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首页> 外文期刊>RSC Advances >Robust catalytically-activated LSM-BCZY-based composite steam electrodes for proton ceramic electrolysis cells
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Robust catalytically-activated LSM-BCZY-based composite steam electrodes for proton ceramic electrolysis cells

机译:用于质子陶瓷电解细胞的鲁棒催化激活的基于LSM-BCZY基蒸汽电极

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摘要

Backbone electrodes based on an electronic conductor and a protonic conductor show advantages for proton ceramic electrolyzer cells (PCECs). This work, aims to shed further light on the nature of the rate determining steps in the anode operation and improve the reaction rate in high steam pressure electrolysis mode by (i) adjusting their catalytic activity through electrode infiltration with catalytic electronic-conducting nanoparticles; and (ii) electrochemical activation of surface species by applying a net current through the electrode. A composite formed by La0.8Sr0.2MnO3-delta (LSM) and BaCe0.2Zr0.7Y0.1O3-delta (BCZY27) was deposited on proton-conducting BCZY27 electrolytes and studied in symmetrical cells to investigate the anode microstructure and electrochemical performance. Electrochemical impedance spectroscopy (EIS) measurements were performed in the 800-500 degrees C range under 3 bar of pressure of wet air (75% of steam). LSM/BCZY27 50/50 vol% showed the best performance with an electrode polarization resistance (R-p) of 6.04 omega cm(2) at 700 degrees C and high steam pressure (0.75 bar of air and 2.25 bar of steam) whereas LSM/BCZY27 60/40 vol% presented a R-p of 18.9 omega cm(2). The backbone electrodes were infiltrated using aqueous solutions of metal precursors to boost the electrocatalytic activity towards water splitting and oxygen evolution. The infiltrated cells were fired at 850 degrees C for 2 h to obtain the desired crystalline nanoparticles (Pr6O11, CeO2, ZrO2 and Pr6O11-CeO2) and electrochemically tested under high steam pressures and bias currents to investigate the influence of catalytic activation on surface exchange kinetics. Among the tested catalysts, the lowest electrode polarization resistances (<0.2 omega cm(2)) were reached for the Pr6O11, CeO2 and Pr6O11-CeO2 catalysts at 700 degrees C by applying current densities ranging from 1.57 to 14.15 mA cm(-2), and the Pr6O11-CeO2-activated LSM/BCZY27 electrode exhibited the best performance. Finally, the effect of pO(2) and pH(2)O was investigated aiming to characterize the rate limiting processes in the electrodes.
机译:基于电子导体的骨干电极和质子导体显示出质子陶瓷电解槽电池(PCEC)的优点。这项工作,旨在进一步发光对阳极操作中的速率确定步骤的性质,并通过(i)通过用催化电子导电纳米颗粒调节其催化活性的高蒸汽压力电解模式的反应速率; (ii)通过将净电流施加通过电极来电化学激活表面物种。由La0.8SR0.2MNO3-DELTA(LSM)和BACE0.2ZR0.7Y0.1O3-DELTA(BCZY27)形成的复合材料沉积在质子传导BCZY27电解质上,并在对称细胞中研究以研究阳极微观结构和电化学性能。电化学阻抗光谱(EIS)测量在800-500摄氏度的范围内进行,湿空气压力的3巴(蒸汽的75%)。 LSM / BCZY27 50/50 Vol%显示最佳性能,电极偏振电阻(RP)为6.04ωcm(2),在700摄氏度和高蒸汽压力(0.75巴的空气和2.25巴的蒸汽),而LSM / BCZY27 60/40 Vol%呈现了18.9毫米厘米(2)的RP。使用金属前体的水溶液渗透骨干电极,以使电催化活性升压到水分裂和氧气进化。在850℃下烧制渗透细胞2小时,得到所需的结晶纳米颗粒(PR6O11,CeO 2,ZrO2和PR6O11-CeO 2),并在高蒸汽压力和偏置电流下电化学测试,以研究催化活化对表面交换动力学的影响。在测试的催化剂中,通过施加从1.57至14.15 mA cm(-2)的电流密度,在700℃下达到最低电极偏振电阻(<0.2ωcm(2)),在700℃下达到PR6O11,CEO2和PR6O11-CEO2催化剂,PR6O11-CEO2激活的LSM / BCZY27电极表现出最佳性能。最后,研究了PO(2)和pH(2)o的效果,旨在表征电极中的速率限制过程。

著录项

  • 来源
    《RSC Advances 》 |2019年第36期| 共10页
  • 作者

    Bausa Nuria; Serra Jose M.;

  • 作者单位

    Univ Politecn Valencia CSIC Inst Tecnol Quim Av Naranjos S-N E-46022 Valencia Spain;

    Univ Politecn Valencia CSIC Inst Tecnol Quim Av Naranjos S-N E-46022 Valencia Spain;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
  • 关键词

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