陆安慧

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教授

博士生导师

硕士生导师

主要任职:校长助理

其他任职:精细化工国家重点实验室副主任,辽宁省低碳资源高值化利用重点实验室主任

性别:男

毕业院校:中科院山西煤化所

学位:博士

所在单位:化工学院

学科:工业催化. 化学工艺. 能源化工

办公地点:大连市凌工路2号大连理工大学西部校区化工楼,邮编:116024

联系方式:0411-84986112

电子邮箱:anhuilu@dlut.edu.cn

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Weak Acid-Base Interaction Induced Assembly for the Synthesis of Diverse Hollow Nanospheres

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论文类型:期刊论文

发表时间:2011-10-25

发表刊物:CHEMISTRY OF MATERIALS

收录刊物:Scopus、SCIE、EI

卷号:23

期号:20

页面范围:4537-4542

ISSN号:0897-4756

关键字:carbon; colloidal catalyst; hollow nanospheres; hydrothermal synthesis; weak acid-base interaction

摘要:We have established a novel and generalizable hydrothermal synthesis for diverse hollow nanospheres, which cover polymer, carbon, graphitic carbon, and metal-doped carbon hollow nanospheres. The synthesis principle is based on the weak acid-base interaction (COO(-)/NH(4)(+)/-COO(-)) induced assembly. That is, the ammonium cations from the reactant ammonia act as a trigger for the assembly of COO(-) group-containing polymer around surfactant oleic acid micelles through the weak interaction between carboxylate anion and ammonium ion. Consequently, hollow polymer nanospheres (HPSs) with diameters ranging from 100 to 200 nm and hollow core sizes ranging from 30 to 80 nm can be synthesized. It was determined that approximately 61% of the added amount of NH(3) participates is retained in the HPS product. Taking these HPSs as the precursor, hollow carbon nanospheres (HCSs) with tunable surface areas can be obtained by varying the preparation conditions. More importantly, owing to the presence of the COO(-) functional groups, a wide range of metal cations (e.g., Fe(3+) and Ag(+)) can be successfully introduced into these HPSs, so that they can then be converted to hollow graphitized nanospheres and Ag-doped catalytically active HCSs.