Gyroidal mesoporous multifunctional nanocomposites via atomic layer deposition

被引:23
|
作者
Werner, Joerg G. [1 ]
Scherer, Maik R. J. [2 ]
Steiner, Ullrich [2 ]
Wiesner, Ulrich [1 ]
机构
[1] Cornell Univ, Dept Mat Sci & Engn, Ithaca, NY 14853 USA
[2] Univ Cambridge, Cavendish Lab, Dept Phys, Cambridge CB3 0HE, England
关键词
NANOSTRUCTURED MATERIALS; STORAGE; ENERGY; STABILITY; ANATASE; TIO2;
D O I
10.1039/c4nr01948b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We demonstrate the preparation of rationally designed, multifunctional, monolithic and periodically ordered mesoporous core-shell nanocomposites with tunable structural characteristics. Three-dimensionally (3D) co-continuous gyroidal mesoporous polymer monoliths are fabricated from a solution-based triblock terpolymer-resol co-assembly and used as the functional templates for the fabrication of free-standing core-shell carbon-titania composites using atomic layer deposition (ALD). The deposition depth into the torturous gyroidal nanonetwork is investigated as a function of ALD conditions and the resulting composites are submitted to different thermal treatments. Results suggest that ALD can homogenously coat mesoporous templates with well defined pore sizes below 50 nm and thicknesses above 10 mu m. Structural tunability like titania shell thickness and pore size control is demonstrated. The ordered nanocomposites exhibit triple functionality; a 3D continuous conductive carbon core that is coated with a crystalline titania shell that in turn is in contact with a 3D continuous mesopore network in a compact monolithic architecture. This materials design is of interest for applications including energy conversion and storage. Gyroidal mesoporous titania monoliths can be obtained through simultaneous titania crystallization and template removal in air.
引用
收藏
页码:8736 / 8742
页数:7
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