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首页> 外文期刊>International journal of hydrogen energy >Ba_(0.5)Sr_(0.5)(Co_(0.8)Fe_(0.2))_(1-x)Ta_xO_(3-δ) perovskite anode in solid oxide electrolysis cell for hydrogen production from high-temperature steam electrolysis
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Ba_(0.5)Sr_(0.5)(Co_(0.8)Fe_(0.2))_(1-x)Ta_xO_(3-δ) perovskite anode in solid oxide electrolysis cell for hydrogen production from high-temperature steam electrolysis

机译:BA_(0.5)SR_(0.5)(CO_(0.8)FE_(0.2))_(1-X)TA_XO_(3-Δ)钙钛矿在高温蒸汽电解中的固体氧化物电解电池中的固体氧化物电解槽阳极

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摘要

Among perovskite anodes in solid oxide electrolysis cell (SOEC), Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) has gained much attention due to its dominantly high performance. However, the BSCF still suffers from chemical instability. In this study, the B-site of BSCF is partially substituted by a higher valence Ta5+ (5, 10, 15 and 20 mol%) to improve its structural stability - Ba0.5Sr0.5(Co0.8Fe0.2)(1-x)TaxO3-delta (BSCFTax, 0 = x = 0.20). It is found that doping with higher valence Ta5+ increases both chemical stability and electrochemical performance of BSCF. Although the BSCFTa0.10 shows the lowest oxygen vacancies indicating by the ratio of adsorbed oxygen vacancies (O-adsorbed) to lattice oxygen (O-lattice), the electrochemical performance increases. The decrease in Co3+/Co4+ ratio results in increasing electronic conductivity in the anode. It is likely that proper amount of Ta5+ doping provide a balance between ionic and electronic conductivity in the anode and improved electrochemical performance. The symmetrical half-cells with electrolyte support (BSCFTa/YSZ/BSCFTa) are fabricated to determine the area specific resistance (ASR) and activation energy of conduction - BSCFTa0.10 shows the best performance. Cathode-supported Ni-YSZ/YSZ/ BSCFTa0.10 also shows higher durability than Ni-YSZ/YSZ/BSCF (operating at current density -0.45 A cm(-2) in electrolysis mode, 80 h, 800 degrees C and H2O to H-2 ratio of 70:30). (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:在固体氧化物电解细胞(SOEC)中的钙钛矿阳极中,Ba0.5SR0.5CO0.8FE0.2O3-DELTA(BSCF)由于其主要高性能而产生了很多关注。然而,BSCF仍然存在化学不稳定。在该研究中,BSCF的B位点被更高的效率Ta 5 +(5,10,15和20mol%)被局部取代,以改善其结构稳定性 - Ba0.5SR0.5(COO.8FE0.2)(1- x)划分税收3-delta(bscftax,0 <= x <= 0.20)。发现具有更高价Ta5 +的掺杂增加了BSCF的化学稳定性和电化学性能。尽管BSCFTA0.10显示了通过吸附的氧空位(O-吸附)与晶格氧(O-晶格)的比率表示的最低氧空位,但电化学性能增加。 CO3 + / CO4 +比率的降低导致阳极中的电子电导率增加。适当量的TA5 +掺杂可能是在阳极中的离子和电子电导率之间的平衡和改善的电化学性能。具有电解质支持(BSCFTA / YSZ / BSCFTA)的对称半电池制造,以确定导通的面积电阻(ASR)和导通的激活能量 - BSCFTA0.10显示了最佳性能。阴极支持的NI-YSZ / YSZ / BSCFTA0.10还显示出比NI-YSZ / YSZ / BSCF更高的耐久性(在电解模式下以电流密度-0.45 a cm(-2)操作,80小时,800℃和H2o至H-2比例为70:30)。 (c)2020氢能源出版物LLC。 elsevier有限公司出版。保留所有权利。

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