Paper
17 April 2000 Nanometer-scale fabrication and data storage on charge transfer complex TEA(TCNQ)2 single crystal
Xinxian Bao, Haifeng Chen, Zhongfan Liu
Author Affiliations +
Abstract
Nanometer-scale holes and words were reproducibly create don a typical organic charge transfer compound, Triethylammonium Bis-7,7,8,8-tetracyanoquinodimethanide (TEA(TCNQ(2) single crystal, using scanning tunneling microscope in ambient conditions by applying a pulse voltage across the tunneling gap. The decomposition products of TEA(TCNQ)2 single crystal were investigated with mass spectroscopy by applying a pulse to the crystal in a vacuum tube. TEA was the sole product being detected. A micro-Raman Spectroscopy was used to fabricate and characterize the sample using a He-Ne laser. A dots array was written by a focused beam and in situ Raman spectra showed the same was decomposited. The most possible mechanism of holes formation appears to be TEA(TCNQ)2 decomposition and TEA evaporation by heating effect of STM current. Comparing data storage in TEA(TCNQ)2 single crystal with a market-sell CD-R disk, the writing threshold value of TEA(TCNQ)2 is much smaller than that of the CD-R disk. This kind of organic conductor may be a promising material for the STM-based high density storage and popular optical storage techniques.
© (2000) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Xinxian Bao, Haifeng Chen, and Zhongfan Liu "Nanometer-scale fabrication and data storage on charge transfer complex TEA(TCNQ)2 single crystal", Proc. SPIE 3937, Micro- and Nano-photonic Materials and Devices, (17 April 2000); https://doi.org/10.1117/12.382808
Lens.org Logo
CITATIONS
Cited by 2 scholarly publications.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Crystals

Scanning tunneling microscopy

Data storage

Optical storage

Micro raman spectroscopy

Raman spectroscopy

Mass spectrometry

Back to Top