纳米片
催化作用
材料科学
4-硝基苯酚
金属
化学工程
色散(光学)
纳米技术
原位
石墨氮化碳
纳米颗粒
选择性催化还原
碳纤维
硝基苯酚
复合数
化学
冶金
复合材料
有机化学
光催化
工程类
物理
光学
作者
Kai Gu,Xueting Pan,Weiwei Wang,Junjie Ma,Yun Sun,Hailong Yang,Heyun Shen,Zhijun Huang,Huiyu Liu
出处
期刊:Small
[Wiley]
日期:2018-07-19
卷期号:14 (33)
被引量:85
标识
DOI:10.1002/smll.201801812
摘要
Abstract Loading novel metal nanosheets onto nanosheet support can improve their catalytic performance, but the morphological incompatibility makes it difficult to construct a well‐contacted interface, which is of particular interest in supported catalysts. Herein, Pd nanosheets (Pd NSs) are supported onto graphitic carbon nitride nanosheets (CNNSs) with intimate face‐to‐face contact through an in situ growth method. This method overcomes the limitations of the morphological incompatibility and ensures the intimate interfacial contact between Pd NSs and CNNSs. The nitrogen‐rich nature of CNNSs endows Pd NSs with abundant anchoring sites, which optimizes the electronic structure and improves the chemical and morphological stability of Pd NSs. The supported Pd NSs demonstrate high dispersion and exhibit largely enhanced activity toward the reduction of 4‐nitrophenol. The concentration‐normalized rate constant is up to 3052 min −1 g −1 L, which is 5.4 times higher than that obtained by unsupported Pd NSs. No obvious deactivation is observed after six runs of the recycling experiments. It is believed that the supported novel metal nanosheets with the intimately contacted interface may show promising applications in catalysis.
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