金属间化合物
纳米结构
高熵合金
催化作用
材料科学
析氧
氧化物
化学工程
陶瓷
无定形固体
纳米孔
纳米技术
电化学
冶金
化学
电极
有机化学
工程类
物理化学
生物化学
合金
作者
Zhaoyi Ding,Juanjuan Bian,Shuo Shuang,Xiaodi Liu,Yuan‐Chao Hu,Chunwen Sun,Yong Yang
标识
DOI:10.1002/adsu.201900105
摘要
Abstract Designing active, stable, yet low cost electrocatalysts for the oxygen evolution reaction (OER) is pivotal to the next generation energy storage technology. However, conventional OER catalysts are of low electrochemical efficiency while the state‐of‐the‐art nanoparticle‐based catalysts require mechanical supports, thereby limiting their wide deployment. Here, it is demonstrated that, due to the excellent corrosion resistance of the Fe–Co–Ni–Cr–Nb high entropy intermetallic Laves phase, fabricating a high entropy bulk porous nanostructure is possible by dealloying the corresponding eutectic alloy precursor. As a result, a core–shell nanostructure with amorphous high entropy oxide ultrathin films wrapped around the nanosized intermetallic ligaments is obtained, which together, exhibits an extraordinarily large active surface area, fast dynamics, and superb long‐term durability, outperforming the existing alloy‐ and ceramic‐based OER electrocatalysts. The outcome of the research suggests that the paradigm of “high entropy” design can be used to develop high performance catalytic materials.
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