硝基苯
材料科学
催化作用
纳米结构
偶氮苯
氧化还原
制作
纳米材料基催化剂
无定形固体
化学工程
纳米技术
有机化学
纳米颗粒
化学
医学
聚合物
替代医学
病理
工程类
冶金
复合材料
作者
Jian Li,Shuyan Song,Long Yan,Lanlan Wu,Xiao Wang,Yan Xing,Rongchao Jin,Xiaogang Liu,Hongjie Zhang
标识
DOI:10.1002/adma.201704416
摘要
Abstract Due to the obvious distinctions in structure, core–shell nanostructures (CSNs) and yolk–shell nanostructures (YSNs) exhibit different catalytic behavior for specific organic reactions. In this work, two unique autoredox routes are developed to the fabrication of CeO 2 ‐encapsulated Au nanocatalysts. Route A is the synthesis of well‐defined CSNs by a one‐step redox reaction. The process involves an interesting phenomenon in which Ce 3+ can act as a weak acid to inhibit the hydrolysis of Ce 4+ under the condition of OH − shortage. Route B is the fabrication of monodispersed YSNs by a two‐step redox reaction with amorphous Co 3 O 4 as an in situ template. Furthermore, the transfer coupling of nitrobenzene is chosen as a probe reaction to investigate their catalytic difference. The CSNs can gradually achieve the conversion of nitrobenzene into azoxybenzene, while the YSNs can rapidly convert nitrobenzene into azobenzene. The different catalytic results are mainly attributed to their structural distinctions.
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