Synthesis and structure of high-purity BaCe0.25Mn0.75O3: an improved material for thermochemical water splitting

Robert T. Bell, Nicholas A. Strange, Dan A. Plattenberger, S. Shulda, J. Park, A. Ambrosini, K. Heinselman, Josh Sugar, P. Parilla, E. Coker, A. McDaniel, D. Ginley
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Abstract

Solar thermochemical hydrogen production (STCH) via redox-active metal oxides is an approach for direct solar-driven hydrogen generation typically using a high-temperature redox cycle involving refractory oxides and steam. Typical cycles involve high-temperature reduction of oxides to form oxygen vacancies, followed by lower temperature reaction between oxygen vacancies and steam where the oxide is re-oxidized and the steam is reduced to hydrogen. Only a few materials have demonstrated reversible cycling under the typically harsh STCH conditions (e.g. 1500°C reduction, 900°C re-oxidation) and critical questions remain on the true reversibility of non-stoichiometric multi-cation oxide systems, significantly hampered by the lack of single-phase samples for these material systems. To date, most STCH processes have relied on CeO2 as a benchmark active material, but more recently, the 12R phase of BaCe0.25Mn0.75O3 (BCM) has demonstrated greater hydrogen-generation potential at lower peak temperatures. However, previous reports of 12R-BCM have included large fractions, > 10 wt%, of secondary phases, which complicate analysis of the stability and performance. A comprehensive understanding of the redox mechanism and reversibility of the process in BCM can only be achieved with nearly single-phase samples which, to date, have been difficult to produce. Here two approaches to BCM synthesis are reported: solid state and sol–gel-based routes. It is demonstrated that both routes can be tuned to produce the 12R structure with > 97 wt% yield when annealed ≥1450°C. Herein synchrotron-based diffraction measurements of rhombohedral 12R-BCM enabled characterization of the anisotropy between thermal expansion along the c-axis and within the ab plane. The impact of high-temperature redox cycling on the stability and phase fraction of the 12R-BCM polytype was also investigated. These results offer two viable routes for synthesis of high-purity 12R-BCM critically needed for evaluating the efficacy of BCM as a STCH material and validate its ability to split water at lower temperatures over extended numbers of redox cycles.
高纯BaCe0.25Mn0.75O3的合成与结构:一种改进的热化学水裂解材料
通过氧化还原活性金属氧化物的太阳能热化学制氢(STCH)是一种直接由太阳能驱动的制氢方法,通常使用包含难熔氧化物和蒸汽的高温氧化还原循环。典型的循环包括氧化物的高温还原形成氧空位,然后氧空位和蒸汽之间的低温反应,氧化物被重新氧化,蒸汽被还原成氢。只有少数材料在典型的恶劣STCH条件下(例如1500°C还原,900°C再氧化)表现出可逆循环,而非化学计量多阳离子氧化物体系的真正可逆性仍然存在关键问题,这些问题由于缺乏这些材料体系的单相样品而受到严重阻碍。迄今为止,大多数STCH工艺都依赖于CeO2作为基准活性材料,但最近,BaCe0.25Mn0.75O3 (BCM)的12R相在较低峰值温度下显示出更大的产氢潜力。然而,之前关于12R-BCM的报道中包含了大于10 wt%的二次相,这使得稳定性和性能的分析变得复杂。对BCM中氧化还原机制和过程可逆性的全面了解只能通过近单相样品来实现,迄今为止,这种样品很难生产。本文报道了两种合成BCM的方法:固态法和溶胶-凝胶法。结果表明,当退火温度≥1450°C时,这两种途径均可调谐产生产率> 97%的12R结构。在这里,基于同步加速器的菱形12R-BCM衍射测量使得沿c轴和ab平面的热膨胀各向异性的表征成为可能。研究了高温氧化还原循环对12R-BCM多型材料稳定性和相分数的影响。这些结果为高纯度12R-BCM的合成提供了两种可行的途径,这对于评估BCM作为STCH材料的功效以及验证其在较低温度下在延长的氧化还原循环中分解水的能力至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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