A New Design Using Metal Wire Brushes as the Current Collector and Catalyst Carrier for Internal Reforming of Micro-Tubular SOFCs

Author(s):  
Jixin Shi ◽  
Junhua Fan ◽  
Yuqing Wang ◽  
Yixiang Shi ◽  
Ningsheng Cai
2021 ◽  
Vol 103 (1) ◽  
pp. 1867-1876
Author(s):  
Jixin Shi ◽  
Junhua Fan ◽  
Yuqing Wang ◽  
Yixiang Shi ◽  
Ningsheng Cai
Keyword(s):  

2021 ◽  
Vol MA2021-03 (1) ◽  
pp. 184-184
Author(s):  
Jixin Shi ◽  
Junhua Fan ◽  
Yuqing Wang ◽  
Yixiang Shi ◽  
Ningsheng Cai
Keyword(s):  

2001 ◽  
Vol 28 (10) ◽  
pp. 937-942 ◽  
Author(s):  
F. Teraoka ◽  
M. Nakagawa ◽  
J. Takahashi
Keyword(s):  

2016 ◽  
Vol 136 (9) ◽  
pp. 733-740 ◽  
Author(s):  
Shin-ichi Tanaka ◽  
Masashi Kotari ◽  
Tomo Tadokoro ◽  
Yutaka Goda
Keyword(s):  

2018 ◽  
Author(s):  
Hakeem K. Henry ◽  
Sang Bok Lee

The PMo<sub>12</sub>-PPy heterogeneous cathode was synthesized electrochemically. In doing so, the PMo<sub>12</sub> redox-active material was impregnated throughout the conductive polymer matrix of the poly(pyrrole) nanowires. All chemicals and reagents used were purchased from Sigma-Aldrich. Anodized aluminum oxide (AAO) purchased from Whatman served as the porous hard template for nanowire deposition. A thin layer of gold of approximately 200nm was sputtered onto the disordered side of the AAO membrane to serve as the current collector. Copper tape was connected to the sputtered gold for contact and the device was sealed in parafilm with heat with an exposed area of 0.32 cm<sup>2</sup> to serve as the electroactive area for deposition. All electrochemical synthesis and experiments were conducted using a Bio-Logic MPG2 potentiostat. The deposition was carried out using a 3-electrode beaker cell setup with a solution of acetonitrile containing 5mM and 14mM of the phosphomolybdic acid and pyrrole monomer, respectively. The synthesis was achieved using chronoamperometry to apply a constant voltage of 0.8V vs. Ag/AgCl (BASi) to oxidatively polymerize the pyrrole monomer to poly(pyrrole). To prevent the POM from chemically polymerizing the pyrrole, an injection method was used in which the pyrrole monomer was added to the POM solution only after the deposition voltage had already been applied. The deposition was well controlled by limiting the amount of charge transferred to 300mC. Following deposition, the AAO template was removed by soaking in 3M sodium hydroxide (NaOH) for 20 minutes and rinsed several times with water. After synthesis, all cathodes underwent electrochemical testing to determine their performance using cyclic voltammetry and constant current charge-discharge cycling in 0.1 M Mg(ClO<sub>4</sub>)<sub>2</sub>/PC electrolyte. The cathodes were further characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and x-ray photoelectron spectroscopy (XPS).


2020 ◽  
pp. 73-83
Author(s):  
L. V. Morozova ◽  
◽  
I. A. Drozdova ◽  

The xerogels in the system 0.88 mol.% ZrO2 − 0.12 mol.% CeO2 were obtained by the method of coprecipitation in a neutral (pH = 7) and slightly alkaline (pH = 9) medium under the influence of ultrasound with the size of the agglomerates 70 – 230 nm. It is shown that the coprecipitation of hydroxides of zirconium and cerium at pH = 9 with the use of ultrasonic treatment facilitates the formation of a primary crystal is symbolic of the particles in the xerogel, whose size is ~ 5 nm, whereas the xerogel synthesized in a neutral environment consists only of the x-ray amorphous phase. The effect of pH-precipitation on deposition processes of dehydration of the xerogels and crystallization solid solution based on zirconia oxide in the metastable pseudocubic modification (с′-ZrO2) was discovered. It was found that in the temperature range 500 – 800 °C there is a phase transition с′-ZrO2 → t-ZrO2, the size of the crystallites of the formed tetragonal solid solutions is 8 and 11 nm. The method of low-temperature nitrogen adsorption were investigated dispersion properties and characteristics of the pore structure of the powders of the solid solution Zr0.88Ce0.12O2. It is determined that the specific surface area of t-ZrO2 samples obtained after firing at 800 °C is 117 and 178 m2/g, the total pore volume reaches 0.300 − 0.325 cm3/g, the pore size distribution is monomodal and is in the range of 2 − 8 nm. The effect of thermal “aging” at a temperature of 800 °C (40 h) on the structure and dispersion of the solid solution t-ZrO2 powders was studied.


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