Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Floating Catalyst CVD Syntheses of SWNTs for Thin Film Devices – Lessons Learned and Future Directions

We discuss (n,m) distributions of our floating catalyst chemical vapor deposition (FFCVD) synthesis of SWCNTs from CO using Fe catalyst clusters made via direct evaporation using hot wire generator as well as via thermal decomposition of ferrocene, and with the addition of trace amount of CO2. Here both the tube diameter as well as length can be tailored by changing the reactor temperature profile as well as CO2 concentration. Helicity i.e. (n,m) distributions as determined with ED/TEM are biased towards large chiral angles with the maximum population at about 23 degrees. Then we proceed to explore the effect of carbon source gas, by adding C2H4 together with CO and looking at the effect of temperature when producing catalysts via ferrocene decomposition. We also discuss Cs-corrected HRTEM results to explore the size and structure of the active Fe catalyst particles responsible for the SWNT growth.

We review our earlier results when growing SWNTs from CO with Fe catalyst clusters made via physical vapor deposition (PVD) i.e. evaporation via resistively heating the iron wire. To explore in more detail the effect of Fe catalyst cluster size and concentration in the floating catalyst synthesis, we have developed a novel catalyst particle production method via PVD, based on arc discharge between two electrodes i.e. the spark generator. This method allows to control separately both the catalyst particle size and concentration when fed into the floating catalyst SWCNT synthesis reactor. Controlling the catalyst gas phase concentration allows us to reduce significantly tube-to-tube collisions i.e. bundling. Preliminary results show that when reducing catalyst particle gas phase number concentration, the bundle size of the produced tubes is significantly reduced, and we reduce the tube diameter below 1 nm and narrow the chiral angle distribution towards armchair when reducing synthesis temperature and CO concentration. Interestingly, the SWNT mean diameter does not significantly change when controlling catalyst number mean diameter from 4 nm to 10 nm. We explore also bundle formation during the SWNT deposition processes.

We present the current status of transparent conducting films and field effect thin film transistors manufactured by direct, dry deposition of SWNT networks. Also, we discuss the use of transparent SWNT films in the EMS applications.

Sponsors

Renu.Sharma [at] nist.gov (Renu Sharma), 301-975-2418

Prof. Esko I. Kauppinen

Department of Applied Physics, Aalto University School of Science, Finland

Created August 31, 2014, Updated September 21, 2016