Parallel fabrication of monolithic nanoscopic tunnel junctions for molecular devices

被引:4
|
作者
Gupta, R. [1 ]
Willis, B. G. [1 ]
机构
[1] Univ Connecticut, Storrs, CT 06269 USA
来源
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY B | 2010年 / 28卷 / 03期
基金
美国国家科学基金会;
关键词
adsorption; atomic layer deposition; desorption; electrodes; molecular electronics; nanofabrication; nanostructured materials; stochastic processes; thermal expansion; tunnelling spectra; ASSISTED NANOSTRUCTURE FORMATION; VIBRATIONAL SPECTROSCOPY; PRECURSOR MOLECULES; MICROSCOPY; FIELD; TEMPERATURE; CHEMISTRY; COPPER; STM;
D O I
10.1116/1.3425629
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Nanoelectrode tunneling devices for molecular level measurements have been grown using atomic layer deposition. These devices are two-terminal nanostructures separated by a free space region on the order of one to several nanometers where molecules can adsorb and be probed with electrical measurements including electron tunneling spectroscopy. Successful fabrication of parallel devices arranged in arrays is achieved by exploiting a nanofeedback mechanism that aids in the convergence of independent devices to tunneling. Independent devices are shown to behave similarly for thermal expansion, adsorption, desorption, and tunneling spectroscopy measurements. Adsorption is shown to be strongly influenced by the large electric fields in the nanoscopic tunnel junctions, and a model based on electric field forces qualitatively captures these effects. Desorption events are observed as stochastic processes for the independent devices and parallel inelastic electron tunneling spectroscopy measurements show features that are similar between independent devices. These data demonstrate parallel operation of nanoelectrode devices and suggest that it may be possible to scale the devices to have many nanojunctions operating in parallel. (C) 2010 American Vacuum Society. [DOI: 10.1116/1.3425629]
引用
收藏
页码:538 / 544
页数:7
相关论文
empty
未找到相关数据