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Engineering Molecular Recognition with Bio-mimetic Polymers on Single Walled Carbon Nanotubes
Published on: January 10, 2017
Large work function difference driven electron transfer from electrides to single-walled carbon nanotubes.
Mini Mol Menamparambath1, Jong-Ho Park, Ho-Sung Yoo
1Center for Integrated Nanostructure Physics, Institute for Basic Science (IBS), Suwon 440-746, Republic of Korea. kimsungwng@skku.edu sbaik@me.skku.ac.kr.
Inorganic electrides facilitate electron transfer to single-walled carbon nanotubes (SWNTs). [Ca(2)N](+)·e(-) significantly enhanced SWNT fluorescence and field emission properties due to its high electron concentration and mobility.
Area of Science:
- Materials Science
- Condensed Matter Physics
- Nanotechnology
Background:
- Work function differences are crucial for charge transfer between materials.
- Inorganic electrides possess unique properties, including very low work functions (2.4-2.6 eV) due to interstitial anionic electrons.
- Single-walled carbon nanotubes (SWNTs) have work functions ranging from 4.73-5.05 eV.
Purpose of the Study:
- To investigate charge transfer between two distinct inorganic electrides, [Ca(2)N](+)·e(-) and [Ca(24)Al(28)O(64)](4+)·4e(-), and SWNTs.
- To evaluate the impact of electride structure on electron donation efficiency to SWNTs.
- To assess the resulting changes in SWNT properties, including fluorescence and field emission.
Main Methods:
- Comparative study of electron transfer from two types of inorganic electrides ([Ca(2)N](+)·e(-) and [Ca(24)Al(28)O(64)](4+)·4e(-)) to SWNTs.
- Characterization of electron concentration and mobility in the electrides.
- Measurement of near-infrared fluorescence enhancement in SWNTs.
- Evaluation of field emission properties of electride-SWNT composites.
Main Results:
- [Ca(2)N](+)·e(-), with its open 2D electron layers, demonstrated more effective electron donation to SWNTs compared to the closed cage structure of [Ca(24)Al(28)O(64)](4+)·4e(-).
- This enhanced donation is attributed to the higher electron concentration (1.3 × 10^22 cm^-3) and mobility (∼200 cm^2 V^-1 s^-1 at RT) of [Ca(2)N](+)·e(-).
- Non-covalent conjugation with electrides resulted in up to a 52% enhancement in SWNT near-infrared fluorescence.
- Field emission current density of electride-SWNT-silver paste increased dramatically by a factor of 46,000, reaching 14.8 mA cm^-2 at 2 V μm^-1, with a low turn-on voltage of 0.85 V μm^-1.
Conclusions:
- The structure of inorganic electrides significantly influences their electron-donating capability.
- [Ca(2)N](+)·e(-) is a highly effective electron donor for modifying SWNT properties.
- Electride-SWNT composites show promising applications in enhanced fluorescence and field emission devices.
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