scholarly journals STRUCTURAL INVESTIGATION OF n-ZnO/p-GaN ULTRAVIOLET LIGHT-EMITTING DIODES GROWN BY ATOMIC LAYER DEPOSITION

2011 ◽  
Vol 04 (03) ◽  
pp. 221-224 ◽  
Author(s):  
W. C. LI ◽  
H. L. TSAI ◽  
H. C. CHEN ◽  
M. K. WU ◽  
H. R. CHEN ◽  
...  

Electron microscopy investigation has been carried for an n- ZnO /p- GaN:Mg heterojunction ultraviolet (UV) light-emitting diode device, where the n- ZnO layer was grown by atomic layer deposition on the p-type GaN:Mg /undoped GaN structure prepared on c- Al 2 O 3 substrate. Threading dislocations, formed at the interface of the GaN/Al2O3 , disappeared at the interface of n- ZnO /p- GaN during post-deposited rapid thermal annealing and accordingly the n- ZnO layer became an almost perfect single crystal including only a few surviving dislocations. An interfacial layer was found along the (0001) interface between the n- ZnO and p- GaN:Mg layers. Scanning transmission microscopy analysis revealed that the interfacial layer was composed of ZnO crystal, which connected coherently with the neighboring n- ZnO and p- GaN:Mg . This interfacial layer contained a few atomic percents of Mg , the atoms of which had been diffused from the p- GaN:Mg . The high quality crystalline n- ZnO and the interfacial layer forming a ZnO/GaN interface states are responsible for the UV electroluminescence from the ZnO .

2016 ◽  
Vol 18 (2) ◽  
pp. 1042-1049 ◽  
Author(s):  
Lae Ho Kim ◽  
Yong Jin Jeong ◽  
Tae Kyu An ◽  
Seonuk Park ◽  
Jin Hyuk Jang ◽  
...  

The shelf-life of the OLED devices passivated with and without PEALD-based films at 60 °C and 90% RH.


Coatings ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1028
Author(s):  
Laura Keskiväli ◽  
Pirjo Heikkilä ◽  
Eija Kenttä ◽  
Tommi Virtanen ◽  
Hille Rautkoski ◽  
...  

The growth mechanism of Atomic Layer Deposition (ALD) on polymeric surfaces differs from growth on inorganic solid substrates, such as silicon wafer or glass. In this paper, we report the growth experiments of Al2O3 and ZnO on nonwoven poly-L-lactic acid (PLLA), polyethersulphone (PES) and cellulose acetate (CA) fibres. Material growth in both ALD and infiltration mode was studied. The structures were examined with a scanning electron microscope (SEM), scanning transmission electron microscope (STEM), attenuated total reflectance-fourier-transform infrared spectroscopy (ATR-FTIR) and 27Al nuclear magnetic resonance (NMR). Furthermore, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) analysis were used to explore the effect of ALD deposition on the thermal properties of the CA polymer. According to the SEM, STEM and ATR-FTIR analysis, the growth of Al2O3 was more uniform than ZnO on each of the polymers studied. In addition, according to ATR-FTIR spectroscopy, the infiltration resulted in interactions between the polymers and the ALD precursors. Thermal analysis (TGA/DSC) revealed a slower depolymerization process and better thermal resistance upon heating both in ALD-coated and infiltrated fibres, more pronounced on the latter type of structures, as seen from smaller endothermic peaks on TA.


Inorganics ◽  
2020 ◽  
Vol 8 (12) ◽  
pp. 69
Author(s):  
Chao Lin ◽  
Alexandre C. Foucher ◽  
Eric A. Stach ◽  
Raymond J. Gorte

Thin, ~1-nm films of CaTiO3, SrTiO3, and BaTiO3 were deposited onto MgAl2O4 by Atomic Layer Deposition (ALD) and then studied as catalyst supports for ~5 wt % of Ni that was added to the perovskite thin films by Atomic Layer Deposition. Scanning Transmission Electron Microscopy demonstrated that both the Ni and the perovskites uniformly covered the surface of the support following oxidation at 1073 K, even after redox cycling, but large Ni particles formed following a reduction at 1073 K. When compared to Ni/MgAl2O4, the perovskite-containing catalysts required significantly higher temperatures for Ni reduction. Equilibrium constants for Ni oxidation, as determined from Coulometric Titration, indicated that the oxidation of Ni shifted to lower PO2 on the perovskite-containing materials. Based on Ni equilibrium constants, Ni interactions are strongest with CaTiO3, followed by SrTiO3 and BaTiO3. The shift in the equilibrium constant was shown to cause reversible deactivation of the Ni/CaTiO3/MgAl2O4 catalyst for CO2 reforming of CH4 at high CO2 pressures, due to the oxidation of the Ni.


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