Mesostructuring layered materials: self-supported mesoporous layered double hydroxide nanotubes

被引:5
|
作者
Morais, Alysson F. [1 ]
Nanclares, Dimy [1 ]
Silva, Ivan G. N. [1 ]
Duarte, Alfredo [2 ]
Garcia, Fernando A. [1 ]
Breynaert, Eric [3 ]
Mustafa, Danilo [1 ]
机构
[1] Univ Sao Paulo, Inst Fis, BR-05508090 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Inst Quim, BR-05508000 Sao Paulo, SP, Brazil
[3] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, B-3001 Leuven, Belgium
基金
巴西圣保罗研究基金会;
关键词
RAY-ABSORPTION SPECTROSCOPY; LANTHANIDE IONS; ROD TRANSITION; LUMINESCENCE; ADSORPTION; ARCHITECTURE; CARBON; LDH; DECOMPOSITION; DELAMINATION;
D O I
10.1039/d1nr02477a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthesis of layered materials exhibiting hierarchical porosity remains challenging, but nevertheless worthwhile because it turns such solids into functional materials with high specific surface area. Using a soft-templating strategy in combination with the incorporation of 8-fold coordinated Eu3+, self-assembly of self-supported layered double hydroxide (LDH) nanotubes has been achieved. Heteromorphic equimolar substitution of Al3+ by Eu3+ in Zn2+/Al3+ LDH solids intercalated with 1,3,5-benzenetricarboxylate anions (BTC) assists precipitation of the double hydroxide layers onto the convex surface of Pluronic (R) P-123 worm-like micelles, yielding multilayer cylinders of BTC-intercalated LDHs. Removal of the micellar template is easily achieved by liquid extraction with methanol, yielding a network of interconnected, well-defined, self-supported, multi-walled, hollow cylindrical nanotubes. Removal of Eu3+ from the synthesis disables formation of the nanotubular morphology, but still yields LDHs containing a network of embedded mesopores, resulting in a specific surface area that is 5-fold higher as compared to standard LDHs.
引用
收藏
页码:11781 / 11792
页数:13
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