Kakinuma
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-03-29
卷期号:8 (14): 13068-13077
被引量:52
标识
DOI:10.1021/acsomega.3c00322
摘要
The rational design of efficient and low-cost electrocatalysts based on earth-abundant materials is imperative for large-scale production of hydrogen by water electrolysis. Here we present a strategy to prepare highly active catalyst materials through modifying the crystallinity of the surface/interface of strongly coupled transition metal-metal oxides. We have thermally activated the catalysts to construct amorphous/crystalline Ni-Fe oxide interfaced with a conductive Ni-Fe alloy and systematically investigated their electrocatalytic performance toward the hydrogen evolution and oxygen evolution reactions (HER and OER) in alkaline solution. It was found that the Ni-Fe/oxide material with a crystalline surface oxide phase showed remarkably superior HER activity in comparison with its amorphous or poorly crystalline counterpart. In contrast, interestingly, the amorphous/poorly crystalline oxide significantly facilitated the OER activity in comparison with the more crystalline counterpart. On one hand, the higher HER activity can be ascribed to a favorable platform for water dissociation and H-H bond formation, enabled by the unique crystalline metal/oxide structure. On the other hand, the enhanced OER catalysis on the amorphous Ni-Fe oxide surfaces can be attributed to the facile activation to form the active oxyhydroxides under OER conditions. Both are explained based on density functional theory calculations. These results thus shed light onto the role of crystallinity in the HER and OER catalysis on heterostructured Ni-Fe/oxide catalysts and provide guidance for the design of new catalysts for efficient water electrolysis.
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