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Surface Structure-Dependent Low Turn-On Electron Field Emission from Polypyrrole/Tin Oxide Hybrid Cathodes
[Image: see text] We present a new surface structure-dependent cold cathode material capable of sustaining high electron emission current suitable for next-generation low turn-on field-emission devices. The low turn-on electric field for electron emission in the cathode materials is critical, which...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645290/ https://www.ncbi.nlm.nih.gov/pubmed/31457313 http://dx.doi.org/10.1021/acsomega.7b01274 |
Sumario: | [Image: see text] We present a new surface structure-dependent cold cathode material capable of sustaining high electron emission current suitable for next-generation low turn-on field-emission devices. The low turn-on electric field for electron emission in the cathode materials is critical, which facilitates the low-power room-temperature operation, a key factor required by the industrial sector. We demonstrate the facile synthesis of polypyrrole (PPy)/tin oxide (SnO(2))-based core–shell hybrid cold cathode materials for large area applications. The technique used here is based on a simple and economical method of surfactant-mediated polymerization. The coupled investigation of X-ray diffraction along with electron microscopy reveals the formation of rutile phase SnO(2) nanoparticles of size ∼15 nm. These SnO(2) nanoparticles act as nucleation sites for the growth of PPy nanofibers, resulting in encapsulated SnO(2) nanoparticles in the PPy amorphous matrix. The coupling of spherical-shaped core–shell structures of PPy/SnO(2) resulted into the particle train-like nanostructured form of the hybrid material. These core–shell structures formed the local p–n junction between the n-type SnO(2) (core) and p-type PPy (shell). The long chains of these p–n junctions in nanofibers result in the modification of the electronic band structure of PPy, leading to a reduction in the work function of the electrons. The significant surface structural modification in PPy/SnO(2) causes a prominent reduction in the turn-on electric field for electron emission in PPy/SnO(2) nanocomposite (∼1.5 V/μm) as compared to the pure PPy (∼3.3 V/μm) without significant loss in current density (∼1 mA/cm(2)). The mechanism of improved field-emission behavior and advantages of using such hybrid nanomaterials as compared to other composite nanomaterials have also been discussed in detail. |
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