首页> 外文期刊>ACS catalysis >Positive Effects of H2O on the Hydrogen Oxidation Reaction on Sr2Fe1.5 Mo0.5O6-delta-Based Perovskite Anodes for Solid Oxide Fuel Cells
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Positive Effects of H2O on the Hydrogen Oxidation Reaction on Sr2Fe1.5 Mo0.5O6-delta-Based Perovskite Anodes for Solid Oxide Fuel Cells

机译:H2O对固体氧化物燃料电池SR2FE1.5 MO0.50.50.5O6-DEROVSKITE阳极氧化反应对固体氧化物燃料电池的正效应

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The steam is commonly supplied with H-2 to the anodes of Ni-based solid oxide fuel cells (SOFCs). Humidified H-2 is also widely used for emerging perovskite anodes of SOFCs, although the influences of H2O on the hydrogen oxidation reaction (HOR) on their surfaces have not been well understood yet. In this work, the effects of H2O on the HOR on Sr2Fe1.5 Mo0.5O6-delta (SF1.5M), La-0.5 Sr-1.5 Fe-1.5 Mo0.5O6-delta (LSFM), and Pr-0.5 Sr-1.5 Fe1.5Mo0.5O6-delta (PSFM) were systematically investigated using the electrochemical impedance spectroscopy (EIS) and electrical conductivity relaxation (ECR) methods. The EIS spectra suggested the possible promotional effect of H2O on decreasing the polarization resistance of SF1.5M. The ECR results confirmed that the presence of H2O in H-2 can significantly increase the oxygen exchange coefficients of SF1.5M, LSFM, and PSFM. To gain a mechanistic understanding of the role of H2O, the density functional theory-based calculations and thermodynamic modeling were performed to unravel the effect of H2O on the HOR on the SF1.5M (001) surfaces. Benefiting from the increment of the oxygen chemical potential and decrement of the free electron concentration upon increasing humidity, the plateau intermediate state in the HOR energy landscape, the step of H2O plus surface oxygen vacancy formation, is reduced on the SF1.5M (001) BO2 (B = Fe and Mo)-terminated surfaces, when decreasing the slab oxygen nonstoichiometry. Furthermore, by comparing the scenarios of the HOR on the dry and hydrated surfaces, the H2O plus surface oxygen vacancy formation energies are lower in the latter case. These two proposed factors, i.e., (i) change of electron chemical potential upon the change of near-surface delta and (ii) enhanced interaction of surface H species with the hydrated perovskite surfaces, contribute to the promoted HOR in the presence of H2O. This work provides important insights into the effects of H2O on the HOR for SOFCs.
机译:蒸汽通常与Ni基固体氧化物燃料电池(SOFC)的阳极供应H-2。加湿的H-2也广泛用于SOFC的钙钛矿阳极,尽管H2O对其表面上的氢氧化反应(HOR)的影响尚未得到很好的理解。在这项工作中,H2O对SR2FE1.5 MO0.5O6-DERTA(SF1.5M),LA-0.5SR-1.5 FE-1.5 MO0.5O6-DERTA(LSFM)和PR-0.5 SR-的影响使用电化学阻抗光谱(EIS)和电导率松弛(ECR)方法系统地研究了1.5 FE1.5MO0.5O6-DERTA(PSFM)。 EIS Spectra提出了H2O在降低SF1.5M的偏振电阻上的可能促进效果。 ECR结果证实,H-2中H2O的存在可以显着增加SF1.5M,LSFM和PSFM的氧交换系数。为了获得对H2O的作用的机械理解,进行密度泛函理论的计算和热力学建模,以解开H2O对SF1.5M(001)表面上HOR的影响。从氧气化学势的增量和自由电子浓度的增量增加,在湿度增加时,HOR能量景观中的平台中间状态,H2O加表面氧空位形成的步骤,降低了SF1.5M(001) Bo2(B = Fe和Mo) - 在减少平板氧不间间计量时的终端表面。此外,通过比较干燥和水合表面上的HOR的场景,在后一种情况下,H2O加表面氧空位形成能量较低。这两个提出的因素,即(i)在近表面δ的变化变化后的电子化学潜力和(ii)与水合钙钛矿表面的表面H种的相互作用,在H 2 O存在下有助于促进的植物。这项工作对H2O对SOFC的影响提供了重要的见解。

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