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Templated growth of carbon nanotubes with controlled diameters using organic-organometallic block copolymers with tailored block lengths

机译:使用具有特定嵌段长度的有机-有机金属嵌段共聚物,对直径受控的碳纳米管进行模板生长

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摘要

Block copolymer thin films fabricated from polystyrene-polyferrocenylsilane (PS-b-PFS) block copolymers on silicon substrates were used as precursors of well-ordered, nanosized growth catalysts for carbon nanotubes (CNTs). The size of the catalytic domains was tuned by changing the molecular weight of the block copolymer, enabling control of the diameter of the CNTs grown from these substrates. CNT growth on catalytic substrates with larger organometallic domain sizes, using acetylene as a carbon source, resulted in enhanced amounts of CNT deposition compared to smaller PFS domains, which exhibited low catalytic activity. The inner and outer diameters of the multi-walled CNTs obtained were typically 8 and 16 nm, respectively, and were not influenced by the catalytic domain sizes. Various annealing strategies in inert or in hydrogen atmosphere were investigated. The use acetylene with an additional hydrogen flow as gas feed resulted in a significant increase in deposition on all PS-b-PFS decorated substrates. Under these conditions, the CNT diameters could be controlled by the catalyst domain sizes, resulting in decreasing diameters with decreasing domain sizes. Multiwalled CNTs with inner and outer diameters of 4 and 7 nm, respectively, and a narrow diameter distribution were obtained.
机译:由聚苯乙烯-聚二茂铁基硅烷(PS-b-PFS)嵌段共聚物在硅基底上制成的嵌段共聚物薄膜用作碳纳米管(CNT)的有序纳米尺寸生长催化剂的前体。通过改变嵌段共聚物的分子量来调节催化域的大小,从而能够控制从这些底物生长的CNT的直径。与较小的PFS域相比,使用乙炔作为碳源,CNT在具有较大有机金属畴尺寸的催化基材上的生长导致CNT沉积量的增加,而较小的PFS域则表现出较低的催化活性。所获得的多壁CNT的内径和外径通常分别为8nm和16nm,并且不受催化域尺寸的影响。研究了惰性或氢气气氛中的各种退火策略。使用乙炔和额外的氢气流作为气体进料会导致在所有PS-b-PFS装饰的基材上的沉积显着增加。在这些条件下,CNT直径可通过催化剂畴尺寸来控制,从而导致直径随着畴尺寸的减小而减小。获得了分别具有4和7nm的内径和外径的窄壁CNT。

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