催化作用
酯交换
碳酸二甲酯
甲醇
基础(拓扑)
碳酸乙烯酯
材料科学
石墨烯
氧化还原
无机化学
化学工程
化学
纳米技术
有机化学
物理化学
电极
工程类
数学分析
数学
电解质
作者
Song‐Song Peng,Yao Nian,Xing-Ru Song,Xiang‐Bin Shao,Chen Gu,Zhi‐Wei Xing,Shi‐Chao Qi,Peng Tan,You Han,Xiao‐Qin Liu,Lin‐Bing Sun
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-02-07
卷期号:17 (6): 4979-4985
被引量:11
标识
DOI:10.1007/s12274-024-6506-8
摘要
Solid strong base catalysts have received considerable attention in various organic reactions due to their facile separation, neglectable corrosion, and environmental friendliness. Although great progress has been made in the preparation of solid strong base catalysts, it is still challenging to avoid basic sites aggregation on support and active sites loss in reaction system. Here, we report a tandem redox strategy to prepare Na single atoms on graphene, producing a new kind of solid strong base catalyst (Na1/G). The base precursor NaNO3 was first reduced to Na2O by graphene (400 °C) and successively to single atoms Na anchored on the graphene vacancies (800 °C). Owing to the atomically dispersed of basicity, the resultant catalyst presents high activity toward the transesterification of methanol and ethylene carbonate to synthesize dimethyl carbonate (turnover frequency (TOF) value: 125.7 h−1), which is much better than the conventional counterpart Na2O/G and various reported solid strong bases (TOF: 1.0–90.1 h−1). Furthermore, thanks to the basicity anchored on graphene, the Na1/G catalyst shows excellent durability during cycling. This work may provide a new direction for the development of solid strong base catalysts.
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