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单壁碳纳米管网络超微电极

Single-walled carbon nanotube network ultramicroelectrodes.

作者信息

Dumitrescu Ioana, Unwin Patrick R, Wilson Neil R, Macpherson Julie V

机构信息

Department of Chemistry, University of Warwick, Coventry, CV4 7AL, UK.

出版信息

Anal Chem. 2008 May 15;80(10):3598-605. doi: 10.1021/ac702518g. Epub 2008 Apr 15.

Abstract

Ultramicroelectrodes (UMEs) fabricated from networks of chemical vapor deposited single-walled carbon nanotubes (SWNTs) on insulating silicon oxide surfaces are shown to offer superior qualities over solid UMEs of the same size and dimensions. Disk shaped UMEs, comprising two-dimensional "metallic" networks of SWNTs, have been fabricated lithographically, with a surface coverage of <1% of the underlying insulating surface. The electrodes are long lasting and give highly reproducible responses (either for repeat runs with the same electrode or when comparing several electrodes with the same size). For redox concentrations <or=1 mM the steady-state behavior of SWNT network UMEs is as expected for conventional solid metal UMEs (e.g., Pt, Au), due to diffusional overlap between neighboring SWNTs. Importantly, the low intrinsic capacitance of the SWNTs and much reduced surface area lead to much faster response times and lower background currents. The well-defined geometry of the SWNT network electrode is also useful for studying electron transfer (ET) kinetics at SWNTs. Given the intrinsically high mass transport rates to SWNTs within a network electrode, the reversible nature of the CVs recorded for Ru(NH 3) 6 (3+/) (2+) and FcTMA (+/) (2+) suggests that ET driven solely by defects on the sidewalls of the SWNTs is highly unlikely.

摘要

由化学气相沉积在绝缘氧化硅表面的单壁碳纳米管(SWNTs)网络制成的超微电极(UMEs),与相同尺寸和维度的固体超微电极相比,具有更优异的性能。通过光刻技术制造出了由二维SWNTs“金属”网络构成的盘状超微电极,其在下层绝缘表面的覆盖率小于1%。这些电极持久耐用,能给出高度可重复的响应(无论是对同一电极的重复测试,还是比较几个相同尺寸的电极)。对于氧化还原浓度小于或等于1 mM的情况,由于相邻SWNTs之间的扩散重叠,SWNT网络超微电极的稳态行为与传统固体金属超微电极(如Pt、Au)预期的一样。重要的是,SWNTs的低固有电容和大幅减小的表面积导致响应时间更快,背景电流更低。SWNT网络电极明确的几何形状对于研究SWNTs上的电子转移(ET)动力学也很有用。鉴于网络电极内SWNTs本质上具有较高的传质速率,记录的Ru(NH₃)₆(³⁺/²⁺)和FcTMA(⁺/²⁺)的循环伏安图(CVs)的可逆性质表明,仅由SWNTs侧壁上的缺陷驱动的电子转移极不可能。

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