Multifunctional three-dimensional nanodiamond-nanoporous alumina nanoarchitectures

被引:40
作者
Aramesh, Morteza [1 ]
Fox, Kate [1 ]
Lau, Desmond W. M. [1 ]
Fang, Jinghua [2 ]
Ostrikov, Kostya [2 ,3 ]
Prawer, Steven [1 ]
Cervenka, Jiri [1 ]
机构
[1] Univ Melbourne, Sch Phys, Melbourne, Vic 3010, Australia
[2] CSIRO Mat Sci & Engn, Plasma Nanosci Ctr Australia, Lindfield, NSW 2070, Australia
[3] Univ Sydney, Sch Phys, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会;
关键词
DIAMOND-LIKE CARBON; POLYCRYSTALLINE DIAMOND; FABRICATION; MEMBRANES; COATINGS; NANOSTRUCTURES; NUCLEATION; GROWTH; ARRAYS; FILMS;
D O I
10.1016/j.carbon.2014.04.025
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hybrid composite nanomaterials provide an attractive and versatile material platform for numerous emerging nano- and biomedical applications by offering the possibility to combine diverse properties which are impossible to obtain within a single material. In this work, we present the fabrication of novel hybrid diamond and amorphous diamond-like carbon (DLC) coated nanoporous alumina materials that exhibit multiple functionalities, such as high surface area, quasi-ordered nanopore structure, tunable surface chemistry and electrical conductivity, excellent biological, chemical and corrosion resistance. These multifunctional nanohybrid materials are fabricated using the plasma-induced carbonization method that effectively modifies the surface and the inside of the nanopores of anodic alumina, producing a homogenous ultrathin DLC protecting layer over the whole external and internal surfaces of the membranes. We demonstrate that the interplay between internal and external carbon supply is a critical factor for the formation of the ultrathin sp(3)-bonded carbon layer in the nanopores. This study brings new insights in the DLC growth mechanisms in confined nanospaces and opens new avenues to fabricate hybrid, chemically resistant and biocompatible carbon-coated nanoarchitectures on other inorganic supports. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:452 / 464
页数:13
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