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Carbon nanotubes (CNTs) have received intense and growing interests since the first discovery in 1991 [32]. Structurally, CNTs are rolled-up graphene nanosheets, the ends of which are capped with a hemisphere of a buckyball [33, 34]. CNTs exist either as single-walled or multi-walled CNTs (SWCNTs or MWCNTs), and MWCNTs are composed of a series of concentric SWCNTs with an inter-tube distance of approximately 0.34 nm [35]. Depending on the atomic arrangement of the hexagonal rings (graphene structure) along the tubular surfaces, CNTs can be metallic and/or semiconducting. SWCNTs are generally regarded as a mixture of metallic and semiconducting material, while MWCNTs are metallic conductors [36]. CNTs offer tremendous exciting opportunities for physicists, chemists, biologists, engineers, and material scientists to develop fundamentally novel material systems, better serving the human being in an accelerating and sustainable fashion. Technically, CNTs can be hybridized with a wide spectrum of inorganic compounds such as oxides, nitrides, carbides, and ceramics, in which metal/metal oxides are currently the most widely exploited species due to their high modulus and strength especially at high temperatures. Consequently, CNT–metal/metal oxide NCs (CMNCs) are considered as promising candidates for many potential applications. CMNCs can be tailored to equip qualities such as lightweight (low density), low thermal expansion coefficient, and high thermal conductivity suitable for use in aerospace, automobile, and many other industries. For example, it is projected that applying CNT–Al and CNT–Mg NCs in automobiles would decrease CO₂ emission by 50% per year, based on the report of Japan Automobile Manufacturers Association (JAMA). Prior to introducing the synthesis methods of CMNCs, it is informative to briefly retrieve the methods for preparation of CNTs first. Various approaches such as arc discharge [37], laser ablation [38], gas phase catalytic growth [39], and chemical vapor deposition (CVD) [40–42] have been commonly used to produce CNTs. To prepare CNTs for application in the NCs, the production of large quantities of CNTs is a prerequisite.

Due to the limitations and high costs associated to large-scale production, the arc discharge and laser ablation techniques are not promising. Often, as produced CNTs contain various degrees of impurities such as fragments of wrapped-up graphene sheets, soot, amorphous C, fullerene, and metal catalyst particles [43], thus purification is needed to purify CNTs because these impurities deteriorate the desired and promising properties and performance of CNTs [44]. Given that gas phase techniques such as CVD method can produce large quantities of CNTs with fewer impurities and particularly, they are superior for in situ assembly of metal oxide nanoparticles (NPs) with CNTs, the gas phase techniques hold the greatest potential for scaling-up manufacturing of CNT-based NCs. Alternatively, derivatization of CNTs with other families of organic interlinker molecules particularly biomolecules (e.g., DNA and biotin streptavidin) offer another promising and versatile route in the assembly of CNTs and metal oxide NPs [45, 46]. The advantage of covalent approach is that various well-defined, structurally tunable interlinkers excel in hybridizing metal oxide NPs and CNTs, projecting the flexibility and versatility of this approach. However, as mentioned above, the electronic and mechanical properties of CNTs would be disrupted because sp2-hybridized C atoms are converted to sp3-hybridized analogues after functionalization. Hydrophobic interactions between long chains of aliphatic compounds and CNTs’ hydrophobic surfaces can be used to assemble metal oxide NPs and CNTs. For instances, phosphonic acid- and alkoxysilane-functionalized MWCNTs were templated to hybridize TiO₂ and SiO₂ NPs; and the resulting NCs show great promise in building blocks for sensors, nanoscale switches, and other nanodevices [47]. Surfactants such as sodium dodecyl sulfate (SDS) and Triton X are also powerful binding motifs for connecting metal oxide NPs (e.g., Pd and ZnO) and CNTs [48, 49]. Particularly, a combination of hydrophobic interaction and hydrogen bonding improves the assembly of CNTs and metal oxide NPs. Au NPs (2–5 nm diameter) covered by a mixed-monolayer of decanethiol and mercaptoundecanoic acid were adjoined strongly with acid-treated CNTs containing carboxylic groups [50]. Both hydrophobic interactions arising from alkyl chains and hydrogen bonding due to carboxylic groups contributed to the formation of stable NCs. The major advantage of hydrophobic assembly is that, in some cases, simple and non-specific physical mixing is suffice to obtain desirable CMNCs [51]. CNTs can be modified to capture either negative or positive surface charges through polyelectrolyte or polymer-wrapping, thereby connecting positively or negatively charged NPs via electrostatically attractive interaction. For example, chemically oxidized CNTs were capped with a thin film of cationic poly(diallyldimethylammonium) (PDDA), serving as the template for anchoring the negatively charged Au NPs (10 nm) [52].

Attributed to the robustness of regulation of nucleation and growth processes, electrochemistry is demonstrated as a powerful way for depositing metal NPs onto CNTs directly, especially for noble metals such as Pd [53, 54], Pt [55], Au, Ag, and bimetallic Pt–Co [56] with potential implications in heterogeneous catalysis, electrocatalysis, biosensors, and fuel cells. Typically, metal NPs can attach onto CNTs’ surface via reduction of metal salts (e.g., AuCl⁻, PtCl62⁻, and PdCl42⁻), with the aid of reducing agents such as H₂ [57], NaBH [58], citric acid [59], or ethylene glycol [60]. The size of the resulting metal NPs and their assembly onto CNTs’ surface can be tailored by adjusting reactant concentration, reaction time and temperature, and nucleation potential and voltage, or by introducing surfactants [61]. An earlier review has addressed potential environmental applications of C-based NMs including CNTs and their composites [62]. Deposition of transition metals (e.g., Au, Ni, Pd, Pt, and Ti) has been achieved on perfect and defective MWCNTs via thermal evaporation of different amounts of metals onto the substrates [63]. Other metal and metallic NMs have also been decorated onto CNTs’ surface including Ag, Cu, and PdO [64]. Confinement of other NPs inside CNTs has been reported including Se [65], Co [66, 67], Pd [68], and magnetite [69]. A more comprehensive review has showcased dozens of inorganic compounds used in CMNCs including synthesis methods, and tested and potential applications. Another review has provided a thorough CNT characterization summary and discussion of adsorption mechanisms of organic contaminants by CNTs as well as the statistical adsorption model development efforts. Other reviews have demonstrated the importance of surface modification of CNTs for removal of heavy metals and organics from industry wastes [69–71]. Specific sensors can be developed for detecting specific analytes. A novel nitrite sensor has been developed by electropolymerization of alizarin red on the surface of glassy C electrode modified with MWCNT–Fe₃O₄ composite nanofilm [72].