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多壁碳纳米管的声化学氧化

Sonochemical oxidation of multiwalled carbon nanotubes.

作者信息

Xing Yangchuan, Li Liang, Chusuei Charles C, Hull Robert V

机构信息

Departments of Chemical & Biological Engineering and Chemistry, University of Missouri-Rolla, Rolla, MO 65409-0010, USA.

出版信息

Langmuir. 2005 Apr 26;21(9):4185-90. doi: 10.1021/la047268e.

DOI:10.1021/la047268e
PMID:15835993
Abstract

Functionalization of carbon nanotubes (CNTs) is important for enhancing deposition of metal nanoparticles in the fabrication of supported catalysts. A facile approach for oxidizing CNTs is presented using a sonochemical method to promote the density of surface functional groups. This was successfully employed in a previous study [J. Phys. Chem. B 2004, 108, 19255] to prepare highly dispersed, high-loading Pt nanoparticles on CNTs as fuel cell catalysts. X-ray photoelectron spectroscopy (XPS), transmission electron microscopy, cyclic voltammetry, and settling speeds were used to characterize the degree of surface functionalization and coverage. The sonochemical method effectively functionalized the CNTs. A mixture of -C-O-/-C=O and -COO- was observed along with evidence for weakly bound CO at longer treatment times. The integrated XPS C 1s core level peak area ratios of the oxidized-to-graphitic C oxidation states, as well as the atom % oxygen from the O 1s level, showed an increase in peak intensity (attributed to -CO(x)()) with increased sonication times from 1 to 8 h; the increase in C surface oxidation correlated well with the measured atom %. Most of the CNT surface oxidation occurred between 1 and 2 h. The sonochemically treated CNTs were also studied by cyclic voltammetry and settling experiments, and the results were consistent with the XPS observations.

摘要

在负载型催化剂的制备过程中,碳纳米管(CNTs)的功能化对于增强金属纳米颗粒的沉积非常重要。本文提出了一种利用声化学方法氧化碳纳米管的简便方法,以提高表面官能团的密度。此前的一项研究[《物理化学杂志B》2004年,第108卷,第19255页]成功地采用了这种方法,在碳纳米管上制备了高度分散、高负载量的铂纳米颗粒作为燃料电池催化剂。利用X射线光电子能谱(XPS)、透射电子显微镜、循环伏安法和沉降速度来表征表面功能化程度和覆盖率。声化学方法有效地使碳纳米管功能化。观察到了-C-O-/-C=O和-COO-的混合物,并且在较长处理时间下有弱结合CO的证据。氧化态碳与石墨态碳的XPS C 1s核心能级峰面积比,以及来自O 1s能级的原子百分比氧,显示随着超声处理时间从1小时增加到8小时,峰强度(归因于-CO(x)())增加;碳表面氧化的增加与测量的原子百分比密切相关。大部分碳纳米管表面氧化发生在1至2小时之间。还通过循环伏安法和沉降实验对经声化学处理的碳纳米管进行了研究,结果与XPS观察结果一致。

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