层状双氢氧化物
剥脱关节
单层
氢氧化物
材料科学
析氧
层状结构
催化作用
化学工程
氧气
蚀刻(微加工)
纳米技术
石墨烯
化学
图层(电子)
电化学
冶金
电极
有机化学
物理化学
工程类
作者
Yanyong Wang,Yiqiong Zhang,Zhijuan Liu,Chao Xie,Feng Shi,Dongdong Liu,Mingfei Shao,Shuangyin Wang
标识
DOI:10.1002/anie.201701477
摘要
Abstract Layered double hydroxides (LDHs) with two‐dimensional lamellar structures show excellent electrocatalytic properties. However, the catalytic activity of LDHs needs to be further improved as the large lateral size and thickness of the bulk material limit the number of exposed active sites. However, the development of efficient strategies to exfoliate bulk LDHs into stable monolayer LDH nanosheets with more exposed active sites is very challenging. On the other hand, the intrinsic activity of monolayer LDH nanosheets can be tuned by surface engineering. Herein, we have exfoliated bulk CoFe LDHs into ultrathin LDH nanosheets through Ar plasma etching, which also resulted in the formation of multiple vacancies (including O, Co, and Fe vacancies) in the ultrathin 2D nanosheets. Owing to their ultrathin 2D structure, the LDH nanosheets expose a greater number of active sites, and the multiple vacancies significantly improve the intrinsic activity in the oxygen evolution reaction (OER).
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