期刊
NANOSCALE
卷 6, 期 15, 页码 8844-8851出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4nr01629g
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资金
- Center for Advanced Soft-Electronics - Ministry of Science, ICT and Future Planning as Global Frontier Project [CASE-2011-0031660]
- KETEP - Korean government Ministry of Knowledge Economy [20124010203270]
- JSPS FIRST-ACCEL Program
- Korea Evaluation Institute of Industrial Technology (KEIT) [20144010200740] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
- Ministry of Science, ICT & Future Planning, Republic of Korea [IBS-R011-D1-2014-A00] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
- National Research Foundation of Korea [2011-0031660] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
A difference in work function plays a key role in charge transfer between two materials. Inorganic electrides provide a unique opportunity for electron transfer since interstitial anionic electrons result in a very low work function of 2.4-2.6 eV. Here we investigated charge transfer between two different types of electrides, (Ca2N](+)center dot e(-) and [Ca24Al28O64](4+)center dot 4e(-), and single-walled carbon nanotubes (SWNTs) with a work function of 4.73-5.05 eV. [Ca2N](+)center dot e(-) with open 2-dimensional electron layers was more effective in donating electrons to SWNTs than closed cage structured [Ca24Al28O64](4+)center dot 4e(-) due to the higher electron concentration (1.3 x 10(22) cm(-3)) and mobility (similar to 200 cm(2) V-1 s(-1) at RT). A non-covalent conjugation enhanced near-infrared fluorescence of SWNTs as high as 52%. The field emission current density of electride-SWNT-silver paste dramatically increased by a factor of 46 000 (14.8 mA cm(-2)) at 2 V mu m(-1) (3.5 wt% (Ca2N](+)center dot e(-)) with a turn-on voltage of 0.85 V mu m(-1).
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