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氨对化学气相沉积和碳纳米管成核机制的影响。

Effect of ammonia on chemical vapour deposition and carbon nanotube nucleation mechanisms.

机构信息

Newcastle Institute for Energy and Resources, The University of Newcastle, Callaghan, 2308 NSW, Australia.

出版信息

Nanoscale. 2017 Jan 26;9(4):1727-1737. doi: 10.1039/c6nr08222j.

Abstract

Chemical vapour deposition (CVD) growth of carbon nanotubes is currently the most viable method for commercial-scale nanotube production. However, controlling the 'chirality', or helicity, of carbon nanotubes during CVD growth remains a challenge. Recent studies have shown that adding chemical 'etchants', such as ammonia and water, to the feedstock gas can alter the diameter and chirality of nanotubes produced with CVD. To date, this strategy for chirality control remains sub-optimal, since we have a poor understanding of how these etchants change the CVD and nucleation mechanisms. Here, we show how ammonia alters the mechanism of methane CVD and single-walled carbon nanotube nucleation on iron catalysts, using quantum chemical molecular dynamics simulations. Our simulations reveal that ammonia is selectively activated by the catalyst, and this enables ammonia to play a dual role during methane CVD. Following activation, ammonia nitrogen removes carbon from the catalyst surface exclusively via the production of hydrogen (iso)cyanide, thus impeding the growth of extended carbon chains. Simultaneously, ammonia hydrogen passivates carbon dangling bonds, which impedes nanotube nucleation and promotes defect healing. Combined, these effects lead to slower, more controllable nucleation and growth kinetics.

摘要

化学气相沉积(CVD)生长碳纳米管是目前最可行的商业规模生产纳米管的方法。然而,在 CVD 生长过程中控制碳纳米管的“手性”或螺旋性仍然是一个挑战。最近的研究表明,向原料气中添加化学“蚀刻剂”,如氨和水,可以改变 CVD 产生的纳米管的直径和手性。迄今为止,这种手性控制策略仍然不是最佳的,因为我们对这些蚀刻剂如何改变 CVD 和成核机制的了解还很有限。在这里,我们使用量子化学分子动力学模拟展示了氨如何改变甲烷 CVD 和铁催化剂上单壁碳纳米管成核的机制。我们的模拟表明,氨被催化剂选择性地激活,这使得氨在甲烷 CVD 过程中可以发挥双重作用。氨氮在激活后通过产生氢(异)氰酸酯将碳原子从催化剂表面上唯一地除去,从而阻碍了扩展碳链的生长。同时,氨氢使碳悬空键失活,从而阻碍了纳米管的成核并促进了缺陷的愈合。这些效应结合起来导致了更慢、更可控的成核和生长动力学。

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