Visible Electroluminescence from Pn Junction Type μc-Sic/ Porous Si / c-Si Structures

1992 ◽  
Vol 283 ◽  
Author(s):  
T. Futagi ◽  
T. Matsumoto ◽  
M. Katsuno ◽  
Y. Ohta ◽  
H. Mimura ◽  
...  

ABSTRACTWe have fabricated two kinds of n-type microcrystalline silicon carbon (μc-SiC) / porous silicon (PS) / p-type crystalline silicon (c-Si) pn junctions and demonstrated a visible light emission from them. We have observed three types of visible light emission; an uniform red light emission at a forward current above 12mA/cm2 for the pn junction using a 0.2–0.4 Qcm c-Si substrate, and a very weak white light emission at a forward current of about 90 mA/mm2 and a strong orange-red light emission at a forward current from 200 to 619 mA/mm2for the pn junction using a 3.5–4.5 Ωcm c-Si substrate.

2013 ◽  
Vol 53 (2) ◽  
pp. 87-91 ◽  
Author(s):  
S. Nishimura ◽  
M. Hirai ◽  
H. Nagayoshi ◽  
K. Terashima

1992 ◽  
Vol 31 (Part 2, No. 5B) ◽  
pp. L616-L618 ◽  
Author(s):  
Toshiro Futagi ◽  
Takahiro Matsumoto ◽  
Masakazu Katsuno ◽  
Yasumitsu Ohta ◽  
Hidenori Mimura ◽  
...  

2010 ◽  
Author(s):  
L. S. Chuah ◽  
Z. Hassan ◽  
H. Abu Hassan ◽  
A. K. Yahya ◽  
Shah Alam

Author(s):  
C. Jacobsen ◽  
J. Fu ◽  
S. Mayer ◽  
Y. Wang ◽  
S. Williams

In scanning luminescence x-ray microscopy (SLXM), a high resolution x-ray probe is used to excite visible light emission (see Figs. 1 and 2). The technique has been developed with a goal of localizing dye-tagged biochemically active sites and structures at 50 nm resolution in thick, hydrated biological specimens. Following our initial efforts, Moronne et al. have begun to develop probes based on biotinylated terbium; we report here our progress towards using microspheres for tagging.Our initial experiments with microspheres were based on commercially-available carboxyl latex spheres which emitted ~ 5 visible light photons per x-ray absorbed, and which showed good resistance to bleaching under x-ray irradiation. Other work (such as that by Guo et al.) has shown that such spheres can be used for a variety of specific labelling applications. Our first efforts have been aimed at labelling ƒ actin in Chinese hamster ovarian (CHO) cells. By using a detergent/fixative protocol to load spheres into cells with permeabilized membranes and preserved morphology, we have succeeded in using commercial dye-loaded, spreptavidin-coated 0.03μm polystyrene spheres linked to biotin phalloidon to label f actin (see Fig. 3).


1992 ◽  
Vol 31 (Part 2, No. 5A) ◽  
pp. L560-L563 ◽  
Author(s):  
Yukinori Ochiai ◽  
Norio Ookubo ◽  
Heiji Watanabe ◽  
Shinji Matsui ◽  
Yasunori Mochizuki ◽  
...  

1991 ◽  
Vol 70 (1) ◽  
pp. 529-531 ◽  
Author(s):  
Enrico Zanoni ◽  
Alessandro Paccagnella ◽  
Pietro Pisoni ◽  
Paolo Telaroli ◽  
Carlo Tedesco ◽  
...  

1999 ◽  
Vol 74 (21) ◽  
pp. 3164-3166 ◽  
Author(s):  
J. P. Wilcoxon ◽  
G. A. Samara

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