Please use this identifier to cite or link to this item: https://doi.org/10.1039/c6nh00071a
Title: Conjugated polyelectrolyte nano field emission adlayers
Authors: Cole, M.T
Parmee, R.J
Kumar, A 
Collins, C.M
Kang, M.H
Xiao, J
Cepek, C
Yuan, X
Milne, W.I
Keywords: Carrier concentration
Electric fields
Electron emission
Field emission
Field emission microscopes
Morphology
Polyelectrolytes
Absorption cross sections
Composite emitters
Conjugated polyelectrolytes
Field electron emissions
Pulsed-mode operation
Scanning anode field emission microscopies
Surface band structures
Vertically aligned
Multiwalled carbon nanotubes (MWCN)
Issue Date: 2016
Citation: Cole, M.T, Parmee, R.J, Kumar, A, Collins, C.M, Kang, M.H, Xiao, J, Cepek, C, Yuan, X, Milne, W.I (2016). Conjugated polyelectrolyte nano field emission adlayers. Nanoscale Horizons 1 (4) : 304-312. ScholarBank@NUS Repository. https://doi.org/10.1039/c6nh00071a
Rights: Attribution 4.0 International
Abstract: Here we report on a straightforward and rapid means of enhancing the field electron emission performance of nascent vertically aligned multi-walled carbon nanotubes by introducing a polar zwitterionic conjugated polyelectrolyte adlayer at the vacuum-emitter interface. We attribute the observed 66% decrease in turn-on electric field to the augmented emitter micro-morphology and shifted surface band structure. The composite emitters can be optically modulated by exploiting the absorption cross-section of the solution cast adlayer, which increases the local carrier concentration which broadens the effective electrostatic shape of the emitter during optical excitation. Assessment via scanning anode field emission microscopy reveals a 25% improvement in DC time stability, a significant reduction in long-term hysteresis shift, and a threefold increase in bandwidth during pulsed mode operation. © The Royal Society of Chemistry 2016.
Source Title: Nanoscale Horizons
URI: https://scholarbank.nus.edu.sg/handle/10635/178893
ISSN: 20556756
DOI: 10.1039/c6nh00071a
Rights: Attribution 4.0 International
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