• 전자공학회논문지A
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• 제31A권5호
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• pp.101-105
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• 1994

The EL lamp have been fabricated by screen printing method. the thickness of BaTiO$_3$ dielectric layer and ZnS:Cu phosphor layer was 20 $\mu$m and 40 $\mu$m, respectively. The threshold voltage of green El lamp was 50 $V_{p-p}$ and the maximum brightness was 13.5 $\mu$ W/cm$^2$ at frequency of 700 Hz and the input voltage of 250 $V_{p-p}$. Also when the Rodamin G6 of 0.02 g was doped, the threshold voltage of white EL lamp was 70 $V_{p-p}$ and the maximum brightness was 34 $\mu$W/cm$^2$.

• 조명전기설비학회논문지
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• 제14권1호
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• pp.1-6
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• 2000

Ethyl hydroxy ethyl cellulose의 고분자를 중심으로 하는 유기 결합제를 사용하고 형광체로서 ZnS:Cu와 유전체로$BaTiO_3$ 사용해 screen printing법에 의해 신광원으로서 많은 연구 개발이 집중되고 있는 유기분산형 백라이트 EL(Electroluminescent) 소자를 제조하였다. 제조된 백라이트용 유기 분산형 EL 소자의 특성은 $25[^{\circ}C]$, 100[V], 400[Hz]에서 $1.98[mA/\m^2]$의 전류밀도, O.075[W]의 power consumption, 정전용량 7.l[nF]를 나타내었다. 소자의 휘도는 50~150[V] 사이에서 $20~110[cd/\m^2]$의 밝기를 나타내였으며, 형광체의 색상변화는 ClE에 공인된 색 좌표에 의해 x=0.1711, y=0.3676의 bluish green의 색상을 나타내었다.

• Nuclear Engineering and Technology
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• 제4권4호
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• pp.331-339
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• 1972

트리티움 표지 형광도료의 원료인 고 비방사능의 트리티움 표지 폴리스타이렌을 얻기 위하여 테슬라 방전법, 윌즈바크 노출법, 감마선 조사법, 자외선 조사법 등 여러 방법들을 비교 검토하였다. 테슬라 방전 또는 자외선 조사법으로 얻은 polystyrene-T(G)의 비방사능은 1-l.2mCi/mg로써 다른 방법에 의한 생성물의 값보다 높았다. Polystyrene-T(G)와 ZnS:Cu 형광체를 무게비로 1:4가 되게 혼합하면 광도가 가장 컸다. 30mg의 형광도료 혼합물을 1ml의 바인다(시판 니스 1g을 100m1의 벤젠에 녹인 것)를 써서 바르는 경우 최대 장도는 약 20$\mu$L이었으며 갱내 표지판이나 암실내 광원으로 유효하게 사용될 수 있음을 확인하였다.

• E2M - 전기 전자와 첨단 소재
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• 제12권7호
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• pp.7-11
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• 1999

Fully sealed field emission display in size of 4.5 inch has been fabricated using single-wall carbon nanotubes-organic vehicle com-posite. The fabricated display were fully scalable at low temperature below 415$^{\circ}C$ and CNTs were vertically aligned using paste squeeze and surface rubbing techniques. The turn-on fields of 1V/${\mu}{\textrm}{m}$ and field emis-sion current of 1.5mA at 3V/${\mu}{\textrm}{m}$ (J=90${\mu}{\textrm}{m}$/$\textrm{cm}^2$)were observed. Brightness of 1800cd/$m^2$ at 3.7V/${\mu}{\textrm}{m}$ was observed on the entire area of 4.5-inch panel from the green phosphor-ITO glass. The fluctuation of the current was found to be about 7% over a 4.5-inch cath-ode area. This reliable result enables us to produce large area full-color flat panel dis-play in the near future. Carbon nanotubes (CNTs) have attracted much attention because of their unique elec-trical properties and their potential applica-tions [1, 2]. Large aspect ratio of CNTs together with high chemical stability. ther-mal conductivity, and high mechanical strength are advantageous for applications to the field emitter [3]. Several results have been reported on the field emissions from multi-walled nanotubes (MWNTs) and single-walled nanotubes (SWNTs) grown from arc discharge [4, 5]. De Heer et al. have reported the field emission from nan-otubes aligned by the suspension-filtering method. This approach is too difficult to be fully adopted in integration process. Recently, there have been efforts to make applications to field emission devices using nanotubes. Saito et al. demonstrated a car-bon nanotube-based lamp, which was oper-ated at high voltage (10KV) [8]. Aproto-type diode structure was tested by the size of 100mm $\times$ 10mm in vacuum chamber [9]. the difficulties arise from the arrangement of vertically aligned nanotubes after the growth. Recently vertically aligned carbon nanotubes have been synthesized using plasma-enhanced chemical vapor deposition(CVD) [6, 7]. Yet, control of a large area synthesis is still not easily accessible with such approaches. Here we report integra-tion processes of fully sealed 4.5-inch CNT-field emission displays (FEDs). Low turn-on voltage with high brightness, and stabili-ty clearly demonstrate the potential applica-bility of carbon nanotubes to full color dis-plays in near future. For flat panel display in a large area, car-bon nanotubes-based field emitters were fabricated by using nanotubes-organic vehi-cles. The purified SWNTs, which were syn-thesized by dc arc discharge, were dispersed in iso propyl alcohol, and then mixed with on organic binder. The paste of well-dis-persed carbon nanotubes was squeezed onto the metal-patterned sodalime glass throuhg the metal mesh of 20${\mu}{\textrm}{m}$ in size and subse-quently heat-treated in order to remove the organic binder. The insulating spacers in thickness of 200${\mu}{\textrm}{m}$ are inserted between the lower and upper glasses. The Y\ulcornerO\ulcornerS:Eu, ZnS:Cu, Al, and ZnS:Ag, Cl, phosphors are electrically deposited on the upper glass for red, green, and blue colors, respectively. The typical sizes of each phosphor are 2~3 micron. The assembled structure was sealed in an atmosphere of highly purified Ar gas by means of a glass frit. The display plate was evacuated down to the pressure level of 1$\times$10\ulcorner Torr. Three non-evaporable getters of Ti-Zr-V-Fe were activated during the final heat-exhausting procedure. Finally, the active area of 4.5-inch panel with fully sealed carbon nanotubes was pro-duced. Emission currents were character-ized by the DC-mode and pulse-modulating mode at the voltage up to 800 volts. The brightness of field emission was measured by the Luminance calorimeter (BM-7, Topcon).