Littérature scientifique sur le sujet « Ag/GDC »
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Articles de revues sur le sujet "Ag/GDC"
Sampath, Deepak, Sylvia Herter, Frank Herting, Ellen Ingalla, Michelle Nannini, Marina Bacac, Wayne J. Fairbrother et Christian Klein. « Combination of the glycoengineered Type II CD20 antibody obinutuzumab (GA101) and The novel Bcl-2 selective Inhibitor GDC-0199 Results in superior In Vitro and In Vivo Anti-tumor activity in models Of B-Cell Malignancies ». Blood 122, no 21 (15 novembre 2013) : 4412. http://dx.doi.org/10.1182/blood.v122.21.4412.4412.
Texte intégralVernoux, Philippe, Benjamin Gilbert, Angel Caravaca, Stéphanie Bruyère, Sylvie Migot, Pauline Vilasi et David Horwat. « Ethylene Electrooxidation into Ethylene Oxide on Nanostructured Ag/GDC Electrocatalysts ». ECS Meeting Abstracts MA2021-02, no 27 (19 octobre 2021) : 837. http://dx.doi.org/10.1149/ma2021-0227837mtgabs.
Texte intégralRehman, Saeed Ur, Muhammad Haseeb Hassan, Syeda Youmnah Batool, Seung Bok Lee, Hye-Sung Kim, Rak-Hyun Song, Tak-Hyoung Lim, Jong-Eun Hong, Seok Joo Park et Dong Woo Joh. « Fabrication of Durable and High-Performance Flat Tubular Anode-Supported Solid Oxide Cells for Stack Application ». ECS Transactions 111, no 6 (19 mai 2023) : 557–64. http://dx.doi.org/10.1149/11106.0557ecst.
Texte intégralRaju, Kati, Muksin et Dang-Hyok Yoon. « Reactive air brazing of GDC–LSCF ceramics using Ag–10 wt% CuO paste for oxygen transport membrane applications ». Ceramics International 42, no 14 (novembre 2016) : 16392–95. http://dx.doi.org/10.1016/j.ceramint.2016.07.042.
Texte intégralRaźniak, Andrzej, Magdalena Dudek et Piotr Tomczyk. « Reduction of oxygen at the interface M|solid oxide electrolyte (M=Pt, Ag and Au, solid oxide electrolyte=YSZ and GDC). Autocatalysis or artifact ? » Catalysis Today 176, no 1 (novembre 2011) : 41–47. http://dx.doi.org/10.1016/j.cattod.2011.04.030.
Texte intégralBiswas, Saheli, Aniruddha P. Kulkarni, Daniel Fini, Sarbjit Giddey et Sankar Bhattacharya. « In situ synthesis of methane using Ag–GDC composite electrodes in a tubular solid oxide electrolytic cell : new insight into the role of oxide ion removal ». Sustainable Energy & ; Fuels 5, no 7 (2021) : 2055–64. http://dx.doi.org/10.1039/d0se01887b.
Texte intégralSakitou, Y., A. Hirano, N. Imanishi, Y. Takeda, Y. Liu et M. Mori. « La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3 – Ag Composite Cathode for Intermediate-Temperature Solid Oxide Fuel Cells ». Journal of Fuel Cell Science and Technology 5, no 3 (27 mai 2008). http://dx.doi.org/10.1115/1.2930764.
Texte intégralLiu, Y., K. Yasumoto, S. Hashimoto, K. Takei, M. Mori, Y. Funahashi, Y. Fijishiro, A. Hirano et Y. Takeda. « Development of Ceria Based SOFCs With a High Performance La0.6Sr0.4Co0.2Fe0.8O3−δ–Ce0.9Gd0.1O1.95–Ag Composite Cathode ». Journal of Fuel Cell Science and Technology 7, no 6 (17 août 2010). http://dx.doi.org/10.1115/1.3176220.
Texte intégralOki, Kentaro, Edward B. Arias et Gregory D. Cartee. « Prior Treatment with the AMPK Activator AICAR Induces Subsequently Enhanced Glucose Uptake in Isolated Skeletal Muscles from Old Rats ». FASEB Journal 31, S1 (avril 2017). http://dx.doi.org/10.1096/fasebj.31.1_supplement.lb726.
Texte intégralThèses sur le sujet "Ag/GDC"
Kaseman, Brian J. « An Investigation of Secondary Formations of High Temperature Solid Oxide Fuel Cells ». Ohio University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1330648584.
Texte intégralGilbert, Benjamin. « Synthèse de films nanocomposites Ag/YSZ, Ag/CGO & ; Ag(Cu)/CGO par pulvérisation cathodique magnétron réactive pour l’électrocatalyse de l’éthylène en oxyde d’éthylène ». Electronic Thesis or Diss., Université de Lorraine, 2020. http://www.theses.fr/2020LORR0257.
Texte intégralEthylene oxide (EO) is an essential building block for the chemical industry. It is produced by the ethylene epoxidation reaction over a silver-based catalyst. Nevertheless, to achieve high selectivity, industrial processes use chloride additives in the gas phase and alkaline moderators on the catalyst. The aim of this study is to increase EO selectivity without chloride additives thanks to Ag/fluorite oxides electrocatalysts synthesized by reactive magnetron sputtering and incorporated in a 3-electrodes configuration cell designed for electrochemical promotion of catalysis, EPOC. Three porous systems (Ag/YSZ, Ag/GDC, Ag(Cu)/GDC) have been synthesized by reactive magnetron sputtering. Ag/YSZ 4 Pa 25 mA nanocomposite thin film exhibits a botryoidal microstructure characteristic of silver segregation inside the YSZ matrix. Ag/GDC 4 Pa 70 mA nanocomposite thin film exhibits a brain like-morphology with open nanoporosities. Ag(Cu)/GDC 4 Pa 70 mA nanocomposite thin film consists of multi-phase hydrophobic entropic nanowires. During catalytic tests under ethylene epoxidation conditions in reducing medium, Ag/GDC 4 Pa 70 mA showed the maximum EO selectivity of 16.55 % at 220 °C and, under polarization, selectivity boost of 2.78 % occur without the appearance of NEMCA effect
Lin, Jhih-ming, et 林志名. « The Study of Sputter-Deposited CeO2,GDC and Ag-CeO2 Thin Films for Resistive Oxygen Sensors ». Thesis, 2008. http://ndltd.ncl.edu.tw/handle/99235907517183812689.
Texte intégral國立臺灣科技大學
材料科技研究所
96
In this thesis, we deposit CeO2,(Gd2O3)x-(CeO2)1-x and Ag- CeO2 thin films on Al2O3 substrate by using magnetron sputtering process, anneal the films, then deposit Pt as electrode to fabricate resistive-type oxygen sensor, analyze its electronal properties, activation energy, and sensors sensitivity of CeO2 thin film, and correlate to their microstruture. Finally, we measure the oxygen sensor’s response time at high temperature(750℃) and low temperature(450℃) and fabricate the resistive oxygen sensors which have good sensitivity and fast response time. The CeO2 thin film deposited on Al2O3 substrate were continuous and dense. Their structure and crystallinity were verified by XRD. The structure and particle sizes of CeO2 films were stablilized by annealing at 750℃,1000℃, and 1250℃ for 5 hours. This approach was also applicable to GDC thin films. Ag-CeO2 composite thin films were deposited by sputtering Ag-CeO2 inlaid targets. Ag particles were dispersed in CeO2 , verified by TEM and Auger. After annealing, the Ag-CeO2 films at 600℃ for 1 hour and 5 hours. Different Ag weight fractions of 5.9%, 3.7% and 2.9% were obtained by EDX analysis. In this study, we measure the sensor’s resistance by changing the oxygen concentration in steady condition, and do the dynamic measurement by changing the oxygen concentration rapidly and recording its response time in osciscope and keithley 2410. We discover that the CeO2 thin film oxygen sensor’s response time is related to it’s heat treatment. The higher heat treatment, temperature the slower response time. With high temperature treatment, CeO2 grain become bigger, the grain boundary become less, so transmitting path become less. In high temperature, GDC sensor has the shortesrresponse time. In low temperature, Ag-CeO2 and GDC sensors have shortresponse time. The CeO2 Oxygen sensors annealed at 750℃, 1000℃ and 1250℃ have response times of 350 ms, 1.5s and 3s tested in 750℃ by changing oxygen partial pressure from 0 Torr to 152 Torr, GDC and Ag-CeO2 oxygen sensors (with 750℃ heat treatment) have response times of 350 ms and 500 ms, tested at 450℃. CeO2 thin films have good sensitivity then GDC and Ag-CeO2 thin films. GDC sensor has better sensitivity in low test temperature than high test temperature. Ag- CeO2 sensors also behave the same, but become unstable in high test temperature because of Ag diffusion and separation. Finally, we calculated the activation energies of CeO2 thin films for different annealing temperature, The higher annealing temperature, the higher activation energy. The activation energy of CeO2 sensor with no heat treatment is 1.23 ev, and the activation energies of CeO2 sensor with 750℃, 1000℃ and 1250℃ heat treatment are 1.55 ev, 1.69 ev and 1.81ev. The activation energy of GDC and Ag-CeO2 thin films are 1.1 ev and 0.73 ev which are lower than those of CeO2 thin film.