Investigation of the Changes in Electronic Properties of Nickel Oxide (NiOx) Due to UV/Ozone Treatment

2017 ◽  
Vol 9 (20) ◽  
pp. 17201-17207 ◽  
Author(s):  
Raisul Islam ◽  
Gang Chen ◽  
Pranav Ramesh ◽  
Junkyo Suh ◽  
Nobi Fuchigami ◽  
...  
2020 ◽  
Vol 64 (1-4) ◽  
pp. 1261-1268
Author(s):  
Shu Otani ◽  
Dang-Trang Nguyen ◽  
Kozo Taguchi

In this study, a portable and disposable paper-based microbial fuel cell (MFC) was fabricated. The MFC was powered by Rhodopseudomonas palustris bacteria (R. palustris). An activated carbon sheet-based anode pre-loaded organic matter (starch) and R. palustris was used. By using starch in the anode, R. palustris-loaded on the anode could be preserved for a long time in dry conditions. The MFC could generate electricity on-demand activated by adding water to the anode. The activated carbon sheet anode was treated by UV-ozone treatment to remove impurities and to improve its hydrophilicity before being loaded with R. palustris. The developed MFC could generate the maximum power density of 0.9 μW/cm2 and could be preserved for long-term usage with little performance degradation (10% after four weeks).


2009 ◽  
Vol 53 (6) ◽  
pp. 621-625 ◽  
Author(s):  
Jae Bon Koo ◽  
Seong Yeol Kang ◽  
In Kyu You ◽  
Kyung Soo Suh

2011 ◽  
Vol 12 (2) ◽  
pp. 279-284 ◽  
Author(s):  
Takahiro Nagata ◽  
Seungjun Oh ◽  
Toyohiro Chikyow ◽  
Yutaka Wakayama

2014 ◽  
Vol 290 ◽  
pp. 381-387 ◽  
Author(s):  
R.O.F. Verkuijlen ◽  
M.H.A. van Dongen ◽  
A.A.E. Stevens ◽  
J. van Geldrop ◽  
J.P.C. Bernards

2013 ◽  
Vol 60 (5) ◽  
pp. 1763-1768 ◽  
Author(s):  
Prajwal Adhikary ◽  
Swaminathan Venkatesan ◽  
Purna P. Maharjan ◽  
David Galipeau ◽  
Qiquan Qiao

2021 ◽  
Vol 21 (8) ◽  
pp. 4418-4422
Author(s):  
Seongwan Kim ◽  
Yunsook Yang ◽  
Sheik Abdur Rahman ◽  
Woo Young Kim

Ag-paste is used as an electrode material in various fields as a manufacturing advantage that enables solution processing. However, when a subsequent thin film is formed on the solidified Ag-paste electrode, there is a fear that the bonding force between the Ag-paste electrode and the subsequent thin film is weakened and peeled off due to the low surface energy of the Agpaste electrode. It is necessary to increase the surface energy of the Ag-paste electrode surface since it ultimately directly affects the yield of the device or product. In this study, the UV/ozone treatment process was introduced to increase the Ag-paste surface energy, thereby making the surface hydrophilic. Additionally, it was confirmed that the UV/ozone treatment process affected only the surface of the Ag-paste electrode by extracting the contact resistance.


2020 ◽  
Vol 59 ◽  
pp. 195-202 ◽  
Author(s):  
Kyungeun Jung ◽  
Du Hyeon Kim ◽  
Jaemin Kim ◽  
Sunglim Ko ◽  
Jae Won Choi ◽  
...  

2003 ◽  
Vol 794 ◽  
Author(s):  
Mark Nowakowski ◽  
Jordana Bandaru ◽  
L.D. Bell ◽  
Shouleh Nikzad

ABSTRACTWe compare various wet chemical treatments, in preparing high-quality Ge (100) surfaces suitable for molecular beam epitaxy (MBE). Various surface treatments are explored such as UV-ozone treatment followed by exposure to chemical solutions such as de-ionized (DI) water, hydrofluoric acid (HF), or hydrochloric acid (HCl). Chemical treatments to remove the oxide are performed in a nitrogen environment to prevent further formation of surface oxide prior to surface analysis. Following chemical treatments, in situ reflection high-energy electron diffraction (RHEED) analysis is performed to observe the surface evolution as a function of temperature. In a separate chamber, we analyze each sample, before and after chemical treatment by x-ray photoelectron spectroscopy (XPS) to directly determine the oxide desorption following each chemical treatment. Our results of this comparative study, the effectiveness of each chemical treatment, and the stability of the passivated surface suggest that UV ozone cleaning, followed by 10% HCl is the best choice for removing most of the oxide. Furthermore, we present evidence of high quality epitaxial growth of SnxGe1−x on wafers prepared by our method.


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