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Supercapacitor performance of nitrogen-doped carbon nanotube arrays

机译:氮掺杂碳纳米管阵列的超级电容器性能

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摘要

Arrays of nitrogen-doped carbon nanotubes (N-CNTs) have been grown on Si substrates by thermolysis of vapors of acetonitrile and ferrocene. To change the content of incorporating nitrogen, carbonyls of Mo, W, and Cr were added in the reaction mixture. The products were comparatively studied using electron microscopy, Raman scattering, X-ray photoelectron spectroscopy, and charge/discharge cycling in an acidic electrolyte. Electrochemical characteristics of N-CNTs were correlated with nanotube length and chemical state of nitrogen. It is found that pyridinic nitrogen has determining effect on the N-CNT performance at low scan rates of potential. The density functional theory calculations of N-CNT models reveal that protonation of pyridinic nitrogen induces a net of negative charges on the neighboring carbon atoms that could increase the electrode capacitance. Cyclic voltammogram of nitrogen-doped carbon nanotube array at a scan rate of 2mVs~(-1) in a 1M H_2SO_4 aqueous solution and possible assignment of redox peaks.
机译:氮掺杂的碳纳米管(N-CNT)的阵列已通过乙腈和二茂铁蒸气的热解在Si衬底上生长。为了改变氮的掺入量,将Mo,W和Cr的羰基加入反应混合物中。使用电子显微镜,拉曼散射,X射线光电子能谱和在酸性电解质中的充电/放电循环对产品进行了比较研究。 N-CNT的电化学特性与纳米管长度和氮的化学状态相关。发现吡啶二氮在低电位扫描速率下对N-CNT性能具有决定性影响。 N-CNT模型的密度泛函理论计算表明,吡啶氮的质子化会在相邻的碳原子上感应出一个负电荷网,这可能会增加电极电容。氮掺杂碳纳米管阵列在1M H_2SO_4水溶液中的扫描速率为2mVs〜(-1)的循环伏安图和氧化还原峰的可能归属。

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