Tunneling Assisted Photocurrent Multiplication in a-Si Based p-i/Sinx/i-n Structure Junction

1990 ◽  
Vol 192 ◽  
Author(s):  
M. Yoshimi ◽  
K. Hattori ◽  
H. Okamoto ◽  
Y. Hamakawa

ABSTRACTPhotocurrent multiplication has been observed in a-Si based p−i/SiNx/i−n junction cells under reverse biased high electric field. An apparent external quantum efficiency exceeds 20. A systematic investigation on electric and optoelectronic properties has been made to clarify the mechanism of photocarrier multiplication. The results indicate the possibility of inter-band tunneling via localized states in the a-SiN layer, which is induced by field-redistribution due to the built-up of trapped charges at the a-SiN/a-Si interface.

2021 ◽  
Vol 21 (7) ◽  
pp. 4037-4041
Author(s):  
Sangshin Park ◽  
Hyukmin Kwon ◽  
Seokwoo Kang ◽  
Sunwoo Park ◽  
Hyocheol Jung ◽  
...  

Molecular size of OLED emitting materials is nano-metric size and when it is applied to the electric field it emits the light based on the energy conversion result. As new green fluorescent emitters, N,N,N',N'-Tetra-m-tolyl-anthracene-9,10-diamine (m-Me-TAD) and N,N,N',N'-Tetra-p-tolyl-anthracene-9,10-diamine (p-Me-TAD) were synthesized and the properties were evaluated. In solution state, photoluminescence (PL) maximum wavelength is 517 nm for m-Me-TAD and 529 nm for p-Me-TAD. In electroluminescence (EL) spectra, EL maximum wavelength of m-Me-TAD is 518 nm and p-Me-TAD is 533 nm. The doped device using m-Me-TAD as green fluorescent dopant exhibited current efficiency (CE) of 17.41 cd/A and external quantum efficiency (EQE) of 7.41%. The doped device with p-Me-TAD was optimized in order to achieve a green OLED with high efficiency.


2002 ◽  
Vol 41 (Part 1, No. 12) ◽  
pp. 7402-7406 ◽  
Author(s):  
Takahiro Inoue ◽  
Shuji Miyamoto ◽  
Sho Amano ◽  
Mitsuyasu Yatsuzuka ◽  
Takayasu Mochizuki

Nanomaterials ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1937
Author(s):  
Tatiana G. Liashenko ◽  
Anatoly P. Pushkarev ◽  
Arnas Naujokaitis ◽  
Vidas Pakštas ◽  
Marius Franckevičius ◽  
...  

Inexpensive perovskite light-emitting devices fabricated by a simple wet chemical approach have recently demonstrated very prospective characteristics such as narrowband emission, low turn-on bias, high brightness, and high external quantum efficiency of electroluminescence, and have presented a good alternative to well-established technology of epitaxially grown III-V semiconducting alloys. Engineering of highly efficient perovskite light-emitting devices emitting green, red, and near-infrared light has been demonstrated in numerous reports and has faced no major fundamental limitations. On the contrary, the devices emitting blue light, in particular, based on 3D mixed-halide perovskites, suffer from electric field-induced phase separation (segregation). This crystal lattice defect-mediated phenomenon results in an undesirable color change of electroluminescence. Here we report a novel approach towards the suppression of the segregation in single-layer perovskite light-emitting electrochemical cells. Co-crystallization of direct band gap CsPb(Cl,Br)3 and indirect band gap Cs4Pb(Cl,Br)6 phases in the presence of poly(ethylene oxide) during a thin film deposition affords passivation of surface defect states and an increase in the density of photoexcited charge carriers in CsPb(Cl,Br)3 grains. Furthermore, the hexahalide phase prevents the dissociation of the emissive grains in the strong electric field during the device operation. Entirely resistant to 5.7 × 106 V·m−1 electric field-driven segregation light-emitting electrochemical cell exhibits stable emission at wavelength 479 nm with maximum external quantum efficiency 0.7%, maximum brightness 47 cd·m−2, and turn-on bias of 2.5 V.


2020 ◽  
Vol 140 (8) ◽  
pp. 650-655
Author(s):  
Shoki Tsuji ◽  
Yoji Fujita ◽  
Hiroaki Urushibata ◽  
Akihiko Kono ◽  
Ryoichi Hanaoka ◽  
...  

2020 ◽  
Vol 14 (1) ◽  
pp. 011004
Author(s):  
Shubhra S. Pasayat ◽  
Chirag Gupta ◽  
Matthew S. Wong ◽  
Ryan Ley ◽  
Michael J. Gordon ◽  
...  

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